Your browser doesn't support javascript.
loading
An 8-year pragmatic observation evaluation of the benefits of allogeneic HCT in older and medically infirm patients with AML.
Sorror, Mohamed L; Gooley, Ted A; Storer, Barry E; Gerds, Aaron T; Sekeres, Mikkael A; Medeiros, Bruno C; Wang, Eunice S; Shami, Paul J; Adekola, Kehinde; Luger, Selina; Baer, Maria R; Rizzieri, David A; Wildes, Tanya M; Koprivnikar, Jamie; Smith, Julie; Garrison, Mitchell; Kojouri, Kiarash; Schuler, Tammy A; Leisenring, Wendy M; Onstad, Lynn E; Becker, Pamela S; McCune, Jeannine S; Lee, Stephanie J; Sandmaier, Brenda M; Appelbaum, Frederick R; Estey, Elihu H.
Afiliação
  • Sorror ML; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Gooley TA; Division of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, WA.
  • Storer BE; Clinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Gerds AT; Department of Biostatistics, School of Public Health, University of Washington, Seattle, WA.
  • Sekeres MA; Clinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Medeiros BC; Department of Biostatistics, School of Public Health, University of Washington, Seattle, WA.
  • Wang ES; Leukemia & Myeloid Disorders Program, Cleveland Clinic, Cleveland, OH.
  • Shami PJ; Division of Hematology, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL.
  • Adekola K; Division of Hematology, Department of Medicine, Stanford University, Stanford, CA.
  • Luger S; Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Baer MR; Division of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
  • Rizzieri DA; Division of Hematology Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL.
  • Wildes TM; Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
  • Koprivnikar J; University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD.
  • Smith J; Division of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC.
  • Garrison M; Division of Hematology & Oncology, University of Nebraska Medical Center, Omaha NE.
  • Kojouri K; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ.
  • Schuler TA; Confluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA.
  • Leisenring WM; Confluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA.
  • Onstad LE; Skagit Valley Hospital, Mount Vernon, WA.
  • Becker PS; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • McCune JS; Clinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Lee SJ; Department of Biostatistics, School of Public Health, University of Washington, Seattle, WA.
  • Sandmaier BM; Clinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Appelbaum FR; Division of Hematology/Oncology, University of California, Irvine, Irvine, CA.
  • Estey EH; Department of Population Sciences, City of Hope, Duarte, CA.
Blood ; 141(3): 295-308, 2023 01 19.
Article em En | MEDLINE | ID: mdl-36260765
ABSTRACT
We designed a prospective, observational study enrolling patients presenting for treatment of acute myeloid leukemia (AML) at 13 institutions to analyze associations between hematopoietic cell transplantation (HCT) and survival, quality of life (QOL), and function in the entire cohort, those aged ≥65 years, those with high comorbidity burden, intermediate cytogenetic risk, adverse cytogenetic risk, and first complete remission with or without measurable residual disease. Patient were assessed 8 times over 2 years. Time-dependent regression models were used. Among 692 patients that were evaluable, 46% received HCT with a 2-year survival of 58%. In unadjusted models, HCT was associated with reduced risks of mortality most of the subgroups. However, after accounting for covariates associated with increased mortality (age, comorbidity burden, disease risks, frailty, impaired QOL, depression, and impaired function), the associations between HCT and longer survival disappeared in most subgroups. Although function, social life, performance status, and depressive symptoms were better for those selected for HCT, these health advantages were lost after receiving HCT. Recipients and nonrecipients of HCT similarly ranked and expected cure as main goal of therapy, whereas physicians had greater expectations for cure than the former. Accounting for health impairments negates survival benefits from HCT for AML, suggesting that the unadjusted observed benefit is mostly owing to selection of the healthier candidates. Considering patients' overall expectations of cure but also the QOL burdens of HCT motivate the need for randomized trials to identify the best candidates for HCT. This trial was registered at www.clinicaltrials.gov as #NCT01929408.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials / Observational_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Clinical_trials / Observational_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article