Dose Optimization in Oncology Drug Development: The Emerging Role of Pharmacogenomics, Pharmacokinetics, and Pharmacodynamics

被引:8
|
作者
Papachristos, Apostolos [1 ]
Patel, Jai [2 ]
Vasileiou, Maria [3 ]
Patrinos, George P. [4 ,5 ,6 ]
机构
[1] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
[2] Atrium Hlth, Levine Canc Inst, Dept Canc Pharmacol & Pharmacogen, Charlotte, NC 28204 USA
[3] Natl & Kapodistrian Univ Athens, Sch Hlth Sci, Dept Pharm, Athens 16121, Greece
[4] Univ Patras, Sch Hlth Sci, Dept Pharm, Lab Pharmacogen & Individualized Therapy, Patras 26504, Greece
[5] United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Genet & Genom, POB 15551, Al Ain, U Arab Emirates
[6] United Arab Emirates Univ, Zayed Ctr Hlth Sci, POB 15551, Al Ain, U Arab Emirates
关键词
dose optimization; clinical trials; TKIs; ADCs; TDM; monoclonal antibodies; FDA; pharmacogenomics; pharmacodynamics; pharmacokinetics; TYROSINE KINASE INHIBITORS; CANCER; DEBRISOQUINE; AXITINIB; TRIAL;
D O I
10.3390/cancers15123233
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Accelerated clinical development of anticancer drugs is crucial to ensure patients' access to the most safe and effective treatments. At the same time, the development process should be designed to ensure that the optimal dose and schedule are administrated. Therefore, pharmacological methods such as pharmacogenomics, pharmacokinetics, and pharmacodynamics must be integrated to inform oncology drug development and dose optimization. Herein we present a summary and some examples of the utility of those methods. Drugs' safety and effectiveness are evaluated in randomized, dose-ranging trials in most therapeutic areas. However, this is only sometimes feasible in oncology, and dose-ranging studies are mainly limited to Phase 1 clinical trials. Moreover, although new treatment modalities (e.g., small molecule targeted therapies, biologics, and antibody-drug conjugates) present different characteristics compared to cytotoxic agents (e.g., target saturation limits, wider therapeutic index, fewer off-target side effects), in most cases, the design of Phase 1 studies and the dose selection is still based on the Maximum Tolerated Dose (MTD) approach used for the development of cytotoxic agents. Therefore, the dose was not optimized in some cases and was modified post-marketing (e.g., ceritinib, dasatinib, niraparib, ponatinib, cabazitaxel, and gemtuzumab-ozogamicin). The FDA recognized the drawbacks of this approach and, in 2021, launched Project Optimus, which provides the framework and guidance for dose optimization during the clinical development stages of anticancer agents. Since dose optimization is crucial in clinical development, especially of targeted therapies, it is necessary to identify the role of pharmacological tools such as pharmacogenomics, therapeutic drug monitoring, and pharmacodynamics, which could be integrated into all phases of drug development and support dose optimization, as well as the chances of positive clinical outcomes.
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页数:13
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