Ariyoshi Y, Sugiura T
Dept. of Hematology and Chemotherapy, Aichi Cancer Center.
Gan To Kagaku Ryoho. 1994 Nov;21(15):2578-84.
New promising anticancer drugs for chemotherapy against lung cancer were reviewed on the basis of the outcomes of clinical trials which were carried out in Japan, USA and Europe. They included irinotecan, 254-S, vinorelubine, gemcitabine, taxol and Taxotere. Response rates of CPT-11 (irinotecan) were evaluated to be approximately 30% for non-small cell lung cancer (NSCLC) and more than 40% for small cell lung cancer (SCLC). Dose limiting toxicities was leukopenia and diarrhea. These toxicities should be managed very carefully because these occasionally might be life-threatening. Efficacy of 254-S, vinorelbine and gemcitabine were thought to be moderately active for NSCLC. Main toxicity was leukopenia and others were tolerable. Clinical trials of taxol and taxotere showed to be promising for NSCLC. Dose limiting factor was leukopenia. As for hypersensitivity seen in the administration of taxol, it is noted that premedication of antiallergic drugs is required. Taxol and Taxotere will be important for combined chemotherapy for advanced stage lung cancer.
基于在日本、美国和欧洲开展的临床试验结果,对用于肺癌化疗的新型有前景的抗癌药物进行了综述。这些药物包括伊立替康、254-S、长春瑞滨、吉西他滨、紫杉醇和多西他赛。CPT-11(伊立替康)对非小细胞肺癌(NSCLC)的缓解率评估约为30%,对小细胞肺癌(SCLC)则超过40%。剂量限制性毒性为白细胞减少和腹泻。这些毒性必须非常谨慎地处理,因为它们偶尔可能危及生命。254-S、长春瑞滨和吉西他滨对NSCLC的疗效被认为中等。主要毒性是白细胞减少,其他毒性可耐受。紫杉醇和多西他赛的临床试验对NSCLC显示出前景。剂量限制因素是白细胞减少。至于紫杉醇给药时出现的超敏反应,需注意要预先使用抗过敏药物。紫杉醇和多西他赛对晚期肺癌的联合化疗将很重要。