Skip to main navigation Skip to search Skip to main content

Ibrutinib added to 10-day decitabine for older patients with AML and higher risk MDS

  • Gerwin Huls*
  • , Dana A. Chitu
  • , Thomas Pabst
  • , Saskia K. Klein
  • , Georg Stussi
  • , Laimonas Griskevicius
  • , Peter J. M. Valk
  • , Jacqueline Cloos
  • , Arjan A. van de Loosdrecht
  • , Dimitri Breems
  • , Danielle van Lammeren-Venema
  • , Isabelle van Zeventer
  • , Rinske Boersma
  • , Mojca Jongen-Lavrencic
  • , Martin Fehr
  • , Mels Hoogendoorn
  • , Markus G. Manz
  • , Maaike Sohne
  • , Rien van Marwijk Kooy
  • , Dries Deeren
  • Marjolein W. M. van der Poel, Marie Cecile Legdeur, Lidwine Tick, Yves Chalandon, Emanuele Ammatuna, Sabine Blum, Bob Lowenberg, Gert J. Ossenkoppele, Dutch-Belgian Hemato-Oncology Cooperative Group (HOVON), Swiss Group for Clinical Cancer Research (SAKK)
*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

The treatment of older, unfit patients with acute myeloid leukemia (AML) is challenging. Based on preclinical data of Bruton tyrosine kinase expression/phosphorylation and ibrutinib cytotoxicity in AML blasts, we conducted a randomized phase 2 multicenter study to assess the tolerability and efficacy of the addition of ibrutinib to 10-day decitabine in unfit (ie, Hematopoietic Cell Transplantation Comorbidity Index >= 3) AML patients and higher risk myelodysplasia patients (HOVON135/SAKK30/15 trial). In total, 144 eligible patients were randomly (1:1) assigned to either 10-day decitabine combined with ibrutinib (560 mg; sequentially given, starting the day after the last dose of decitabine) (n = 72) or to 10-day decitabine (n = 72). The addition of ibrutinib was well tolerated, and the number of adverse events was comparable for both arms. In the decitabine plus ibrutinib arm, 41% reached complete remission/complete remission with incomplete hematologic recovery (CR/CRi), the median overall survival (OS) was 11 months, and 2-year OS was 27%; these findings compared with 50% CR/CRi, median OS of 11.5months, and 2-year OS of 21% for the decitabine group (not significant). Extensive molecular profiling at diagnosis revealed that patients with STAG2, IDH2, and ASXL1 mutations had significantly lower CR/CRi rates, whereas patients with mutations in TP53 had significantly higher CR/CRi rates. Furthermore, multicolor flow cytometry revealed that after 3 cycles of treatment, 28 (49%) of 57 patients with available bone marrow samples had no measurable residual disease. In this limited number of cases, measurable residual disease revealed no apparent impact on event-free survival and OS. In conclusion, the addition of ibrutinib does not improve the therapeutic efficacy of decitabine. This trial was registered at the Netherlands Trial Register (NL5751 [NTR6017]) and has EudraCT number 2015-002855-85.

Original languageEnglish
Pages (from-to)4267-4277
Number of pages11
JournalBlood advances
Volume4
Issue number18
DOIs
Publication statusPublished - 22 Sept 2020

Keywords

  • ACUTE MYELOID-LEUKEMIA
  • MINIMAL RESIDUAL DISEASE
  • HYPOMETHYLATING AGENT THERAPY
  • CONVENTIONAL CARE REGIMENS
  • MYELODYSPLASTIC SYNDROME
  • AZACITIDINE THERAPY
  • TREATMENT RESPONSE
  • CLINICAL-RESPONSE
  • SURVIVAL
  • TRIAL

Fingerprint

Dive into the research topics of 'Ibrutinib added to 10-day decitabine for older patients with AML and higher risk MDS'. Together they form a unique fingerprint.

Cite this