Department of General and Visceral Surgery, Endocrine Surgery, and Coloproctology, Municipal Hospital of Munich-Neuperlach, Germany.
Department of Surgery, Carl-Thiem-Klinikum, Cottbus, Germany.
J Am Coll Surg. 2020 Oct;231(4):413-425.e2. doi: 10.1016/j.jamcollsurg.2020.06.023. Epub 2020 Jul 19.
Neoadjuvant chemoradiotherapy (nCRT) in patients with rectal cancer carries a high risk of adverse effects. The aim of this study was to examine the selective application of nCRT based on patient risk profile, as determined by MRI, to find the optimal range between undertreatment and overtreatment.
In this prospective multicenter observational study, nCRT before total mesorectal excision (TME) was indicated in high-risk patients with involved or threatened mesorectal fascia (≤1 mm), or cT4 or cT3 carcinomas of the lower rectal third. All other patients received primary surgery.
Of the 1,093 patients, 878 (80.3%) were treated according to the protocol, 526 patients (59.9%) underwent primary surgery, and 352 patients (40.1%) underwent nCRT followed by surgery. The 3-year locoregional recurrence (LR) rate was 3.1%. Of 604 patients with clinical stages II and III, 267 (44.2%) had primary surgery; 337 (55.8%) received nCRT followed by TME. The 3-year LR rate was 3.9%, without significant differences between groups. In patients with clinical stages II and III who underwent primary surgery, 27.3% were diagnosed with pathological stage I.
The results justify the restriction of nCRT to high-risk patients with rectal cancer classified by pretreatment MRI. Provided that a high-quality MRI diagnosis, TME surgery, and standardized examination of the resected specimen are performed, nCRT, with its adverse effects, costs, and treatment time can be avoided in more than 40% of patients with stage II or III rectal cancer with minimal risk of undertreatment. (clinicaltrials.gov NCT325649).
新辅助放化疗(nCRT)在直肠癌患者中存在发生不良反应的高风险。本研究旨在根据 MRI 确定的患者风险特征,选择性地应用 nCRT,以找到治疗不足和过度治疗之间的最佳范围。
在这项前瞻性多中心观察性研究中,nCRT 适用于高危患者,包括累及或侵犯中直肠筋膜(≤1mm)、cT4 或 cT3 下段直肠癌。所有其他患者均接受初始手术治疗。
在 1093 例患者中,878 例(80.3%)按方案治疗,526 例(59.9%)接受初始手术,352 例(40.1%)接受 nCRT 后手术。3 年局部区域复发(LR)率为 3.1%。在 604 例临床分期 II 期和 III 期患者中,267 例(44.2%)接受初始手术;337 例(55.8%)接受 nCRT 后行 TME 手术。3 年 LR 率为 3.9%,两组之间无显著差异。在接受初始手术的临床分期 II 期和 III 期患者中,27.3%的患者被诊断为病理分期 I 期。
这些结果支持将 nCRT 限制用于经术前 MRI 分类的高危直肠癌患者。只要能够进行高质量的 MRI 诊断、TME 手术以及对切除标本的标准化检查,就可以避免在超过 40%的 II 期或 III 期直肠癌患者中应用 nCRT,这些患者的治疗不足风险极小,但同时需要承担不良反应、成本和治疗时间方面的风险。(clinicaltrials.gov NCT0325649)