慢性淋巴细胞白血病
医学
药品
疾病
白血病
内科学
药理学
作者
Cathrine Korsholm,Cille Bülow,Mikkel Christensen,Kim Dalhoff,Joshua Feinberg,Trine Meldgaard Lund,Carsten Utoft Niemann,Tonny Studsgaard Petersen,Michael Asger Andersen
标识
DOI:10.1080/10428194.2024.2412289
摘要
For fixed-duration therapies against chronic lymphocytic leukemia (CLL), undetectable measurable residual disease (MRD) predicts overall and progression-free survival more accurately than complete remission. For indefinite therapies, MRD status can direct discontinuation of treatment. We systematically reviewed the relationship between antineoplastic drug exposures and undetectable MRD in CLL. Seventeen trials from MEDLINE and EMBASE met the inclusion criteria; four of which evaluated drug exposures in relation to MRD status. Undetectable MRD was associated with higher trough concentrations of ofatumumab and alemtuzumab, as well as increased maximum concentration and area under the plasma concentration curve (AUC) of ibrutinib. One study found an association between high rituximab AUC and undetectable MRD until adjusting for tumor burden. The limited studies, lack of exposure measurements of concomitant drugs, and high heterogeneity in designs limit the results' generalizability. Further research is needed to explore the exposure-MRD relationship and the possibility for therapeutic drug monitoring in CLL.
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