Abstract

Irinotecan (CPT-11) is widely used for the treatment of unresectable colorectal cancer in combination with fluoropyrimidines, such as 5-fluorouracil and S-1. Diarrhea is one of the adverse effects associated with CPT-11 and frequently reported by patients treated with CPT-11-containing regimens combined with oral fluoropyrimidines. However, the mechanisms involved in this process, as well as whether fluctuations in the frequency and differences in the onset time of diarrhea with each CPT-11-containing regimen are caused by drug interactions remain unclear. Therefore, we examined the incidence of diarrhea caused by each CPT-11-containing regimen in patients with colorectal cancer using data from the large voluntary reporting Japanese Adverse Drug Event Report (JADER) database. Firstly, we searched for suspected drugs related to the occurrence of diarrhea using reported odds ratio and calculated the signal score to assess drug–drug interactions. Subsequently, we conducted a time-to-onset analysis using Weibull distribution. The results showed that the combination of CPT-11 with S-1 increased the frequency of diarrhea due to a pharmacological interaction but delayed its onset. The present results may contribute to the appropriate management of drug-induced adverse effects by healthcare professionals.

Highlights

  • Colorectal cancer (CRC) remains the second most common cause of cancer-related mortality worldwide

  • The results showed that the combination of CPT-11 and S-1 increased the risk of diarrhea as drug-drug interaction (Table 3)

  • 0.005 study yielded two important findings regarding CPT-11-induced major finding is that the combination of CPT-11 plus S-1 increases the incidence of diarrhea due to CPT-11 plus a pharmacological interaction

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Summary

Introduction

Colorectal cancer (CRC) remains the second most common cause of cancer-related mortality worldwide. In Japan, irinotecan (CPT-11) is widely used for the treatment of unresectable CRC in combination with fluoropyrimidines, such as 5-fluorouracil (5-FU). The latter is an oral anticancer drug that combines tegafur with 5-chloro-2,4-dihydropyrimidine (CDHP) and potassium oxonate in a molar ratio of 1.0:0.4:1.0 [1,2]. CPT-11 hydrochloride is a prodrug of 7-ethyl-10-hydroxycamptothecin (SN-38), which is approximately 100- to 1000-fold more cytotoxic than the parent compound. SN-38 prevents DNA recombination by topoisomerase I. DNA damage is not efficiently repaired and apoptosis ensues due to the induction of replication arrest and DNA doublestrand breaks [3,4]

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