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机构地区:[1]广州市中西医结合医院肿瘤科,广州510800
出 处:《临床肿瘤学杂志》2010年第7期640-642,共3页Chinese Clinical Oncology
摘 要:目的观察洛铂联合伊立替康方案治疗经EP方案初治后3~6个月内复发的广泛期晚期小细胞肺癌(SCLC)的疗效和安全性。方法选取24例SCLC患者予洛铂35mg/m^2,d1;伊立替康200mg/m^2,d1,21d为1周期。2个周期后评价疗效和毒副反应,并随访总生存时间(0S)和疾病进展时间(TTP)。结果24例均可评价疗效,完全缓解2例,部分缓解8例,总有效率为41.7%;稳定5例,进展9例,中位TTP为4.3个月,中位OS为7.4个月。毒副反应主要为血液学毒性和消化道反应,3、4级白细胞减少、中性粒细胞减少和血小板减少发生率分别为50.0%(12/24)、41.7%(10/24)和20.8%(5/24);腹泻发生率为87.5%(21/24),其中3、4级腹泻为58.3%(14/24)。全组无毒性相关死亡。结论洛铂联合伊立替康方案作为中度敏感复发性SCLC的挽救治疗方案有较好的疗效,毒副反应可以耐受。Objective To observe the efficacy and safety of chemotherapy consisted of lobaplatin and irinotecan for Chinese patients with advanced small cell lung cancer(SCLC). Methods Eligible patients with SCLC who had relapsed in 3-6 months after the first line therapeutic regimen of EP were done with lobaplatin and irinotecan. The regimen consisted of lobaplatin 35mg/m^2 on d1 and irinotecan 200mg/m^2 on dl, the plan was given every 21 days. Results Twenty-four patients were evaluable for response, in which 2 achieved complete response and 8 partial responses, namely the objective responses rate was 41.7%, 5 patients had stable disease and 9 progressive diseases. Thus the disease control rate was 62. 5%. The median time to progression and overall survival was 4. 3 months and 7.4 months, respectively. The main toxicity was the matological toxicity and gastrointestinal tract side reaction. Grade Ⅲ, Ⅳ- leucopenia was seen in 12 patients(50. 0% ), neutropenia in 10 patients(41.7% ), and thrombocytopenia in 5 patients(20. 8% ). Diarrhea was seen in 21 patients(87.5% ), 14 of who were grade Ⅲ,Ⅳ. There was no treatment-related death. Conclusion The combination of lobaplatin and irinotecan is highly active and tolerable in patients with chemotherapy mediate sensitive relapsed SCLC when it is administered as rescue treatment.
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