Matsui Y, Satake N, Kusume K, Kado M, Ohshima S, Yamamoto Y, Ishida H, Matsubara Y, Ikeda S
Second Dept. of Internal Medicine, Chest Disease Research Institute, Kyoto University, Japan.
Gan To Kagaku Ryoho. 1991 Dec;18(15):2567-72.
Sixteen untreated patients with small cell lung cancer were treated with a combination of Etoposide (70 mg/m2 i.v., day 3-5), Cisplatin (40 mg/m2 i.v., days 1 and 8) and THP (20 mg/m2 i.v., days 1 and 8). Cycles were repeated every 4 weeks and 15 patients received more than two cycles. The objective response rate was 80% (12 of 15) in complete cases, 91% (10 of 11) in limited disease and 50% (2 of 4) in extensive disease. CR rate was 33% in complete cases, 46% in limited disease. The median duration of response was 22.6 weeks. The median survival was more than 12 months in complete cases. Toxicity was primarily myelosuppression. Three of 15 patients had leukopenia of grade 4, 3 of 15 of grade 3, and 7 of 15 of grade 2. Nausea and vomiting were well tolerated by metoclopromide and methylprednisolone. The renal toxicity was minimal. There were no chemotherapy-related lethal complications. This schedule of Etoposide, split-dose Cisplatin and THP is effective and safe for patients with small cell lung cancer. However, the advantage of THP is still controversial.
16例未经治疗的小细胞肺癌患者接受了依托泊苷(70mg/m²静脉注射,第3 - 5天)、顺铂(40mg/m²静脉注射,第1天和第8天)和吡柔比星(20mg/m²静脉注射,第1天和第8天)联合治疗。每4周重复一个周期,15例患者接受了两个以上周期的治疗。完全缓解病例的客观缓解率为80%(15例中的12例),局限性疾病患者为91%(11例中的10例),广泛性疾病患者为50%(4例中的2例)。完全缓解病例的CR率为33%,局限性疾病患者为46%。缓解的中位持续时间为22.6周。完全缓解病例的中位生存期超过12个月。毒性主要为骨髓抑制。15例患者中有3例出现4级白细胞减少,3例为3级,7例为2级。甲氧氯普胺和甲泼尼龙对恶心和呕吐有良好的耐受性。肾毒性极小。无化疗相关的致命并发症。依托泊苷、分剂量顺铂和吡柔比星的这种治疗方案对小细胞肺癌患者有效且安全。然而,吡柔比星的优势仍存在争议。