Minimal residual disease–driven treatment intensification with sequential addition of ibrutinib to venetoclax in R/R CLL

•A sequential MRD-guided addition of ibrutinib to venetoclax led to uMRD in 33 (87%) of 38 patients with relapsed/refractory CLL.•This MRD-driven strategy allowed identical depth of response to be reached in each patient with an individualized time-limited approach. [Display omitted] Undetectable me...

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Veröffentlicht in:Blood 2022-12, Vol.140 (22), p.2348-2357
Hauptverfasser: Scarfò, Lydia, Heltai, Silvia, Albi, Elisa, Scarano, Eloise, Schiattone, Luana, Farina, Lucia, Moia, Riccardo, Deodato, Marina, Ferrario, Andrea, Motta, Marina, Reda, Gianluigi, Sancetta, Rosaria, Coscia, Marta, Rivela, Paolo, Laurenti, Luca, Varettoni, Marzia, Perotta, Eleonora, Capasso, Antonella, Ranghetti, Pamela, Colia, Maria, Ghia, Paolo
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Sprache:eng
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Zusammenfassung:•A sequential MRD-guided addition of ibrutinib to venetoclax led to uMRD in 33 (87%) of 38 patients with relapsed/refractory CLL.•This MRD-driven strategy allowed identical depth of response to be reached in each patient with an individualized time-limited approach. [Display omitted] Undetectable measurable residual disease (uMRD) is achievable in patients with chronic lymphocytic leukemia (CLL) with the BCL2-inhibitor venetoclax alone or combined with the Bruton’s tyrosine kinase inhibitor ibrutinib. This phase 2, multicenter, MRD-driven study was designed to discontinue treatment upon reaching uMRD4 (
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.2022016901