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Immunotherapy utilization in stage IIIA melanoma: less may be more.
Frey, Alexander E; Kerekes, Daniel M; Khan, Sajid A; Tran, Thuy T; Kluger, Harriet M; Clune, James E; Ariyan, Stephan; Sznol, Mario; Ishizuka, Jeffrey J; Olino, Kelly L.
Afiliação
  • Frey AE; Department of Surgery, Yale University School of Medicine, New Haven, CT, United States.
  • Kerekes DM; Department of Surgery, Yale University School of Medicine, New Haven, CT, United States.
  • Khan SA; Department of Surgery, Yale University School of Medicine, New Haven, CT, United States.
  • Tran TT; Department of Medicine (Medical Oncology), Yale University School of Medicine, New Haven, CT, United States.
  • Kluger HM; Department of Medicine (Medical Oncology), Yale University School of Medicine, New Haven, CT, United States.
  • Clune JE; Department of Surgery, Yale University School of Medicine, New Haven, CT, United States.
  • Ariyan S; Department of Surgery, Yale University School of Medicine, New Haven, CT, United States.
  • Sznol M; Department of Medicine (Medical Oncology), Yale University School of Medicine, New Haven, CT, United States.
  • Ishizuka JJ; Department of Medicine (Medical Oncology), Yale University School of Medicine, New Haven, CT, United States.
  • Olino KL; Department of Surgery, Yale University School of Medicine, New Haven, CT, United States.
Front Oncol ; 14: 1336441, 2024.
Article em En | MEDLINE | ID: mdl-38380358
ABSTRACT

Background:

Immunotherapy agents are approved for adjuvant treatment of stage III melanoma; however, evidence for survival benefit in early stage III disease is lacking. Current guidelines for adjuvant immunotherapy utilization in stage IIIA rely on clinician judgment, creating an opportunity for significant variation in prescribing patterns. This study aimed to characterize current immunotherapy practice variations and to compare patient outcomes for different prescribing practices in stage IIIA melanoma. Study

design:

Patients with melanoma diagnosed from 2015-2019 that met American Joint Committee on Cancer 8th edition criteria for stage IIIA and underwent resection were identified in the National Cancer Database. Multiple imputation by chained equations replaced missing values. Factors associated with receipt of adjuvant immunotherapy were identified. Multivariable Cox proportional hazards regression compared overall survival across groups.

Results:

Of 4,432 patients included in the study, 34% received adjuvant immunotherapy. Patients had lower risk-adjusted odds of receiving immunotherapy if they were treated at an academic center (OR=0.48, 95%CI=0.33-0.72, p<0.001 vs. community facility) or at a high-volume center (OR=0.69, 0.56-0.84, p<0.001 vs. low-volume). Immunotherapy receipt was not associated with risk-adjusted survival (p=0.095). Moreover, patients treated at high-volume centers experienced longer overall risk-adjusted survival than those treated at low-volume centers (HR=0.52, 0.29-0.93, p=0.030). Risk-adjusted survival trended toward being longer at academic centers than at community centers, but the difference was not statistically significant.

Conclusion:

Academic and high-volume centers utilize significantly less adjuvant immunotherapy in stage IIIA melanoma than community and low-volume centers without compromise in overall survival. These findings suggest that this population may benefit from more judicious immunotherapy utilization.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos
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