Department of Surgery, UCLA School of Public Health, Los Angeles, CA, USA.
Surgery. 2011 Sep;150(3):466-73. doi: 10.1016/j.surg.2011.07.006.
Neoadjuvant treatment has proven beneficial for many gastrointestinal (GI) malignancies, but no phase III trials have been completed examining this approach in pancreatic cancer. This meta-analysis examines the best available phase II trials using neoadjuvant treatment for resectable and borderline/unresectable pancreatic adenocarcinoma.
Phase II trials were identified using a MEDLINE search, and the Cochrane Central Register of Controlled Trials from 1960 to July 2010. Patients were divided into 2 groups: Patients with initially resectable tumors (group A), and patients with borderline/unresectable tumors (group B). Primary outcome measures were rate of resection and survival. Pooled proportions and 95% confidence intervals (CIs) were calculated using random-effects or fixed-effects models based on the heterogeneity of included studies.
A total of 14 phase II clinical trials including 536 patients were analyzed. After treatment, resectability was 65.8% (95% CI, 55.4-75.6%) compared with 31.6% in group B (95% CI, 14.0-52.5%). A partial response was observed in patients with borderline/unresectable tumors; 31.8 (95% CI, 24.2-39.8%) in group B and 9.5% (95% CI, 2.9-19.4%) in group A (P = .003). Progressive disease was seen in 17.0% (95% CI, 11.9-22.7) of patients in group A versus 21.8% (95% CI, 10.1-36.5%) in group B (P = .006). Median survival in resected patients was 23 months for group A and 22 months for group B.
Neoadjuvant treatment seems to have some activity in patients with borderline/unresectable pancreatic adenocarcinoma. Nearly one third of tumors initially deemed marginal for operative intervention were able to be ultimately resected after treatment. Until more effective targeted chemotherapeutics are developed, the only group of patients with pancreatic cancer that may benefit from neoadjuvant treatment are those with locally advanced disease.
新辅助治疗已被证明对许多胃肠道(GI)恶性肿瘤有益,但尚未完成评估新辅助治疗在胰腺癌中应用的 III 期临床试验。本荟萃分析旨在研究可切除和局部进展/不可切除胰腺腺癌的最佳新辅助治疗的 II 期临床试验。
通过 MEDLINE 检索,结合 Cochrane 中心对照试验注册库(1960 年至 2010 年 7 月),确定 II 期临床试验。患者分为 2 组:初始可切除肿瘤患者(A 组)和局部进展/不可切除肿瘤患者(B 组)。主要观察指标为切除率和生存率。根据纳入研究的异质性,采用随机效应或固定效应模型计算汇总比例及其 95%置信区间(CI)。
共纳入 14 项包含 536 例患者的 II 期临床试验。治疗后,可切除率为 65.8%(95%CI,55.4-75.6%),B 组为 31.6%(95%CI,14.0-52.5%)。B 组中有部分缓解的患者,其中 31.8%(95%CI,24.2-39.8%);A 组为 9.5%(95%CI,2.9-19.4%)(P =.003)。A 组进展性疾病发生率为 17.0%(95%CI,11.9-22.7%),B 组为 21.8%(95%CI,10.1-36.5%)(P =.006)。可切除患者的中位生存时间为 A 组 23 个月,B 组 22 个月。
新辅助治疗似乎对局部进展/不可切除胰腺腺癌患者有一定疗效。近三分之一初始手术干预边缘性肿瘤在治疗后可获得最终切除。在开发出更有效的靶向化疗药物之前,新辅助治疗可能受益的唯一一组胰腺癌患者是局部进展期疾病患者。