Tumor primary site as a prognostic factor for Merkel cell carcinoma disease-specific death.

Merkel cell carcinoma Merkel cell carcinoma survival tumor primary site tumor site unknown primary site

Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
11 2021
Historique:
received: 20 01 2021
revised: 12 06 2021
accepted: 20 06 2021
pubmed: 2 7 2021
medline: 5 3 2022
entrez: 1 7 2021
Statut: ppublish

Résumé

Merkel cell carcinoma (MCC) primary site has not been fully investigated as a potential prognostic factor. To determine the incidence by tumor primary site of death due to MCC. We undertook a retrospective analysis of the Survival, Epidemiology, and End Results database. MCC patients treated between 1973 and 2016 were grouped by tumor primary site and a competing risks analysis was performed to test the impact of primary site on disease-specific death. Cumulative incidence of Merkel cell carcinoma-specific mortality (CMMI) at 5 years was estimated for each primary site. Of 9407 MCC patients identified, 6305 (67.0%) had localized disease, 2397 (25.5%) had regional metastasis, and 705 (7.5%) had distant metastasis. Tumor primary site was predictive of CMMI and varied by stage at diagnosis. Tumors involving the scalp/neck carried the highest CMMI among localized MCC (26.0%). Tumors involving the lip had the highest CMMI among MCC with regional metastasis (56.7%) and distant metastasis (82.1%). Tumor size data were missing for a large proportion of patients, precluding stratification by stage according to current American Joint Committee on Cancer guidelines. Probability of MCC disease-specific death varies by primary site. The primary site of the tumor may be useful as a prognostic indicator for MCC.

Sections du résumé

BACKGROUND
Merkel cell carcinoma (MCC) primary site has not been fully investigated as a potential prognostic factor.
OBJECTIVE
To determine the incidence by tumor primary site of death due to MCC.
METHODS
We undertook a retrospective analysis of the Survival, Epidemiology, and End Results database. MCC patients treated between 1973 and 2016 were grouped by tumor primary site and a competing risks analysis was performed to test the impact of primary site on disease-specific death. Cumulative incidence of Merkel cell carcinoma-specific mortality (CMMI) at 5 years was estimated for each primary site.
RESULTS
Of 9407 MCC patients identified, 6305 (67.0%) had localized disease, 2397 (25.5%) had regional metastasis, and 705 (7.5%) had distant metastasis. Tumor primary site was predictive of CMMI and varied by stage at diagnosis. Tumors involving the scalp/neck carried the highest CMMI among localized MCC (26.0%). Tumors involving the lip had the highest CMMI among MCC with regional metastasis (56.7%) and distant metastasis (82.1%).
LIMITATIONS
Tumor size data were missing for a large proportion of patients, precluding stratification by stage according to current American Joint Committee on Cancer guidelines.
CONCLUSIONS
Probability of MCC disease-specific death varies by primary site. The primary site of the tumor may be useful as a prognostic indicator for MCC.

Identifiants

pubmed: 34197874
pii: S0190-9622(21)02009-0
doi: 10.1016/j.jaad.2021.06.863
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1259-1266

Informations de copyright

Copyright © 2021 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest None disclosed.

Auteurs

Christopher R Cullison (CR)

Department of Dermatology, Case Western Reserve University School of Medicine, Cleveland, Ohio. Electronic address: cxc886@case.edu.

David X Zheng (DX)

Department of Dermatology, Case Western Reserve University School of Medicine, Cleveland, Ohio.

Melissa A Levoska (MA)

Department of Dermatology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, Ohio.

Jeffrey F Scott (JF)

Department of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Jeremy S Bordeaux (JS)

Department of Dermatology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, Ohio.

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