Digestive Disease Institute, Virginia Mason Medical Center, Seattle, WA, USA.
Section of General Thoracic, and Vascular Surgery, Virginia Mason Medical Center, Seattle, WA, USA.
Ann Surg Oncol. 2018 Apr;25(4):1052-1060. doi: 10.1245/s10434-018-6334-8. Epub 2018 Jan 17.
Gemcitabine-taxane combination chemotherapy has demonstrated a survival benefit clinically in metastatic pancreatic cancer (PC). The authors present their experience with gemcitabine and docetaxel (gem/tax)-based adjuvant treatment (Rx) after surgery with curative intent.
Patients with de novo resectable PC from January 2010 to December 2015 were identified from the authors' institutional database and registry. The study included only patients who received gem/tax as their initial Rx administered exclusively at the authors' institution with or without chemoradiation (CRTx). Survival analysis was performed using Kaplan-Meier methods, and prognostic factors were investigated by Cox proportional hazard modeling.
Of 102 patients identified, 58 met the study criteria. The median age at diagnosis was 65 years, with 55% of the patients undergoing an R1 resection (margin ≤ 1 mm). Tumor characteristics included a median tumor size of 28 mm, a poor differentiation rate of 54%, and a lymph node positivity of 67%. Most of the patients (90%, 52/58) completed 80% or more of the 24 week Rx. Of these patients, 71% received post-gem/tax CRTx Rx. Grade 3 or 4 toxicity was observed in 52% of the patients. The median follow-up period was 51.2 months, and the observed median overall survival (OS) was 52 months [95% confidence interval (CI) 27.4-not reached]. The actuarial 5-year OS was 49% (95% CI 33.7-63.4%). In the multivariate analysis, an R1 resection and American Joint Committee on Cancer (AJCC) stage 2 versus stage 1 disease were negatively associated with OS, whereas administration of CRTx was positively associated with OS.
Adjuvant gem/tax with or without CRTx is feasible, with a favorable OS. Future prospective studies of gem/taxane-based adjuvant Rx for PC are warranted.
吉西他滨联合紫杉醇化疗在转移性胰腺癌(PC)的临床治疗中显示出了生存获益。作者介绍了他们对具有治愈性意图的手术后接受吉西他滨和多西他赛(吉西他滨/多西他赛)为基础的辅助治疗(Rx)的经验。
从作者的机构数据库和登记处确定了 2010 年 1 月至 2015 年 12 月新诊断为可切除 PC 的患者。该研究仅包括在作者所在机构接受吉西他滨/多西他赛初始 Rx 治疗的患者,这些 Rx 单独或联合放化疗(CRTx)应用。使用 Kaplan-Meier 方法进行生存分析,并通过 Cox 比例风险模型研究预后因素。
在确定的 102 名患者中,58 名符合研究标准。诊断时的中位年龄为 65 岁,55%的患者行 R1 切除术(切缘≤1mm)。肿瘤特征包括中位肿瘤大小 28mm、低分化率 54%、淋巴结阳性率 67%。大多数患者(90%,52/58)完成了 24 周 Rx 的 80%或更多。这些患者中,71%接受了吉西他滨/多西他赛 Rx 后 CRTx。观察到 52%的患者出现 3 级或 4 级毒性。中位随访时间为 51.2 个月,观察到的中位总生存期(OS)为 52 个月[95%置信区间(CI)27.4-未达到]。5 年总生存率的估计值为 49%(95%CI 33.7-63.4%)。多变量分析显示,R1 切除术和美国癌症联合委员会(AJCC)分期 2 期与 1 期疾病与 OS 呈负相关,而 CRTx 的应用与 OS 呈正相关。
吉西他滨/多西他赛联合或不联合 CRTx 的辅助治疗是可行的,具有良好的 OS。有必要进行前瞻性研究以评估吉西他滨联合紫杉烷类药物作为 PC 的辅助治疗方案。