Rabin Medical Center, Petach Tikva, Israel; Faculty of Medicine, Tel Aviv University, Israel.
Princess Margaret Cancer Centre, Toronto, Canada; Department of Medicine, University of Toronto, Toronto, Canada.
Cancer Treat Rev. 2018 Feb;63:71-78. doi: 10.1016/j.ctrv.2017.12.003. Epub 2017 Dec 6.
Despite a lack of improvement in overall survival (OS) with doxorubicin-based combinations over doxorubicin alone in advanced STS, the role of multi-agent chemotherapy remains poorly defined.
We conducted a systematic review and meta-analysis to evaluate benefits and harms of multi-agent chemotherapy in advanced STS. Eligible studies were randomized trials of chemotherapy in advanced STS comparing single agent to multi-agent therapy. Data from studies reporting a hazard ratio (HR) and 95% confidence intervals (CI) for OS and progression-free survival (PFS) were pooled in a meta-analysis. Meta-regression was utilized to explore the association between efficacy (OS and PFS) and both toxicity and dose intensity.
We identified 22 trials published between 1974 and April 2016 and comprising 5044 patients. Overall, multi-agent chemotherapy was associated with improved OS (HR:0.79, p = 0.02), and borderline improvement in PFS (HR:0.86, p = 0.05). While the effect on OS was similar in trials with non-anthracycline controls compared to those with anthracycline controls (HR for OS 0.73 vs. 0.82, p for difference = 0.63) there was a non-significantly greater effect for multi-agent chemotherapy on PFS in non-anthracycline RCT (HR for PFS 0.73 vs. 0.91, p for difference = 0.13). Compared to studies with cytotoxic therapy-based multi-agent therapy, a non-significantly greater magnitude of effect among studies with biological/cytostatic experimental groups was seen (HR for OS 0.64 vs. 0.86, p for difference = 0.37). There was a borderline significant association between dose reductions (which were more common in combination arms) and worse PFS (beta = 0.70, p = 0.053).
Multi-agent chemotherapy is associated with a modest, but statistically significant improvement in outcomes in STS. Combining chemotherapy with non-cytotoxic agents might represent a promising strategy.
尽管蒽环类药物联合化疗在晚期 STS 中并未改善总体生存(OS),但多药化疗的作用仍未得到明确界定。
我们进行了系统评价和荟萃分析,以评估多药化疗在晚期 STS 中的获益和危害。纳入的研究是比较单药与多药化疗治疗晚期 STS 的化疗随机试验。对报告 OS 和无进展生存期(PFS)的危险比(HR)和 95%置信区间(CI)的研究数据进行荟萃分析。采用荟萃回归来探讨疗效(OS 和 PFS)与毒性和剂量强度之间的关联。
我们确定了 1974 年至 2016 年 4 月期间发表的 22 项试验,共纳入 5044 例患者。总体而言,多药化疗与 OS 改善相关(HR:0.79,p=0.02),并且 PFS 略有改善(HR:0.86,p=0.05)。尽管与非蒽环类对照试验相比,多药化疗对 OS 的影响在蒽环类对照试验中相似(OS 的 HR 为 0.73 对 0.82,差异的 p 值=0.63),但在非蒽环类 RCT 中,多药化疗对 PFS 的影响更大(PFS 的 HR 为 0.73 对 0.91,差异的 p 值=0.13)。与以细胞毒性疗法为基础的多药化疗研究相比,以生物/细胞抑制性实验组为基础的研究中观察到的效应幅度更大(OS 的 HR 为 0.64 对 0.86,差异的 p 值=0.37)。剂量减少(在联合治疗组中更为常见)与 PFS 较差之间存在临界显著关联(β=0.70,p=0.053)。
多药化疗与 STS 结局的适度但具有统计学意义的改善相关。将化疗与非细胞毒性药物联合使用可能是一种有前途的策略。