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


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
22 09 2020
Historique:
received: 02 07 2020
accepted: 17 07 2020
entrez: 11 9 2020
pubmed: 12 9 2020
medline: 15 5 2021
Statut: ppublish

Résumé

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 11.5 months, 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.

Identifiants

pubmed: 32915972
pii: S2473-9529(20)31507-X
doi: 10.1182/bloodadvances.2020002846
pmc: PMC7509861
doi:

Substances chimiques

Piperidines 0
ibrutinib 1X70OSD4VX
Decitabine 776B62CQ27
Adenine JAC85A2161

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4267-4277

Informations de copyright

© 2020 by The American Society of Hematology.

Références

Cell Rep. 2017 Jul 18;20(3):572-585
pubmed: 28723562
Blood. 2009 Apr 30;113(18):4179-87
pubmed: 19008455
Blood Adv. 2018 Dec 26;2(24):3608-3617
pubmed: 30567725
J Clin Oncol. 2010 Feb 1;28(4):562-9
pubmed: 20026804
Br J Haematol. 2022 Aug;198(3):535-544
pubmed: 35438802
J Clin Oncol. 2013 Nov 1;31(31):3889-97
pubmed: 24062400
Blood. 2015 Jul 16;126(3):291-9
pubmed: 25987659
J Clin Oncol. 2012 Jul 20;30(21):2670-7
pubmed: 22689805
Leuk Lymphoma. 2014 Jul;55(7):1533-7
pubmed: 24144313
Leuk Lymphoma. 2013 Nov;54(11):2385-91
pubmed: 23425038
N Engl J Med. 2018 Mar 29;378(13):1189-1199
pubmed: 29601269
N Engl J Med. 2009 Sep 24;361(13):1235-48
pubmed: 19776405
Proc Natl Acad Sci U S A. 2010 Apr 20;107(16):7473-8
pubmed: 20368434
Leukemia. 2017 Apr;31(4):872-881
pubmed: 27740633
N Engl J Med. 2004 Apr 15;350(16):1617-28
pubmed: 15084694
Oncotarget. 2014 Oct 30;5(20):9930-8
pubmed: 25294819
N Engl J Med. 2016 Nov 24;375(21):2023-2036
pubmed: 27959731
Blood. 2015 Jan 29;125(5):767-74
pubmed: 25515963
Leukemia. 2018 Jan;32(1):241-244
pubmed: 28919634
J Clin Oncol. 2014 Apr 20;32(12):1242-8
pubmed: 24663049
Leuk Lymphoma. 2013 Sep;54(9):2003-7
pubmed: 23270581
Cancer. 2017 May 15;123(6):994-1002
pubmed: 28094841
J Clin Oncol. 2017 Aug 20;35(24):2745-2753
pubmed: 28486043
Leukemia. 2019 Jan;33(1):75-87
pubmed: 29977015
Blood. 2019 Jan 3;133(1):7-17
pubmed: 30361262
Br J Haematol. 2007 Feb;136(4):624-7
pubmed: 17223919
Am J Hematol. 2015 May;90(5):E77-9
pubmed: 25651001
J Clin Oncol. 2013 Nov 10;31(32):4123-31
pubmed: 24062403
Haematologica. 2016 Nov;101(11):e457-e460
pubmed: 27418649
Blood. 2017 Jan 26;129(4):424-447
pubmed: 27895058
Leukemia. 2014 Jan;28(1):78-87
pubmed: 24045501
Br J Haematol. 2017 Sep;178(5):810-812
pubmed: 27431572
Clin Lymphoma Myeloma Leuk. 2019 Aug;19(8):509-515.e1
pubmed: 31227358
Blood. 2014 Feb 20;123(8):1229-38
pubmed: 24307721
Sci Rep. 2015 Aug 21;5:12949
pubmed: 26292723
N Engl J Med. 2020 Aug 13;383(7):617-629
pubmed: 32786187
Clin Cancer Res. 2017 Nov 1;23(21):6430-6440
pubmed: 28765326
N Engl J Med. 2017 Aug 3;377(5):454-464
pubmed: 28644114
Cancer. 2015 Feb 15;121(4):556-61
pubmed: 25336333
Blood. 2018 Mar 22;131(12):1275-1291
pubmed: 29330221

Auteurs

Gerwin Huls (G)

Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands.

Dana A Chitu (DA)

Department of Hematology, HOVON Data Center, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Thomas Pabst (T)

Department of Oncology, University Hospital, Inselspital, and University of Bern, Bern, Switzerland.

Saskia K Klein (SK)

Department of Hematology, Meander Hospital Amersfoort, Amersfoort, The Netherlands.

Georg Stussi (G)

Department of Hematology, Ospedale Regionale, Bellinzona, Switzerland.

Laimonas Griskevicius (L)

Hematology, Oncology and Transfusion Medicine Center, Vilnius University Hospital Santaros Klinikos, Vilnius University, Vilnius, Lithuania.

Peter J M Valk (PJM)

Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Jacqueline Cloos (J)

Department of Hematology, Amsterdam UMC, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Arjan A van de Loosdrecht (AA)

Department of Hematology, Amsterdam UMC, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Dimitri Breems (D)

Department of Hematology, ZNA Stuivenberg/Middelheim, Antwerp, Belgium.

Danielle van Lammeren-Venema (D)

Department of Hematology, Hagaziekenhuis, Den Haag, The Netherlands.

Isabelle van Zeventer (I)

Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands.

Rinske Boersma (R)

Department of Hematology, Amphia Hospital, Breda, The Netherlands.

Mojca Jongen-Lavrencic (M)

Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Martin Fehr (M)

Department of Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Mels Hoogendoorn (M)

Department of Hematology, Medical Center Leeuwarden, Leeuwarden, The Netherlands.

Markus G Manz (MG)

Department of Medical Oncology and Hematology, Universitätsspital Zurich, Zurich, Switzerland.

Maaike Söhne (M)

Department of Hematology, Antonius Hospital, Nieuwegein, The Netherlands.

Rien van Marwijk Kooy (R)

Department of Hematology, Isala Hospital, Zwolle, The Netherlands.

Dries Deeren (D)

Department of Hematology, AZ Delta Roeselare, Roeselare, Belgium.

Marjolein W M van der Poel (MWM)

Department of Hematology, Maastricht University Medical Center, Maastricht, The Netherlands.

Marie Cecile Legdeur (MC)

Department of Hematology, Medical Spectrum Twente, Enschede, The Netherlands.

Lidwine Tick (L)

Department of Hematology, Maxima Medical Center, Veldhoven, The Netherlands.

Yves Chalandon (Y)

Division of Hematology, University Hospital Genève and Faculty of Medicine, University of Genève, Genève, Switzerland; and.

Emanuele Ammatuna (E)

Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands.

Sabine Blum (S)

Service and Central Laboratory of Hematology, Department of Oncology and Department of Laboratory Medicine and Pathology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.

Bob Löwenberg (B)

Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Gert J Ossenkoppele (GJ)

Department of Hematology, Amsterdam UMC, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands.

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