Evaluation of utility of pharmacokinetic studies in phase I trials of two oncology drugs

Clin Cancer Res. 2013 Nov 1;19(21):6039-43. doi: 10.1158/1078-0432.CCR-13-0597. Epub 2013 Sep 20.

Abstract

Purpose: There are many phase I trials of oncology drug combinations, very few of which report clinically significant pharmacokinetic interactions. We hypothesized that the utility of such pharmacokinetic drug-drug interaction (DDI) studies is low in the absence of a mechanistic hypothesis.

Experimental design: We retrospectively reviewed 152 phase I (two drug) combination studies published between 2007 and 2011.

Results: Only 28 (18%) studies had an implicit or explicit rationale, either inhibition/induction of a drug-metabolizing enzyme or transporter, cosubstrates for the same enzyme or transporter, potential for end-organ toxicity, or protein binding. Only 12 (8%) studies demonstrated a statistically significant DDI, on the basis of change in clearance (or area under the curve) of parent drug and/or active metabolite. There was a strong association between a rationale and a demonstrable drug interaction, as only 2% of studies without a rationale demonstrated a DDI, compared with 32% of studies with a rationale (Fisher exact test; P < 10(-6)).

Conclusion: DDI studies should not be routinely performed as part of phase I trials of oncology combinations.

Publication types

  • Meta-Analysis
  • Research Support, N.I.H., Extramural

MeSH terms

  • Antineoplastic Agents / pharmacokinetics*
  • Antineoplastic Agents / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Clinical Trials, Phase I as Topic
  • Drug Interactions*
  • Humans

Substances

  • Antineoplastic Agents