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Development and testing of a lymphoma clinical trial-specific frailty index: a secondary analysis of the NCIC-CTG LY.12 clinical trial.
Vijenthira, Abi; Li, Xinzhi; Crump, Michael; Hay, Annette E; Shepherd, Lois; Meyer, Ralph M; Djurfeldt, Marina; Chen, Bingshu E; Prica, Anca.
Afiliação
  • Vijenthira A; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, USA.
  • Li X; School of Pharmacy, Macau University of Science and Technology, Macau, China.
  • Crump M; Canadian Cancer Trials Group, Cancer Research Institute, Kingston, ON, USA.
  • Hay AE; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, USA.
  • Shepherd L; Canadian Cancer Trials Group, Cancer Research Institute, Kingston, ON, USA.
  • Meyer RM; Department of Medicine, Queen's University, Kingston, Canada.
  • Djurfeldt M; Canadian Cancer Trials Group, Cancer Research Institute, Kingston, ON, USA.
  • Chen BE; Department of Pathology and Molecular Medicine, Kingston, Canada.
  • Prica A; Department of Oncology, Juravinski Hospital and Cancer Centre, Queen's University, Hamilton, Canada.
Leuk Lymphoma ; : 1-8, 2024 Jul 09.
Article em En | MEDLINE | ID: mdl-38982633
ABSTRACT
The prevalence of frailty in clinical trials of lymphoma is unknown. We conducted a secondary analysis of the phase III LY.12 trial in which patients with relapsed aggressive non-Hodgkin lymphoma were randomized to different salvage regimens before autologous stem cell transplant. The primary objective was to construct a lymphoma clinical trials-specific frailty index (LyFI) using previously described methods. The secondary objective was to describe the association of frailty withover all and event-free survival (OS, EFS). The LyFI was constructed using 619 patients, and11% (N = 70) were classified as frail. Frailty was associated with EFS (HR 1.94, 95%CI 1.53-2.46) and OS (HR 2.01, 95%CI 1.57-2.58) in univariable analysis, but was only significant as a continuous (not binary) variable in multivariable analysis controlling for prognostic score, suggesting limitations of a FI in this trial population. Future work could validate the FI using clinical assessments and/or apply it to an older trial population.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Leuk Lymphoma Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Leuk Lymphoma Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos