Zhao Jing, Liu Xiaoliang, Wang Weiping, Hu Ke, Zhang Fuquan, Hou Xiaorong, Meng Qingyu
Department of Oncology, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Department of Radiation Oncology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, People's Republic of China,
Cancer Manag Res. 2019 Feb 15;11:1579-1586. doi: 10.2147/CMAR.S193657. eCollection 2019.
The purpose of this study was to evaluate the efficacy and toxicity of concomitant dose-escalated Tomotherapy in locally advanced mid-low rectal cancer.
Patients with locally advanced (T3/T4 or N+), low-mid (≤10 cm from anal verge) rectal carcinoma treated with neoadjuvant chemoradiotherapy followed by surgery between May 2012 and October 2017 in Peking Union Medical College Hospital were included in this study. A dose of 45/50 Gy in 25 fractions was delivered to the pelvis with Tomotherapy, and 55 Gy was prescribed for the primary tumor with a simultaneous, integrated boost. Megavolt computed tomography was performed before every delivery. The concurrent chemotherapy regimen included capecitabine alone and XELOX.
A total of 141 patients were enrolled; 129 patients (91.5%) had stage cT3 or cT4, and 121 patients (85.8%) had positive lymph nodes. The location of the tumors was in the lower rectum in 88 patients (62.4%). After neoadjuvant chemoradiotherapy, 113 patients (80.1%) underwent sphincter-preserving resection. Downstaging was observed in 121 patients (85.8%), including 80 patients (56.7%) with T downstaging and 101 patients (83.5%) with N downstaging. Thirty-two patients (22.7%) obtained pathological complete response (pCR). The median follow-up was 38.5 months (range, 9.3-73.6 months). Only 36 patients (25.5%) experienced treatment failure, including distant metastasis in 29 patients (20.6%) and pelvic recurrent in 7 patients (5.0%). The estimated 5-year overall survival (OS), disease-free survival (DFS), and local control (LC) rates of patients were 75.1%, 70.9%, and 95.5%, respectively. pCR was an independent prognostic factor for DFS (HR 0.13, 95% CI: 0.02-0.93, = 0.043), but it did not improve OS or LC. Grade 3 or greater acute leukopenia and diarrhea rates were 5.7% and 7.8%, respectively, and 15 patients (10.6%) developed postoperative complications.
This study indicates that neoadjuvant, image-guided Tomotherapy with 55 Gy boosted to the primary tumor was well tolerated and resulted in high rates of sphincter-preserving surgery, pCR, LC, and DFS for locally advanced rectal cancer.
本研究旨在评估同步剂量递增的螺旋断层放疗对局部晚期中低位直肠癌的疗效和毒性。
纳入2012年5月至2017年10月在北京协和医院接受新辅助放化疗后手术治疗的局部晚期(T3/T4或N+)、中低位(距肛缘≤10 cm)直肠癌患者。采用螺旋断层放疗对盆腔给予45/50 Gy分25次照射,对原发肿瘤给予55 Gy同步整合加量照射。每次照射前均进行兆伏级计算机断层扫描。同步化疗方案包括单药卡培他滨和XELOX方案。
共纳入141例患者;129例(91.5%)为cT3或cT4期,121例(85.8%)有阳性淋巴结。88例(62.4%)肿瘤位于直肠下段。新辅助放化疗后,113例(80.1%)患者接受了保肛手术。121例(85.8%)患者实现降期,其中80例(56.7%)实现T降期,101例(83.5%)实现N降期。32例(22.7%)患者获得病理完全缓解(pCR)。中位随访时间为38.5个月(范围9.3 - 73.6个月)。仅36例(25.5%)患者出现治疗失败,包括29例(20.6%)远处转移和7例(5.0%)盆腔复发。患者的5年总生存率(OS)、无病生存率(DFS)和局部控制率(LC)分别估计为75.1%、70.9%和95.5%。pCR是DFS的独立预后因素(HR 0.13,95%CI:0.02 - 0.93,P = 0.043),但未改善OS或LC。3级及以上急性白细胞减少和腹泻发生率分别为5.7%和7.8%,15例(10.6%)患者发生术后并发症。
本研究表明,对原发肿瘤加量至55 Gy的新辅助影像引导螺旋断层放疗耐受性良好,可使局部晚期直肠癌患者获得较高的保肛手术率、pCR率、LC率和DFS率。