Department of Surgery, Erasmus MC - University Medical Centre, Suite Z-839, P.O. Box 2040 3000, CA, Rotterdam, The Netherlands.
Department of Gastroenterology, Leiden University Medical Centre, Leiden, the Netherlands.
BMC Cancer. 2018 Feb 6;18(1):142. doi: 10.1186/s12885-018-4034-1.
Neoadjuvant chemoradiotherapy (nCRT) plus surgery is a standard treatment for locally advanced oesophageal cancer. With this treatment, 29% of patients have a pathologically complete response in the resection specimen. This provides the rationale for investigating an active surveillance approach. The aim of this study is to assess the (cost-)effectiveness of active surveillance vs. standard oesophagectomy after nCRT for oesophageal cancer.
This is a phase-III multi-centre, stepped-wedge cluster randomised controlled trial. A total of 300 patients with clinically complete response (cCR, i.e. no local or disseminated disease proven by histology) after nCRT will be randomised to show non-inferiority of active surveillance to standard oesophagectomy (non-inferiority margin 15%, intra-correlation coefficient 0.02, power 80%, 2-sided α 0.05, 12% drop-out). Patients will undergo a first clinical response evaluation (CRE-I) 4-6 weeks after nCRT, consisting of endoscopy with bite-on-bite biopsies of the primary tumour site and other suspected lesions. Clinically complete responders will undergo a second CRE (CRE-II), 6-8 weeks after CRE-I. CRE-II will include 18F-FDG-PET-CT, followed by endoscopy with bite-on-bite biopsies and ultra-endosonography plus fine needle aspiration of suspected lymph nodes and/or PET- positive lesions. Patients with cCR at CRE-II will be assigned to oesophagectomy (first phase) or active surveillance (second phase of the study). The duration of the first phase is determined randomly over the 12 centres, i.e., stepped-wedge cluster design. Patients in the active surveillance arm will undergo diagnostic evaluations similar to CRE-II at 6/9/12/16/20/24/30/36/48 and 60 months after nCRT. In this arm, oesophagectomy will be offered only to patients in whom locoregional regrowth is highly suspected or proven, without distant dissemination. The main study parameter is overall survival; secondary endpoints include percentage of patients who do not undergo surgery, quality of life, clinical irresectability (cT4b) rate, radical resection rate, postoperative complications, progression-free survival, distant dissemination rate, and cost-effectiveness. We hypothesise that active surveillance leads to non-inferior survival, improved quality of life and a reduction in costs, compared to standard oesophagectomy.
If active surveillance and surgery as needed after nCRT leads to non-inferior survival compared to standard oesophagectomy, this organ-sparing approach can be implemented as a standard of care.
新辅助放化疗(nCRT)加手术是治疗局部晚期食管癌的标准治疗方法。采用这种治疗方法,29%的患者在切除标本中病理完全缓解。这为探索主动监测方法提供了依据。本研究旨在评估 nCRT 后主动监测与标准食管癌切除术的(成本)效益。
这是一项多中心、三阶段、阶梯式楔形集群随机对照试验。总共 300 例 nCRT 后临床完全缓解(cCR,即组织学无局部或播散性疾病)的患者将被随机分为主动监测组和标准食管癌切除术组,以证明主动监测不劣于标准食管癌切除术(非劣效性边界为 15%,组内相关系数为 0.02,效能为 80%,双侧 α 为 0.05,脱落率为 12%)。患者将在 nCRT 后 4-6 周进行第一次临床反应评估(CRE-I),包括内镜检查和原发肿瘤部位及其他可疑病变的咬活检。临床完全缓解者将进行第二次 CRE(CRE-II),在 CRE-I 后 6-8 周进行。CRE-II 将包括 18F-FDG-PET-CT,然后进行内镜检查和咬活检以及超内镜超声加细针抽吸可疑淋巴结和/或 PET 阳性病变。在 CRE-II 时 cCR 的患者将被分配到食管癌切除术(第一阶段)或主动监测(研究的第二阶段)。第一阶段的持续时间将在 12 个中心随机确定,即阶梯式楔形集群设计。主动监测组的患者将在 nCRT 后 6/9/12/16/20/24/30/36/48 和 60 个月进行类似于 CRE-II 的诊断评估。在该组中,仅当局部区域复发高度可疑或证实且无远处播散时,才会对患者进行食管癌切除术。主要研究参数为总生存率;次要终点包括未行手术的患者比例、生活质量、临床不可切除性(cT4b)率、根治性切除率、术后并发症、无进展生存率、远处播散率和成本效益。我们假设与标准食管癌切除术相比,nCRT 后主动监测和按需手术可导致非劣效生存,改善生活质量并降低成本。
如果 nCRT 后主动监测和必要时的手术与标准食管癌切除术相比导致非劣效生存,那么这种保留器官的方法可以作为一种标准的治疗方法。