Huang Ou, Wu Dandan, Zhu Li, Li Yafen, Chen Weiguo, Shen Kunwei
Department of Surgery, Ruijin Hospital, Medical School of Shanghai Jiaotong University, Shanghai, China.
J Cancer Res Ther. 2016 Jan-Mar;12(1):84-9. doi: 10.4103/0973-1482.148702.
To compare the efficacy of concurrent and sequential administration of radiotherapy and chemotherapy on patients with operable breast cancer after breast.conserving surgery. (BCS).
We searched MEDLINE (National Library of Medicine, Bethesda, Maryland) and EMBASE (Elsevier, Amsterdam, Netherlands) databases for eligible studies. Clinical outcomes (such as overall and locoregional recurrence-free survival, toxicity related complications) used as evaluation indexes of efficacy. Odds ratios (ORs) with 95% confidence intervals (CI) of each index was calculated and analyzed with the RevMan Version 5.2 software.
Three articles (two trials), which compared the clinical efficacy of concurrent and sequential administration of radiotherapy and chemotherapy for operable breast cancer patients, were eligible in this meta-analysis. There were significant differences between concurrent and sequential treatments in 5-year loco-regional recurrence free survival (OR: 0.39, 95% CI: 0.20-0.75, P = 0.005) and late skin toxicity of telangiectasia (OR: 2.00, 95% CI: 1.39-2.87, P = 0.0002). However, no significant difference was discovered in five-year overall survival (OR: 0.62, 95% CI: 0.35-1.11, P > 0.05), acute skin toxicity (OR: 1.73, 95% CI: 0.98-3.04, P > 0.05) and late skin toxicity of lymphedema (OR: 1.27, 95% CI: 0.88-1.83, P > 0.05).
Our study demonstrated that the concurrent administration of chemotherapy (anthracycline-based) and radiotherapy was superior to the sequential administration in locoregional recurrence-free survival for the operable node positive breast cancer patients. However, choose of treatment for operable breast cancer patients must be cautious due to high risk of lymphedema.
比较保乳手术后可手术乳腺癌患者同步和序贯放化疗的疗效。
检索MEDLINE(美国国立医学图书馆,马里兰州贝塞斯达)和EMBASE(爱思唯尔,荷兰阿姆斯特丹)数据库中的符合条件的研究。将临床结局(如总生存和局部区域无复发生存率、毒性相关并发症)作为疗效评估指标。计算各指标的比值比(OR)及其95%置信区间(CI),并使用RevMan 5.2软件进行分析。
三篇文章(两项试验)比较了同步和序贯放化疗对可手术乳腺癌患者的临床疗效,符合本荟萃分析的要求。同步和序贯治疗在5年局部区域无复发生存率(OR:0.39,95%CI:0.20 - 0.75,P = 0.005)和晚期皮肤毛细血管扩张毒性(OR:2.00,95%CI:1.39 - 2.87,P = 0.0002)方面存在显著差异。然而,在5年总生存率(OR:0.62,95%CI:0.35 - 1.11,P > 0.05)、急性皮肤毒性(OR:1.73,95%CI:0.98 - 3.04,P > 0.05)和晚期皮肤淋巴水肿毒性(OR:1.27,95%CI:0.88 - 1.83,P > 0.05)方面未发现显著差异。
我们的研究表明,对于可手术的淋巴结阳性乳腺癌患者,同步(基于蒽环类)放化疗在局部区域无复发生存率方面优于序贯治疗。然而,由于淋巴水肿风险高,对可手术乳腺癌患者的治疗选择必须谨慎。