Department of Surgery, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
J Surg Oncol. 2013 Sep;108(4):213-9. doi: 10.1002/jso.23394. Epub 2013 Aug 1.
This study evaluated the safety and efficiency of preoperative chemoradiation therapy (CRT) with the XELOX or FOLFOX regimen in locally advanced rectal cancer patients.
One hundred forty-four patients (T3/T4 or N+) were enrolled between 2005 and 2011. The patients received preoperative concomitant CRT (XELOX or FOLFOX regimen). Patients were divided into four groups: pCR (pT0N0), downstaging, no-downstaging, and progression group. Clinical outcome with overall survival (OS) and disease-free survival (DFS) were compared for each group.
One hundred thirty-eight patients received radical resection after preoperative CRT. Twenty-seven patients (20%) achieved pCR. The response rate (pCR + downstaging) was 67%. The most common side effects were nausea (64%), diarrhea (49%), and leucopenia (49%). The overall estimated 5-year OS was 86% for all patients. The estimated 5-year OS was significantly better in the responders (pCR + downstaging) than the non-responders (no-downstaging + progression, 94% vs. 68%, P = 0.001). There was also statistical difference in 3-year DFS between the two groups (93% vs. 68%, P = 0.000).
pCR and downstaging after neoadjuvant CRT are associated with improved survival for locally advanced rectal cancer patients. Preoperative CRT with the XELOX or FOLFOX regimen is well tolerated and has mild adverse events.
本研究评估了术前 XELOX 或 FOLFOX 方案放化疗(CRT)治疗局部进展期直肠癌患者的安全性和有效性。
2005 年至 2011 年间,共纳入 144 例 T3/T4 或 N+患者。患者接受术前同期 CRT(XELOX 或 FOLFOX 方案)。患者分为四组:完全病理缓解(pCR)组、降期组、未降期组和进展组。比较各组的临床结局,包括总生存(OS)和无病生存(DFS)。
138 例患者在术前 CRT 后接受了根治性切除术。27 例(20%)达到了 pCR。总缓解率(pCR+降期)为 67%。最常见的副作用是恶心(64%)、腹泻(49%)和白细胞减少(49%)。所有患者的总体 5 年 OS 估计为 86%。与非缓解者(未降期+进展,94% vs. 68%,P=0.001)相比,缓解者(pCR+降期)的 5 年 OS 显著更好。两组 3 年 DFS 也存在统计学差异(93% vs. 68%,P=0.000)。
新辅助 CRT 后的 pCR 和降期与局部进展期直肠癌患者的生存改善相关。XELOX 或 FOLFOX 方案的术前 CRT 耐受性良好,不良反应轻微。