Skarlos D V, Samantas E, Kosmidis P, Fountzilas G, Angelidou M, Palamidas P, Mylonakis N, Provata A, Papadakis E, Klouvas G
Hellenic Co-operative Oncology Group, Athens/Ambelokipi, Greece.
Ann Oncol. 1994 Sep;5(7):601-7. doi: 10.1093/oxfordjournals.annonc.a058931.
To compare the efficacy and toxicity of etoposide and cisplatin (EP) with etoposide and carboplatin (EC) in combination with irradiation in small-cell lung cancer (SCLC).
Previously untreated patients (pts) with SCLC and measurable or evaluable disease were randomized to receive either cisplatin 50 mg/m2 on days 1-2 or carboplatin 300 mg/m2 on day 1, both combined with etoposide 300 mg/m2 on days 1-3 every 21 days for 6 treatment cycles. The vast majority of responding limited disease (LD) pts and complete responders (CR) with extensive disease (ED), also received thoracic irradiation (TI) and prophylactic cranial irradiation (PCI) concurrently with the third cycle.
Of the 147 patients registered, 143 were eligible; median performance status (PS, WHO) was 1, and tumour stage was LD in 41 pts of each treatment group. The mean delay between cycles was 8 days in the EP group and 9 in the EC group increasing in both arms with the number of treatment courses. The drug dose administered per unit time as a proportion of the protocol dose was 74% and 80% for the two groups respectively. Leukopenia, neutropenic infections, nausea, vomiting, neurotoxicity and hyperergic reactions were more frequent and/or severe in the EP group. The CR rates were 57% and 58% for EP and EC respectively. Median survival for all pts was 12.5 and 11.8 months, respectively.
Both treatments proved to be effective, with no differences in response and survival between the two treatment arms. The EC regimen was associated with significantly less toxicity.
比较依托泊苷和顺铂(EP)与依托泊苷和卡铂(EC)联合放疗治疗小细胞肺癌(SCLC)的疗效和毒性。
将既往未接受过治疗、患有SCLC且疾病可测量或可评估的患者随机分为两组,一组在第1 - 2天接受顺铂50 mg/m²,另一组在第1天接受卡铂300 mg/m²,两组均在第1 - 3天联合依托泊苷300 mg/m²,每21天为一个周期,共进行6个治疗周期。绝大多数有反应的局限期(LD)患者以及广泛期(ED)的完全缓解者(CR)在第三个周期时同时接受胸部放疗(TI)和预防性颅脑照射(PCI)。
在登记的147例患者中,143例符合条件;中位体能状态(PS,WHO标准)为1,每个治疗组各有41例患者为LD期。EP组周期之间的平均间隔为8天,EC组为9天,两组均随着治疗疗程数增加。两组每单位时间给予的药物剂量占方案剂量的比例分别为74%和80%。EP组白细胞减少、中性粒细胞感染、恶心、呕吐、神经毒性和过敏反应更频繁和/或更严重。EP组和EC组的CR率分别为57%和58%。所有患者的中位生存期分别为12.5个月和11.8个月。
两种治疗方法均有效,两个治疗组在反应和生存方面无差异。EC方案的毒性明显较小。