| Literature DB >> 31077412 |
Jennifer H Martin1, Simon Dimmitt1,2.
Abstract
Drug development for cancer chemotherapy has an interesting history. A mix of serendipity, animal, cell line, and standard pharmacological principles of dose, dose-response, dose-concentration, dose intensity and combination therapies have been used to develop optimal dosing schedules. However in practice, significant gaps in the translation of preclinical to clinical dosing schedules persist, and clinical development has instead moved to new drug development. A older chemotherapies are still the backbone of most solid tumour schedules, therapeutic drug monitoring has emerged as a method for optimising the dose for individual patients.Entities:
Keywords: body surface area; cancer; dose-response; flat dosing; log-dose; surrogate outcome
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Year: 2019 PMID: 31077412 PMCID: PMC6783605 DOI: 10.1111/bcp.13979
Source DB: PubMed Journal: Br J Clin Pharmacol ISSN: 0306-5251 Impact factor: 4.335