Lee D H, Kim S-W, Suh C, Lee J-S, Lee J H, Lee S-J, Ryoo B Y, Park K, Kim J S, Heo D S, Kim N K
Division of Oncology, Department of Internal medicine, Asan Medical Center, Seoul, Korea.
Ann Oncol. 2008 Jan;19(1):123-7. doi: 10.1093/annonc/mdm437. Epub 2007 Sep 6.
Belotecan (Camtobell, Chong Keun Dang Corp, Seoul, Korea; CKD602) is a new camptothecin analogue. This study aimed to investigate the safety and efficacy of single-agent belotecan for small-cell lung cancer (SCLC).
Twenty-seven patients with chemotherapy-naive or chemosensitive SCLC were treated with belotecan 0.5 mg/m(2)/day on days 1-5 of a 3-week cycle. All 27 patients were assessable for toxicity, and 21 patients assessable for response.
Nine patients (42.9%) showed objective tumor responses including one complete response; seven (63.6%) in 11 chemotherapy-naive patients; and two (20.0%) in 10 chemosensitive patients. With a median follow-up of 5 years, median progression-free and survival time for chemotherapy-naive patients were 4.8 months and 11.9 months, respectively, while the corresponding values for chemosensitive patients were 3.3 months and 10.5 months, respectively. The most common toxicity was neutropenia.
Belotecan was active in SCLC patients as a single agent, warranting further investigations of belotecan in combination with platinum or other active agents.
倍喜康(Camtobell,韩国首尔崇根堂制药公司;CKD602)是一种新型喜树碱类似物。本研究旨在探讨单药倍喜康治疗小细胞肺癌(SCLC)的安全性和疗效。
27例初治或化疗敏感的小细胞肺癌患者接受倍喜康治疗,剂量为0.5mg/m²/天,在3周周期的第1 - 5天给药。所有27例患者均可评估毒性,21例患者可评估疗效。
9例患者(42.9%)出现客观肿瘤反应,包括1例完全缓解;11例初治患者中有7例(63.6%);10例化疗敏感患者中有2例(20.0%)。中位随访5年,初治患者的中位无进展生存期和总生存期分别为4.8个月和11.9个月,而化疗敏感患者的相应值分别为3.3个月和10.5个月。最常见的毒性是中性粒细胞减少。
倍喜康作为单药在小细胞肺癌患者中具有活性,值得进一步研究倍喜康与铂类或其他活性药物联合使用的情况。