Herman Joseph M, Swartz Michael J, Hsu Charles C, Winter Jordan, Pawlik Timothy M, Sugar Elizabeth, Robinson Ray, Laheru Daniel A, Jaffee Elizabeth, Hruban Ralph H, Campbell Kurtis A, Wolfgang Christopher L, Asrari Fariba, Donehower Ross, Hidalgo Manuel, Diaz Luis A, Yeo Charles, Cameron John L, Schulick Richard D, Abrams Ross
Department of Radiation Oncology & Molecular Radiation Sciences, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins Hospital, Baltimore, MD, USA.
J Clin Oncol. 2008 Jul 20;26(21):3503-10. doi: 10.1200/JCO.2007.15.8469.
To examine the efficacy of adjuvant chemoradiotherapy after pancreaticoduodenectomy (PD) for pancreatic adenocarcinoma (PC) in patients undergoing resection at Johns Hopkins Hospital (JHH; Baltimore, MD).
Between August 30, 1993, and February 28, 2005, a total of 908 patients underwent PD for PC at JHH. A prospective database was reviewed to determine which patients received fluorouracil (FU) -based CRT. Excluded patients had metastatic disease, died 60 or fewer days after PD, received preoperative therapy, an experimental vaccine, adjuvant chemotherapy or radiation alone. The final cohort includes 616 patients.
The median follow-up was 17.8 months (interquartile range, 9.7 to 33.5 months). Overall median survival was 17.9 months (95% CI, 16.3 to 19.5 months). Groups were similar with respect to tumor size, nodal status, and margin status, but the CRT group was younger (P < .001), and less likely to present with a severe comorbid disease (P = .001). Patients with carcinomas larger than 3 cm (P = .001), grade 3 and 4 (P < .001), margin-positive resection (P = .001), and complications after surgery (P = .017) had poor long-term survival. Patients receiving CRT experienced an improved median (21.2 v 14.4 months; P < .001), 2-year (43.9% v 31.9%), and 5-year (20.1% v 15.4%) survival compared with no CRT. After controlling for high-risk features, CRT was still associated with improved survival (relative risk = 0.74; 95% CI, 0.62 to 0.89).
These data suggest that adjuvant concurrent FU-based CRT significantly improves survival after PD for PC when compared with patients not receiving CRT. These data support the use of combined adjuvant CRT for PC.
在约翰霍普金斯医院(位于马里兰州巴尔的摩市),研究胰腺癌(PC)患者行胰十二指肠切除术(PD)后辅助放化疗的疗效。
1993年8月30日至2005年2月28日期间,共有908例患者在约翰霍普金斯医院接受了胰腺癌的胰十二指肠切除术。回顾前瞻性数据库,以确定哪些患者接受了以氟尿嘧啶(FU)为基础的同步放化疗。排除有转移性疾病、胰十二指肠切除术后60天内死亡、接受术前治疗、实验性疫苗、单纯辅助化疗或放疗的患者。最终队列包括616例患者。
中位随访时间为17.8个月(四分位间距为9.7至33.5个月)。总体中位生存期为17.9个月(95%可信区间为16.3至19.5个月)。两组在肿瘤大小、淋巴结状态和切缘状态方面相似,但同步放化疗组患者更年轻(P < 0.001),出现严重合并症的可能性更小(P = 0.001)。肿瘤大于3cm(P = 0.001)、病理分级为3级和4级(P < 0.001)、切缘阳性切除(P = 0.001)以及术后出现并发症(P = 0.017)的患者长期生存率较差。与未接受同步放化疗的患者相比,接受同步放化疗的患者中位生存期(21.2个月对14.4个月;P < 0.001)、2年生存率(43.9%对31.9%)和5年生存率(20.1%对15.4%)均有所提高。在控制了高危因素后,同步放化疗仍与生存率提高相关(相对危险度 = 0.74;95%可信区间为0.62至0.89)。
这些数据表明,与未接受同步放化疗的患者相比,辅助性基于氟尿嘧啶的同步放化疗显著提高了胰腺癌患者胰十二指肠切除术后的生存率。这些数据支持对胰腺癌采用联合辅助同步放化疗。