Grunberg S M, Crowley J J, Livingston R B, Muggia F M, MacDonald J S, Williamson S K, Stephens R L
University of Southern California School of Medicine, Los Angeles.
Cancer Chemother Pharmacol. 1991;28(3):211-3. doi: 10.1007/BF00685511.
Suggestions of a dose-response effect for cisplatin in non-small-cell lung cancer have contributed to the development of very high-dose cisplatin regimens (200 mg/m2 per cycle). We treated 53 eligible patients with metastatic or recurrent non-small-cell lung cancer with a combination of 100 mg/m2 cisplatin and 4 mg/m2 vinblastine, each given on days 1 and 8 of a 28-day cycle. We observed no complete response and 4 partial responses (8%). Median survival was 6 months. Toxicities of grade III or greater included leukopenia (11 cases), nausea/vomiting (6 cases), thrombocytopenia (2 cases), anemia (2 cases), and elevation of transaminase (1 case). Neurotoxicity has been reported to be a major problem in several other very high-dose cisplatin regimens. The low level of neurotoxicity observed in this study may be attributable to the median cumulative cisplatin dose of less than 600 mg/m2. This vinblastine/very high-dose cisplatin regimen showed minor activity against non-small-cell lung cancer. The level of activity did not surpass that of standard-dose (100 mg/m2 per cycle) cisplatin-containing regimens.
顺铂在非小细胞肺癌中的剂量反应效应的相关建议促使了极高剂量顺铂方案(每周期200mg/m²)的发展。我们用100mg/m²顺铂和4mg/m²长春花碱联合治疗了53例符合条件的转移性或复发性非小细胞肺癌患者,两种药物均在28天周期的第1天和第8天给药。我们未观察到完全缓解,有4例部分缓解(8%)。中位生存期为6个月。3级或更高级别的毒性包括白细胞减少(11例)、恶心/呕吐(6例)、血小板减少(2例)、贫血(2例)和转氨酶升高(1例)。在其他几种极高剂量顺铂方案中,神经毒性据报道是一个主要问题。本研究中观察到的低水平神经毒性可能归因于顺铂的中位累积剂量低于600mg/m²。这种长春花碱/极高剂量顺铂方案对非小细胞肺癌显示出轻微活性。活性水平未超过含标准剂量(每周期100mg/m²)顺铂方案。