Division of Surgical Oncology, Tufts University School of Medicine, Boston, MA, USA.
Maine Medical Center. Portland, ME, USA.
Am Surg. 2023 Dec;89(12):5535-5544. doi: 10.1177/00031348231156756. Epub 2023 Feb 28.
This study is a retrospective cohort study of National Cancer Data Base (NCDB) data for pancreatic cancer with vascular involvement.
A total of 23 903 patients with vascular involvement were included and divided into 3 groups; no treatment (40.6%), medical treatment (36.6%), and resection (22.8%). Of the patients undergoing resection, 31.3% received neoadjuvant multiagent chemotherapy (N-MAC). The remainder were treated with postoperative adjuvant treatment (33.8%), surgery alone (24.9%), preoperative radiotherapy (8.3%), or single-agent preoperative chemotherapy (1.7%). Median survival for N-MAC was superior (28.42 months) when compared to neoadjuvant radiotherapy (20.73 months), neoadjuvant single-agent chemotherapy (20.8 months), postoperative adjuvant therapy (17.87 months), and surgery alone (10.12 months). N-MAC was associated with improved survival compared to postoperative multiagent chemotherapy (P-MAC) (28.4 vs 16.95, HR 1.82; CI 1.64-2.02, < .0010) (Figure 1). The addition of radiation therapy to N-MAC did not improve survival (27.4 vs 29.8, HR .93; CI .83-1.05, = .3). Clinical downstaging occurred in 40% of patients treated with N-MAC, and downstaging was associated with improved survival (HR .74; CI .64-.85, < .001). N-MAC patients were more likely to undergo an R0 resection than P-MAC (74% v. 48, < .001).
Most resected pancreatic cancer patients in this study with vascular involvement receive either postoperative or no adjuvant therapy. N-MAC increases downstaging, R0 resection rates, and survival.
本研究是一项基于国家癌症数据库(NCDB)数据的回顾性队列研究,纳入了伴有血管侵犯的胰腺癌患者。
共纳入 23903 例伴有血管侵犯的患者,分为 3 组:未治疗组(40.6%)、药物治疗组(36.6%)和手术切除组(22.8%)。在接受手术切除的患者中,31.3%接受了新辅助多药化疗(N-MAC)。其余患者接受了术后辅助治疗(33.8%)、单纯手术治疗(24.9%)、术前放疗(8.3%)或单药术前化疗(1.7%)。与新辅助放疗(20.73 个月)、新辅助单药化疗(20.8 个月)、术后辅助治疗(17.87 个月)和单纯手术治疗(10.12 个月)相比,N-MAC 的中位生存时间更长(28.42 个月)。与术后多药化疗(P-MAC)相比,N-MAC 可改善生存(28.4 比 16.95,HR 1.82;CI 1.64-2.02, <.0010)(图 1)。在 N-MAC 中添加放疗并不能提高生存(27.4 比 29.8,HR.93;CI.83-1.05, =.3)。接受 N-MAC 治疗的患者中有 40%发生临床降期,降期与生存改善相关(HR.74;CI.64-.85, <.001)。与 P-MAC 相比,N-MAC 患者更有可能接受 R0 切除术(74%比 48%, <.001)。
在这项研究中,大多数伴有血管侵犯的接受手术切除的胰腺癌患者要么接受术后辅助治疗,要么不接受辅助治疗。N-MAC 可增加降期、R0 切除率和生存。