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Keeping up with venetoclax for leukemic malignancies: key findings, optimal regimens, and clinical considerations

Authors :
Marina Konopleva
Maria Tariq Siddiqui
Source :
Expert Review of Clinical Pharmacology. 14:1497-1512
Publication Year :
2021
Publisher :
Informa UK Limited, 2021.

Abstract

Introduction Venetoclax has transformed the treatment landscape in hematologic malignancies, especially in elderly population. With high rates of remission, deep and durable responses, and safe toxicity profile, venetoclax in combination therapy has been extremely effective, garnering accelerated approval and becoming standard of care in lymphoid and myeloid malignancies. Areas covered The role of venetoclax in the intrinsic apoptotic pathway is covered. This includes preclinical and clinical experience of venetoclax monotherapy and combination therapy in relapsed/refractory and frontline CLL, AML, ALL and high-risk MDS, with an emphasis on key clinical trials and efficacy of combination regimens in distinct mutational landscapes. Strategies to mitigate myelosuppression, manage dose adjustments and infectious complications are addressed. Expert opinion Targeting BCL-2 offers a safe and highly effective adjunct to available therapies in hematologic malignancies. Despite success and frequent utilization of venetoclax, several resistance mechanisms have been elucidated, prompting development of novel combinatorial strategies. Further, on-target myelosuppression of venetoclax is a key obstacle in clinical practice, requiring diligent monitoring and practice-based knowledge of dose modifications. Despite these limitations, venetoclax has gained tremendous popularity in hematologic-oncology, becoming an integral component of numerous combination regimes, with ongoing plethora of clinical trials encompassing standard chemotherapy, targeted agents and immune-based approaches.

Details

ISSN :
17512441 and 17512433
Volume :
14
Database :
OpenAIRE
Journal :
Expert Review of Clinical Pharmacology
Accession number :
edsair.doi.dedup.....635cef7c6582f88f54d46ffe2b6ff6ac