TY - JOUR
T1 - Drug exposure and measurable residual disease in chronic lymphocytic leukemia
T2 - a systematic review
AU - Korsholm, Cathrine
AU - Bülow, Cille
AU - Christensen, Mikkel
AU - Dalhoff, Kim
AU - Feinberg, Joshua Buron
AU - Lund, Trine Meldgaard
AU - Niemann, Carsten Utoft
AU - Petersen, Tonny Studsgaard
AU - Andersen, Michael Asger
PY - 2024/11/7
Y1 - 2024/11/7
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85208985389&partnerID=8YFLogxK
U2 - 10.1080/10428194.2024.2412289
DO - 10.1080/10428194.2024.2412289
M3 - Review
C2 - 39509142
SN - 1042-8194
SP - 1
EP - 11
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
ER -