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...
Gespeichert in:
Veröffentlicht in: | Blood 2022-12, Vol.140 (22), p.2348-2357 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |