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Survival outcomes in patients with acute myeloid leukaemia who received subsequent therapy for relapse in QUAZAR AML-001.
Ravandi, Farhad; Döhner, Hartmut; Wei, Andrew H; Montesinos, Pau; Pfeilstöcker, Michael; Papayannidis, Cristina; Lai, Yinzhi; Wang, Kefeng; See, Wendy L; de Menezes, Daniel Lopes; Petrlik, Erica; Prebet, Thomas; Roboz, Gail J.
Afiliação
  • Ravandi F; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Döhner H; Ulm University Hospital, Ulm, Germany.
  • Wei AH; Peter MacCallum Cancer Centre, Melbourne, Australia.
  • Montesinos P; The Royal Melbourne Hospital, Melbourne, Australia.
  • Pfeilstöcker M; Hematology Department, Hospital Universitari i Politècnic, La Fe, València, Spain.
  • Papayannidis C; CIBERONC, Instituto Carlos III, Madrid, Spain.
  • Lai Y; Third Medical Department for Hematology and Oncology, Hanusch Hospital, Vienna, Austria.
  • Wang K; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
  • See WL; IRCCS, Azienda Ospedaliero Universitaria di Bologna, Istituto di Ematologia "L. e A. Seràgnoli", Bologna, Italy.
  • de Menezes DL; Bristol Myers Squibb, Princeton, New Jersey, USA.
  • Petrlik E; Bristol Myers Squibb, Princeton, New Jersey, USA.
  • Prebet T; Bristol Myers Squibb, San Francisco, California, USA.
  • Roboz GJ; Bristol Myers Squibb, San Francisco, California, USA.
Br J Haematol ; 204(3): 877-886, 2024 Mar.
Article em En | MEDLINE | ID: mdl-37952982
ABSTRACT
In the phase 3 QUAZAR AML-001 trial (NCT01757535) of patients with acute myeloid leukaemia (AML) in remission following intensive chemotherapy (IC) and ineligible for haematopoietic stem cell transplant (HSCT), oral azacitidine (Oral-AZA) maintenance significantly prolonged overall survival (OS) versus placebo. The impact of subsequent treatment following maintenance has not been evaluated. In this post hoc analysis, OS was estimated for patients who received subsequent AML therapy, and by regimen received (IC or lower-intensity therapy). First subsequent therapy (FST) was administered after treatment discontinuation in 134/238 Oral-AZA and 173/234 placebo patients. OS from randomization in patients who received FST after Oral-AZA versus placebo was 17.8 versus 12.9 months (HR 0.82 [95% CI 0.64-1.04], median follow-up 56.7 months); OS from FST was similar between arms. Among patients who received injectable hypomethylating agents as FST, median OS was 8.2 versus 4.9 months in the Oral-AZA versus placebo groups (HR 0.66 [95% CI 0.41-1.06]). Forty-eight patients (16/238 Oral-AZA, 32/234 placebo) received HSCT following treatment discontinuation, including six Oral-AZA patients still in first remission; Oral-AZA OS benefit persisted when censoring these patients. Oral-AZA maintenance can prolong AML remission duration without negatively impacting survival outcomes after salvage therapies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Azacitidina / Leucemia Mieloide Aguda Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Azacitidina / Leucemia Mieloide Aguda Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article