Irinotecan-induced Neutropenia: A Comprehensive Review of Pathogenesis, Risk Factors, and Management

Irinotecan is a camptothecin derivative that exerts its antitumor effects by metabolizing into the active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38). It is widely used clinically for treating various advanced solid tumors. However, irinotecan frequently induces neutropenia, predisposing patients to infection and even death. This review aims to provide a theoretical basis for the clinical management of irinotecan-induced neutropenia (IIN). Irinotecan and SN-38 mainly induce hematopoietic stem cell damage and dysfunction by inhibiting topoisomerase I and triggering mitochondrial injury, which ultimately results in neutropenia. Notably, the risk factors of IIN include irinotecan dosage, gene polymorphism, individual baseline characteristics, and drug combination. And several strategies effectively prevent IIN, such as adjustment of drug dosage, genotype testing, oral alkalinizing drugs, supplement of granulocyte colony-stimulating factor, and regulation of intestinal microorganisms. In summary, this review systematically elaborates on the classification, epidemiology, pathogenesis, risk factors, and management strategies of IIN, with the goal of providing references for the clinical prevention and management of irinotecan-related adverse reactions.

Authors

Publication Details

Journal
Journal of Exploratory Research in Pharmacology
Published
2026-05-21
DOI
https://doi.org/10.14218/jerp.2026.00002
Primary Topic
Cancer therapeutics and mechanisms
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Irinotecan-induced Neutropenia: A Comprehensive Review of Pathogenesis, Risk Factors, and Management

Lan Yan, Chengliang Zhang, Cheng Tian, Chengren Shu et al.
Journal of Exploratory Research in Pharmacology
Cancer therapeutics and mechanisms
article

Irinotecan-induced Neutropenia: A Comprehensive Review of Pathogenesis, Risk Factors, and Management

Lan Yan, Chengliang Zhang, Cheng Tian, Chengren Shu, Li, Wei, 1970 May 26-, Lijuan Zhang
article en

Abstract

Irinotecan is a camptothecin derivative that exerts its antitumor effects by metabolizing into the active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38). It is widely used clinically for treating various advanced solid tumors. However, irinotecan frequently induces neutropenia, predisposing patients to infection and even death. This review aims to provide a theoretical basis for the clinical management of irinotecan-induced neutropenia (IIN). Irinotecan and SN-38 mainly induce hematopoietic stem cell damage and dysfunction by inhibiting topoisomerase I and triggering mitochondrial injury, which ultimately results in neutropenia. Notably, the risk factors of IIN include irinotecan dosage, gene polymorphism, individual baseline characteristics, and drug combination. And several strategies effectively prevent IIN, such as adjustment of drug dosage, genotype testing, oral alkalinizing drugs, supplement of granulocyte colony-stimulating factor, and regulation of intestinal microorganisms. In summary, this review systematically elaborates on the classification, epidemiology, pathogenesis, risk factors, and management strategies of IIN, with the goal of providing references for the clinical prevention and management of irinotecan-related adverse reactions.

Journal of Exploratory Research in PharmacologyVol. 11(2)
Natural Science Foundation of Hubei Province
Good health and well-being
Openalex Percentile: Top 8%
Cancer therapeutics and mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.