A real-world comparison of treatment and survival outcomes with zanubrutinib (zanu) and acalabrutinib (acala) monotherapy among patients with relapsed or refractory (R/R) mantle cell lymphoma (MCL) in the United States

ASCO 2026MCLZanubrutinibPoster

Yucai Wang, MD, PhD

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SUMMARY

This retrospective cohort study evaluated realworld effectiveness of zanubrutinib versus acalabrutinib monotherapy in adults with relapsed or refractory mantle cell lymphoma treated in the secondline or later setting. Using Komodo administrative claims data, 2,219 patients were included (zanubrutinib, n=931; acalabrutinib, n=1,288). The primary effectiveness outcomes were overall survival and time to next treatment. Median followup was 14.8 months for zanubrutinib and 18.2 months for acalabrutinib. Median overall survival was not reached for zanubrutinib and was 60.6 months for acalabrutinib, while median time to next treatment was 26.7 and 20.8 months, respectively. In unadjusted analyses, zanubrutinib was associated with longer overall survival (hazard ratio [HR], 0.74; 95% CI, 0.62-0.88; P<0.001) and time to next treatment (HR, 0.86; 95% CI, 0.76-0.97; P=0.012). After inverse probability of treatment weighting adjustment, both overall survival (HR, 0.81; 95% CI, 0.68-0.98; P=0.03) and time to next treatment (HR, 0.86; 95% CI, 0.76-0.98; P=0.025) favored zanubrutinib compared with acalabrutinib.

Population Intervention Comparator Outcome Measures
Adults (≥18 years) in the United States with relapsed or refractory mantle cell lymphoma identified in Komodo Health administrative claims data who received second-line or later therapy Zanubrutinib Acalabrutinib Overall survival and time to next treatment

FAQs

The objective of the study was to evaluate realworld effectiveness of zanubrutinib compared with acalabrutinib in adults with relapsed or refractory mantle cell lymphoma treated in the secondline or later setting in the United States.

This was a retrospective cohort study using administrative claims data from the Komodo database. Adults with at least two diagnoses of mantle cell lymphoma who initiated zanubrutinib or acalabrutinib monotherapy as secondline or later therapy were included. Patients with prior stem cell transplant, endstage renal disease, or clinical trial participation were excluded. The assessed endpoints were overall survival, measured from index date to allcause mortality, and time to next treatment, measured from index date to subsequent therapy with an allowable gap of 120 days.

A total of 2,219 patients were included (zanubrutinib, n=931; acalabrutinib, n=1,288). Median followup was 14.8 months for zanubrutinib and 18.2 months for acalabrutinib. Median time to next treatment was 26.7 months with zanubrutinib and 20.8 months with acalabrutinib, while median overall survival was not reached for zanubrutinib and was 60.6 months for acalabrutinib. In unadjusted analyses, zanubrutinib was associated with longer overall survival (hazard ratio [HR], 0.74; 95% CI, 0.62-0.88; P<0.001) and time to next treatment (HR, 0.86; 95% CI, 0.76-0.97; P=0.012). After inverse probability of treatment weighting adjustment, both overall survival (HR, 0.81; 95% CI, 0.68-0.98; P=0.03) and time to next treatment (HR, 0.86; 95% CI, 0.76-0.98; P=0.025) favored zanubrutinib compared with acalabrutinib.

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