Sørensen J B, Hansen H H
Department of Oncology, Rigshospitalet, Copenhagen, Denmark.
Invest New Drugs. 1993 May-Aug;11(2-3):103-33. doi: 10.1007/BF00874146.
Vindesine is a semisynthetic derivative of vinblastine which has been evaluated in clinical studies since the late 1970's. The literature on vindesine in the treatment of non-small cell lung cancer has been reviewed and all aspects of vindesine treatment in this disease has been covered. It is concluded that vindesine as a single agent yields a response rate of 18% based on the treatment of 295 patients included in phase II trials (95% confidence limits 13%-22%). No difference was observed among the three major histologic types of non-small cell lung cancer. In phase III trials, the response rate and confidence limits are at a similar level. Combination chemotherapy including vindesine plus cisplatin ranks among the most active treatments in non-small cell lung cancer and is as active as etoposide plus cisplatin, both with respect to response rate and survival. It has not been documented that the addition of one or two other drugs to the combination of vindesine yields an increase in survival. When best supportive care was compared with a combination of vindesine plus cisplatin, the group with chemotherapy was attributed a survival advantage in all three studies published, and the difference was statistically significant in two of these three studies. Thus, vindesine has a well documented activity in non-small cell lung cancer and ranks among the most active single agents in this disease. Vindesine is also part of several active combination chemotherapies among which the combination of vindesine plus cisplatin is particularly interesting, because it has been repeatedly shown to prolong survival as compared to supportive care. Especially this latter point leads to the conclusion that there is a role for vindesine in the treatment of non-small cell lung cancer. However, the concept of chemotherapy in this disease remains investigational even though the advances seen in recent years clearly merit further studies.
长春地辛是长春碱的半合成衍生物,自20世纪70年代末以来一直在临床研究中进行评估。本文回顾了长春地辛治疗非小细胞肺癌的相关文献,并涵盖了长春地辛治疗该疾病的各个方面。基于纳入II期试验的295例患者的治疗情况得出结论,长春地辛作为单一药物的缓解率为18%(95%置信区间为13%-22%)。在非小细胞肺癌的三种主要组织学类型之间未观察到差异。在III期试验中,缓解率和置信区间处于相似水平。包括长春地辛加顺铂的联合化疗是治疗非小细胞肺癌最有效的疗法之一,在缓解率和生存率方面与依托泊苷加顺铂一样有效。尚未有文献证明在长春地辛联合方案中添加一两种其他药物能提高生存率。当将最佳支持治疗与长春地辛加顺铂联合治疗进行比较时,在已发表的三项研究中,化疗组均显示出生存优势,其中两项研究的差异具有统计学意义。因此,长春地辛在非小细胞肺癌中具有充分记录的活性,是该疾病最有效的单一药物之一。长春地辛也是几种有效的联合化疗方案的组成部分,其中长春地辛加顺铂的联合方案尤其引人注目,因为与支持治疗相比,它已多次显示出能延长生存期。特别是后一点得出结论,长春地辛在非小细胞肺癌治疗中具有一定作用。然而,尽管近年来取得的进展显然值得进一步研究,但该疾病的化疗概念仍处于研究阶段。