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Development and validation of time-to-event models to predict metastatic recurrence of localized cutaneous melanoma.
Wan, Guihong; Leung, Bonnie W; DeSimone, Mia S; Nguyen, Nga; Rajeh, Ahmad; Collier, Michael R; Rashdan, Hannah; Roster, Katie; Zhou, Xu; Moseley, Cameron B; Nirmal, Ajit J; Pelletier, Roxanne J; Maliga, Zoltan; Marko-Varga, Gyorgy; Németh, István Balázs; Tsao, Hensin; Asgari, Maryam M; Gusev, Alexander; Stagner, Anna M; Lian, Christine G; Hurlbert, Marc S; Liu, Feng; Yu, Kun-Hsing; Sorger, Peter K; Semenov, Yevgeniy R.
Afiliação
  • Wan G; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Systems Biology, Harvard Medical School, Boston, Massachusetts; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts.
  • Leung BW; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • DeSimone MS; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Nguyen N; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Rajeh A; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Collier MR; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Rashdan H; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Roster K; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Zhou X; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; School of Systems and Enterprises, Stevens Institute of Technology, Hoboken, New Jersey.
  • Moseley CB; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Nirmal AJ; Department of Systems Biology, Harvard Medical School, Boston, Massachusetts.
  • Pelletier RJ; Department of Systems Biology, Harvard Medical School, Boston, Massachusetts.
  • Maliga Z; Department of Systems Biology, Harvard Medical School, Boston, Massachusetts.
  • Marko-Varga G; Department of Translational Medicine, Lund University, Lund, Sweden.
  • Németh IB; Department of Dermatology and Allergology, University of Szeged, Szeged, Hungary.
  • Tsao H; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Asgari MM; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Population Medicine, Harvard Pilgrim Healthcare, Boston, Massachusetts.
  • Gusev A; Department of Medicine, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Stagner AM; Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Lian CG; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Hurlbert MS; Melanoma Research Alliance, Washington, District of Columbia.
  • Liu F; School of Systems and Enterprises, Stevens Institute of Technology, Hoboken, New Jersey.
  • Yu KH; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Sorger PK; Department of Systems Biology, Harvard Medical School, Boston, Massachusetts.
  • Semenov YR; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Systems Biology, Harvard Medical School, Boston, Massachusetts. Electronic address: ysemenov@mgh.harvard.edu.
J Am Acad Dermatol ; 90(2): 288-298, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37797836
ABSTRACT

BACKGROUND:

The recent expansion of immunotherapy for stage IIB/IIC melanoma highlights a growing clinical need to identify patients at high risk of metastatic recurrence and, therefore, most likely to benefit from this therapeutic modality.

OBJECTIVE:

To develop time-to-event risk prediction models for melanoma metastatic recurrence.

METHODS:

Patients diagnosed with stage I/II primary cutaneous melanoma between 2000 and 2020 at Mass General Brigham and Dana-Farber Cancer Institute were included. Melanoma recurrence date and type were determined by chart review. Thirty clinicopathologic factors were extracted from electronic health records. Three types of time-to-event machine-learning models were evaluated internally and externally in the distant versus locoregional/nonrecurrence prediction.

RESULTS:

This study included 954 melanomas (155 distant, 163 locoregional, and 636 12 matched nonrecurrences). Distant recurrences were associated with worse survival compared to locoregional/nonrecurrences (HR 6.21, P < .001) and to locoregional recurrences only (HR 5.79, P < .001). The Gradient Boosting Survival model achieved the best performance (concordance index 0.816; time-dependent AUC 0.842; Brier score 0.103) in the external validation.

LIMITATIONS:

Retrospective nature and cohort from one geography.

CONCLUSIONS:

These results suggest that time-to-event machine-learning models can reliably predict the metastatic recurrence from localized melanoma and help identify high-risk patients who are most likely to benefit from immunotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans 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 / Melanoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2024 Tipo de documento: Article