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多柔比星为主的化疗与铂类为主的化疗治疗小细胞肺癌的Ⅲ期随机试验

Phase III randomised trial of doxorubicin-based chemotherapy compared with platinum-based chemotherapy in small-cell lung cancer.

作者信息

Baka S, Califano R, Ferraldeschi R, Aschroft L, Thatcher N, Taylor P, Faivre-Finn C, Blackhall F, Lorigan P

机构信息

Department of Medical Oncology, Christie Hospital NHS Foundation Trust, Wilmslow Road, Manchester M20 4BX, UK.

出版信息

Br J Cancer. 2008 Aug 5;99(3):442-7. doi: 10.1038/sj.bjc.6604480.

Abstract

This randomised trial compared platinum-based to anthracycline-based chemotherapy in patients with small-cell lung cancer (limited or extensive stage) and <or=2 adverse prognostic factors. Patients were randomised to receive six cycles of either ACE (doxorubicin 50 mg/m(2) i.v., cyclophosphamide 1 g/m(2) i.v. and etoposide 120 mg/m(2) i.v. on day 1, then etoposide 240 mg/m(2) orally for 2 days) or PE (cisplatin 80 mg/m(2) and etoposide 120 mg/m(2) i.v. on day 1, then etoposide 240 mg/m(2) orally for 2 days) given for every 3 weeks. For patients where cisplatin was not suitable, carboplatin (AUC6) was substituted. A total of 280 patients were included (139 ACE, 141 PE). The response rates were 72% for ACE and 77% for PE. One-year survival rates were 34 and 38% (P=0.497), respectively and 2-year survival was the same (12%) for both arms. For LD patients, the median survival was 10.9 months for ACE and 12.6 months for PE (P=0.51); for ED patients median survival was 8.3 months and 7.5 months, respectively. More grades 3 and 4 neutropenia (90 vs 57%, P<0.005) and grades 3 and 4 infections (73 vs 29%, P<0.005) occurred with ACE, resulting in more days of hospitalisation and greater i.v. antibiotic use. ACE was associated with a higher risk of neutropenic sepsis than PE and with a trend towards worse outcome in patients with LD, and should not be studied further in this group of patients.

摘要

这项随机试验比较了铂类化疗与蒽环类化疗在小细胞肺癌(局限期或广泛期)且不良预后因素≤2个的患者中的疗效。患者被随机分为两组,分别接受六个周期的ACE方案(第1天静脉注射阿霉素50mg/m²、环磷酰胺1g/m²和依托泊苷120mg/m²,随后连续2天口服依托泊苷240mg/m²)或PE方案(第1天静脉注射顺铂80mg/m²和依托泊苷120mg/m²,随后连续2天口服依托泊苷240mg/m²),每3周进行一次治疗。对于不适合使用顺铂的患者,用卡铂(AUC6)替代。共纳入280例患者(139例接受ACE方案,141例接受PE方案)。ACE方案的缓解率为72%,PE方案为77%。一年生存率分别为34%和38%(P = 0.497),两组的两年生存率相同(均为12%)。对于局限期患者,ACE方案的中位生存期为10.9个月,PE方案为12.6个月(P = 0.51);对于广泛期患者,中位生存期分别为8.3个月和7.5个月。ACE方案出现更多3级和4级中性粒细胞减少(90%对57%,P<0.005)以及3级和4级感染(73%对29%,P<0.005),导致住院天数更多且静脉使用抗生素更多。与PE方案相比,ACE方案发生中性粒细胞减少性败血症的风险更高,且局限期患者有预后更差的趋势,因此不应在这类患者中进一步研究该方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0126/2527803/a210db825a58/6604480f1.jpg

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