Cersosimo R J
Bouvé College of Pharmacy & Health Sciences, Northeastern University, Boston, MA 02115, USA.
Ann Pharmacother. 1998 Dec;32(12):1324-33. doi: 10.1345/aph.17462.
To review the pharmacologic, pharmacokinetic, therapeutic, and safety aspects of irinotecan, a new antineoplastic agent, and to assess its role in the treatment of colorectal and lung cancer.
English-language articles from the MEDLINE database, January 1990-March 1998; Pharmacia & Upjohn Company; published articles and meeting abstracts.
Studies in humans with cancer, clinical case reports, and open clinical studies were reviewed. Efficacy studies were limited to trials with at least 20 evaluable patients.
Relevant data were extracted from published reports and abstracts.
Irinotecan is an effective agent for the treatment of advanced colorectal cancer. It demonstrates significant activity as a first-line agent and in patients with disease that is refractory to fluorouracil-containing regimens. Activity against lung cancer has also been demonstrated. Limited data indicate activity against cancers of the ovary, cervix, stomach, and in non-Hodgkin's lymphomas. Major toxicity consists of myelosuppression and diarrhea.
Irinotecan is a useful addition to the antineoplastic drug family and offers significant efficacy for treatment of patients with fluorouracil-refractory colorectal cancer.
回顾新型抗肿瘤药物伊立替康的药理学、药代动力学、治疗学及安全性等方面,并评估其在结直肠癌和肺癌治疗中的作用。
1990年1月至1998年3月MEDLINE数据库中的英文文章;法玛西亚普强公司;已发表文章及会议摘要。
对癌症患者的研究、临床病例报告及开放性临床研究进行了综述。疗效研究仅限于至少有20例可评估患者的试验。
从已发表的报告和摘要中提取相关数据。
伊立替康是治疗晚期结直肠癌的有效药物。作为一线药物以及在对含氟尿嘧啶方案耐药的患者中,它都显示出显著活性。对肺癌也有活性。有限的数据表明对卵巢癌、宫颈癌、胃癌及非霍奇金淋巴瘤也有活性。主要毒性包括骨髓抑制和腹泻。
伊立替康是抗肿瘤药物家族中的有益补充,对氟尿嘧啶耐药的结直肠癌患者的治疗具有显著疗效。