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Comparable outcomes of patients eligible vs ineligible for SWOG leukemia studies.
Statler, Abby; Othus, Megan; Erba, Harry P; Chauncey, Thomas R; Radich, Jerald P; Coutre, Steven; Advani, Anjali; Nand, Sucha; Ravandi, Farhad; Mukherjee, Sudipto; Sekeres, Mikkael A.
Afiliação
  • Statler A; Leukemia Program, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
  • Othus M; Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Erba HP; SWOG Leukemia Committee, Portland, OR.
  • Chauncey TR; Division of Hematology and Oncology, University of Alabama, Birmingham, AL.
  • Radich JP; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Coutre S; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Advani A; Stanford Cancer Center, Stanford University School of Medicine, Stanford, CA.
  • Nand S; Leukemia Program, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
  • Ravandi F; Division of Hematology/Oncology, Department of Medicine, Loyola University Medical Center, Maywood, IL; and.
  • Mukherjee S; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Sekeres MA; Leukemia Program, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
Blood ; 131(25): 2782-2788, 2018 06 21.
Article em En | MEDLINE | ID: mdl-29618479
Patients may be deemed ineligible for a clinical trial for reasons that do not directly impact efficacy or safety. We identified reasons for ineligibility and compared outcomes of ineligible with eligible patients treated on Southwest Oncology Group (SWOG) Leukemia Committee protocols. Patients enrolled in SWOG phase 2, 2/3, or 3 protocols open since 2005 were analyzed for eligibility status, reasons for ineligibility, baseline characteristics, Eastern Cooperative Oncology Group (ECOG) performance status (PS), serious adverse events (SAEs), complete remission (CR) status, and overall survival. A total of 2361 patients were enrolled in the 13 included studies. Of these, 247 (10%) were deemed ineligible; 78 were excluded from analyses, and 169 were included. Of the 169 included in analyses, 60% (101/169) were excluded due to missing baseline documentation. Baseline characteristics comparing ineligible to eligible patients were similar, with the exception of ECOG PS for S0325 (P = .02) and S0530 (P = .002). In multivariable analyses, neither the proportion of patients with ECOG PS ≥ 2 (P = .12) nor the rate of grade 5 SAEs (P = .62) differed between groups. There was no difference in survival between eligible and ineligible patients (P = .25), and CR rates were similar, with the exception of S0325 (P < .001) and S0703 (P = .004). The findings of this study suggest that nonessential eligibility criteria can be less restrictive, thus expanding patient enrollment and avoiding protocol deviations. The clinical trials included in this study were registered at www.clincialtrials.gov as #NCT00085709, #NCT00066794, #NCT00070499, #NCT00109837, #NCT00093418, #NCT00492856, #NCT00337168, #NCT00352365, #NCT00658814, #NCT00792948, #NCT00945815, #NCT00840177, and #NCT01522976.
Assuntos

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Leucemia / Ensaios Clínicos Fase III como Assunto / Ensaios Clínicos Fase II como Assunto Tipo de estudo: Guideline / Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Leucemia / Ensaios Clínicos Fase III como Assunto / Ensaios Clínicos Fase II como Assunto Tipo de estudo: Guideline / Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article