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伊立替康与替吉奥联合治疗结肠癌致致命性骨髓抑制、腹泻及神经毒性1例报告

A fatal myelosuppression, diarrhea and neurotoxicity induced by combination of irinotecan and tegafur-gimeracil-oteracil potassium in the treatment of colon cancer: a case report.

作者信息

Liu Yang-Xi, Le Ke-Jia, Zhang Chi, Cui Min, Zhou Hong, Su Ying-Jie, Gu Zhi-Chun

机构信息

Department of Pharmacyy, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200127, China.

Department of Gastrointestinal Surgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200127, China.

出版信息

Transl Cancer Res. 2020 Jan;9(1):382-387. doi: 10.21037/tcr.2019.11.39.

Abstract

Chemical treatment is the vital pattern for colon cancer patients after surgery. Irinotecan and tegafur-gimeracil-oteracil potassium (S-1) combined chemotherapy is effective on metastatic colorectal cancer (mCRC). Nevertheless, patients receiving this combined chemotherapy might suffer the adverse drug reaction (ADR), such as myelosuppression and/or diarrhea, which could lead to poor prognosis. Here, we report a 76-year-old Chinese female who died due to the toxicity of combined therapy with irinotecan and S-1. This patient received irinotecan and S-1 combined therapy for 6 sessions after laparoscopic radical operation on colon cancer. After 6 sessions of chemotherapy, myelosuppression and severe diarrhea appeared with delirious accompanied. Antineoplastic agents were stopped immediately due to the appearance of III grade myelosuppression and IV grade diarrhea. Loperamide and octreotide were used to stop diarrhea, while granulocyte colony-stimulating factor (G-CSF) and recombinant human IL (IL-11) were used to improve blood cell count. Meanwhile, intravenous fluid replacement was continuously transfused to maintain water electrolyte balance. The patient remained continuous insanity and died 4 days after admission because of multiple organ failure, cardiac insufficiency, sever myelosuppression and ascending colon cancer. Myelosuppression is the principal toxicity associated with chemotherapy. And delayed-onset diarrhea is most frequently reported ADR of irinotecan, which could also be induced by S-1. Moreover, neurotoxicity is rarely reported as ADR for both irinotecan and S-1. Postoperative adjuvant chemotherapy should be carefully selected according to specific condition of patient. Blood routine examination should be monitored, and clinical manifestations should be carefully observed to ensure the safety and effectiveness of chemotherapy during the treatment.

摘要

化学治疗是结肠癌患者术后的重要治疗方式。伊立替康与替吉奥联合化疗对转移性结直肠癌(mCRC)有效。然而,接受这种联合化疗的患者可能会出现药物不良反应(ADR),如骨髓抑制和/或腹泻,这可能导致预后不良。在此,我们报告一名76岁的中国女性因伊立替康和替吉奥联合治疗的毒性死亡。该患者在结肠癌腹腔镜根治术后接受了6个疗程的伊立替康和替吉奥联合治疗。6个疗程化疗后,出现骨髓抑制和严重腹泻并伴有谵妄。由于出现Ⅲ级骨髓抑制和Ⅳ级腹泻,立即停用抗肿瘤药物。使用洛哌丁胺和奥曲肽止泻,同时使用粒细胞集落刺激因子(G-CSF)和重组人白细胞介素(IL-11)提高血细胞计数。同时,持续静脉补液以维持水电解质平衡。患者持续神志不清,入院4天后因多器官功能衰竭、心功能不全、严重骨髓抑制和升结肠癌死亡。骨髓抑制是与化疗相关的主要毒性。迟发性腹泻是伊立替康最常报道的ADR,替吉奥也可能诱发。此外,神经毒性作为伊立替康和替吉奥的ADR很少报道。术后辅助化疗应根据患者具体情况谨慎选择。应监测血常规检查,并仔细观察临床表现,以确保治疗期间化疗的安全性和有效性。

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本文引用的文献

1
NCCN Guidelines Insights: Colon Cancer, Version 2.2018.NCCN 指南解读:结肠癌,第 2.2018 版。
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S-1: a promising new oral fluoropyrimidine derivative.S-1:一种有前景的新型口服氟嘧啶衍生物。
Expert Opin Investig Drugs. 2009 Mar;18(3):335-48. doi: 10.1517/13543780902729412.

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