But-Hadzic Jasna, Velenik Vaneja
Department of Radiotherapy, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Radiol Oncol. 2018 Feb 8;52(1):23-29. doi: 10.1515/raon-2018-0007. eCollection 2018 Mar.
The aim of the study was to investigate the feasibility and safety of experimental fractionation using intensity modulated radiation therapy with a simultaneous integrated boost (IMRT-SIB) to shorten the overall treatment time without dose escalation in preoperative radiochemotherapy of locally advanced rectal cancer.
Between January 2014 and November 2015, a total of 51 patients with operable stage II-III rectal adenocarcinoma were treated. The preoperative treatment with intensity modulated radiation therapy (IMRT) and a pelvic dose of 41.8 Gy and simultaneously delivered 46.2 Gy to T2/3 and 48.4 Gy to T4 tumour in 22 fractions, with standard concomitant capecitabine, was completed in 50 patients out of whom 47 were operated. The median follow-up was 35 months.
The rate of acute toxicity G ≥ 3 was 2.4%. The total downstaging rate was 89% and radical resection was achieved in 98% of patients. Pathologic complete response (pCR) was observed in 25.5% of patients, with 2-year local control (LC), disease free survival (DFS), and overall survival (OS) of 100% for this patient group. An intention-to-treat analysis revealed pN to be a significant prognostic factor for DFS and OS (P = 0.005 and 0.030, respectively). LC for the entire group was 100%, and 2-year DFS and OS were 90% (95 % CI 98.4-81.6) and 92.2% (95% CI 99.6-84.7), respectively.
The experimental regime in this study resulted in a high rate of pCR with a low acute toxicity profile. Excellent early results translated into encouraging 2-year LC, DFS, and OS.
本研究的目的是探讨在局部晚期直肠癌术前放化疗中,使用调强放射治疗同步整合加量(IMRT-SIB)进行实验性分割放疗以缩短总治疗时间且不增加剂量的可行性和安全性。
2014年1月至2015年11月期间,共治疗了51例可手术的II-III期直肠腺癌患者。50例患者完成了术前调强放射治疗(IMRT),盆腔剂量为41.8 Gy,同时分22次给予T2/3肿瘤46.2 Gy、T4肿瘤48.4 Gy,并同步给予标准的卡培他滨,其中47例接受了手术。中位随访时间为35个月。
3级及以上急性毒性发生率为2.4%。总降期率为89%,98%的患者实现了根治性切除。25.5%的患者观察到病理完全缓解(pCR),该患者组的2年局部控制(LC)、无病生存率(DFS)和总生存率(OS)均为100%。意向性分析显示pN是DFS和OS的显著预后因素(分别为P = 0.005和0.030)。整个组的LC为100%,2年DFS和OS分别为90%(95%CI 98.4-81.6)和92.2%(95%CI 99.6-84.7)。
本研究中的实验方案导致了高pCR率和低急性毒性特征。优异的早期结果转化为令人鼓舞的2年LC、DFS和OS。