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首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Cisplatin-etoposide alternating with topotecan in patients with extensive stage small cell lung cancer (SCLC). A multicenter phase II study.
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Cisplatin-etoposide alternating with topotecan in patients with extensive stage small cell lung cancer (SCLC). A multicenter phase II study.

机译:顺铂-依托泊苷与拓扑替康交替治疗广泛期小细胞肺癌(SCLC)患者。多中心II期研究。

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PURPOSE: In order to investigate the feasibility of a potentially non-cross resistant drug regimen, we alternated cycles of cisplatin-etoposide with topotecan as front-line treatment in patients with extensive stage small cell lung cancer (SCLC). PATIENTS AND METHODS: Thirty-six previously untreated patients with extensive stage SCLC received cisplatin 75 mg/m(2) IV on day 1 and etoposide 100 mg/m(2) IV on days 1-3 on cycles one, three, five and seven and topotecan 1.5 mg/m(2) IV on days 1-5 on cycles two, four, six and eight. Cycles were repeated every 21 days. Patients' median age was 60 years and performance status (WHO) was 0 for 13, 1 for 20 and 2 for three patients. All patients were evaluable for response and toxicity. RESULTS: Five (14%) patients achieved a complete response and 18 (50%) a partial response for an overall response rate of 64% (95% confidence interval: 48.2-79.6%). After a median follow up of 10 months, the median duration of response was 5.5 months, the time to tumor progression8 months and the probability of 1-year survival 48.9%. A total of 126 cycles of cisplatin-etoposide and 117 cycles of topotecan were administered with a median number of 4 cycles/patient for each regimen. There were no toxic deaths. Treatment delays due to toxicity occurred in 13 (10%) cycles after cisplatin-etoposide and 16 (14%) cycles after topotecan while doses were reduced in seven (6%) and five (4%) cycles, respectively. Grade 3-4 neutropenia, thrombocytopenia and febrile neutropenia complicated 13, 1 and 3% of cisplatin-etoposide cycles and 28, 6 and 1% of topotecan, respectively. Non-hematologic toxicity was mild. The delivered dose intensity was 96% for cisplatin and etoposide and 98% for topotecan. CONCLUSIONS: The alternating administration of cisplatin-etoposide and topotecan is a feasible, active and well-tolerated regimen in patients with extensive stage SCLC.
机译:目的:为了研究潜在的非交叉耐药性药物治疗方案的可行性,我们将顺铂-依托泊苷与托泊替康交替使用作为广泛期小细胞肺癌(SCLC)患者的一线治疗。患者和方法:36例先前未经治疗的SCLC广泛分期患者在第1、3、5和1周期的第1天接受顺铂75 mg / m(2)IV,在1-3天接受依托泊苷100 mg / m(2)IV。第七和托泊替康1.5 mg / m(2)在第二,第四,第六和第八个周期的1-5天静脉​​注射。每21天重复一次循环。患者的中位年龄为60岁,表现状态(WHO)为13的0、1的20和2的3位。所有患者的反应和毒性均可以评估。结果:五名(14%)患者获得完全缓解,部分(18%)患者获得部分缓解,总缓解率为64%(95%置信区间:48.2-79.6%)。中位随访10个月后,中位缓解时间为5.5个月,肿瘤进展时间为8个月,一年生存的可能性为48.9%。总共给药126个周期的顺铂-依托泊苷和117个周期的拓扑替康,每种方案的中位数为4个周期/患者。没有中毒死亡。由于毒性导致的治疗延迟发生在顺铂-依托泊苷之后的13(10%)个周期和托泊替康之后的16(14%)周期,而剂量分别减少了七个(6%)和五个(4%)周期。 3-4级中性粒细胞减少症,血小板减少症和发热性中性粒细胞减少症分别使​​顺铂-依托泊苷周期的13%,1%和3%以及拓扑替康的28%,6%和1%复杂化。非血液学毒性轻微。顺铂和依托泊苷的递送剂量强度为96%,托泊替康为98%。结论:顺铂-依托泊苷和拓扑替康交替给药对SCLC广泛期患者是一种可行,积极且耐受性良好的方案。

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