Relative efficacy of systemic treatments for patients with relapsed/refractory chronic lymphocytic leukemia: a

Jinchul Kim1, Jinhyun Cho1, Joo Han Lim1

  • 1Department of Hematology-Oncology, Inha University College of Medicine and Hospital, 7-206 Third Street, Shinheung-Dong Jung-Gu, Incheon, Republic of Korea.

Blood Research
|January 3, 2025
PubMed
Abstract

Insights

Venetoclax plus rituximab and zanubrutinib are superior treatments for relapsed/refractory chronic lymphocytic leukemia (R/R CLL). Treatment effectiveness varies based on specific genetic mutations like 17p deletion and TP53.

Area of Science:

  • Hematology
  • Oncology
  • Pharmacology

Background:

  • Chronic lymphocytic leukemia (CLL) is a common B-cell malignancy.
  • Relapsed/refractory (R/R) CLL presents treatment challenges, particularly with specific genetic mutations.
  • Identifying optimal systemic treatments is crucial for improving patient outcomes.

Purpose of the Study:

  • To conduct a network meta-analysis evaluating systemic treatments for R/R CLL.
  • To compare treatment efficacy, focusing on patients with 17p deletion and TP53 mutations.

Main Methods:

  • Systematic literature review of randomized controlled trials (RCTs) through December 2023.
  • Bayesian network meta-analysis to estimate hazard ratios (HRs) for progression-free survival (PFS).
  • Ranking of treatment regimens using surface under the cumulative ranking curve (SUCRA).

Main Results:

  • Twelve trials with 4,437 patients and 13 treatments were analyzed.
  • Venetoclax plus rituximab and zanubrutinib showed superior PFS compared to ibrutinib in the overall R/R CLL population.
  • Zanubrutinib was most effective in the 17p deletion/TP53 mutation subgroup (HR 0.52), while venetoclax plus rituximab was most effective in patients without these mutations (HR 0.49).

Conclusions:

  • Venetoclax plus rituximab and zanubrutinib demonstrate superior efficacy in R/R CLL.
  • Treatment selection should consider the patient's specific genetic mutation profile.
  • These findings offer guidance for optimizing R/R CLL therapy.