Ibrutinib-Venetoclax Combination Found Effective Against Mantle Cell Lymphoma
Ibrutinib-venetoclax combination shows superior progression-free survival and higher complete response rate than ibrutinib and placebo
LBA-2: Ibrutinib Combined with Venetoclax in Patients with Relapsed/Refractory Mantle Cell Lymphoma: Primary Analysis Results from the Randomized Phase 3 Sympatico Study
"Ibrutinib plus venetoclax has been shown to be very effective, safe, and well tolerated, and could benefit many patients with relapsed MCL," said
MCL is a rare non-Hodgkin lymphoma, a cancer of white blood cells, that is most common in older adults. Patients affected with this cancer often have swollen lymph nodes, enlarged spleen, and abnormal blood counts due to damage to the bone marrow by the cancer. After frontline therapies, a majority of patients see this cancer relapse after initially responding to treatment. Ibrutinib is currently approved for relapsed MCL in many countries but was withdrawn for MCL in the
Ibrutinib and venetoclax are oral cancer drugs that are designed to affect different biochemical pathways. Ibrutinib targets Bruton tyrosine kinase (BTK), an enzyme involved in cell signaling, whereas venetoclax inhibits BCL2 proteins, which are involved in cell survival and growth.
For the phase III trial, researchers enrolled 267 patients with MCL whose cancer had not responded to previous treatments or had returned after an initial response. After a median follow-up of 51 months, the results showed significantly better outcomes with the ibrutinib-venetoclax combination. The median progression-free survival, the trial's primary endpoint, was significantly longer with 31.9 months in the combination group compared with 22.1 months in the placebo group.
Treatment with ibrutinib and venetoclax was also associated with a significantly better rate of complete response (CR, or the eradication of cancer as measured with standard imaging methods), which was achieved in 54% of those assigned to the combination therapy and 32% of those in the placebo group.
"The combination was synergistic, with a CR rate that is higher than the additive CR rate of the two drugs," said
The benefits of the combination therapy were consistent across subgroups of patients with high-risk features. The overall survival rate was numerically higher in the group that received the combination therapy, but the difference was not statistically significant.
Adverse events were more common among patients who received the combination therapy, with the most frequent events including low white blood cell count, low platelet count, pneumonia, and anemia. About 60% of participants in both study arms experienced adverse events that were considered serious. Adverse events of grade three or higher were more common among those receiving the combination therapy, 84% of whom experienced such events compared to 76% in the control arm.
The study was funded by AbbVie, maker of ibrutinib.
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The American Society of Hematology (ASH) (hematology.org) is the world's largest professional society of hematologists dedicated to furthering the understanding, diagnosis, treatment, and prevention of disorders affecting the blood. For more than 60 years, the Society has led the development of hematology as a discipline by promoting research, patient care, education, training, and advocacy in hematology.
ASH's flagship journal, Blood (bloodjournal.org) is the most cited peer-reviewed publication in the field, and Blood Advances (bloodadvances.org) is an open-access, online journal that publishes more peer-reviewed hematology research than any other academic journal worldwide. Two new journals will be joining the Blood Journals portfolio in 2024, Blood Neoplasia (bloodneoplasia.org) and Blood Vessels, Thrombosis & Hemostasis (bloodvth.org).
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SOURCE American Society of Hematology
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