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Research progress of chemotherapy-related diarrhea induced by molecularly targeted anti-tumor drugs
- ZHONGGUO YAOFANG Vol. 35, Issue 4, Pages: 506-512(2024)
- 作者机构：
1.北京医院药学部/国家老年医学中心/中国医学科学院老年医学研究院，北京 100730
2.中国航天科工集团七三一医院药学部，北京 100074
- 作者简介：
- 基金信息：
DOI：10.6039/j.issn.1001-0408.2024.04.23
CLC： R979.1;R442.2Published：29 February 2024，
Received：29 August 2023，
Revised：24 January 2024，
扫 描 看 全 文
孙雪林,郑丽,李鸿升等.抗肿瘤分子靶向药物致化疗相关性腹泻的研究进展 Δ[J].中国药房,2024,35(04):506-512.
SUN Xuelin,ZHENG Li,LI Hongsheng,et al.Research progress of chemotherapy-related diarrhea induced by molecularly targeted anti-tumor drugs[J].ZHONGGUO YAOFANG,2024,35(04):506-512.
孙雪林,郑丽,李鸿升等.抗肿瘤分子靶向药物致化疗相关性腹泻的研究进展 Δ[J].中国药房,2024,35(04):506-512. DOI： 10.6039/j.issn.1001-0408.2024.04.23.
SUN Xuelin,ZHENG Li,LI Hongsheng,et al.Research progress of chemotherapy-related diarrhea induced by molecularly targeted anti-tumor drugs[J].ZHONGGUO YAOFANG,2024,35(04):506-512. DOI： 10.6039/j.issn.1001-0408.2024.04.23.
摘要
化疗相关性腹泻（CRD）可导致治疗效果和患者依从性降低，影响肿瘤患者的长期治疗结局，甚至危及生命。除传统化疗药物外，许多分子靶向药物也可导致CRD，包括小分子表皮生长因子受体（EGFR）抑制剂、抗EGFR单克隆抗体、磷酸肌醇3-激酶抑制剂、血管内皮细胞生长因子受体小分子抑制剂、
BCR-ABL1
和KIT抑制剂、人表皮生长因子受体2靶点抑制剂、周期蛋白依赖性激酶抑制剂、抗体-药物偶联物等多种分子靶向药物。其发生机制可能与分子靶向治疗药物引起肠黏膜损伤或肠炎等有关，临床表现为大便频率增加和/或松散不成形，患者常伴有产气过多和/或肠绞痛。不同药物引起的CRD发生率不同，临床应重视病史采集和鉴别诊断，积极干预并进行动态评估，加强患者教育，以及时发现和预防肠毒性的发生。
Abstract
Diarrhea caused by chemotherapy is called chemotherapy-related diarrhea （CRD）. CRD can lead to reduced treatment effectiveness and compliance， affect the long-term outcome of tumor patients， and can be life-threatening in severe cases. In addition to conventional chemotherapy drugs， many molecularly targeted drugs are also associated with CRD， including small molecule epidermal growth factor receptor （EGFR） inhibitors， anti-EGFR monoclonal antibodies， phosphoinositide 3-kinase inhibitors， small molecule inhibitors of vascular endothelial growth factor receptor，
BCR-ABL1
and KIT inhibitors， human epidermal growth factor receptor 2 target inhibitors， cyclin-dependent protein kinase inhibitors， antibody-drug conjugates and other molecularly targeted drugs. The occurrence mechanism may be related to the intestinal mucosal injury or enteritis caused by molecularly targeted drugs. The clinical manifestations are increased stool frequency and/or loose imposition， and patients are often associated with excess hyperproduction and/or colic. The incidence of CRD varies with different drugs. Great importance should be attached to collecting medical history and differential diagnosis， actively intervening and conducting dynamic evaluation， strengthening patient education， and timely detecting and preventing the occurrence of intestinal toxicity.
关键词
化疗相关性腹泻肿瘤靶向治疗肠毒性不良反应
Keywords
tumortargeted therapyintestinal toxicityadverse drug reactions
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