Clinical Outcomes and Risk Stratification of Early-Stage Melanoma Micrometastases From an International Multicenter Study: Implications for the Management of American Joint Committee on Cancer IIIA Disease.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 12 2022
Historique:
pubmed: 19 7 2022
medline: 1 12 2022
entrez: 18 7 2022
Statut: ppublish

Résumé

Indications for offering adjuvant systemic therapy for patients with early-stage melanomas with low disease burden sentinel node (SN) micrometastases, namely, American Joint Committee on Cancer (AJCC; eighth edition) stage IIIA disease, are presently controversial. The current study sought to identify high-risk SN-positive AJCC stage IIIA patients who are more likely to derive benefit from adjuvant systemic therapy. Patients were recruited from an intercontinental (Australia/Europe/North America) consortium of nine high-volume cancer centers. All were adult patients with pathologic stage pT1b/pT2a primary cutaneous melanomas who underwent SN biopsy between 2005 and 2020. Patient data, primary tumor and SN characteristics, and survival outcomes were analyzed. Three thousand six hundred seven patients were included. The median follow-up was 34 months. Pairwise disease comparison demonstrated no significant survival difference between N1a and N2a subgroups. Survival analysis identified a SN tumor deposit maximum dimension of 0.3 mm as the optimal cut point for stratifying survival. Five-year disease-specific survival rates were 80.3% and 94.1% for patients with SN metastatic tumor deposits ≥ 0.3 mm and < 0.3 mm, respectively (hazard ratio, 1.26 [1.11 to 1.44]; Patients with AJCC IIIA melanoma with SN tumor deposits ≥ 0.3 mm in maximum dimension are at higher risk of disease progression and may benefit from adjuvant systemic therapy or enrollment into a clinical trial. Patients with SN deposits < 0.3 mm in maximum dimension can be managed similar to their SN-negative, AJCC IB counterparts, thereby avoiding regular radiological surveillance and more intensive follow-up.

Identifiants

pubmed: 35849790
doi: 10.1200/JCO.21.02488
doi:

Types de publication

Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3940-3951

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

Marc D Moncrieff (MD)

Norfolk and Norwich University Hospital NHS Trust, Norwich, United Kingdom.

Serigne N Lo (SN)

Melanoma Institute of Australia, The University of Sydney, Sydney, New South Wales, Australia.

Richard A Scolyer (RA)

Melanoma Institute of Australia, The University of Sydney, Sydney, New South Wales, Australia.
Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
NSW Health Pathology, Sydney, New South Wales, Australia.
Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.

Martin J Heaton (MJ)

Norfolk and Norwich University Hospital NHS Trust, Norwich, United Kingdom.

Jenny P Nobes (JP)

Norfolk and Norwich University Hospital NHS Trust, Norwich, United Kingdom.

Andrew P Snelling (AP)

Norfolk and Norwich University Hospital NHS Trust, Norwich, United Kingdom.

Michael J Carr (MJ)

H. Lee Moffitt Cancer Center, Tampa, FL.

Carolyn Nessim (C)

The Ottawa Hospital, University of Ottawa, Ottawa, Ontario, Canada.

Ryckie Wade (R)

Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.

A Howard Peach (AH)

Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.

Rumi Kisyova (R)

North Bristol Hospital NHS Trust, Bristol, United Kingdom.

Jennifer Mason (J)

North Bristol Hospital NHS Trust, Bristol, United Kingdom.

Ewan D Wilson (ED)

North Bristol Hospital NHS Trust, Bristol, United Kingdom.

Grant Nolan (G)

St Helens and Knowsley NHS Teaching Hospitals Trust, Liverpool, United Kingdom.

Rowan Pritchard Jones (R)

St Helens and Knowsley NHS Teaching Hospitals Trust, Liverpool, United Kingdom.

Iva Johansson (I)

Sahlgrenska Centre for Cancer Research, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Sahlgrenska University Hospital, Gothenburg, Sweden.

Roger Olofsson Bagge (R)

Sahlgrenska Centre for Cancer Research, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Sahlgrenska University Hospital, Gothenburg, Sweden.

Lucie J Wright (LJ)

United Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Nakul G Patel (NG)

United Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Vernon K Sondak (VK)

H. Lee Moffitt Cancer Center, Tampa, FL.

John F Thompson (JF)

Melanoma Institute of Australia, The University of Sydney, Sydney, New South Wales, Australia.
Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.

Jonathan S Zager (JS)

H. Lee Moffitt Cancer Center, Tampa, FL.

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Classifications MeSH