Measure ID: MIPS 397|Oncology|2026 Performance Year

Melanoma Reporting

Pathology reports for primary malignant cutaneous melanoma that include the pT category, thickness, ulceration and mitotic rate, peripheral and deep margin status and presence or absence of microsatellitosis for invasive tumors.

Process – High PriorityOncologyDermatology

Last updated: January 15, 2026

⚙️

Measure Specification

Denominator (Eligible Population)

Patients ≥ 18 years of age on date of service
ANDDiagnosis for malignant cutaneous melanoma
ANDPatient procedure during performance period

Denominator Exclusions1

G9430Specimen site other than anatomic cutaneous location

Numerator

Pathology reports for primary malignant cutaneous melanoma that include the pT category, thickness, ulceration and mitotic rate, peripheral and deep margin status and presence or absence of microsatellitosis for invasive tumors.

Submission Codes (QDCs)

✓ Performance Met
G9428Pathology report includes the pT Category, thickness, ulceration and mitotic rate, peripheral and deep margin status and presence or absence of microsatellitosis for invasive tumors
✗ Performance Not Met
G9431Pathology report does not include the pT Category, thickness, ulceration and mitotic rate, peripheral and deep margin status and presence or absence of microsatellitosis for invasive tumors

Denominator Exceptions

G9429Denominator Exception: Documentation of medical reason(s) for not including pT Category, thickness, ulceration and mitotic rate, peripheral and deep margin status and presence or absence of microsatellitosis for invasive tumors (e.g., negative skin biopsies, insufficient tissue, or other documented medical reasons)

🧮MIPS Score Simulator

Estimate only — actual CMS scoring may vary based on reporting method, data completeness, and annual rule updates.

%Benchmarks vary by collection type
💡 Tip: Enter your performance rate to compare MIPS points across all collection types. The same rate can score differently depending on how you submit.
VBCA Insights

💡Why This Measure Matters

Melanoma pathology reports should document tumor thickness (to 0.1 mm precision), ulceration, mitotic rate, and margin status—elements that determine stage and prognosis under current AJCC guidelines. These details guide whether patients need sentinel lymph node biopsy, adjuvant therapy, or surveillance intensity. Thorough reporting takes time but prevents understaging (missing adjuvant therapy that could improve survival) and overstaging (unnecessary aggressive treatment). Precision here directly impacts cancer outcomes.

📖Clinical Rationale

Research and the publication of new guidelines in 2017 indicate newer tumor characteristics for more precise staging, with implications for treatment outcomes. In 2017, the American Joint Committee on Cancer (AJCC) Melanoma Expert Panel introduced several important changes to the Tumor, Nodes, Metastasis (TNM) classification. The relevant change for this measure in the eighth edition AJCC Cancer Staging Manual include: 1) tumor thickness measurements to be recorded to the nearest 0.

1 mm, not 0.01 mm; 2) definitions of T1a and T1b are revised (T1a, <0.8 mm without ulceration; T1b, 0.8-1.0 mm with or without ulceration or <0.8 mm with ulceration), with mitotic rate no longer a T category criterion. (Gershenwald et al.) The new guidelines state: “As supported by this univariate analysis and previous reports, the mitotic rate is likely an important prognostic determinant when evaluated using its dynamic range across melanomas of all tumor thickness categories.

Therefore, the AJCC Melanoma Expert Panel strongly recommends that mitotic rate be assessed and recorded for all primary melanomas, although it is not used for T1 staging in the eighth edition. The mitotic rate will likely be an important parameter for inclusion in the future development of prognostic models applicable to individual patients.” (http://onlinelibrary.

wiley.com/doi/10.3322/caac.21409/pdf ) The American Academy of Dermatology updated guidelines for management of primary cutaneous melanoma. In addition to re-affirming the importance of thickness, ulceration and mitotic rate (“There is strong evidence that at least 3 histologic features of the primary tumor are dominant predictors of outcome: Breslow thickness, ulceration, and dermal mitotic rate”), these guidelines also emphasized the importance of other elements include peripheral and deep margin status, microsatellitosis and lymphovascular invasion (Swetter et al).

For margin status, the guidelines note that “An additional essential element of the pathology report is the status of the peripheral and deep margins (positive or negative) of the specimen. Presence or absence of tumor at the surgical margin indicates whether the entire lesion was available for histologic evaluation and provides guidance for further management.

” Microsatellites, or tumors nests in the vicinity of the main invasive tumor, are an important component of the eighth edition of the AJCC staging system and per the AAD guideline “the presence or absence of microscopic satellites must be reported for accurate staging.

📝Clinical Recommendations

There is strong evidence that at least 3 histologic features of the primary tumor are dominant predictors of outcome: Breslow thickness, ulceration, and dermal mitotic rate. An additional essential element of the pathology report is the status of the peripheral and deep margins (positive or negative) of the specimen. Depending on the specific T- and N-category criteria, such patients would be staged as either stage IIIC or IIID.

Therefore, the presence or absence of microscopic satellites must be reported for accurate staging.

📋Implementation Notes

This measure contains one strata defined by a single submission criteria. This measure produces a single performance rate. For purposes of MIPS implementation, this procedure measure is submitted each time a procedure is performed during the performance period. Only one quality data code (QDC) per date of service for a patient is required. In instances where multiple specimens from different/unique lesions are submitted and resulted in a single report, each eligible specimen must be Met in order for the case to be considered Met (Denominator Exclusions and Denominator Exceptions are not considered eligible specimens).

If any eligible specimen is Not Met, the quality data code for Not Met should be submitted for this report.

Report this measure through VBCA

Our QCDR handles measure selection, data validation, and submission—so you can focus on clinical performance.

Learn About Our QCDR →
© 2025 College of American Pathologists. All Rights Reserved