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Merkel cell carcinoma recurrence risk estimation is improved by integrating factors beyond cancer stage: A multivariable model and web-based calculator.
McEvoy, Aubriana M; Hippe, Daniel S; Lachance, Kristina; Park, Song; Cahill, Kelsey; Redman, Mary; Gooley, Ted; Kattan, Michael W; Nghiem, Paul.
Afiliação
  • McEvoy AM; Department of Dermatology, University of Washington, Seattle, Washington; Division of Dermatology, Department of Medicine, Washington University in St. Louis, St. Louis, Missouri.
  • Hippe DS; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
  • Lachance K; Department of Dermatology, University of Washington, Seattle, Washington.
  • Park S; Department of Dermatology, University of Washington, Seattle, Washington.
  • Cahill K; Department of Dermatology, University of Washington, Seattle, Washington.
  • Redman M; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
  • Gooley T; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
  • Kattan MW; Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.
  • Nghiem P; Department of Dermatology, University of Washington, Seattle, Washington; Fred Hutchinson Cancer Center, Seattle, Washington. Electronic address: pnghiem@uw.edu.
J Am Acad Dermatol ; 90(3): 569-576, 2024 Mar.
Article em En | MEDLINE | ID: mdl-37984720
ABSTRACT

BACKGROUND:

Merkel cell carcinoma (MCC) recurs in 40% of patients. In addition to stage, factors known to affect recurrence risk include sex, immunosuppression, unknown primary status, age, site of primary tumor, and time since diagnosis.

PURPOSE:

Create a multivariable model and web-based calculator to predict MCC recurrence risk more accurately than stage alone.

METHODS:

Data from 618 patients in a prospective cohort were used in a competing risk regression model to estimate recurrence risk using stage and other factors.

RESULTS:

In this multivariable model, the most impactful recurrence risk factors were American Joint Committee on Cancer stage (P < .001), immunosuppression (hazard ratio 2.05; P < .001), male sex (1.59; P = .003) and unknown primary (0.65; P = .064). Compared to stage alone, the model improved prognostic accuracy (concordance index for 2-year risk, 0.66 vs 0.70; P < .001), and modified estimated recurrence risk by up to 4-fold (18% for low-risk stage IIIA vs 78% for high-risk IIIA over 5 years).

LIMITATIONS:

Lack of an external data set for model validation. CONCLUSION/RELEVANCE As demonstrated by this multivariable model, accurate recurrence risk prediction requires integration of factors beyond stage. An online calculator based on this model (at merkelcell.org/recur) integrates time since diagnosis and provides new data for optimizing surveillance for MCC patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neoplasias Primárias Desconhecidas / Carcinoma de Célula de Merkel Limite: Humans / Male Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neoplasias Primárias Desconhecidas / Carcinoma de Célula de Merkel Limite: Humans / Male Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2024 Tipo de documento: Article