Therapeutic Drug Monitoring of Oral Anticancer Drugs: The Dutch Pharmacology Oncology Group–Therapeutic Drug Monitoring Protocol for a Prospective Study

医学 药品 加药 药代动力学 耐受性 药理学 治疗药物监测 相伴的 毒性 血液取样 内科学 不利影响
作者
Stefanie L. Groenland,Ruben A.G. van Eerden,Remy B. Verheijen,Stijn L.W. Koolen,Dirk Jan A. R. Moes,Ingrid M.E. Desar,Anna K.L. Reyners,Hans Gelderblom,Nielka P. van Erp,Ron H.J. Mathijssen,Alwin D. R. Huitema,Neeltje Steeghs
出处
期刊:Therapeutic Drug Monitoring [Lippincott Williams & Wilkins]
卷期号:41 (5): 561-567 被引量:44
标识
DOI:10.1097/ftd.0000000000000654
摘要

Background: Oral anticancer drugs show a high interpatient variability in pharmacokinetics (PK), leading to large differences in drug exposure. For many of these drugs, exposure has been linked to efficacy and toxicity. Despite this knowledge, these drugs are still administered in a one-size-fits-all approach. Consequently, individual patients have a high probability to be either underdosed, which can lead to decreased antitumor efficacy, or overdosed, which could potentially result in increased toxicity. Therapeutic drug monitoring (TDM), personalized dosing based on measured drug levels, could be used to circumvent underdosing and overdosing and thereby optimize treatment outcomes. Methods: In this prospective clinical study (www.trialregister.nl; NL6695), the feasibility, tolerability, and efficacy of TDM of oral anticancer drugs will be evaluated. In total, at least 600 patients will be included for (at least) 23 different compounds. Patients starting regular treatment with one of these compounds at the approved standard dose can be included. PK sampling will be performed at 4, 8, and 12 weeks after the start of treatment and every 12 weeks thereafter. Drug concentrations will be measured, and trough concentrations (C min ) will be calculated. In cases where C min falls below the predefined target and acceptable toxicity, a PK-guided intervention will be recommended. This could include emphasizing compliance, adapting concomitant medication (due to drug–drug interactions), instructing to take the drug concomitant with food, splitting intake moments, or recommending a dose increase. Discussion: Despite a strong rationale for the use of TDM for oral anticancer drugs, this is currently not yet widely adopted in routine patient care. This prospective study will be a valuable contribution to demonstrate the additional value of dose optimization on treatment outcome for these drugs.
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