Sørensen J B, Hansen H H
Department of Oncology ONB, Finsen Institute, Copenhagen, Denmark.
Cancer Chemother Pharmacol. 1988;21(2):103-16. doi: 10.1007/BF00257355.
Combination chemotherapy has been used widely in the treatment of inoperable adenocarcinoma of the lung (ACL), but without uniform success. This review summarizes current knowledge of combination chemotherapy in ACL, with the aim of establishing critical background material for future studies. Not all the numerous combinations applied in non-randomized studies have produced response rates above 20% when evaluated in randomized trials. This holds true for the following regimens: cyclophosphamide + lomustine + methotrexate (response rates 14%-38%), hexamethylmelamine + doxorubicin + methotrexate (13%-32%), methotrexate + doxorubicin + cyclophosphamide + lomustine (13%-24%), cyclophosphamide + doxorubicin + cisplatin (0-36%), cyclophosphamide + bleomycin + cisplatin (20%), mitomycin C + vinblastine + cisplatin (26%-33%), cyclophosphamide + doxorubicin + etoposide + cisplatin (29%) and vindesine + cisplatin (33%). None of these combinations has been shown to be clearly superior to single-agent treatment. Nor has any specific regimen been shown to have clear advantages over other active combination chemotherapy regimens or over the sequential administration of either single agents or combined treatments. The prognosis for patients with inoperable ACL remains dismal. None of the studies considered in this review revealed median survival times exceeding 47 weeks. High priority should therefore be given to the identification of new compounds with significant activity against ACL.
联合化疗已广泛应用于不可切除的肺腺癌(ACL)的治疗,但并非都取得了一致的成功。本综述总结了目前关于ACL联合化疗的知识,目的是为未来的研究建立关键的背景资料。在非随机研究中应用的众多联合方案,在随机试验评估时,并非所有方案的缓解率都高于20%。以下方案均是如此:环磷酰胺+洛莫司汀+甲氨蝶呤(缓解率14%-38%)、六甲蜜胺+阿霉素+甲氨蝶呤(13%-32%)、甲氨蝶呤+阿霉素+环磷酰胺+洛莫司汀(13%-24%)、环磷酰胺+阿霉素+顺铂(0-36%)、环磷酰胺+博来霉素+顺铂(20%)、丝裂霉素C+长春碱+顺铂(26%-33%)、环磷酰胺+阿霉素+依托泊苷+顺铂(29%)和长春地辛+顺铂(33%)。这些联合方案均未显示明显优于单药治疗。也没有任何一种特定方案显示出比其他有效的联合化疗方案或比单药序贯给药或联合治疗有明显优势。不可切除的ACL患者的预后仍然很差。本综述中考虑的所有研究均未显示中位生存时间超过47周。因此,应高度优先寻找对ACL有显著活性的新化合物。