Oncology: Step-by-Step Guide on How to Write SOAP Notes

Updated January 2026

Oncology documentation demands exceptional precision, comprehensive detail, and strict adherence to evidence-based protocols. Cancer care SOAP notes must capture complex staging information, treatment regimens, toxicity assessments, and response evaluations while supporting multidisciplinary coordination and clinical trial compliance. This guide provides comprehensive instructions for documenting oncology encounters, from initial diagnosis through treatment and survivorship, ensuring compliance with NCCN guidelines and optimal patient care.

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What Makes Oncology Documentation Unique

Oncology documentation differs from other specialties in several critical ways:

  1. Cancer Staging: Documentation must precisely capture TNM staging, histopathologic features, and molecular/genomic markers essential for treatment planning
  2. Treatment Protocols: Chemotherapy, immunotherapy, and targeted therapy regimens require exact documentation of drugs, doses, cycles, and modifications
  3. Toxicity Monitoring: Systematic assessment and grading of treatment-related adverse events using CTCAE (Common Terminology Criteria for Adverse Events)
  4. Response Assessment: Standardized evaluation using RECIST criteria for solid tumors or disease-specific response criteria
  5. Performance Status: Regular documentation of ECOG or Karnofsky performance status to guide treatment decisions
  6. Survivorship Care: Long-term monitoring for late effects, secondary malignancies, and quality of life
  7. Clinical Trial Documentation: Rigorous documentation requirements for patients enrolled in research protocols
  8. Multidisciplinary Coordination: Integration of surgery, radiation, and medical oncology treatment plans

Subjective Section (S)

The Subjective section in oncology captures treatment tolerance, symptom burden, functional status, and psychosocial factors essential for cancer care management.

Subjective Section (S) Components

  1. Chief Complaint:

    • Primary reason for visit (treatment, surveillance, symptom management)
    • Current point in treatment course
    • Example: "Cycle 4 Day 1 of FOLFOX chemotherapy for stage III colon cancer"
  2. Treatment Tolerance Assessment:

    • How patient tolerated previous treatment cycle
    • New or worsening symptoms since last treatment
    • Symptom severity and impact on function
    • Example: "Patient reports moderate fatigue for 5 days following last cycle, resolved by day 10. Mild nausea controlled with ondansetron."
  3. Symptom Assessment with CTCAE Grading: Document each symptom with severity grade:

    • Grade 1: Mild; asymptomatic or mild symptoms
    • Grade 2: Moderate; minimal intervention indicated
    • Grade 3: Severe; medically significant, hospitalization indicated
    • Grade 4: Life-threatening; urgent intervention indicated
    • Grade 5: Death related to adverse event

    Common symptoms to assess:

    • Fatigue: Severity, duration, impact on ADLs
    • Nausea/Vomiting: Frequency, triggers, response to antiemetics
    • Neuropathy: Location, character (numbness, tingling, pain), functional impact
    • Mucositis/Stomatitis: Severity, impact on oral intake
    • Diarrhea/Constipation: Frequency, volume, need for intervention
    • Myelosuppression symptoms: Infections, bleeding, fatigue from anemia
    • Skin reactions: Rash, hand-foot syndrome, nail changes
    • Cognitive changes: "Chemo brain," concentration difficulties

    Example: "Peripheral neuropathy - Grade 2: Moderate symptoms limiting instrumental ADLs (difficulty with buttons, writing). Numbness and tingling in fingertips and toes bilaterally, present since cycle 3."

  4. Functional Status Assessment:

    ECOG Performance Status:

    • 0: Fully active, no restrictions
    • 1: Restricted in strenuous activity, ambulatory, light work capable
    • 2: Ambulatory, capable of self-care, unable to work, up >50% of waking hours
    • 3: Capable of limited self-care, confined to bed/chair >50% of waking hours
    • 4: Completely disabled, no self-care, totally confined to bed/chair
    • 5: Dead

    Karnofsky Performance Status (alternative scale, 0-100%):

    • 100: Normal, no complaints
    • 90: Able to carry on normal activity; minor signs/symptoms
    • 80: Normal activity with effort; some signs/symptoms
    • 70: Cares for self; unable to carry on normal activity
    • 60: Requires occasional assistance but cares for most needs
    • 50: Requires considerable assistance and frequent medical care
    • 40: Disabled; requires special care and assistance
    • 30: Severely disabled; hospitalization indicated
    • 20: Very sick; active supportive treatment necessary
    • 10: Moribund

    Example: "ECOG Performance Status: 1 (baseline 0). Patient reports increased fatigue limiting ability to exercise but continues working part-time from home."

  5. Nutritional Status:

    • Current weight and weight change
    • Appetite assessment
    • Dietary intake adequacy
    • Need for nutritional support
    • Example: "Weight 165 lbs, down 8 lbs (4.6%) from treatment start. Appetite decreased, eating approximately 50% of usual intake. No dysphagia. Using nutritional supplements twice daily."
  6. Pain Assessment:

    • Location, quality, intensity (0-10 scale)
    • Cancer-related vs. treatment-related
    • Current pain regimen and effectiveness
    • Breakthrough pain frequency
    • Example: "Right hip pain 6/10, constant, aching quality. Known bone metastasis. Currently on extended-release morphine 30mg BID with morphine IR 15mg for breakthrough (using 2-3 doses daily). Partial relief with current regimen."
  7. Psychosocial Assessment:

    • Emotional coping and adjustment
    • Anxiety and depression screening
    • Social support system
    • Financial/insurance concerns
    • Work/functional impact
    • Caregiver burden
    • Example: "Patient reports increased anxiety regarding upcoming restaging scans. PHQ-2 positive, PHQ-9 score 12 (moderate depression). Living with spouse who provides good support. Concerned about medical expenses despite insurance coverage."
  8. Review of Systems (Cancer-Focused):

    • Constitutional: Fever, night sweats, weight loss
    • New or changing masses
    • Neurological symptoms (concerning for CNS involvement)
    • Respiratory symptoms (pulmonary metastases, effusions)
    • GI symptoms (obstruction, bleeding)
    • Bone pain (metastatic disease)
  9. Medication Review:

    • Current chemotherapy/immunotherapy regimen
    • Supportive medications (antiemetics, growth factors, pain management)
    • Adherence to oral oncolytics if applicable
    • OTC medications and supplements
    • Example: "Current regimen: FOLFOX (cycle 4). Supportive meds: Ondansetron 8mg TID PRN, dexamethasone per protocol, pegfilgrastim day 2. Taking all medications as prescribed."

Example Subjective Section for Oncology

Subjective (Oncology)
 
 
CHIEF COMPLAINT: Cycle 4 Day 1 of FOLFOX chemotherapy for stage IIIB (pT3N2M0) colon adenocarcinoma, adjuvant setting
 
TREATMENT HISTORY:
- Diagnosis: Sigmoid colon adenocarcinoma, diagnosed September 2025
- Surgery: Low anterior resection October 2025, R0 resection
- Pathology: Moderately differentiated adenocarcinoma, pT3N2a (4/18 nodes positive), MSS, KRAS wild-type
- Current treatment: FOLFOX adjuvant chemotherapy, planned 12 cycles (6 months)
- Cycles completed: 3
 
TREATMENT TOLERANCE (since last cycle):
Patient reports tolerable side effects from cycle 3:
- Fatigue: Grade 2 - Moderate fatigue days 1-7, required afternoon rest daily, improved by day 10
- Nausea: Grade 1 - Mild nausea days 1-3, controlled with ondansetron, no vomiting
- Diarrhea: Grade 1 - 3-4 loose stools daily for days 2-4, self-limited
- Peripheral neuropathy: Grade 1 progressing to Grade 2 - Cold sensitivity with mild numbness/tingling in fingertips, noticed difficulty with fine motor tasks (buttoning shirts)
- Mucositis: Grade 1 - Mild mouth soreness, no ulcerations, able to maintain oral intake
- No fevers, infections, or bleeding episodes
 
SYMPTOM ASSESSMENT WITH CTCAE GRADING:
1. Fatigue - Grade 2: Moderate; limits instrumental ADLs
2. Peripheral sensory neuropathy - Grade 2: Moderate symptoms; limiting instrumental ADL
3. Nausea - Grade 1: Mild; loss of appetite without alteration in eating habits
4. Diarrhea - Grade 1: Resolved; was <4 stools/day over baseline
5. Oral mucositis - Grade 1: Asymptomatic or mild symptoms
6. Hand-foot syndrome - Grade 0: None
7. Neutropenia - Not assessed clinically; labs pending
 
FUNCTIONAL STATUS:
- ECOG Performance Status: 1 (baseline prior to treatment: 0)
- Karnofsky: 80%
- Patient is ambulatory and independent in all ADLs
- Working from home part-time (reduced from full-time due to fatigue)
- Decreased exercise tolerance - previously ran 3 miles, now walks 1 mile
 
NUTRITIONAL STATUS:
- Current weight: 172 lbs (78 kg)
- Weight at diagnosis: 180 lbs
- Weight change: -8 lbs (-4.4%) over 3 months
- Appetite: Decreased, eating ~75% of usual portions
- Diet: Tolerating regular diet, avoiding cold foods due to cold sensitivity
- Nutritional supplements: Ensure Plus once daily
- Hydration: Drinking 6-8 glasses water daily
 
PAIN ASSESSMENT:
- Surgical site: Healed, no pain (0/10)
- Abdominal pain: None
- No bone pain, headaches, or other pain complaints
 
PSYCHOSOCIAL:
- Mood: Some anxiety about treatment, generally coping well
- PHQ-2: Negative (score 1)
- Support system: Strong; spouse accompanies to all appointments, adult children nearby
- Work: Able to work from home part-time as financial analyst
- Insurance: Covered, no financial distress reported
 
REVIEW OF SYSTEMS:
- Constitutional: Fatigue as above, no fever, chills, or night sweats. 8 lb weight loss.
- HEENT: Mild mouth soreness, no dysphagia, no vision changes
- Respiratory: No cough, dyspnea, or chest pain
- Cardiovascular: No chest pain, palpitations, or edema
- GI: Mild intermittent nausea, resolved diarrhea, no constipation, no abdominal pain, no blood in stool
- GU: No dysuria, hematuria, or changes in urination
- Neurological: Peripheral neuropathy as described, no headaches, weakness, or cognitive changes
- Musculoskeletal: No bone pain, joint pain, or muscle weakness
- Skin: No rash, no hand-foot syndrome, mild hair thinning
- Hematologic: No easy bruising, bleeding, or signs of infection
 
CURRENT MEDICATIONS:
Chemotherapy:
- FOLFOX regimen: Oxaliplatin, leucovorin, 5-fluorouracil (per protocol)
 
Supportive Care:
- Ondansetron 8mg PO TID PRN nausea
- Dexamethasone 12mg PO pre-chemo per protocol
- Prochlorperazine 10mg PO Q6H PRN breakthrough nausea
- Loperamide 4mg initial then 2mg after each loose stool PRN
 
Other Medications:
- Lisinopril 10mg daily (hypertension)
- Vitamin D3 2000 IU daily
- Multivitamin daily
 
ALLERGIES: Penicillin (hives)
 

Objective Section (O)

The oncology Objective section requires comprehensive physical examination with attention to treatment-related effects, performance status verification, tumor markers, and imaging results.

Objective Section (O) Components

  1. Vital Signs:

    • Blood pressure, heart rate, temperature
    • Respiratory rate, oxygen saturation
    • Weight with comparison to prior visits
    • Height (for BSA calculation)
    • Body Surface Area (BSA) for dosing
    • Example: "BP 128/78, HR 72, Temp 98.4F, RR 16, SpO2 98% RA. Weight 172 lbs (78 kg), Height 5'10' (178 cm), BSA 1.96 m2"
  2. Performance Status (Verified):

    • ECOG score with supporting observations
    • Comparison to baseline and prior visits
    • Example: "ECOG 1: Patient walked independently to exam room, appears mildly fatigued but in no distress. Baseline ECOG 0."
  3. General Appearance:

    • Overall condition
    • Nutritional status
    • Signs of distress
    • Example: "Alert, well-groomed male appearing stated age. Mild pallor. No acute distress. Appears well-nourished despite modest weight loss."
  4. Treatment-Specific Physical Examination:

    Port/Central Line Assessment:

    • Site inspection (erythema, swelling, drainage)
    • Patency verification
    • Example: "Right chest port site: Well-healed, no erythema, warmth, tenderness, or drainage. Port accessed without difficulty, good blood return."

    Neuropathy Assessment:

    • Sensory examination (light touch, pinprick, vibration)
    • Motor strength testing
    • Deep tendon reflexes
    • Functional assessment
    • Example: "Peripheral sensory neuropathy: Decreased light touch and pinprick sensation in stocking-glove distribution to mid-feet and fingertips bilaterally. Vibration sense intact at ankles. Motor strength 5/5 throughout. DTRs 1+ at ankles (baseline 2+). Gait steady. Fine motor: Mild difficulty with rapid alternating movements."

    Skin Examination:

    • Hand-foot syndrome assessment
    • Rash (including immune-related)
    • Nail changes
    • Injection site reactions
    • Example: "Skin: No hand-foot syndrome. No rash. Mild nail ridging and discoloration on fingernails. No injection site reactions."

    Oral Cavity:

    • Mucositis grading
    • Thrush assessment
    • Hydration status
    • Example: "Oral mucosa: Grade 1 mucositis with mild erythema of buccal mucosa, no ulcerations. No thrush. Moist membranes."
  5. System-Based Examination (Cancer-Specific):

    • Lymph Nodes: All accessible nodal basins
    • Abdomen: Hepatomegaly, masses, ascites
    • Lungs: Breath sounds, effusion signs
    • Extremities: Edema, DVT signs
    • Neurological: Focal deficits, mental status
  6. Laboratory Results:

    Complete Blood Count (Critical for Treatment):

    • WBC with ANC (Absolute Neutrophil Count)
    • Hemoglobin and Hematocrit
    • Platelet count
    • Example: "CBC: WBC 4.2 (ANC 2,100), Hgb 11.2, Hct 33.8, Plt 156. Nadir labs from cycle 3 day 10: ANC 800, Hgb 10.1, Plt 98."

    Comprehensive Metabolic Panel:

    • Renal function (dosing adjustments)
    • Hepatic function (metabolism, metastatic disease)
    • Electrolytes

    Tumor Markers:

    • CEA for colorectal cancer
    • CA-125 for ovarian cancer
    • PSA for prostate cancer
    • CA 19-9 for pancreatic cancer
    • AFP, HCG for germ cell tumors
    • Example: "CEA: 2.8 ng/mL (baseline pre-surgery 45.2, post-surgery 3.1, prior cycle 3.0) - within normal limits, stable"
  7. Imaging Results with RECIST Assessment:

    RECIST 1.1 Criteria (Response Evaluation Criteria in Solid Tumors):

    • Complete Response (CR): Disappearance of all target lesions
    • Partial Response (PR): >=30% decrease in sum of diameters of target lesions
    • Progressive Disease (PD): >=20% increase in sum of diameters OR new lesions
    • Stable Disease (SD): Neither sufficient shrinkage nor sufficient increase

    Document:

    • Target lesions with measurements
    • Non-target lesions
    • New lesions
    • Overall response
    • Example: "CT Chest/Abdomen/Pelvis (12/20/2025): No evidence of recurrent disease. Surgical site unremarkable. No lymphadenopathy. Liver, lungs clear. RECIST Assessment: Not applicable (adjuvant setting, no measurable disease)."
  8. Pathology/Molecular Results:

    • Histopathology
    • Immunohistochemistry
    • Molecular markers (KRAS, BRAF, MSI, HER2, etc.)
    • Genomic profiling results
    • Example: "Pathology (surgical specimen): Moderately differentiated adenocarcinoma, pT3N2aM0, 4/18 lymph nodes positive. LVI present, PNI present. Margins negative (R0). IHC: MSS (MLH1+, MSH2+, MSH6+, PMS2+). Molecular: KRAS wild-type, BRAF wild-type."

Example Objective Section for Oncology

Objective (Oncology)
 
 
VITAL SIGNS:
- Blood Pressure: 128/78 mmHg
- Heart Rate: 72 bpm, regular
- Temperature: 98.4 F (36.9 C)
- Respiratory Rate: 16/min
- SpO2: 98% on room air
- Weight: 172 lbs (78 kg) - DOWN 2 lbs from last visit (cycle 3)
- Height: 5'10' (178 cm)
- BSA: 1.96 m2
 
PERFORMANCE STATUS:
- ECOG: 1 (verified - patient walked independently, mild fatigue, no distress)
- Baseline ECOG: 0
- Trend: Stable at ECOG 1 since cycle 2
 
GENERAL APPEARANCE:
Alert, cooperative male appearing stated age of 62 years. Mild pallor. Well-groomed. No acute distress. Appears mildly fatigued but comfortable. No cachexia.
 
HEENT:
- Head: Normocephalic, atraumatic. Mild hair thinning, no alopecia
- Eyes: PERRL, EOMI, conjunctivae pale pink, sclera anicteric
- Ears: TMs clear bilaterally
- Nose: No epistaxis
- Oral cavity: Grade 1 mucositis - mild erythema of buccal mucosa bilaterally, no ulcerations, no thrush. Dentition intact. Moist membranes. Pharynx clear.
 
NECK:
- Supple, no lymphadenopathy
- No JVD
- Thyroid: Normal size, no nodules
 
PORT ASSESSMENT:
- Location: Right anterior chest (subclavian)
- Site appearance: Well-healed incision, no erythema, warmth, induration, or drainage
- Palpation: Port easily palpable, no tenderness
- Access: Port accessed with 3/4 inch Huber needle, good blood return, flushes easily
- Status: Functional, appropriate for chemotherapy administration
 
LYMPH NODE EXAMINATION:
- Cervical: No lymphadenopathy
- Supraclavicular: No lymphadenopathy
- Axillary: No lymphadenopathy
- Inguinal: No lymphadenopathy
 
CARDIOVASCULAR:
- Regular rate and rhythm
- S1, S2 normal, no murmurs, rubs, or gallops
- No peripheral edema
- Distal pulses 2+ bilaterally
 
PULMONARY:
- Clear to auscultation bilaterally
- No wheezes, rales, or rhonchi
- No respiratory distress
- No dullness to percussion
 
ABDOMEN:
- Soft, non-distended
- Non-tender to palpation
- Surgical scar (low anterior resection): Well-healed midline incision, no hernia
- No hepatomegaly or splenomegaly
- No masses palpable
- Bowel sounds: Normal
- No ascites
 
EXTREMITIES:
- No lower extremity edema
- No calf tenderness or signs of DVT
- Warm, well-perfused
- Pulses intact
 
SKIN:
- No hand-foot syndrome (palms and soles normal)
- No rash
- Mild nail changes: Horizontal ridging on fingernails (likely treatment-related)
- No petechiae or ecchymoses
- No injection site reactions
 
NEUROLOGICAL:
Peripheral Neuropathy Assessment:
- Mental status: Alert and oriented x 4
- Cranial nerves II-XII: Intact
- Motor: Strength 5/5 in all extremities, no weakness
- Sensory:
- Light touch: Decreased in stocking-glove distribution (feet to mid-shin, hands to wrist)
- Pinprick: Decreased in same distribution
- Vibration: Intact at ankles and wrists
- Proprioception: Intact
- Deep tendon reflexes: 1+ at ankles (decreased from baseline 2+), 2+ at knees and biceps
- Coordination: Mild difficulty with rapid alternating movements in hands, finger-to-nose intact
- Gait: Steady, no ataxia, heel-to-toe walk intact
 
NEUROPATHY GRADING: CTCAE Grade 2 - Moderate symptoms; limiting instrumental ADL
 
LABORATORY RESULTS (today):
Complete Blood Count:
- WBC: 4.2 x 10^9/L (normal 4.5-11.0)
- ANC: 2,100/uL (normal >1,500)
- Hemoglobin: 11.2 g/dL (low; baseline 14.5)
- Hematocrit: 33.8%
- Platelets: 156 x 10^9/L (normal 150-400)
- Nadir values (cycle 3, day 10): ANC 800, Hgb 10.1, Plt 98
 
Comprehensive Metabolic Panel:
- Sodium: 139 mEq/L
- Potassium: 4.2 mEq/L
- Chloride: 102 mEq/L
- CO2: 24 mEq/L
- BUN: 18 mg/dL
- Creatinine: 0.9 mg/dL (eGFR >60)
- Glucose: 98 mg/dL
- Calcium: 9.1 mg/dL
- Total Protein: 6.8 g/dL
- Albumin: 3.8 g/dL
- AST: 28 U/L
- ALT: 32 U/L
- Alkaline Phosphatase: 72 U/L
- Total Bilirubin: 0.8 mg/dL
 
TUMOR MARKERS:
- CEA: 2.8 ng/mL (normal <3.0)
- Baseline (pre-surgery): 45.2 ng/mL
- Post-surgery (October 2025): 3.1 ng/mL
- Prior cycle: 3.0 ng/mL
- Trend: Normalized, stable
 
Hepatic Function Panel: Within normal limits
 
IMAGING:
Most Recent CT Chest/Abdomen/Pelvis (December 20, 2025):
- Lungs: Clear, no nodules or masses
- Mediastinum: No lymphadenopathy
- Liver: No focal lesions, normal size
- Surgical site: Post-operative changes at sigmoid colon anastomosis, no recurrence
- Retroperitoneum: No lymphadenopathy
- Pelvis: Unremarkable
- Bones: No suspicious lesions
- IMPRESSION: No evidence of recurrent or metastatic disease
 
RECIST ASSESSMENT: Not applicable (adjuvant setting - no measurable disease)
 
PATHOLOGY (October 2025 - Surgical Specimen):
- Procedure: Low anterior resection
- Tumor: Sigmoid colon adenocarcinoma
- Histology: Moderately differentiated adenocarcinoma
- Tumor size: 4.2 cm
- Depth of invasion: pT3 (invasion through muscularis propria into pericolorectal tissues)
- Lymph nodes: 4 of 18 positive (pN2a)
- Margins: Negative (proximal 8 cm, distal 5 cm, radial negative)
- Lymphovascular invasion: Present
- Perineural invasion: Present
- MMR/MSI status: Mismatch repair proficient (pMMR), microsatellite stable (MSS)
- Molecular: KRAS wild-type, BRAF wild-type
 
AJCC 8TH EDITION STAGING: pT3N2aM0 - Stage IIIB
 

Assessment Section (A)

The oncology Assessment synthesizes clinical findings, documents staging, evaluates treatment response and toxicity, and informs treatment decisions.

Assessment Section (A) Components

  1. Cancer Diagnosis with Complete Staging:

    • Primary diagnosis with ICD-10 code
    • TNM staging (clinical and/or pathologic)
    • AJCC stage and edition
    • Key prognostic factors
    • Example: "Sigmoid colon adenocarcinoma, pT3N2aM0, Stage IIIB (AJCC 8th edition). MSS, KRAS wild-type. High-risk features: N2 disease, LVI, PNI."
  2. Treatment Status:

    • Current treatment regimen
    • Cycle number and day
    • Treatment intent (curative, adjuvant, neoadjuvant, palliative)
    • Example: "Currently receiving adjuvant FOLFOX chemotherapy, Cycle 4 of planned 12 cycles (6 months). Curative intent."
  3. Treatment Response Assessment: For patients with measurable disease:

    • RECIST 1.1 category (CR, PR, SD, PD)
    • Tumor marker trends
    • Clinical response
    • Example: "RECIST: Partial response with 45% decrease in sum of target lesions. CEA decreased from 125 to 28. Clinical improvement in symptoms."
  4. Toxicity Assessment Summary: Document all treatment-related toxicities with CTCAE grades:

    • List each toxicity with grade
    • Comparison to prior cycle
    • Impact on dose/schedule
    • Example:
      • "Peripheral neuropathy: Grade 2 (progressed from Grade 1) - limiting instrumental ADL"
      • "Fatigue: Grade 2 - stable from prior cycle"
      • "Nausea: Grade 1 - improved from Grade 2 with antiemetic adjustment"
      • "Myelosuppression: Nadir ANC 800 (Grade 3) - recovered"
  5. Dose Modification Assessment:

    • Need for dose reduction
    • Need for treatment delay
    • Supportive care adjustments
    • Example: "Oxaliplatin dose reduction indicated per protocol for Grade 2 neuropathy. Recommend 25% dose reduction (from 85 to 65 mg/m2)."
  6. Performance Status Trend:

    • Current ECOG with change from baseline
    • Functional implications
    • Example: "ECOG 1 (baseline 0). Decline attributable to treatment-related fatigue; no evidence of disease progression."
  7. Supportive Care Assessment:

    • Pain control adequacy
    • Antiemetic efficacy
    • Growth factor needs
    • Nutritional status
    • Psychosocial needs

Cancer Staging Documentation Requirements

TNM Staging Components:

  • T (Tumor): Size and extent of primary tumor
  • N (Nodes): Regional lymph node involvement
  • M (Metastasis): Distant metastasis

Prefixes:

  • c: Clinical staging (pre-treatment imaging and exam)
  • p: Pathologic staging (post-surgical)
  • y: Post-neoadjuvant therapy
  • r: Recurrent tumor

Document:

  • Staging edition (e.g., AJCC 8th edition)
  • Stage grouping (I, II, III, IV)
  • Key histopathologic features
  • Molecular/genomic markers

Example Assessment Section for Oncology

Assessment (Oncology)
 
 
ASSESSMENT:
 
1. SIGMOID COLON ADENOCARCINOMA, STAGE IIIB (pT3N2aM0) - AJCC 8TH EDITION (C18.7)
 
Staging Summary:
- Primary tumor: pT3 (through muscularis propria into pericolorectal tissues)
- Regional nodes: pN2a (4 of 18 positive)
- Distant metastasis: M0 (no evidence of distant disease)
- Stage Group: IIIB
 
Prognostic Factors:
- High-risk features: N2 disease (>3 positive nodes), lymphovascular invasion, perineural invasion
- Favorable: R0 resection, MSS (not eligible for immunotherapy), KRAS/BRAF wild-type
- MSI Status: Microsatellite stable (MSS)
- Molecular: KRAS wild-type, BRAF wild-type
 
Treatment Intent: CURATIVE - Adjuvant chemotherapy
 
2. ADJUVANT CHEMOTHERAPY - FOLFOX REGIMEN
- Current: Cycle 4 Day 1 of planned 12 cycles
- Duration: 6 months total planned
- Completion: 25% complete
- On schedule: Yes
 
3. TREATMENT RESPONSE ASSESSMENT
- No measurable disease (adjuvant setting post-R0 resection)
- CEA: 2.8 ng/mL - normalized and stable (baseline 45.2 pre-surgery)
- CT imaging (December 20): No evidence of recurrence
- Clinical status: No signs or symptoms of recurrent disease
 
4. TREATMENT TOXICITY SUMMARY (CTCAE v5.0)
 
| Toxicity | Current Grade | Prior Grade | Trend | Action |
|----------|---------------|-------------|-------|--------|
| Peripheral sensory neuropathy | Grade 2 | Grade 1 | Worsening | Dose reduce oxaliplatin |
| Fatigue | Grade 2 | Grade 2 | Stable | Supportive care |
| Nausea | Grade 1 | Grade 1 | Stable | Continue antiemetics |
| Diarrhea | Grade 1 (resolved) | Grade 1 | Resolved | PRN loperamide |
| Oral mucositis | Grade 1 | Grade 1 | Stable | Oral hygiene |
| Neutropenia (nadir) | Grade 3 (recovered) | Grade 2 | Worsening nadir | Monitor closely |
| Anemia | Grade 1 | Grade 1 | Stable | Monitor |
| Thrombocytopenia | Grade 1 (recovered) | Grade 0 | New | Monitor |
 
Dose-Limiting Toxicity: Grade 2 peripheral neuropathy
- Symptoms: Numbness and tingling in fingers and toes, difficulty with fine motor tasks
- Functional impact: Limiting instrumental ADLs (buttons, writing)
- Duration: Progressive since cycle 3
- Recommendation: 25% oxaliplatin dose reduction per FOLFOX protocol
 
5. PERFORMANCE STATUS
- Current ECOG: 1
- Baseline ECOG: 0
- Trend: Stable at ECOG 1 since cycle 2
- Assessment: Decline from baseline attributable to cumulative treatment-related fatigue; no evidence suggesting disease progression
 
6. HEMATOLOGIC TOXICITY
- Current counts: ANC 2,100 (adequate for treatment), Hgb 11.2 (Grade 1 anemia), Plt 156 (normal)
- Nadir (Cycle 3, Day 10): ANC 800 (Grade 3), Hgb 10.1, Plt 98 (Grade 1)
- Recovery: Full count recovery prior to cycle 4
- Assessment: Increased myelosuppression with cumulative cycles; monitoring indicated
 
7. NUTRITIONAL STATUS
- Weight: 172 lbs (8 lbs below diagnosis weight, 4.4% loss)
- Trend: Gradual decline, 2 lbs since last visit
- Oral intake: Approximately 75% of baseline
- Assessment: Mild treatment-related anorexia; nutritional counseling reinforced
 
8. SUPPORTIVE CARE
- Antiemetics: Effective - nausea well-controlled on current regimen
- Pain: No cancer-related pain, no analgesics required
- Growth factors: Not currently indicated (ANC adequate)
- Psychosocial: Mild anxiety, coping well with good support system
 
9. ELIGIBILITY FOR CONTINUED TREATMENT
- ANC: 2,100 (>1,500 required) - ADEQUATE
- Platelets: 156K (>100K required) - ADEQUATE
- Creatinine: 0.9 (normal renal function) - ADEQUATE
- Hepatic function: Normal - ADEQUATE
- Performance status: ECOG 1 - ADEQUATE
- CONCLUSION: Eligible to proceed with Cycle 4 with dose modification
 
TREATMENT DECISION:
Proceed with FOLFOX Cycle 4 with 25% oxaliplatin dose reduction (85 mg/m2 to 65 mg/m2) due to Grade 2 peripheral neuropathy. Continue 5-FU and leucovorin at full dose.
 

Plan Section (P)

The oncology Plan must comprehensively address treatment administration, dose modifications, supportive care, monitoring, and follow-up while maintaining compliance with protocols and guidelines.

Plan Section (P) Components

  1. Chemotherapy/Immunotherapy Administration:

    • Regimen name and cycle/day
    • Individual drug doses (with dose modifications noted)
    • BSA-based calculations
    • Infusion schedule
    • Pre-medications
    • Example:
      • "FOLFOX Cycle 4 Day 1:"
      • "Oxaliplatin 127 mg (65 mg/m2 x 1.96 m2) - 25% dose reduction for Grade 2 neuropathy"
      • "Leucovorin 784 mg (400 mg/m2 x 1.96 m2)"
      • "5-FU bolus 784 mg (400 mg/m2 x 1.96 m2)"
      • "5-FU infusion 4,704 mg (2400 mg/m2 x 1.96 m2) over 46 hours"
  2. Dose Modifications:

    • Specific modifications made
    • Rationale (toxicity grade, per protocol)
    • Reference to treatment protocol
    • Example: "Oxaliplatin dose reduced 25% (from 85 to 65 mg/m2) per FOLFOX protocol for Grade 2 peripheral neuropathy. 5-FU and leucovorin continued at full dose."
  3. Supportive Care Medications:

    • Antiemetics (acute and delayed)
    • Growth factors (G-CSF if indicated)
    • Pain management
    • Anti-diarrheals
    • Neuropathy management
    • Example:
      • "Pre-medications: Ondansetron 8mg IV, Dexamethasone 12mg IV"
      • "Post-chemo: Ondansetron 8mg PO TID PRN x 3 days, then PRN"
      • "Pegfilgrastim 6mg SC on Day 2 (if indicated)"
  4. Clinical Trial Documentation (if applicable):

    • Protocol number
    • Study drug administration
    • Protocol-specific assessments
    • Adverse event reporting
    • Example: "Patient enrolled in Protocol ABC-123. Study drug administered per protocol. Grade 2 neuropathy reported to sponsor per protocol requirements."
  5. Laboratory Monitoring:

    • Labs ordered and timing
    • Specific parameters to follow
    • Thresholds for notification
    • Example:
      • "CBC with differential: Prior to each cycle"
      • "CMP: Prior to each cycle"
      • "Nadir labs: Day 10 of each cycle (CBC)"
      • "CEA: Every 3 cycles (with restaging)"
  6. Imaging and Restaging:

    • Next imaging scheduled
    • Tumor marker schedule
    • Response assessment timing
    • Example: "CT Chest/Abdomen/Pelvis at completion of chemotherapy (after Cycle 12) for restaging. CEA to be checked with restaging labs."
  7. Toxicity Management Plan:

    • Specific interventions for ongoing toxicities
    • Patient instructions
    • When to call/return
    • Example:
      • "Neuropathy: Avoid cold exposure, use gloves for cold items. Gabapentin 100mg TID may be initiated if symptoms worsen."
      • "Diarrhea: Loperamide 4mg initially, then 2mg after each loose stool (max 16mg/day). Call if >6 stools/day or fever."
  8. Referrals and Consultations:

    • Multidisciplinary team involvement
    • Supportive services
    • Example:
      • "Nutrition: Referral to oncology dietitian for weight loss"
      • "Palliative care: Not indicated at this time"
      • "Survivorship: Will refer at completion of treatment"
  9. Patient Education:

    • Treatment expectations
    • Side effect management
    • Emergency instructions
    • Example: "Reviewed signs/symptoms requiring immediate attention: fever >100.4F, severe diarrhea, uncontrolled nausea/vomiting, bleeding, new or worsening neurological symptoms."
  10. Follow-Up:

    • Next treatment date
    • Monitoring appointments
    • Restaging schedule
    • Example:
      • "Cycle 4 Day 1: Today"
      • "Pump disconnect: Day 3 (home health or return to clinic)"
      • "Nadir labs: Day 10"
      • "Cycle 5 Day 1: January 10, 2026"

Example Plan Section for Oncology

Plan (Oncology)
 
 
PLAN:
 
1. CHEMOTHERAPY ADMINISTRATION - FOLFOX CYCLE 4 DAY 1
 
Regimen: Modified FOLFOX6 (adjuvant)
BSA: 1.96 m2
 
| Drug | Standard Dose | Modified Dose | Actual Dose | Route | Schedule |
|------|---------------|---------------|-------------|-------|----------|
| Oxaliplatin | 85 mg/m2 | 65 mg/m2 (-25%) | 127 mg | IV over 2 hrs | Day 1 |
| Leucovorin | 400 mg/m2 | 400 mg/m2 | 784 mg | IV over 2 hrs | Day 1 |
| 5-FU bolus | 400 mg/m2 | 400 mg/m2 | 784 mg | IV push | Day 1 |
| 5-FU infusion | 2400 mg/m2 | 2400 mg/m2 | 4704 mg | CIV over 46 hrs | Day 1-3 |
 
Dose Modification Rationale:
- Oxaliplatin reduced 25% for Grade 2 peripheral sensory neuropathy per FOLFOX protocol guidelines
- 5-FU and leucovorin continued at full dose (no dose-limiting 5-FU toxicity)
 
2. PRE-MEDICATIONS (Day 1):
- Ondansetron 8 mg IV x 1
- Dexamethasone 12 mg IV x 1
- Diphenhydramine 25 mg IV PRN (available)
 
3. SUPPORTIVE CARE MEDICATIONS:
 
Antiemetics:
- Ondansetron 8 mg PO TID PRN days 1-3, then PRN (continue current supply)
- Prochlorperazine 10 mg PO Q6H PRN breakthrough nausea (continue current supply)
 
Diarrhea:
- Loperamide 4 mg PO initially, then 2 mg after each loose stool (max 16 mg/day)
- Call if >6 stools/day, bloody stool, or fever
 
Neuropathy Management:
- Avoid cold exposure during and for 3 days after oxaliplatin
- Use gloves when handling cold/frozen items
- Room temperature or warm beverages only
- Gabapentin 100 mg PO TID - NEW START for neuropathy symptoms
- Consider dose increase to 300 mg TID if inadequate relief
 
Mucositis:
- Magic mouthwash (lidocaine/Maalox/Benadryl) swish and spit QID PRN
- Soft toothbrush, gentle oral hygiene
 
Growth Factors:
- Not indicated at this time (ANC 2,100, nadir ANC 800 with recovery)
- If nadir ANC <500 or febrile neutropenia occurs, will initiate pegfilgrastim
 
4. PORT CARE:
- Port accessed for treatment today
- De-access after pump disconnect (Day 3)
- Flush with heparin per protocol
 
5. PUMP DISCONNECT:
- 5-FU pump disconnect: Day 3 (January 2, 2026)
- Patient to return to infusion center for disconnect OR
- Home health nurse to disconnect if arranged
- Bring pump to next appointment if disconnected at home
 
6. LABORATORY MONITORING:
 
Today (Cycle 4 Day 1):
- CBC with differential: COMPLETED - adequate for treatment
- CMP: COMPLETED - adequate for treatment
 
Nadir Labs (Day 10 - January 7, 2026):
- CBC with differential
- CMP
- Note: If ANC <500 or febrile, patient should go to ED and call oncology
 
Pre-Cycle 5 (January 10, 2026):
- CBC with differential
- CMP
 
7. TUMOR MARKER MONITORING:
- CEA: Check every 3 cycles (next: Cycle 6)
- Current CEA: 2.8 ng/mL (normal, stable)
 
8. IMAGING/RESTAGING:
- CT Chest/Abdomen/Pelvis: After completion of Cycle 12 (approximately April 2026)
- Earlier imaging only if clinical concern for recurrence
 
9. NEUROPATHY MONITORING AND MANAGEMENT:
- Current Grade: 2
- Action taken: 25% oxaliplatin dose reduction
- If neuropathy progresses to Grade 3: Discontinue oxaliplatin, continue 5-FU/LV
- Reassess at each visit with neurological exam
- Document functional impact (buttoning, writing, walking, balance)
 
10. NUTRITIONAL SUPPORT:
- Weight loss: 8 lbs (4.4%) - continue monitoring
- Continue Ensure Plus or equivalent 1-2 daily
- Small, frequent meals
- Referral to oncology dietitian: ORDERED
- Call if unable to maintain oral intake or continued weight loss
 
11. PSYCHOSOCIAL SUPPORT:
- PHQ-2 negative today - continue monitoring
- Social work available if needed
- Support group information provided
- Cancer navigation services available
 
12. PATIENT EDUCATION PROVIDED:
- Reviewed neuropathy precautions (cold avoidance)
- Reviewed gabapentin initiation for neuropathy
- Reviewed signs/symptoms requiring immediate medical attention:
* Fever >100.4F or chills
* Uncontrolled nausea/vomiting
* Diarrhea >6 stools/day or bloody stool
* Signs of infection
* Unusual bleeding or bruising
* Severe mouth sores preventing oral intake
* Chest pain or shortness of breath
* New or severe abdominal pain
* Worsening neuropathy (weakness, difficulty walking)
- After-hours oncology contact number provided
 
13. EMERGENCY INSTRUCTIONS:
- Fever >100.4F: Go to ED, call oncology on-call
- Severe symptoms: Go to ED or call 911
- Non-urgent questions: Call clinic during business hours
 
14. FOLLOW-UP SCHEDULE:
| Date | Visit | Purpose |
|------|-------|---------|
| January 2, 2026 | Day 3 | Pump disconnect |
| January 7, 2026 | Day 10 | Nadir labs (lab only) |
| January 10, 2026 | Cycle 5 Day 1 | Treatment + physician visit |
 
15. LONG-TERM PLAN:
- Complete 12 cycles FOLFOX (adjuvant)
- Restaging CT after Cycle 12
- Transition to surveillance protocol after treatment completion
- Surveillance: CEA every 3 months x 2 years, CT every 6-12 months x 3 years
- Colonoscopy: 1 year post-surgery, then per findings
 
16. TREATMENT TEAM:
- Medical Oncologist: [Name, MD]
- Oncology NP/PA: [Name]
- Oncology Nurse Navigator: [Name]
- Oncology Pharmacist: [Name]
- Surgeon (if needed): [Name, MD]
 
Next appointment: January 10, 2026 - Cycle 5 Day 1 with Dr. [Name]
 

AI-Assisted Documentation for Oncology

As of 2025, 66% of healthcare providers utilize AI tools in their practice. AI scribes and ambient clinical intelligence can significantly reduce documentation burden for oncologists while maintaining comprehensive cancer care records.

How AI Can Help with Oncology Documentation

  • Treatment tracking: Accurately captures chemotherapy cycles, dates, and regimen changes
  • Symptom documentation: Records patient-reported symptoms with severity descriptions
  • Medication reconciliation: Documents complex supportive care regimens
  • Template population: Generates structured notes following oncology documentation standards
  • Follow-up scheduling: Captures treatment schedules and monitoring plans

Oncology-Specific AI Considerations

What AI captures well:

  • Patient-reported symptoms and treatment tolerance
  • Performance status descriptions
  • Medication lists including supportive care
  • Treatment schedule discussions
  • Patient education topics covered
  • Follow-up plans

What requires careful review:

  • CTCAE grading: Verify AI-assigned toxicity grades match clinical assessment
  • Dose calculations: Confirm BSA-based dosing and dose modifications are accurate
  • Staging information: Verify TNM staging and stage grouping accuracy
  • Tumor marker values: Confirm exact values and trends
  • RECIST assessments: Verify response categorization matches imaging reports
  • Protocol-specific documentation: Ensure clinical trial requirements are met
  • Drug doses and modifications: Double-check all chemotherapy doses

Tips for Using AI with Oncology Documentation

  1. State CTCAE grades explicitly: "The patient has Grade 2 peripheral neuropathy, limiting instrumental ADLs"
  2. Verbalize dose modifications: "Due to Grade 2 neuropathy, we are reducing oxaliplatin by 25 percent, from 85 to 65 milligrams per meter squared"
  3. Dictate performance status clearly: "ECOG performance status is 1, unchanged from last visit"
  4. Specify tumor marker values: "CEA is 2.8, which is normalized and stable from the prior value of 3.0"
  5. State treatment intent: "This is adjuvant chemotherapy with curative intent"
  6. Review staging carefully: Verify all TNM components and stage grouping
AI-Assisted Oncology Documentation Checklist
 
 
AI DOCUMENTATION REVIEW CHECKLIST - ONCOLOGY
 
Before signing AI-generated notes, verify:
 
TREATMENT INFORMATION:
[ ] Correct regimen name and cycle number
[ ] Accurate drug doses (verify BSA calculation)
[ ] Dose modifications documented with rationale
[ ] Treatment intent stated (curative, adjuvant, palliative)
 
STAGING AND DIAGNOSIS:
[ ] Complete TNM staging with correct edition
[ ] Stage grouping accurate
[ ] Key molecular markers documented
[ ] Histology and grade correct
 
TOXICITY ASSESSMENT:
[ ] Each toxicity listed with CTCAE grade
[ ] Grades match clinical assessment
[ ] Comparison to prior cycle documented
[ ] Functional impact of toxicities noted
 
PERFORMANCE STATUS:
[ ] ECOG score stated and verified
[ ] Comparison to baseline documented
[ ] Supporting clinical observations included
 
LABORATORY VALUES:
[ ] ANC and counts verified for treatment eligibility
[ ] Tumor markers with trends documented
[ ] Organ function adequate for treatment
 
RESPONSE ASSESSMENT:
[ ] RECIST category correct (if applicable)
[ ] Imaging findings accurately summarized
[ ] Tumor marker trends documented
 
PLAN VERIFICATION:
[ ] Treatment eligible - counts adequate
[ ] Supportive care medications complete
[ ] Lab monitoring schedule correct
[ ] Follow-up appointments accurate
[ ] Emergency instructions documented
 

For more details, see our complete AI-Assisted Documentation Guide.

Telehealth Oncology Documentation

Virtual oncology care has expanded significantly for symptom monitoring, treatment tolerance assessments, and survivorship follow-up. Per CMS 2026 guidelines, telehealth services continue with specific documentation requirements.

Telehealth-Appropriate Oncology Services

  1. Treatment Tolerance Monitoring:

    • Between-cycle symptom assessment
    • Toxicity monitoring and grading
    • Medication adjustments
    • Supportive care optimization
  2. Survivorship Follow-Up:

    • Post-treatment surveillance
    • Late effects monitoring
    • Quality of life assessment
    • Psychosocial support
  3. Symptom Management:

    • Pain assessment and management
    • Nausea/emesis management
    • Fatigue counseling
    • Depression/anxiety screening
  4. Results Review:

    • Laboratory result review
    • Tumor marker trending
    • Imaging review and discussion
    • Pathology result discussion

Telehealth Oncology Documentation Requirements

For virtual oncology visits, document:

  1. Visit logistics:

    • Platform used (HIPAA-compliant)
    • Patient and provider locations
    • Consent for telehealth services
    • Audio/video quality
  2. Modified physical examination:

    • Visual assessment of performance status
    • Patient self-reported findings (weight, temperature if available)
    • Visible examination (skin, port site if visible, visible lymphadenopathy)
    • Limitations clearly documented
  3. Toxicity assessment via telehealth:

    • Patient-reported symptoms with grades
    • Functional status assessment via observation and report
    • Clear documentation of what could not be assessed
  4. Treatment eligibility assessment:

    • Review of recent laboratory values
    • Performance status assessment
    • Determination if in-person visit needed before treatment

Example Telehealth Oncology Documentation

Telehealth Oncology Visit - Symptom Check
 
 
TELEHEALTH ONCOLOGY VISIT
 
SESSION DETAILS:
- Platform: Epic MyChart Video (HIPAA-compliant)
- Patient Location: Home in [State]
- Provider Location: Cancer Center, [State]
- Consent: Patient verbally consented to telehealth oncology visit
- Technical Quality: Good audio and video quality
- Visit Type: Between-cycle symptom assessment (Cycle 3, Day 10)
 
PATIENT: [Name], [DOB]
DIAGNOSIS: Stage IIIB sigmoid colon adenocarcinoma on FOLFOX (Cycle 3)
 
SUBJECTIVE (via telehealth):
Chief Concern: Routine symptom check between treatment cycles
 
Treatment Tolerance Review:
- Fatigue: Moderate (Grade 2) - requiring afternoon rest daily, similar to prior cycle
- Nausea: Mild (Grade 1) - occasional, well-controlled with ondansetron
- Diarrhea: Resolved - had 3-4 loose stools days 2-4, now resolved
- Neuropathy: Mild cold sensitivity (Grade 1), no functional impairment
- Mucositis: None
- No fever, chills, or signs of infection
- No bleeding or bruising
- Appetite: Fair, eating approximately 70% of usual intake
- Weight: Patient reports 173 lbs (home scale) - stable
 
Functional Status:
- Able to perform all ADLs independently
- Walking daily, approximately 1 mile
- Working from home part-time
- Patient-reported ECOG: 1
 
OBJECTIVE (Modified for Telehealth):
General: Patient appears comfortable, seated in well-lit room. Alert and oriented. No visible distress. Speaking in complete sentences without shortness of breath.
 
Visual Assessment:
- Skin color: Normal, no pallor or jaundice visible
- Visible skin: No rash observed on face, neck, or arms
- Mucous membranes: Unable to visualize oral mucosa via video
- Functional mobility: Patient stood and walked across room without difficulty
 
Unable to Assess via Telehealth:
- Vital signs (no home blood pressure or thermometer available)
- Auscultation of heart and lungs
- Abdominal examination
- Detailed neurological examination
- Port site examination
- Lymph node palpation
 
LABORATORY RESULTS (Reviewed - obtained at local lab today):
- WBC: 3.8 (nadir expected)
- ANC: 850 (Grade 3 neutropenia - no fever)
- Hemoglobin: 10.8 (Grade 1 anemia)
- Platelets: 108 (Grade 1 thrombocytopenia)
- BMP: Electrolytes normal, creatinine 0.9
 
ASSESSMENT:
1. Stage IIIB colon adenocarcinoma on adjuvant FOLFOX - Cycle 3, Day 10
- Expected nadir occurring - counts appropriate for day 10
- ANC 850 (Grade 3 neutropenia) - no fever, no signs of infection
- Treatment tolerance: Acceptable
 
2. Treatment-related toxicities - all stable or improving:
- Fatigue: Grade 2
- Neuropathy: Grade 1
- Nausea: Grade 1, controlled
- Diarrhea: Resolved
- Anemia: Grade 1
- Neutropenia: Grade 3 at nadir (expected)
- Thrombocytopenia: Grade 1
 
3. Performance Status: ECOG 1 per patient report and visual assessment
 
PLAN:
1. Counts recovering as expected - continue monitoring
2. Neutropenic precautions: Reviewed with patient
- Avoid crowds and sick contacts
- Hand hygiene
- Temperature monitoring - call immediately if fever >100.4F
3. Continue supportive medications as prescribed
4. Next treatment (Cycle 4 Day 1): Scheduled for January 10, 2026
- Pre-treatment labs: Morning of appointment
- Expect count recovery by day 14
5. Call clinic immediately for:
- Fever >100.4F
- Worsening symptoms
- Signs of infection
- Bleeding
 
TELEHEALTH APPROPRIATENESS:
This between-cycle symptom check was appropriate for telehealth. Patient is clinically stable with expected toxicities. No in-person evaluation required at this time. Next in-person visit scheduled for Cycle 4 treatment on January 10, 2026.
 
Follow-up: Cycle 4 Day 1 - January 10, 2026 (in-person for treatment)
 

Survivorship Telehealth Visit

Survivorship Telehealth Follow-Up
 
 
TELEHEALTH ONCOLOGY VISIT - SURVIVORSHIP
 
SESSION DETAILS:
- Platform: Doxy.me (HIPAA-compliant video)
- Patient Location: Home in [State]
- Provider Location: Cancer Center, [State]
- Consent: Verbal consent for telehealth obtained
- Visit Type: 6-month survivorship follow-up
 
PATIENT: [Name], [DOB]
DIAGNOSIS: Stage IIIB sigmoid colon adenocarcinoma
TREATMENT: Low anterior resection (October 2024), adjuvant FOLFOX x 12 cycles (completed April 2025)
STATUS: Surveillance
 
SUBJECTIVE:
Time from Treatment Completion: 8 months
Current Concerns: Routine 6-month surveillance visit
 
Symptom Review - Late Effects:
- Peripheral neuropathy: Persistent Grade 1 - numbness in fingertips, stable
- Fatigue: Resolved - returned to baseline energy level
- Bowel function: 2-3 formed stools daily, no urgency or incontinence, minimal dietary modifications needed
- Appetite: Normal, weight stable
 
Functional Status:
- ECOG: 0 - returned to baseline
- Work: Returned to full-time work
- Exercise: Running 3 miles 3x/week
- Quality of life: Good, reports return to pre-diagnosis function
 
Psychosocial:
- Mood: Good, minimal anxiety about surveillance
- PHQ-2: Negative
- Support: Strong family support
 
Review of Systems:
- No weight loss, fever, night sweats
- No abdominal pain or change in bowel habits
- No rectal bleeding
- No new palpable masses
- No shortness of breath or cough
- No bone pain
- No neurological symptoms beyond baseline neuropathy
 
OBJECTIVE (Modified for Telehealth):
General: Well-appearing, healthy-appearing individual. No visible distress. Animated and engaged.
Visual assessment: No pallor, jaundice, or visible masses
Functional: Appears fully functional via observation
 
Unable to Assess via Telehealth:
- Complete physical examination
- Lymph node examination
- Abdominal examination
 
SURVEILLANCE RESULTS (Reviewed):
CEA (last week): 2.1 ng/mL (normal, baseline range 1.8-2.8 since treatment completion)
 
CT Chest/Abdomen/Pelvis (last month):
- No evidence of recurrent disease
- Post-surgical changes stable
- No lymphadenopathy
- Liver, lungs clear
- No new findings
 
Colonoscopy (6 months post-surgery - April 2025):
- Anastomosis intact, no recurrence
- 2 small tubular adenomas removed
- Recommend repeat in 1 year
 
ASSESSMENT:
1. Stage IIIB sigmoid colon adenocarcinoma - IN REMISSION
- 8 months post-completion of adjuvant therapy
- No evidence of recurrence
- CEA normal and stable
- CT surveillance negative
- Surveillance on track per NCCN guidelines
 
2. Chemotherapy-induced peripheral neuropathy - Stable Grade 1
- Persistent but not progressive
- No functional impairment
- Expected to continue gradual improvement
 
3. Post-treatment surveillance per NCCN Colon Cancer Guidelines
 
PLAN:
1. Continue surveillance per NCCN guidelines:
- CEA: Every 3-6 months for 2 years, then every 6 months years 3-5
- CT Chest/Abdomen/Pelvis: Every 6-12 months for 3 years
- Colonoscopy: 1 year post-surgery (completed), repeat in 1 year (3-year interval due to adenomas)
 
2. Next surveillance labs and imaging:
- CEA: 3 months (order placed)
- CT: 6 months (order placed)
- Colonoscopy: April 2026 (1 year from prior, due to adenoma findings)
 
3. Late effects monitoring:
- Peripheral neuropathy: Stable, continue observation
- No intervention needed at this time
 
4. Preventive care:
- Age-appropriate cancer screening (lung, prostate per PCP)
- Healthy lifestyle counseling: Continue exercise, balanced diet
- Smoking: Lifelong non-smoker - continue abstinence
 
5. Return to oncology:
- In-person visit: 6 months for physical examination and surveillance review
- Sooner if concerning symptoms develop
 
6. Concerning symptoms - call immediately:
- Unexplained weight loss
- New abdominal pain or change in bowel habits
- Rectal bleeding
- New masses
- Persistent cough or shortness of breath
- Bone pain
 
TELEHEALTH APPROPRIATENESS:
This routine survivorship visit was appropriate for telehealth given patient is in remission with no symptoms of recurrence. Recent imaging and labs reviewed. In-person physical examination recommended at next 6-month visit.
 
Follow-up: 6 months - in-person survivorship visit
 

For complete telehealth documentation guidance, see our Telehealth SOAP Notes Guide.

Specialty Documentation Templates

Chemotherapy Treatment Visit Template

Chemotherapy Treatment Visit Documentation
 
 
CHEMOTHERAPY TREATMENT VISIT
 
PATIENT: _______________ DOB: ___________ MRN: ___________
DATE: _______________ CYCLE: ___ DAY: ___
 
DIAGNOSIS:
- Cancer type: _______________
- Stage: _______________ (AJCC Edition: ___)
- Histology: _______________
- Key molecular markers: _______________
 
TREATMENT:
- Regimen: _______________
- Treatment intent: [ ] Curative [ ] Adjuvant [ ] Neoadjuvant [ ] Palliative
- Total planned cycles: ___
- Current cycle: ___
 
TREATMENT TOLERANCE (since last cycle):
Symptom assessment with CTCAE grades:
| Symptom | Grade (0-4) | Comments |
|---------|-------------|----------|
| Fatigue | | |
| Nausea/vomiting | | |
| Diarrhea | | |
| Constipation | | |
| Mucositis | | |
| Neuropathy | | |
| Hand-foot syndrome | | |
| Rash | | |
| Pain | | |
| Other: | | |
 
PERFORMANCE STATUS:
- ECOG today: ___
- Baseline ECOG: ___
- Trend: [ ] Stable [ ] Improved [ ] Declined
 
VITAL SIGNS:
- BP: ___/___ HR: ___ Temp: ___ RR: ___ SpO2: ___%
- Weight: ___ (Change: ___ since last visit)
- BSA: ___ m2
 
LABORATORY RESULTS:
- WBC: ___ ANC: ___ (adequate if >1,500)
- Hemoglobin: ___ Platelets: ___
- Creatinine: ___ (CrCl: ___)
- Liver function: AST ___ ALT ___ Bili ___
- Other: _______________
 
TUMOR MARKERS (if applicable):
- Marker: ___ Value: ___ (Prior: ___ Trend: ___)
 
PHYSICAL EXAMINATION:
- General: _______________
- Port/line site: _______________
- HEENT/Oral: _______________
- Lungs: _______________
- CV: _______________
- Abdomen: _______________
- Extremities: _______________
- Neuro (neuropathy assessment): _______________
- Skin: _______________
 
TREATMENT ELIGIBILITY ASSESSMENT:
[ ] ANC adequate (>1,500)
[ ] Platelets adequate (>100,000)
[ ] Organ function adequate
[ ] Performance status adequate
[ ] Toxicities manageable
[ ] ELIGIBLE FOR TREATMENT
 
DOSE MODIFICATIONS:
[ ] None - continue at full dose
[ ] Dose reduction: ___ (Drug: ___, New dose: ___, Reason: ___)
[ ] Treatment delay: ___ (Reason: ___, Resume date: ___)
[ ] Drug discontinuation: ___ (Drug: ___, Reason: ___)
 
CHEMOTHERAPY ORDERS (today):
| Drug | Dose (mg/m2) | Actual Dose | Route | Duration |
|------|--------------|-------------|-------|----------|
| | | | | |
| | | | | |
| | | | | |
 
PRE-MEDICATIONS:
- _______________
- _______________
 
SUPPORTIVE CARE MEDICATIONS:
- Antiemetics: _______________
- Growth factors: _______________
- Pain management: _______________
- Other: _______________
 
PATIENT EDUCATION:
[ ] Side effects reviewed
[ ] When to call instructions reviewed
[ ] Medication instructions reviewed
[ ] Emergency contact provided
 
NEXT STEPS:
- Labs before next cycle: ___
- Next treatment date: ___
- Imaging/restaging: ___
 
Provider: _______________ Date: _______________
 

Toxicity Assessment Template

CTCAE Toxicity Assessment Template
 
 
CTCAE v5.0 TOXICITY ASSESSMENT
 
Patient: _______________ Date: _______________
Diagnosis: _______________ Current Treatment: _______________
Cycle: ___ Day: ___
 
GRADING SCALE:
Grade 1: Mild; asymptomatic or mild symptoms; clinical or diagnostic observations only
Grade 2: Moderate; minimal, local, or noninvasive intervention indicated
Grade 3: Severe; medically significant but not immediately life-threatening; hospitalization or prolongation indicated
Grade 4: Life-threatening; urgent intervention indicated
Grade 5: Death related to adverse event
 
HEMATOLOGIC TOXICITIES:
| Toxicity | Current Grade | Nadir Grade | Prior Cycle Grade |
|----------|---------------|-------------|-------------------|
| Anemia (Hgb) | | | |
| Neutropenia (ANC) | | | |
| Thrombocytopenia | | | |
| Febrile neutropenia | | | |
 
GASTROINTESTINAL:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| Nausea | | |
| Vomiting | | |
| Diarrhea | | |
| Constipation | | |
| Mucositis/stomatitis | | |
| Anorexia | | |
| Dysphagia | | |
 
NEUROLOGICAL:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| Peripheral sensory neuropathy | | |
| Peripheral motor neuropathy | | |
| Cognitive disturbance | | |
| Headache | | |
 
DERMATOLOGIC:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| Rash | | |
| Hand-foot syndrome | | |
| Nail changes | | |
| Alopecia | | |
| Pruritus | | |
 
CONSTITUTIONAL:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| Fatigue | | |
| Fever | | |
| Weight loss | | |
 
CARDIOVASCULAR:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| Hypertension | | |
| Hypotension | | |
| Cardiac (specify) | | |
 
PULMONARY:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| Dyspnea | | |
| Cough | | |
| Pneumonitis | | |
 
HEPATIC:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| AST/ALT elevation | | |
| Bilirubin elevation | | |
 
RENAL:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| Creatinine elevation | | |
| Proteinuria | | |
 
IMMUNE-RELATED (if on immunotherapy):
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| irAE - specify: | | |
 
OTHER TOXICITIES:
| Toxicity | Current Grade | Comments |
|----------|---------------|----------|
| | | |
 
DOSE-LIMITING TOXICITIES:
[ ] None identified
[ ] Present: _______________
Recommended action: _______________
 
TOXICITY MANAGEMENT PLAN:
1. _______________
2. _______________
3. _______________
 
NEW MEDICATIONS FOR TOXICITY:
_______________
 
DOSE MODIFICATIONS INDICATED:
[ ] None
[ ] Dose reduction: _______________
[ ] Treatment delay: _______________
[ ] Drug discontinuation: _______________
 
Assessed by: _______________ Date: _______________
 

Free Oncology SOAP Note Template

ONCOLOGY SOAP NOTE TEMPLATE
 
PATIENT: _______________ DOB: ___________ MRN: ___________
DATE: _______________ PROVIDER: _______________
VISIT TYPE: [ ] New [ ] Follow-up [ ] Treatment [ ] Surveillance
 
DIAGNOSIS:
- Primary cancer: _______________
- Histology: _______________
- Stage: ___ (TNM: ___) AJCC Edition: ___
- Key markers: _______________
- Date of diagnosis: _______________
 
TREATMENT HISTORY:
- Surgery: _______________
- Radiation: _______________
- Systemic therapy: _______________
- Current regimen: _______________ Cycle: ___
 
===================================================
SUBJECTIVE
===================================================
 
CHIEF COMPLAINT:
_______________
 
TREATMENT TOLERANCE (since last treatment):
_______________
 
SYMPTOM ASSESSMENT (with CTCAE grades):
- Fatigue: Grade ___
- Nausea/vomiting: Grade ___
- Diarrhea/constipation: Grade ___
- Neuropathy: Grade ___
- Mucositis: Grade ___
- Pain: ___ /10, Location: ___
- Other: _______________
 
FUNCTIONAL STATUS:
- ECOG Performance Status: ___
- Baseline ECOG: ___
- Functional changes: _______________
 
NUTRITIONAL STATUS:
- Current weight: ___ Change: ___
- Appetite: _______________
- Dietary intake: _______________
 
PSYCHOSOCIAL:
- Mood/coping: _______________
- Depression screening: PHQ-2 ___
- Support system: _______________
 
REVIEW OF SYSTEMS:
[ ] Constitutional: _______________
[ ] HEENT: _______________
[ ] Respiratory: _______________
[ ] Cardiovascular: _______________
[ ] GI: _______________
[ ] GU: _______________
[ ] Neurological: _______________
[ ] Musculoskeletal: _______________
[ ] Skin: _______________
[ ] Hematologic: _______________
 
CURRENT MEDICATIONS:
- Chemotherapy/targeted/immunotherapy: _______________
- Supportive care: _______________
- Other medications: _______________
 
ALLERGIES: _______________
 
===================================================
OBJECTIVE
===================================================
 
VITAL SIGNS:
- BP: ___/___ HR: ___ Temp: ___ RR: ___ SpO2: ___%
- Weight: ___ (Change from last: ___)
- Height: ___ BSA: ___ m2
 
PERFORMANCE STATUS: ECOG ___ (verified by observation)
 
GENERAL: _______________
 
HEENT: _______________
- Oral cavity (mucositis assessment): _______________
 
PORT/LINE ASSESSMENT:
_______________
 
LYMPH NODES: _______________
 
CARDIOVASCULAR: _______________
 
PULMONARY: _______________
 
ABDOMEN: _______________
 
EXTREMITIES: _______________
 
SKIN: _______________
 
NEUROLOGICAL (neuropathy assessment):
- Sensory: _______________
- Motor: _______________
- Reflexes: _______________
- Gait: _______________
 
LABORATORY RESULTS:
CBC: WBC ___ ANC ___ Hgb ___ Plt ___
CMP: Na ___ K ___ Cr ___ AST ___ ALT ___ Bili ___
Tumor markers: _______________
 
IMAGING:
_______________
RECIST Assessment (if applicable): _______________
 
===================================================
ASSESSMENT
===================================================
 
1. [Cancer diagnosis with stage] (ICD-10: ___)
- Disease status: _______________
- Treatment status: _______________
 
2. Treatment toxicities:
- _______________: Grade ___
- _______________: Grade ___
- Dose modifications indicated: _______________
 
3. Performance status: ECOG ___
- Trend: _______________
 
4. Other diagnoses:
- _______________
 
TREATMENT ELIGIBILITY:
[ ] ANC adequate [ ] Platelets adequate [ ] Organ function adequate
[ ] Performance status adequate [ ] ELIGIBLE FOR TREATMENT
 
===================================================
PLAN
===================================================
 
1. TREATMENT:
Regimen: _______________
| Drug | Dose | Route | Schedule |
|------|------|-------|----------|
| | | | |
 
Dose modifications: _______________
 
2. SUPPORTIVE CARE:
- Antiemetics: _______________
- Growth factors: _______________
- Pain management: _______________
- Other: _______________
 
3. TOXICITY MANAGEMENT:
_______________
 
4. LABORATORY MONITORING:
- Next labs: _______________
- Tumor markers: _______________
 
5. IMAGING/RESTAGING:
_______________
 
6. REFERRALS:
_______________
 
7. PATIENT EDUCATION:
[ ] Treatment plan reviewed
[ ] Side effects discussed
[ ] When to call reviewed
[ ] Emergency instructions provided
 
8. FOLLOW-UP:
- Next treatment: _______________
- Next visit: _______________
- Restaging: _______________
 
Emergency contact: _______________
 
Provider Signature: _______________ Date: _______________
 

Frequently Asked Questions

Oncology notes must include complete TNM staging with: T (tumor size/extent), N (nodal involvement), M (metastasis), staging prefix (c for clinical, p for pathologic, y for post-neoadjuvant), AJCC edition used, and stage grouping (I-IV). Also document key histopathologic features, grade, and molecular/genomic markers (KRAS, BRAF, MSI status, HER2, etc.). Both clinical and pathologic staging should be included when available.

Document each treatment-related toxicity using CTCAE (Common Terminology Criteria for Adverse Events) grading: Grade 1 (mild/asymptomatic), Grade 2 (moderate, minimal intervention needed), Grade 3 (severe, hospitalization indicated), Grade 4 (life-threatening), Grade 5 (death). Include the specific toxicity name, current grade, comparison to prior cycle, functional impact, and any dose modifications indicated. Example: 'Peripheral neuropathy: Grade 2 (progressed from Grade 1) - limiting instrumental ADLs, recommending 25% oxaliplatin dose reduction.'

RECIST 1.1 documentation should include: target lesions with specific measurements, non-target lesions status, presence of new lesions, and overall response category. Categories are: Complete Response (CR) - disappearance of all lesions; Partial Response (PR) - 30% or greater decrease; Stable Disease (SD) - neither sufficient shrinkage nor increase; Progressive Disease (PD) - 20% or greater increase or new lesions. Include date of imaging and comparison to baseline or nadir measurements.

Document: the specific drug being modified, original dose and new dose (with mg/m2 calculations), percent reduction, rationale for modification (toxicity type and CTCAE grade), reference to treatment protocol guidelines, and any delays required before resuming treatment. Example: 'Oxaliplatin dose reduced 25% (from 85 to 65 mg/m2) per FOLFOX protocol for Grade 2 peripheral sensory neuropathy. 5-FU and leucovorin continued at full dose.'

Document ECOG or Karnofsky performance status with: numerical score, supporting clinical observations that verify the score, comparison to baseline, and trend over time. ECOG scale ranges from 0 (fully active) to 4 (completely disabled). Document functional examples that support your assessment: 'ECOG 1: Patient walked independently to exam room, reports fatigue limiting strenuous activity but continues working part-time. Baseline ECOG 0, stable at ECOG 1 since cycle 2.'

Yes, SOAPNoteAI.com provides AI-assisted documentation that's ideal for oncology practice. It's HIPAA-compliant with a Business Associate Agreement (BAA), available on iPhone, iPad, and web browsers, and works for any medical specialty. The platform can capture complex treatment regimens, toxicity assessments, staging information, and treatment discussions while you focus on patient care. It significantly reduces the documentation burden while maintaining the comprehensive detail required for oncology notes.

Oncology telehealth notes must include: platform used and patient/provider locations, consent for telehealth, visual assessment of performance status and general appearance, patient-reported symptoms with CTCAE grades, review of recent laboratory and imaging results, limitations of virtual examination clearly stated, and determination of whether in-person visit is needed before next treatment. Document telehealth appropriateness assessment explaining why the visit type was suitable for the clinical situation.

Medical Disclaimer: This content is for educational purposes only and should not replace professional medical judgment. Always consult current clinical guidelines and your institution's policies.

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