Summary & Overview
HCPCS Level II M1386: Excisional Surgery Cohort for Melanoma Stages 0–II
HCPCS Level II code M1386 designates patients who underwent excisional surgery for melanoma or melanoma in situ within the prior five years and who began the performance period with an AJCC stage of 0, I, or II. The code matters nationally as a way to identify a surgical melanoma cohort for quality measurement, surveillance programs, and performance reporting across payers. Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare.
Readers will learn the clinical context for the code, expected sites of service, and the kinds of benchmarks and policy-related details typically associated with cohort-based HCPCS reporting. The publication outlines how M1386 is used to define eligible patient populations for follow-up or quality measurement, summarizes common modifiers and billing considerations provided in the input, and notes where input data are not available. This content is written for a national audience seeking concise guidance on the clinical scope and administrative use of HCPCS Level II code M1386.
Billing Code Overview
HCPCS Level II code M1386 applies to patients who have undergone an excisional surgery for melanoma or melanoma in situ within the past five years and who had an initial AJCC staging of 0, I, or II at the start of the performance period. This code identifies a defined cohort of melanoma surgical patients for programmatic tracking or quality measurement.
-
Service type: Surgical follow-up and post-excision surveillance cohort identification
-
Typical site of service: Outpatient surgical clinics, dermatologic surgery centers, and ambulatory oncology or dermatology follow-up settings
Clinical & Coding Specifications
Clinical Context
A typical patient is a middle-aged adult who underwent an excisional surgery for cutaneous melanoma or melanoma in situ within the past five years and had an initial American Joint Committee on Cancer (AJCC) stage of 0, I, or II at the start of the performance period. The clinical workflow begins with a dermatology or surgical oncology evaluation for a suspicious pigmented lesion, biopsy confirming melanoma or melanoma in situ, and a definitive excisional procedure with clear margins. Postoperative pathology establishes tumor thickness (Breslow depth), ulceration status, and margin status to confirm AJCC stage 0–II.
Following excision, the patient enters a surveillance and care management period that may include wound care visits, scar management, periodic dermatologic skin checks, education on self-skin exams and sun protection, and documentation of absence of recurrence. Encounters occur in outpatient dermatology or surgical oncology clinics, with possible involvement of primary care for coordination. Imaging and sentinel lymph node biopsy may have been performed during the original treatment episode if clinically indicated for stage II; ongoing visits focus on surveillance for local recurrence, new primary melanomas, and management of surgical sequelae over the five-year performance window.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 | Increased procedural services | When work, time, or complexity substantially exceeds usual for excisional surgery or related visits. |