Tang Junwei, Zhang Yue, Zhang Dongsheng, Zhang Chuan, Jin Kangpeng, Ji Dongjian, Peng Wen, Feng Yifei, Sun Yueming
Colorectal Surgery Division, Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Front Surg. 2022 Feb 1;9:812343. doi: 10.3389/fsurg.2022.812343. eCollection 2022.
Transanal endoscopic microsurgery (TEM) is an organ-preserving treatment alternative for patients with early rectal cancer. However, TEM alone is associated with greater risk of local recurrence and inferior survival in comparison with total meso-rectal excision (TME). As an important adjuvant therapy, radiotherapy can effectively reduce the local recurrence rate of rectal cancer. This study aimed to investigate whether TEM followed by radiotherapy can be a valid alternative to TME in T2N0M0 distal rectal cancer treatment.
We plan to recruit 168 participants meeting established inclusion criteria. Following informed consent, participants will randomly receive treatment protocols of TEM followed by radiotherapy (a total dose of 45-50.4 Gy given in 25-28 factions) or TME. Depending on post-operative pathology, the participants will receive either long-term follow-up or further treatment. The primary endpoint of this trial is 3-year local recurrence rate. The secondary end points include 3-year disease-free survival rate, 3-year overall survival rate, 3-year mortality rate, post-operative quality of life, post-operative safety index, intraoperative evaluation index and post-operative short-term evaluation index.
This trial is the first prospective randomized trial to investigate the rectum preserving treatment by using transanal local excision followed by radiotherapy.
The trial was prospectively registered at ClinicalTrials.gov NCT04098471 on September 20, 2019.
经肛门内镜显微手术(TEM)是早期直肠癌患者保留器官的一种治疗选择。然而,与全直肠系膜切除术(TME)相比,单纯TEM局部复发风险更高,生存率更低。作为一种重要的辅助治疗,放疗可有效降低直肠癌的局部复发率。本研究旨在探讨TEM联合放疗在T2N0M0期低位直肠癌治疗中是否可作为TME的有效替代方案。
我们计划招募168名符合既定纳入标准的参与者。在获得知情同意后,参与者将随机接受TEM联合放疗(总剂量45 - 50.4 Gy,分25 - 28次给予)或TME的治疗方案。根据术后病理情况,参与者将接受长期随访或进一步治疗。本试验的主要终点是3年局部复发率。次要终点包括3年无病生存率、3年总生存率、3年死亡率、术后生活质量、术后安全指数、术中评估指标和术后短期评估指标。
本试验是首个前瞻性随机试验,旨在研究经肛门局部切除联合放疗保留直肠的治疗方法。
该试验于2019年9月20日在ClinicalTrials.gov上进行前瞻性注册,注册号为NCT04098471。