Acalabrutinib and its use in the treatment of chronic lymphocytic leukemia

Future Oncol. 2022 Mar;18(7):755-769. doi: 10.2217/fon-2021-0602. Epub 2022 Feb 10.

Abstract

Bruton's tyrosine kinase inhibitors have changed the treatment landscape for chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL) and lymphoplasmacytic lymphoma dramatically. In 2019, acalabrutinib was approved by the US FDA for the treatment of treatment-naive and relapsed/refractory CLL and MCL. Acalabrutinib monotherapy was found to be effective and safe in CLL patients. In ASCEND and ELEVATE treatment-naive studies, acalabrutinib monotherapy and the combination with obinutuzumab demonstrated improved efficacy and an acceptable safety profile. The triple combination with venetoclax showed a high rate of molecular remission without an impaired safety profile. Adverse events, with an occurrence rate of >20%, were as follows: grade 1-2 myelosuppression, gastrointestinal toxicity, rash, constitutional symptoms; grade 3 or 4 toxicities were syncope, pneumonia, hypertension, atrial fibrillation, neutropenia and thrombocytopenia.

Keywords: BTK inhibitors; CLL; acalabrutinib; ibrutinib toxicity; relapsed/refractory CLL; treatment-naive CLL.

Publication types

  • Review

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / therapeutic use
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Benzamides / therapeutic use*
  • Clinical Trials as Topic
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell / drug therapy*
  • Piperidines / therapeutic use
  • Pyrazines / therapeutic use*
  • Pyrazoles / therapeutic use
  • Pyrimidines / therapeutic use

Substances

  • Antineoplastic Agents
  • Benzamides
  • Piperidines
  • Pyrazines
  • Pyrazoles
  • Pyrimidines
  • ibrutinib
  • zanubrutinib
  • acalabrutinib
  • Adenine