Venetoclax plus low-dose cytarabine in Japanese patients with untreated acute myeloid leukaemia ineligible for intensive chemotherapy.


Journal

Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225

Informations de publication

Date de publication:
30 Aug 2021
Historique:
received: 13 05 2021
accepted: 26 06 2021
pubmed: 30 7 2021
medline: 25 11 2021
entrez: 29 7 2021
Statut: ppublish

Résumé

In a multinational phase 3 trial (VIALE-C), venetoclax plus low-dose cytarabine prolonged overall survival vs placebo plus low-dose cytarabine in patients with newly diagnosed acute myeloid leukaemia ineligible for intensive chemotherapy, although it was not statistically significant. Herein, we assess the benefit of venetoclax plus low-dose cytarabine in the Japanese subgroup of VIALE-C patients (n = 27). VIALE-C, a randomized (2:1), double-blind study (NCT03069352), enrolled untreated patients (≥18 years) with acute myeloid leukaemia. Patients received venetoclax (600 mg days 1-28, 4-day ramp-up in cycle 1) or placebo in 28-day cycles with low-dose cytarabine (20 mg/m2 days 1-10). The primary endpoint was median overall survival. In the Japanese subgroup, at a 6-month follow-up from the primary analysis, median overall survival for venetoclax (n = 18) and placebo (n = 9), plus low-dose cytarabine, was 4.7 and 8.1 months, respectively (hazard ratio, 0.928, 95% confidence intervals : 0.399, 2.156). The rate of complete remission plus complete remission with incomplete blood count recovery was higher with venetoclax plus low-dose cytarabine (44.4%) vs placebo plus low-dose cytarabine (11.1%). All patients experienced at least 1 adverse event. The most common grade ≥3 adverse events with venetoclax or placebo, plus low-dose cytarabine, were febrile neutropenia (50.0% vs 44.4%, respectively) and thrombocytopenia (27.8% vs 44.4%, respectively). Serious adverse events were reported in 50.0 and 33.3% of patients in the venetoclax and placebo, plus low-dose cytarabine arms, respectively; pneumonia was the most common (22.2% each). Limited survival benefit in the Japanese subgroup can be attributed to small patient numbers and to baseline imbalances observed between treatment arms, with more patients in the venetoclax plus low-dose cytarabine arm presenting poor prognostic factors. Venetoclax plus low-dose cytarabine was well tolerated in Japanese patients with acute myeloid leukaemia ineligible for intensive chemotherapy.

Sections du résumé

BACKGROUND BACKGROUND
In a multinational phase 3 trial (VIALE-C), venetoclax plus low-dose cytarabine prolonged overall survival vs placebo plus low-dose cytarabine in patients with newly diagnosed acute myeloid leukaemia ineligible for intensive chemotherapy, although it was not statistically significant. Herein, we assess the benefit of venetoclax plus low-dose cytarabine in the Japanese subgroup of VIALE-C patients (n = 27).
METHODS METHODS
VIALE-C, a randomized (2:1), double-blind study (NCT03069352), enrolled untreated patients (≥18 years) with acute myeloid leukaemia. Patients received venetoclax (600 mg days 1-28, 4-day ramp-up in cycle 1) or placebo in 28-day cycles with low-dose cytarabine (20 mg/m2 days 1-10). The primary endpoint was median overall survival.
RESULTS RESULTS
In the Japanese subgroup, at a 6-month follow-up from the primary analysis, median overall survival for venetoclax (n = 18) and placebo (n = 9), plus low-dose cytarabine, was 4.7 and 8.1 months, respectively (hazard ratio, 0.928, 95% confidence intervals : 0.399, 2.156). The rate of complete remission plus complete remission with incomplete blood count recovery was higher with venetoclax plus low-dose cytarabine (44.4%) vs placebo plus low-dose cytarabine (11.1%). All patients experienced at least 1 adverse event. The most common grade ≥3 adverse events with venetoclax or placebo, plus low-dose cytarabine, were febrile neutropenia (50.0% vs 44.4%, respectively) and thrombocytopenia (27.8% vs 44.4%, respectively). Serious adverse events were reported in 50.0 and 33.3% of patients in the venetoclax and placebo, plus low-dose cytarabine arms, respectively; pneumonia was the most common (22.2% each).
CONCLUSIONS CONCLUSIONS
Limited survival benefit in the Japanese subgroup can be attributed to small patient numbers and to baseline imbalances observed between treatment arms, with more patients in the venetoclax plus low-dose cytarabine arm presenting poor prognostic factors. Venetoclax plus low-dose cytarabine was well tolerated in Japanese patients with acute myeloid leukaemia ineligible for intensive chemotherapy.

Identifiants

pubmed: 34322703
pii: 6329815
doi: 10.1093/jjco/hyab112
pmc: PMC8405845
doi:

Substances chimiques

Bridged Bicyclo Compounds, Heterocyclic 0
Sulfonamides 0
Cytarabine 04079A1RDZ
venetoclax N54AIC43PW

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1372-1382

Subventions

Organisme : AbbVie and Genentech

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Takahiro Yamauchi (T)

Department of Hematology and Oncology, University of Fukui Hospital, Fukui, Japan.

Chikashi Yoshida (C)

Department of Hematology, National Hospital Organization, Mito Medical Center, Ibaraki, Japan.

Kensuke Usuki (K)

Department of Hematology, NTT Medical Center Tokyo, Tokyo, Japan.

Satoru Takada (S)

Leukemia Research Center, Saiseikai Maebashi Hospital, Maebashi, Japan.

Itaru Matsumura (I)

Department of Hematology and Rheumatology, Kindai University Hospital, Osaka, Japan.

Nobuaki Dobashi (N)

Division of Clinical Oncology/Hematology, The Jikei University Daisan Hospital, Tokyo, Japan.

Yasushi Miyazaki (Y)

Department of Hematology, Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, Japan.

Toshihiro Miyamoto (T)

Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Hiroatsu Iida (H)

Department of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Norio Asou (N)

Department of Hematology, Saitama Medical University International Medical Center, Hidaka, Japan.

Junya Kuroda (J)

Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Satoshi Ichikawa (S)

Department of Hematology, Tohoku University Hospital, Sendai, Japan.

Norio Komatsu (N)

Department of Hematology, Juntendo University School of Medicine, Tokyo, Japan.

Wellington Mendes (W)

AbbVie Inc., North Chicago, IL, USA.

Hideyuki Honda (H)

AbbVie GK, Tokyo, Japan.

Sumiko Okubo (S)

AbbVie GK, Osaka, Japan.

Misaki Kurokawa (M)

AbbVie GK, Tokyo, Japan.

Qi Jiang (Q)

AbbVie Inc., North Chicago, IL, USA.

Andrew Wei (A)

Department of Clinical Haematology, The Alfred Hospital and Monash University, Melbourne, VIC, Australia.

Kenichi Ishizawa (K)

Department of Third Internal Medicine, Yamagata University Hospital, Yamagata, Japan.

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