Summary & Overview
HCPCS M1393: Nonrecurrent Melanoma Status
HCPCS Level II code M1393 denotes patients who were not diagnosed with recurrent melanoma during the current performance period. The code is used to classify and report patient status for melanoma surveillance and quality reporting programs, supporting measurement of recurrence-free cohorts and related outcome metrics. Nationally, clear identification of nonrecurrent status informs quality assessment, performance measurement, and care coordination across oncology and dermatology services.
Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of the clinical context for M1393, typical service settings where the code is applied, and what its use signifies for melanoma surveillance and reporting. The publication also outlines typical benchmarks, common billing modifiers, and programmatic considerations relevant to payers and providers. Where input data are incomplete, the text indicates "Data not available in the input." The aim is to provide a concise reference for clinicians, billing professionals, and policy analysts seeking to understand how M1393 is used in national reporting and care pathways for patients without recurrent melanoma.
Billing Code Overview
HCPCS Level II code M1393 designates patients who were not diagnosed with recurrent melanoma during the current performance period. This code pertains to assessment and reporting of melanoma recurrence status and is used to identify patients without documented recurrent disease in the defined performance window.
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Service type: Surveillance and outcome assessment related to melanoma recurrence status
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Typical site of service: Oncology clinic, dermatology clinic, outpatient surgical follow-up, or ambulatory care settings
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult with a prior history of primary cutaneous melanoma who presents for routine surveillance during the current performance period. The patient has no clinical signs, symptoms, or imaging findings suggestive of recurrent melanoma; pathology review and clinical examination do not identify new suspicious lesions. The clinical workflow includes: pre-visit chart review of prior melanoma staging and treatment, focused skin and lymph node physical examination, review of interval history (new lumps, weight loss, or persistent symptoms), coordination of surveillance imaging if indicated by prior stage (for example chest CT for stage II/III per institutional protocol), and documentation that there is no recurrence. If no recurrence is found, the billing entry M1393 is used to indicate the patient was not diagnosed with recurrent melanoma during the performance period. Typical sites of service are outpatient dermatology, surgical oncology, medical oncology, or survivorship clinics. A realistic scenario: a 58-year-old male five years post wide local excision and sentinel lymph node biopsy for stage II melanoma attends a scheduled surveillance visit; exam and review of interval studies show no evidence of recurrence and the clinician documents no recurrent melanoma for the current performance period.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 | Increased procedural services | Use when work required is substantially greater than typically required (document rationale). |