Department of Gastroenterological Surgery, Yokohama City University School of Medicine, Yokohama, Japan.
Department of Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Ann Surg. 2022 Jul 1;276(1):140-145. doi: 10.1097/SLA.0000000000004494. Epub 2020 Sep 15.
We conducted the first prospective clinical trial of neoadjuvant chemotherapy for patients with obstructive colon cancer.
Obstructive colorectal cancer is locally advanced colorectal cancer with a poor prognosis. The effect of neoadjuvant chemotherapy for obstructive colon cancer is unclear.
We conducted a single arm, multicenter trial involving patients from the Yokohama Clinical Oncology Group with obstructive colon cancer. All eligible patients underwent diverting stoma formation before neoadjuvant chemotherapy. Patient received 6 cycles of mFOLFOX6 followed by primary tumor surgery and then 6 cycles of adjuvant chemotherapy. The primary endpoint was the objective response rate of all intended neoadjuvant therapy. The study was registered with the Japanese Clinical Trials Registry as UMIN000013198.
Between April 2014, and July 2016, 50 patients were registered, and 46 received neoadjuvant chemotherapy. The objective response rate as the primary endpoint was 67.4%. The most common grade >3 adverse event associated with neoadjuvant chemotherapy was neutropenia (28.3%). Forty-five patients underwent surgical resection of the primary lesion (R0 resection in all cases). Grade >2 surgery-related complications occurred in 7 patients (15.6%). The downstaging rate was 48.9%, and the moderate or greater regression rate was 52.2%; no cases showed pathological complete response. Adjuvant chemotherapy with mFOLFOX6 was performed in 34 patients (75.6%). The 3-year relapse-free and overall survival rates were 76.5% and 95.4%, respectively.
Neoadjuvant chemotherapy using mFOLFOX6 was feasible and might be a treatment option for patients with obstructive colon cancer. Further large-scale studies are warranted to confirm the present findings.
我们进行了首例针对梗阻性结肠癌患者的新辅助化疗的前瞻性临床试验。
梗阻性结直肠癌是局部晚期结直肠癌,预后较差。新辅助化疗对梗阻性结肠癌的疗效尚不清楚。
我们进行了一项单臂、多中心试验,纳入了来自横浜临床肿瘤学组的梗阻性结肠癌患者。所有符合条件的患者在新辅助化疗前均接受了转流造口术。患者接受 6 个周期的 mFOLFOX6 治疗,然后进行原发肿瘤手术,再进行 6 个周期的辅助化疗。主要终点是所有意向性新辅助治疗的客观缓解率。该研究在日本临床试验注册中心注册为 UMIN000013198。
2014 年 4 月至 2016 年 7 月,共登记了 50 例患者,其中 46 例接受了新辅助化疗。作为主要终点的客观缓解率为 67.4%。与新辅助化疗相关的最常见的 3 级以上不良事件是中性粒细胞减少症(28.3%)。45 例患者接受了原发肿瘤切除术(均为 R0 切除)。7 例患者(15.6%)发生了 2 级以上手术相关并发症。降期率为 48.9%,中度或以上退缩率为 52.2%;无病例出现病理完全缓解。34 例患者(75.6%)接受了 mFOLFOX6 辅助化疗。3 年无复发生存率和总生存率分别为 76.5%和 95.4%。
使用 mFOLFOX6 的新辅助化疗是可行的,可能是梗阻性结肠癌患者的一种治疗选择。需要进一步的大规模研究来证实目前的发现。