Zanubrutinib Elicits Meaningful Benefit in B-Cell Malignancy Population

News
Article

Treatment with zanubrutinib may be a viable option for patients with B-cell malignancies who are intolerant to acalabrutinib, says Mazyar Shadman, MD.

“The results of this study demonstrated that zanubrutinib may be a viable option for patients who are intolerant of acalabrutinib,” according to Mazyar Shadman, MD.

“The results of this study demonstrated that zanubrutinib may be a viable option for patients who are intolerant of acalabrutinib,” according to Mazyar Shadman, MD.

Zanubrutinib (Brukinsa) produced meaningful activity in patients with B-cell malignancies intolerant to previous therapy with acalabrutinib (Calquence), according to findings from the phase 2 BGB-3111-215 study (NCT04116437) presented at the 2023 American Society of Hematology (ASH) Annual Meeting and Exposition.1

Results from the ongoing phase 2 BGB-3111-215 study (NCT04116437) showed data from cohort 2 of patients intolerant to acalabrutinib (n = 27). The median exposure to zanubrutinib lasted 6 months longer than the patient’s cumulative exposure to acalabrutinib before treatment discontinuation at 11.4 months (range, 0.5-32.2) vs 5.4 months (range, 0.5-33.7), respectively.

Further, 70% of the acalabrutinib intolerance events experienced by patients did not reoccur at any grade with zanubrutinib. Of those that did recur, no events recurred at a higher severity. The most common grade 2 or higher of these acalabrutinib intolerance events that recurred during treatment with zanubrutinib included arthralgia (n = 6), headache (n = 5), myalgia (n = 5), diarrhea (n = 3), rash (n = 3), fatigue (n = 2), and hemorrhage (n = 2).

According to Mazyar Shadman, MD, who presented these data at the 2023 ASH meeting, no adverse events (AEs) led to death, but 2 AEs led to treatment discontinuation of zanubrutinib. Other patients discontinued zanubrutinib due to physician decision (n = 2), patient withdrawal (n = 2), and progressive disease ([PD] n = 1). The AEs that led to discontinuation of zanubrutinib were a recurrence of grade 2 myalgia in 1 patient and grade 3 diarrhea in another.

Looking at grade 3 or higher AEs, 3 patients experienced a neutrophil count decrease after zanubrutinib, but anemia, thrombocytopenia, nor platelet count decrease occurred. Overall, 7 patients had a serious AE with 16 events leading to dose interruption and 6 leading to dose reduction.

In the phase 2 study, patients with previously treated B-cell malignances included those with chronic lymphocytic leukemia (CLL; n = 17), small lymphocytic lymphoma (SLL; n = 2), Waldenström’s macroglobulinemia (n = 4), mantle cell lymphoma (n = 2), or marginal zone lymphoma (n = 2). To be enrolled in the study, they had to be deemed intolerant of a prior Bruton tyrosine kinase (BTK) inhibitor treatment and could not have either Richter transformation or PD while on BTK treatment. In the first cohort of the study, 57 patients intolerant to ibrutinib (Imbruvica) were enrolled. In cohort 1 and 2, patients were given either 160 mg of zanubrutinib twice a day or 320 mg once a day.

The median age of patients in cohort 2 was 73 years (range, 51-87), with a majority of male patients (63%); most had an ECOG performance status of 0 (67%).

According to Shadman, associate professor in the clinical research division and innovators Network Endowed Chair at the Fred Hutchinson Cancer Center, previous findings from the first cohort showed similar promise with zanubrutinib after ibrutinib.2 In cohort 2, 19 of the acalabrutinib-intolerant patients received the 160 mg dose and 8 received the 320 mg dose. Thirteen of the 27 patients intolerant to acalabrutinib were also intolerant to previous use of ibrutinib, with 12 given a prior ibrutinib monotherapy and 1 patient on an ibrutinib combination therapy.1 Twenty-six patients intolerant to acalabrutinib received the BTK as a monotherapy and 1 patient was intolerant to an acalabrutinib combination regimen.

Twenty-five of the patients in cohort 2 were evaluable for efficacy after zanubrutinib treatment. Investigators observed a 96% disease control rate (95% CI, 80%-100%), defined as patients with stable disease (SD) or better with zanubrutinib. There was an overall response rate of 64% (95% CI, 43%-82%), defined as having a minor response or better, to the next-generation BTK inhibitor.

Overall, 48% of patients had a PR, 4% had a very good partial response, 4% had a minor response, 32% had SD, and 4% had PD. The median time to best overall response was 3.0 months (range, 2.7-11.1) and time to the first overall response was seen at a median of 2.9 months (range, 2.7-11.1). Of the patients with either CLL or SLL, 71% had a partial response (PR) with lymphocytosis or better.

“The results of this study demonstrated that zanubrutinib may be a viable option for patients who are intolerant of acalabrutinib,” concluded Shadman.

References

  1. Shadman M, Flinn IW, Kingsley E, et al. Zanubrutinib in acalabrutinib-intolerant patients (pts) with B-cell malignancies. Blood. 2023;142(suppl 1):3279. doi:10.1182/blood-2023-174096
  2. Shadman M, Flinn IW, Levy MY, et al. Zanubrutinib in patients with previously treated B-cell malignancies intolerant of previous Bruton tyrosine kinase inhibitors in the USA: a phase 2, open-label, single-arm study. Lancet Haematol. 2023;10(1):e35-e45. doi:10.1016/S2352-3026(22)00320-9
Recent Videos
Paolo Tarantino, MD discusses updated breast cancer trial findings presented at ESMO 2024 supporting the use of agents such as T-DXd and ribociclib.
Higher, durable rates of response to frontline therapy are needed to potentially improve long-term survival among patients with non–small cell lung cancer.
A retrospective study sought to assess CRS and ICANS onset and duration, as well as non-relapse mortality causes in patients infused with CAR T-cell therapies.
A retrospective study sought to assess CRS and ICANS onset and duration, as well as non-relapse mortality causes in patients infused with CAR T-cell therapies.
A retrospective study sought to assess CRS and ICANS onset and duration, as well as non-relapse mortality causes in patients infused with CAR T-cell therapies.
Although no responses were observed in 11 patients receiving abemaciclib monotherapy, combination therapies with abemaciclib may offer clinical benefit.
Findings show no difference in overall survival between various treatments for metastatic RCC previously managed with immunotherapy and TKIs.
An epigenomic profiling approach may help pick up the entire tumor burden, thereby assisting with detecting sarcomatoid features in those with RCC.
Future meetings may address how immunotherapy, bispecific agents, and CAR T-cell therapies can further impact the AML treatment paradigm.
Related Content