Venetoclax and hypomethylating agent therapy in high risk myelodysplastic syndromes: a retrospective evaluation of a real-world experience.


Journal

Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422

Informations de publication

Date de publication:
11 2020
Historique:
pubmed: 17 6 2020
medline: 28 4 2021
entrez: 17 6 2020
Statut: ppublish

Résumé

Treatment with hypomethylating agents (HMAs) azacitidine or decitabine is the current standard of care for high risk myelodysplastic syndromes (MDSs) but is associated with low rates of response. The limited number of treatment options for patients with high risk MDS highlights a need for new therapeutic options. Venetoclax is an inhibitor of the BCL-2 protein which, when combined with an HMA, has shown high response rates in unfit and previously untreated acute myeloid leukemia. We performed a retrospective study of high risk MDS patients receiving combination HMA plus venetoclax in order to determine their effectiveness in this context. We show that in our cohort, the combination results in high response rates but is associated with a high frequency of myelosuppression. These data highlight the efficacy of combination HMA plus venetoclax in high risk MDS, warranting further prospective evaluation in clinical trials.

Identifiants

pubmed: 32543932
doi: 10.1080/10428194.2020.1775214
doi:

Substances chimiques

Bridged Bicyclo Compounds, Heterocyclic 0
Sulfonamides 0
Decitabine 776B62CQ27
Azacitidine M801H13NRU
venetoclax N54AIC43PW

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2700-2707

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL120824
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA188055
Pays : United States

Auteurs

Armon Azizi (A)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Asiri Ediriwickrema (A)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Ritika Dutta (R)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Shyam A Patel (SA)

Department of Medicine, Division of Hematology-Oncology, UMass Memorial Medical Center, University of Massachusetts Medical School, Worcester, MA, USA.

William Shomali (W)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Bruno Medeiros (B)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

David Iberri (D)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Jason Gotlib (J)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Gabriel Mannis (G)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Peter Greenberg (P)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Ravindra Majeti (R)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Tian Zhang (T)

Department of Medicine, Division of Hematology, Cancer Institute, Stanford University, Stanford, CA, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH