Tas Faruk, Derin Duygu, Guney Nese, Camlica Hakan, Aydiner Adnan, Topuz Erkan
Institute of Oncology, Istanbul University, Turkey.
Lung Cancer. 2007 Jul;57(1):79-83. doi: 10.1016/j.lungcan.2007.02.009. Epub 2007 Mar 26.
Topotecan is an active agent for the management of untreated and recurrent extensive-disease small cell lung cancer (ED-SCLC). This study was designed to evaluate the efficacy and safety of a triplet combination with topotecan added to the standard PE regimen in previously untreated patients with ED-SCLC.
Twenty-one patients (median age 55 years, and 18 male) with chemotherapy-naive ED-SCLC were enrolled into the study. PET treatment consisted of etoposide 80mg/m(2), cisplatin 20mg/m(2) and topotecan 0.75mg/m(2) and all were given intravenously on days 1 to 3 for every 3 weeks.
Leucopoenia and/or neutropenia and to a lesser extent thrombocytopenia were the main dose-limiting toxicities. Severe leucopenia/neutropenia were observed in 14 (67%)/12 (57%) patients, and only two (10%) developed febrile neutropenia. Severe thrombocytopenia was observed in 6 (29%) patients and one patient died due to orbital and cerebral haemorrhage. Dose reductions were required in 13 (62%) patients, delays in 8 (38%) patients and early treatment discontinuation in 3 (14%) patients. The overall response rate was 52.6% (95% CI: 28, 9-75.6) with 2 (10.5%) complete and 8 (42.1%) partial responses. The overall median survival time was 6.6 months (range 0.5-16.5 months) and the 6-month overall survival was 65.3%+/-11.7. The overall median survival time of responders was 9.7 months compared to 5.7 months in non-responders (p=0.026).
Topotecan combined with PE regimen with this schedule and dosage does not seem to provide any benefit in terms of response and survival in ED-SCLC patients and does not deserve further studies.
拓扑替康是治疗初治及复发的广泛期小细胞肺癌(ED-SCLC)的一种有效药物。本研究旨在评估在标准PE方案基础上加用拓扑替康的三联方案对初治ED-SCLC患者的疗效和安全性。
21例初治ED-SCLC患者(中位年龄55岁,男性18例)入组本研究。PET治疗方案为依托泊苷80mg/m²、顺铂20mg/m²和拓扑替康0.75mg/m²,均于每3周的第1至3天静脉给药。
白细胞减少和/或中性粒细胞减少以及程度较轻的血小板减少是主要的剂量限制性毒性。14例(67%)/12例(57%)患者出现严重白细胞减少/中性粒细胞减少,仅2例(10%)发生发热性中性粒细胞减少。6例(29%)患者出现严重血小板减少,1例患者因眼眶和脑出血死亡。13例(62%)患者需要减量,8例(38%)患者出现治疗延迟,3例(14%)患者提前终止治疗。总缓解率为52.6%(95%CI:28.9-75.6),其中2例(10.5%)完全缓解,8例(42.1%)部分缓解。总中位生存时间为6.6个月(范围0.5-16.5个月),6个月总生存率为65.3%±11.7。缓解者的总中位生存时间为9.7个月,未缓解者为5.7个月(p=0.026)。
拓扑替康联合PE方案采用此给药方案和剂量,在ED-SCLC患者的缓解率和生存率方面似乎未带来任何益处,不值得进一步研究。