Navigating the post–covalent Bruton tyrosine kinase inhibitor (cBTKi) landscape in mantle cell lymphoma (MCL): Real-world insights on treatment patterns, discontinuation, and healthcare resource utilization (HCRU)

ASCO 2026MCLZanubrutinibPoster

Alvaro Alencar, MD

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SUMMARY

This retrospective realworld evidence analysis evaluated treatment patterns, time to treatment discontinuation, and healthcare resource utilization among adults with mantle cell lymphoma who previously received covalent Bruton tyrosine kinase inhibitors. Using claims data from the Symphony Integrated Dataverse (January 2020 to August 2025), 571 patients who discontinued a covalent Bruton tyrosine kinase inhibitor and initiated a subsequent therapy were identified. Reported outcomes included treatment patterns, time to discontinuation, and healthcare resource utilization per patient per month. Subsequent treatments included covalent and noncovalent BTK inhibitors, chemo±immunotherapy, BCL2 inhibitors, CART therapy, and other regimens. Median time to discontinuation was longest with covalent BTK inhibitors (365 days), followed by noncovalent BTK inhibitors (206 days) and BCL2 inhibitors (140 days). Mean monthly healthcare utilization was lowest with covalent BTK inhibitors (outpatient, 1.21; inpatient, 0.20; other medical visits, 1.07) and highest with CART therapy (outpatient, 10.63; inpatient, 1.89; other medical visits, 1.55).

Population Intervention Comparator Outcome Measures
Adults in the United States with mantle cell lymphoma who had previously received covalent Bruton tyrosine kinase inhibitors and subsequently initiated another line of therapy, identified using claims data from the Symphony Integrated Dataverse (January 2020 to August 2025) Post–covalent Bruton tyrosine kinase inhibitor treatment regimens N/A Treatment patterns, time to treatment discontinuation, and healthcare resource utilization

FAQs

The objective of the study was to evaluate realworld treatment patterns, time to treatment discontinuation, and healthcare resource utilization among adults with mantle cell lymphoma (MCL) who had previously received covalent Bruton tyrosine kinase inhibitors (cBTKi) and subsequently initiated another therapy.

This retrospective observational study used claims data from the Symphony Integrated Dataverse (January 2020 to August 2025) to identify adults with MCL who had received a cBTKi in any line of therapy and, after discontinuation, initiated a subsequent treatment. The reported outcomes included treatment patterns, time to treatment discontinuation, and healthcare resource utilization measured per patient per month.

Of 10,519 total patients with MCL, 571 had been previously treated with cBTKis and received a subsequent line of therapy. Subsequent regimens included cBTKis (38%), noncovalent BTK inhibitors (32%), chemotherapy with or without immunotherapy (11%), BCL2 inhibitors (9%, including 7% monotherapy), CART therapy (2%), and other treatments (8%). Median time to discontinuation was longest with cBTKis (365 days) and shorter with noncovalent BTK inhibitors (206 days) and BCL2 inhibitors (140 days). Mean HCRU per patient per month was lowest with cBTKis (outpatient, 1.21; inpatient, 0.20; other medical visits, 1.07) and highest with CART therapy (outpatient, 10.63; inpatient, 1.89; other medical visits, 1.55).

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