首页> 美国卫生研究院文献>British Journal of Cancer >Mitomycin-ifosfamide-cisplatinum (MIP) vs MIP-interferon vs cisplatinum-carboplatin in metastatic non-small-cell lung cancer: a FONICAP randomised phase II study. Italian Lung Cancer Task Force.
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Mitomycin-ifosfamide-cisplatinum (MIP) vs MIP-interferon vs cisplatinum-carboplatin in metastatic non-small-cell lung cancer: a FONICAP randomised phase II study. Italian Lung Cancer Task Force.

机译:转移性非小细胞肺癌中的丝裂霉素-异环磷酰胺-顺铂(MIP)vs MIP干扰素vs顺铂-carboplatin:一项FONICAP随机II期研究。意大利肺癌工作队。

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摘要

The FONICAP group is screening, with randomised phase II studies, the activity of new chemotherapy programmes for advanced non-small-cell lung cancer (NSCLC) looking for regimens with > 30% activity. In the present study, three regimens were tested: MIP (mitomycin 6 mg m-2, ifosfamide 3 g m-2, cisplatinum 80 mg m-2 on day 1 every 28 days); MIP-IFN (MIP and interferon alpha-2b 3 MU s.c. three times a week); and PC (cisplatinum 60 mg m-2 and carboplatin 400 mg m-2 on day 1 every 28 days). Overall 93 chemotherapy-naive patients were enrolled: 23 received MIP, 27 received MIP-IFN and 43 received PC. Eighty per cent of the patients had stage IV and 20% stage IIIb disease (positive pleural effusion or supraclavicular nodes). Response rates were as follows: MIP = 9% (95% CI 1-28%), MIP-IFN = 7% (95% CI 1-24%) and PC = 14% (95% CI 5-28%). The overall median survival was 183 days. Grade III-IV leucopenia was observed in 36% of patients treated with MIP-IFN vs 10% in the other two arms, and thrombocytopenia grade III-IV was reported in nearly 10% of patients overall. In conclusion, (1) all three regimens investigated have poor activity (< 30%); (2) when tested in multicentre randomised phase II trials, MIP displays lower activity than in phase II trials; (3) PC has similar activity to other platinum-containing regimens; (4) randomised phase II studies are a reliable and quick method of determining the anti-tumour activity of novel chemotherapeutic regimens in NSCLC.
机译:FONICAP研究小组正在通过II期随机研究筛查晚期非小细胞肺癌(NSCLC)新化疗方案的活性,以寻找活性> 30%的方案。在本研究中,测试了三种方案:MIP(丝裂霉素6 mg m-2,异环磷酰胺3 g m-2,顺铂80 mg m-2每28天在第1天); MIP-IFN(MIP和干扰素α-2b3 MU s.c.每周三次);和PC(第28天第1天的顺铂60 mg m-2和卡铂400 mg m-2)。共有93名未接受过化疗的患者入组:23例接受MIP,27例接受MIP-IFN,43例接受PC。 80%的患者患有IV期和20%的IIIb期疾病(阳性胸腔积液或锁骨上淋巴结)。响应率如下:MIP = 9%(95%CI 1-28%),MIP-IFN = 7%(95%CI 1-24%)和PC = 14%(95%CI 5-28%)。总体中位生存期为183天。在接受MIP-IFN治疗的患者中观察到III-IV级白细胞减少症,而在另外两个组中观察到10%,而据报告,总体上将近10%的患者发生了血小板减少症III-IV级。总之,(1)所研究的所有三种方案的活动均较差(<30%); (2)在多中心随机II期试验中进行测试时,MIP的活性低于II期试验; (3)PC具有与其他含铂方案相似的活性; (4)II期随机研究是确定NSCLC新型化疗方案抗肿瘤活性的可靠且快速的方法。

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