Utilizing risk factors to guide treatment decisions in chronic lymphocytic leukemia.

Expert Rev Anticancer Ther

Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA, USA.

Published: October 2024

AI Article Synopsis

  • High-risk factors traditionally predicted poor outcomes for CLL patients, but the use of BTK inhibitors has improved survival rates even for those with these high-risk features.
  • Continuous treatment with BTK inhibitors has positively affected survival, while finite-duration therapies like venetoclax combinations haven't shown the same results.
  • Ongoing research and new treatments emphasize the importance of understanding prognostic factors to guide therapy decisions and encourage participation in clinical trials for patients with high-risk CLL.

Article Abstract

Introduction: In the era of chemo-immunotherapy, high-risk factors unequivocally predicted inferior outcomes for patients with CLL. The widespread adoption of BTK inhibitors has challenged the practical implications of such testing, as many patients have improved outcomes despite the presence of high-risk features. The impact of adverse prognostic factors, such as unmutated , on survival has been ameliorated by continuous treatment with BTK inhibitors, but not by finite-duration therapy with venetoclax-based combinations. Furthermore, abnormalities continue to be associated with worse outcomes in the era of novel agents. New treatment modalities, such as pirtobrutinib, lisocabtagene maraleucel, and ongoing studies combining BTK inhibitors with venetoclax, raise new questions on the significance of prognostic factors of survival for patients with CLL.

Areas Covered: Herein, we summarized the available literature on patients with CLL harboring high-risk biomarkers, with a focus on data from key clinical trials.

Expert Opinion: Testing for prognostic biomarkers will remain relevant to identify patients who may have increased benefit from novel therapeutic strategies, such as combination therapies and novel agents. Patients with high-risk disease should be encouraged to participate in clinical trials.

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Source
http://dx.doi.org/10.1080/14737140.2024.2398483DOI Listing

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