Hellenic Oncology Research Group (HORG), 55 Lomvardou Str, 11470, Athens, Greece.
Anticancer Res. 2010 Jul;30(7):3031-8.
To compare the efficacy and tolerance of sequential versus alternate front-line administration of cisplatin-etoposide (PE) and topotecan (T) in patients with extensive stage small cell lung cancer (SCLC).
Patients were randomized to receive either 4 cycles PE (cisplatin 80 mg/m(2) i.v. day 1 and etoposide100 mg/m(2)/d i.v. days 1-3 every 21 days) followed by 4 cycles T (1.5 mg/m(2)/d i.v. days 1-5 every 21 days) (arm A, 183 patients) or the same regimens using an alternate sequence (arm B, 181 patients).
There was no significant difference in terms of compliance with treatment, overall response rates (51.4% vs. 55.2%; p=0.458), median response duration (4.3 vs. 5.2 months; p=0.780), median time to tumour progression (5.7 vs. 6.4 months; p=0.494), median overall survival (10.9 vs. 9.8 months; p=0.186) and 1-year survival (43.8% vs. 36.5%) between the two arms. The incidence of severe grade 3-4 haematological and grade 2-4 non-haematological (asthenia, mucositis, diarrhoea and neurotoxicity) toxicity was comparable between the two arms.
The comparison of sequential versus alternate administration of cisplatin-etoposide and topotecan as front-line treatment of patients with extensive stage SCLC revealed no clinically meaningful differences in terms of efficacy and tolerance.
比较广泛期小细胞肺癌(SCLC)患者顺铂-依托泊苷(PE)序贯与交替一线治疗,以及拓扑替康(T)的疗效和耐受性。
患者随机接受 4 周期 PE(顺铂 80mg/m2,iv,第 1 天,依托泊苷 100mg/m2/d,iv,第 1-3 天,每 21 天 1 周期),随后 4 周期 T(1.5mg/m2/d,iv,第 1-5 天,每 21 天 1 周期)(A 组,183 例),或采用交替序列的相同方案(B 组,181 例)。
两组患者在治疗依从性、总缓解率(51.4%对 55.2%;p=0.458)、中位缓解持续时间(4.3 对 5.2 个月;p=0.780)、肿瘤进展时间(5.7 对 6.4 个月;p=0.494)、中位总生存时间(10.9 对 9.8 个月;p=0.186)和 1 年生存率(43.8%对 36.5%)方面,均无统计学差异。两组间严重度 3-4 级血液学毒性和 2-4 级非血液学毒性(乏力、黏膜炎、腹泻和神经毒性)发生率相当。
广泛期 SCLC 患者顺铂-依托泊苷序贯与交替一线治疗拓扑替康比较,疗效和耐受性方面无临床意义差异。