Drug exposure and measurable residual disease in chronic lymphocytic leukemia: a systematic review.

IF 2.2 4区 医学 Q3 HEMATOLOGY
Cathrine Korsholm, Cille Bülow, Mikkel Christensen, Kim Dalhoff, Joshua Buron Feinberg, Trine Meldgaard Lund, Carsten Utoft Niemann, Tonny Studsgaard Petersen, Michael Asger Andersen
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引用次数: 0

Abstract

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.

慢性淋巴细胞白血病的药物暴露与可测量残留病:系统综述。
对于慢性淋巴细胞白血病(CLL)的固定疗程疗法,检测不到可测量残留疾病(MRD)比完全缓解更能准确预测总生存期和无进展生存期。对于无限期疗法,MRD 状态可以指导治疗的中止。我们系统回顾了CLL中抗肿瘤药物暴露与检测不到的MRD之间的关系。来自 MEDLINE 和 EMBASE 的 17 项试验符合纳入标准;其中 4 项试验评估了药物暴露与 MRD 状态之间的关系。检测不到MRD与ofatumumab和阿仑妥珠单抗较高的谷浓度以及伊布替尼较高的最大浓度和血浆浓度曲线下面积(AUC)有关。一项研究发现,在调整肿瘤负荷之前,高利妥昔单抗 AUC 与检测不到 MRD 之间存在关联。有限的研究、缺乏伴随药物的暴露测量以及设计的高度异质性限制了结果的普遍性。还需要进一步研究来探讨暴露与MRD之间的关系以及对CLL进行治疗药物监测的可能性。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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