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Cutaneous immune-related adverse events are associated with longer overall survival in advanced cancer patients on immune checkpoint inhibitors: A multi-institutional cohort study.
Zhang, Shijia; Tang, Kimberly; Wan, Guihong; Nguyen, Nga; Lu, Chenyue; Ugwu-Dike, Pearl; Raval, Neel; Seo, Jayhyun; Alexander, Nora A; Jairath, Ruple; Phillipps, Jordan; Leung, Bonnie W; Roster, Kathleen; Chen, Wenxin; Zubiri, Leyre; Boland, Genevieve; Chen, Steven T; Tsao, Hensin; Demehri, Shadmehr; LeBoeuf, Nicole R; Reynolds, Kerry L; Yu, Kun-Hsing; Gusev, Alexander; Kwatra, Shawn G; Semenov, Yevgeniy R.
Afiliación
  • Zhang S; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts.
  • Tang K; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Wan G; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts.
  • Nguyen N; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Lu C; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts.
  • Ugwu-Dike P; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Raval N; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Seo J; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Alexander NA; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Jairath R; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Phillipps J; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Leung BW; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Roster K; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Chen W; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts.
  • Zubiri L; Division of Oncology and Hematology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Boland G; Department of Surgery, Massachusetts General Hospital, Boston, Massachusetts.
  • Chen ST; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Tsao H; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Demehri S; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; Department of Dermatology, Center for Cancer Immunology and Cutaneous Biology Research Center, Center for Cancer Research, Massachusetts General Hospital Cancer Center, Massachusetts General Hos
  • LeBoeuf NR; Department of Dermatology, Center for Cutaneous Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Reynolds KL; Division of Oncology and Hematology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
  • Yu KH; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts.
  • Gusev A; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Kwatra SG; Department of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Semenov YR; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts. Electronic address: ysemenov@mgh.harvard.edu.
J Am Acad Dermatol ; 88(5): 1024-1032, 2023 05.
Article en En | MEDLINE | ID: mdl-36736626
ABSTRACT

BACKGROUND:

Cutaneous immune-related adverse events (cirAEs) occur in up to 40% of immune checkpoint inhibitor (ICI) recipients. However, the association of cirAEs with survival remains unclear.

OBJECTIVE:

To investigate the association of cirAEs with survival among ICI recipients.

METHODS:

ICI recipients were identified from the Mass General Brigham healthcare system and Dana-Farber Cancer Institute. Patient charts were reviewed for cirAE development within 2 years after ICI initiation. Multivariate time-varying Cox proportional hazards models, adjusted for age, sex, race/ethnicity, Charlson Comorbidity Index, ICI type, cancer type, and year of ICI initiation were utilized to investigate the impact of cirAE development on overall survival.

RESULTS:

Of the 3731 ICI recipients, 18.1% developed a cirAE. Six-month landmark analysis and time-varying Cox proportional hazards models demonstrated that patients who developed cirAEs were associated with decreased mortality (hazardratio [HR] = 0.87, P = .027), particularly in patients with melanoma (HR = 0.67, P = .003). Among individual morphologies, lichenoid eruption (HR = 0.51, P < .001), psoriasiform eruption (HR = 0.52, P = .005), vitiligo (HR = 0.29, P = .007), isolated pruritus without visible manifestation of rash (HR = 0.71, P = .007), acneiform eruption (HR = 0.34, P = .025), and non-specific rash (HR = 0.68, P < .001) were significantly associated with better survival after multiple comparisons adjustment.

LIMITATIONS:

Retrospective design; single geography.

CONCLUSION:

CirAE development is associated with improved survival among ICI recipients, especially patients with melanoma.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Exantema / Melanoma Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Am Acad Dermatol Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Exantema / Melanoma Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Am Acad Dermatol Año: 2023 Tipo del documento: Article