Ives Natalie J, Stowe Rebecca L, Lorigan Paul, Wheatley Keith
Birmingham Clinical Trials Unit, Division of Medical Sciences, Robert Aitken Institute, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
J Clin Oncol. 2007 Dec 1;25(34):5426-34. doi: 10.1200/JCO.2007.12.0253.
To assess the effect of adding interferon-alpha (IFN) +/- interleukin-2 (IL-2) to chemotherapy in patients with metastatic melanoma. METHODS A published data meta-analysis of trials of biochemotherapy versus chemotherapy in patients with metastatic melanoma was undertaken. End points evaluated were rates of partial response (PR), complete response (CR) and overall (partial + complete) response (OR); response duration; progression-free survival; overall survival (OS); and toxicity. The only subgroup analysis performed was by type of immunotherapy, with trials divided according to whether IFN only or IFN and IL-2 were administered in the biochemotherapy arm.
Eighteen randomized trials were identified: 11 trials of chemotherapy +/- IFN and seven trials of chemotherapy +/- IFN and IL-2. More than 2,600 patients were entered onto the trials, with 555 responses and 2,039 deaths. There was a clear benefit for biochemotherapy for PR (odds ratio = 0.66; 95% CI, 0.53 to 0.82; P = .0001), CR (odds ratio = 0.50; 95% CI, 0.35 to 0.73; P = .0003) and OR (odds ratio = 0.59; 95% CI, 0.49 to 0.72; P < .00001). For OR, these benefits were significant for both the IFN (odds ratio = 0.60; 95% CI, 0.46 to 0.79; P = .0002) and IFN + IL-2 (odds ratio = 0.58; 95% CI, 0.44 to 0.77; P = .0001) subgroups. In contrast, there was no benefit overall in OS (odds ratio = 0.99; 95% CI, 0.91 to 1.08; P = .9), but there was evidence of heterogeneity of treatment effect between the individual trials (P = .006).
This meta-analysis provides a comprehensive summary of all the data currently available, and shows that although biochemotherapy clearly improves response rates, this does not appear to translate into a survival benefit.
评估在转移性黑色素瘤患者中,化疗联合α-干扰素(IFN)±白细胞介素-2(IL-2)的疗效。方法:对已发表的转移性黑色素瘤患者生物化疗与化疗试验的数据进行荟萃分析。评估的终点指标包括部分缓解率(PR)、完全缓解率(CR)和总缓解率(部分缓解 + 完全缓解,OR);缓解持续时间;无进展生存期;总生存期(OS);以及毒性。唯一进行的亚组分析是根据免疫治疗类型,将试验分为生物化疗组中仅使用IFN或使用IFN和IL-2两类。
共纳入18项随机试验:11项化疗±IFN试验和7项化疗±IFN及IL-2试验。超过2600例患者参与试验,其中555例有缓解,2039例死亡。生物化疗在PR(优势比 = 0.66;95%置信区间,0.53至0.82;P = 0.0001)、CR(优势比 = 0.50;95%置信区间,0.35至0.73;P = 0.0003)和OR(优势比 = 0.59;95%置信区间,0.49至0.72;P < 0.00001)方面有明显益处。对于OR,这些益处在IFN亚组(优势比 = 0.60;95%置信区间,0.46至0.79;P = 0.0002)和IFN + IL-2亚组(优势比 = 0.58;95%置信区间,0.44至0.77;P = 0.0001)中均显著。相比之下,OS总体上无益处(优势比 = 0.99;95%置信区间,0.91至1.08;P = 0.9),但各试验间存在治疗效果异质性的证据(P = 0.006)。
这项荟萃分析全面总结了目前所有可用数据,表明尽管生物化疗明显提高了缓解率,但这似乎并未转化为生存获益。