Preventing oxaliplatin-induced neurotoxicity: rationale and design of phase Ib randomized, double-blind, placebo-controlled, cross-over trials for early clinical evaluation of investigational therapeutics

被引:17
作者
Han, Catherine H. [1 ,2 ,3 ]
Kilfoyle, Dean H. [4 ]
Hill, Andrew G. [5 ]
Jameson, Michael B. [6 ,7 ]
McKeage, Mark J. [1 ,2 ,3 ]
机构
[1] Univ Auckland, Fac Med & Hlth Sci, Dept Pharmacol & Clin Pharmacol, Auckland, New Zealand
[2] Univ Auckland, Fac Med & Hlth Sci, Auckland Canc Soc Res Ctr, Sch Med Sci, Auckland, New Zealand
[3] Auckland City Hosp, Dept Med Oncol, Auckland, New Zealand
[4] Auckland City Hosp, Dept Neurophysiol, Auckland, New Zealand
[5] Tasman Oncol Res, Southport, Qld, Australia
[6] Waikato Hosp, Dept Oncol, Hamilton, New Zealand
[7] Univ Auckland, Fac Med & Hlth Sci, Waikato Clinical Campus, Hamilton, New Zealand
关键词
Oxaliplatin; chemotherapy neurotoxicity; nerve hyperexcitability; pharmacokinetics; phase I clinical trial design; chemoprotection; crossover trial; INDUCED PERIPHERAL NEUROPATHY; III COLON-CANCER; COLORECTAL-CANCER; MAGNESIUM INFUSIONS; IN-VITRO; STAGE-II; CHEMOTHERAPY; LEUCOVORIN; FLUOROURACIL; PLATINUM;
D O I
10.1080/17425255.2016.1223625
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Oxaliplatin-based chemotherapy has become the standard treatment for colorectal cancer and other gastrointestinal tumor types. Oxaliplatin- induced neurotoxicity is a major treatment-limiting side effect that compromizes the delivery of cancer treatment and causes long-standing neurological deficits that negatively impact upon patient quality of life Areas covered: The prevention of oxaliplatin-induced neurotoxicity represents an important opportunity for new therapeutic product development to address this major unmet medical need. In this article, we describe a phase Ib clinical trial design, and study procedures and protocols, that we have developed and now propose for the early clinical evaluation of investigational therapeutics for preventing oxaliplatin-induced neurotoxicity. Expert opinion: Recently, several advances have been made in the development of research methodologies applicable to the clinical evaluation of investigational drugs for preventing oxaliplatin-induced neurotoxicity. As we gain better understanding of the mechanisms of oxaliplatin-induced neurotoxicity, we will be able to use these methods to develop and test more effective and targeted neuroprotective agents that may not only improve patients' quality of life but also improve treatment delivery and survival outcomes.
引用
收藏
页码:1479 / 1490
页数:12
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