Phase II Study of Venetoclax Added to Cladribine Plus Low-Dose Cytarabine Alternating With 5-Azacitidine in Older Patients With Newly Diagnosed Acute Myeloid Leukemia.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 11 2022
Historique:
pubmed: 16 6 2022
medline: 19 11 2022
entrez: 15 6 2022
Statut: ppublish

Résumé

The combination of venetoclax and 5-azacitidine (5-AZA) for older or unfit patients with acute myeloid leukemia (AML) improves remission rates and survival compared with 5-AZA alone. We hypothesized that the addition of venetoclax to cladribine (CLAD)/low-dose araC (low-dose cytarabine [LDAC]) alternating with 5-AZA backbone may further improve outcomes for older patients with newly diagnosed AML. This is a phase II study investigating the combination of venetoclax and CLAD/LDAC alternating with venetoclax and 5-AZA in older (≥ 60 years) or unfit patients with newly diagnosed AML. The primary objective was composite complete response (CR) rate (CR plus CR with incomplete blood count recovery); secondary end points were overall survival, disease-free survival (DFS), overall response rate, and toxicity. A total of 60 patients were treated; median age was 68 years (range, 57-84 years). By European LeukemiaNet, 23%, 33%, and 43% were favorable, intermediate, and adverse risk, respectively. Fifty-six of 60 evaluable patients responded (composite CR: 93%) and 84% were negative for measurable residual disease. There was one death (2%) within 4 weeks. With a median follow-up of 22.1 months, the median overall survival and DFS have not yet been reached. The most frequent grade 3/4 nonhematologic adverse events were febrile neutropenia (n = 33) and pneumonia (n = 14). One patient developed grade 4 tumor lysis syndrome. Venetoclax and CLAD/LDAC alternating with venetoclax and 5-AZA is an effective regimen among older or unfit patients with newly diagnosed AML. The rates of overall survival and DFS are encouraging. Further study of this non-anthracycline-containing backbone in younger patients, unfit for intensive chemotherapy, as well as comparisons to standard frontline therapies is warranted.

Identifiants

pubmed: 35704787
doi: 10.1200/JCO.21.02823
pmc: PMC9671758
doi:

Substances chimiques

Azacitidine M801H13NRU
Bridged Bicyclo Compounds, Heterocyclic 0
Cladribine 47M74X9YT5
Cytarabine 04079A1RDZ
venetoclax N54AIC43PW

Banques de données

ClinicalTrials.gov
['NCT03586609']

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

3848-3857

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA100632
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009666
Pays : United States

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Auteurs

Tapan M Kadia (TM)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Patrick K Reville (PK)

Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Xuemei Wang (X)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX.

Caitlin R Rausch (CR)

Department of Pharmacy, The University of Texas MD Anderson Cancer Center, Houston, TX.

Gautam Borthakur (G)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Naveen Pemmaraju (N)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Naval G Daver (NG)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Courtney D DiNardo (CD)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Koji Sasaki (K)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Ghayas C Issa (GC)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Maro Ohanian (M)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Guillermo Montalban-Bravo (G)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Nicholas J Short (NJ)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Nitin Jain (N)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Alessandra Ferrajoli (A)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Kapil N Bhalla (KN)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Elias Jabbour (E)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Koichi Takahashi (K)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Rashmi Malla (R)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Kelly Quagliato (K)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Rashmi Kanagal-Shamanna (R)

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Uday R Popat (UR)

Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX.

Michael Andreeff (M)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Guillermo Garcia-Manero (G)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Marina Y Konopleva (MY)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Farhad Ravandi (F)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Hagop M Kantarjian (HM)

Departments of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

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Classifications MeSH