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胃肠道恶性肿瘤的新型药物:第1部分:伊立替康的临床应用

New agents in gastrointestinal malignancies: Part 1: Irinotecan in clinical practice.

作者信息

Stucky-Marshall L

机构信息

Northwestern Memorial Hospital, Chicago, IL 60611, USA.

出版信息

Cancer Nurs. 1999 Jun;22(3):212-9. doi: 10.1097/00002820-199906000-00004.

Abstract

In 1996 two chemotherapy agents were introduced by the U.S. Food and Drug Administration (FDA) with indications for the gastrointestinal malignancies for advanced colon and pancreatic cancers. The agents approved were irinotecan hydrochloride (CAMPTOSAR Injection, Pharmacia & Upjohn Company, Kalamazoo, MI; also investigated under the name CPT-11) for the second-line treatment of metastatic colorectal cancer, recurrent or relapsed, after 5-fluorouracil (5-FU)-based therapy, and gemcitabine hydrochloride (GEMZAR for injection, Eli Lilly and Company, Indianapolis, IN; also referred to as dFdC) for first-line treatment of locally advanced and metastatic cancer of the pancreas. Irinotecan and gemcitabine, with demonstrated activity in colorectal and pancreatic cancer, respectively, are generally well tolerated and can be administered safely on an outpatient basis. Clinically relevant activity is documented for both single agents. Therapy-related side effects are manageable with appropriate monitoring and intervention, and reversible with dose modification or discontinuation. This article is one of a two-part series on new chemotherapeutic agents for gastrointestinal malignancies. The first in the series, this article addresses the agent irinotecan hydrochloride (CAMPTOSAR Injection). The second article, appearing in a subsequent issue, will review gemcitabine hydrochloride (Gemzar for Injection). Both articles review the current clinical use, safety profile, and key patient management guidelines for these new and novel cytotoxics. As clinical and investigational use of irinotecan and gemcitabine increases, the oncology nurse and other members of the health care team will need to anticipate potential treatment associated toxicities and be knowledgeable in their early identification and management. As patient advocates, oncology nurses play a key role in treatment outcome and related quality of life through expert patient education, symptom recognition, and intervention individualized to patient tolerance. This first article of the series addresses irinotecan, which in 1996 was approved for the second-line therapy of metastatic colorectal cancer, recurrent or elapsed, after 5-fluorouracil (5-FU).

摘要

1996年,美国食品药品监督管理局(FDA)批准了两种化疗药物,用于治疗晚期结肠癌和胰腺癌等胃肠道恶性肿瘤。获批的药物包括盐酸伊立替康(商品名:开普拓注射剂,法玛西亚普强公司,密歇根州卡拉马祖市;也曾以CPT - 11的名称进行研究),用于在基于5 - 氟尿嘧啶(5 - FU)的治疗后,对复发或转移性结直肠癌进行二线治疗;以及盐酸吉西他滨(商品名:健择注射剂,礼来公司,印第安纳波利斯市;也称为dFdC),用于局部晚期和转移性胰腺癌的一线治疗。伊立替康和吉西他滨分别在结直肠癌和胰腺癌中显示出活性,通常耐受性良好,可在门诊安全给药。两种单药均有临床相关活性记录。通过适当的监测和干预,与治疗相关的副作用是可控的,通过调整剂量或停药可逆转。本文是关于胃肠道恶性肿瘤新型化疗药物系列文章的第一篇。作为该系列的第一篇文章,本文介绍盐酸伊立替康(开普拓注射剂)。后续期刊将发表第二篇文章,回顾盐酸吉西他滨(健择注射剂)。两篇文章均回顾了这些新型细胞毒性药物的当前临床应用、安全性概况以及关键的患者管理指南。随着伊立替康和吉西他滨临床及研究应用的增加,肿瘤护士和医疗团队的其他成员需要预测潜在的治疗相关毒性,并了解其早期识别和管理方法。作为患者的支持者,肿瘤护士通过专业的患者教育、症状识别以及根据患者耐受性进行个体化干预,在治疗结果和相关生活质量方面发挥关键作用。本系列的第一篇文章介绍伊立替康,它于1996年被批准用于在5 - 氟尿嘧啶(5 - FU)治疗后,对复发或转移性结直肠癌进行二线治疗。

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