Department of Surgery, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, 892 Dongnam-ro, Gangdong-gu, Seoul, 05278, South Korea.
Department of Medicine, the Graduate School of Yonsei University, 50-1 Yonsei-ro, Seoul, South Korea.
BMC Cancer. 2018 May 8;18(1):538. doi: 10.1186/s12885-018-4466-7.
BACKGROUND: Neoadjuvant chemoradiotherapy (CRT) followed by total mesorectal excision (TME) has been a standard treatment option for locally advanced rectal cancer with improved local control. However, systemic recurrence despite neoadjuvant CRT remained unchanged. The only significant prognostic factor proven to be important was pathologic complete response (pCR) after neoadjuvant CRT. Several efforts have been tried to improve survival of patients who treated with neoadjuvant CRT and to achieve more pCR including adding cytotoxic chemotherapeutic agents, chronologic modification of chemotherapy schedule or adding chemotherapy during the perioperative period. Consolidation chemotherapy is adding several cycles of chemotherapy between neoadjuvant CRT and TME. It could increase pCR rate, subsequently could show better oncologic outcomes. METHODS: Patients with advanced mid or low rectal cancer who received neoadjuvant CRT will be included after screening. They will be randomized and assigned to undergo TME followed by 8 cycles of adjuvant chemotherapy (control arm) or receive 3 cycles of consolidation chemotherapy before TME, and receive 5 cycles of adjuvant chemotherapy (experimental arm). The primary endpoints are pCR and 3-year disease-free survival (DFS), and the secondary endpoints are radiotherapy-related complications, R0 resection rate, tumor response rate, surgery-related morbidity, and peripheral neuropathy at 3 year after the surgery. The authors hypothesize that the experimental arm would show a 15% improvement in pCR (15 to 30%) and in 3-year DFS (65 to 80%), compared with the control arm. The accrual period is 2 years and the follow-up period is 3 years. Based on the superiority design, one-sided log-rank test with α-error of 0.025 and a power of 80% was conducted. Allowing for a drop-out rate of 10%, 358 patients (179 per arm) will need to be recruited. Patients will be followed up at every 3 months for 2 years and then every 6 months for 3 years after the last patient has been randomized. DISCUSSION: KONCLUDE trial aims to investigate whether consolidation chemotherapy shows better pCR and 3-year DFS than adjuvant chemotherapy alone for the patients who received neoadjuvant CRT for locally advanced rectal cancer. This trial is expected to provide evidence to support clear treatment guidelines for patients with locally advanced rectal cancer. TRIAL REGISTRATION: Clinicaltrials.gov NCT02843191 (First posted on July 25, 2016).
背景:新辅助放化疗(CRT)后全直肠系膜切除术(TME)已成为局部晚期直肠癌的标准治疗选择,可提高局部控制率。然而,尽管进行了新辅助 CRT,全身复发率仍保持不变。唯一被证明具有重要意义的显著预后因素是新辅助 CRT 后的病理完全缓解(pCR)。为了提高接受新辅助 CRT 治疗的患者的生存率并实现更多的 pCR,人们已经尝试了几种方法,包括添加细胞毒性化疗药物、化疗方案的时间调整或在围手术期添加化疗。巩固化疗是在新辅助 CRT 和 TME 之间添加几个周期的化疗。它可以提高 pCR 率,从而显示出更好的肿瘤学结果。
方法:筛选后将纳入接受新辅助 CRT 的中低位局部晚期直肠腺癌患者。他们将被随机分配接受 TME 后接受 8 个周期的辅助化疗(对照组)或在 TME 前接受 3 个周期的巩固化疗,然后接受 5 个周期的辅助化疗(实验组)。主要终点是 pCR 和 3 年无病生存率(DFS),次要终点是放疗相关并发症、R0 切除率、肿瘤反应率、手术相关发病率和手术后 3 年的周围神经病。作者假设实验组在 pCR(15%至 30%)和 3 年 DFS(65%至 80%)方面将显示出 15%的改善,与对照组相比。入组期为 2 年,随访期为 3 年。基于优势设计,进行单侧 log-rank 检验,α 错误为 0.025,效能为 80%。考虑到 10%的脱落率,需要招募 358 名患者(每组 179 名)。患者将在 2 年内每 3 个月随访一次,然后在最后一名患者随机分组后 3 年内每 6 个月随访一次。
讨论:KONCLUDE 试验旨在研究对于接受新辅助 CRT 的局部晚期直肠腺癌患者,巩固化疗是否比单独辅助化疗显示出更好的 pCR 和 3 年 DFS。该试验有望提供支持局部晚期直肠腺癌患者明确治疗指南的证据。
试验注册:Clinicaltrials.gov NCT02843191(首次发布于 2016 年 7 月 25 日)。
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