Final Version of 2009 AJCC Melanoma Staging and Classification

Author:

Balch Charles M.1,Gershenwald Jeffrey E.1,Soong Seng-jaw1,Thompson John F.1,Atkins Michael B.1,Byrd David R.1,Buzaid Antonio C.1,Cochran Alistair J.1,Coit Daniel G.1,Ding Shouluan1,Eggermont Alexander M.1,Flaherty Keith T.1,Gimotty Phyllis A.1,Kirkwood John M.1,McMasters Kelly M.1,Mihm Martin C.1,Morton Donald L.1,Ross Merrick I.1,Sober Arthur J.1,Sondak Vernon K.1

Affiliation:

1. From Johns Hopkins Medical Institutions, Baltimore, MD; The University of Texas M. D. Anderson Cancer Center, Houston, TX; University of Alabama at Birmingham, Birmingham, AL; Beth Israel Deaconess Medical Center; Massachusetts General Hospital, Harvard Medical School, Boston, MA; University of Washington, Seattle, WA; Hospital Sirio Libanes, Sao Paulo, Brazil; David Geffen School of Medicine at the University of California at Los Angeles, Los Angeles; John Wayne Cancer Institute at Saint John's Health...

Abstract

Purpose To revise the staging system for cutaneous melanoma on the basis of data from an expanded American Joint Committee on Cancer (AJCC) Melanoma Staging Database. Methods The melanoma staging recommendations were made on the basis of a multivariate analysis of 30,946 patients with stages I, II, and III melanoma and 7,972 patients with stage IV melanoma to revise and clarify TNM classifications and stage grouping criteria. Results Findings and new definitions include the following: (1) in patients with localized melanoma, tumor thickness, mitotic rate (histologically defined as mitoses/mm2), and ulceration were the most dominant prognostic factors. (2) Mitotic rate replaces level of invasion as a primary criterion for defining T1b melanomas. (3) Among the 3,307 patients with regional metastases, components that defined the N category were the number of metastatic nodes, tumor burden, and ulceration of the primary melanoma. (4) For staging purposes, all patients with microscopic nodal metastases, regardless of extent of tumor burden, are classified as stage III. Micrometastases detected by immunohistochemistry are specifically included. (5) On the basis of a multivariate analysis of patients with distant metastases, the two dominant components in defining the M category continue to be the site of distant metastases (nonvisceral v lung v all other visceral metastatic sites) and an elevated serum lactate dehydrogenase level. Conclusion Using an evidence-based approach, revisions to the AJCC melanoma staging system have been made that reflect our improved understanding of this disease. These revisions will be formally incorporated into the seventh edition (2009) of the AJCC Cancer Staging Manual and implemented by early 2010.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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