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EHA 2023 | Phase I/II BRUIN update: efficacy of pirtobrutinib in R/R Waldenström’s macroglobulinemia

Lydia Scarfò, MD, Vita-Salute San Raffaele University & IRCCS San Raffaele Scientific Institute, Milan, Italy, discusses the treatment efficacy of pirtobrutinib in lymphoproliferative disorders, specifically Waldenström’s macroglobulinemia (WM), based on findings from the Phase I/II BRUIN trial (NCT03740529). Dr. Scarfò highlights the high activity and tolerability of pirtobrutinib treatment for WM, with low treatment discontinuation rates. This interview took place at the 28th Congress of the European Hematology Association (EHA) 2023 in Frankfurt, Germany.

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Transcript (edited for clarity)

I’m very excited about this, this non-covalent BTK inhibitor that has been recently approved in the US for the treatment of Mantle cell lymphoma, but in the original BRUIN study also patients with other lymphoproliferative disorders were enrolled. And Waldenström Macroglobulinemia is a rare disease and patients relapsing after covalent BTK inhibitor are for sure an unmet need in this field...

I’m very excited about this, this non-covalent BTK inhibitor that has been recently approved in the US for the treatment of Mantle cell lymphoma, but in the original BRUIN study also patients with other lymphoproliferative disorders were enrolled. And Waldenström Macroglobulinemia is a rare disease and patients relapsing after covalent BTK inhibitor are for sure an unmet need in this field. So around 70 patients with Waldenström Macroglobulinemia were enrolled in the BRUIN study. Basically, 80% of them were previously exposed to covalent BTK inhibitor and pirtobrutinib was able to achieve a very high overall response rate in 70% of them and in the whole cohort was very well tolerated, meaning that we had very few adverse events. Only 2.5% of patients, among more than 700 patients, interrupting treatment, discontinuing treatment because of tolerability issue, and, in the vast majority, they could continue treatment at the standard dose while on study. So it’s a very powerful drug that I hope can become available for many other lymphoproliferative disorders soon.

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Disclosures

Advisory board: AbbVie, AstraZeneca, BeiGene, Janssen, Lilly
Speaker bureau: Octapharma