Department of General, Visceral, Cancer and Transplantation Surgery, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Department of General and Visceral Surgery, Helios University Hospital of Wuppertal, Wuppertal, Germany.
Br J Cancer. 2023 Jun;128(11):2025-2035. doi: 10.1038/s41416-023-02232-y. Epub 2023 Mar 25.
Histopathologic regression following neoadjuvant treatment (NT) of oesophageal cancer is a prognostic factor of survival, but the nodal status is not considered. Here, a score combining both to improve prediction of survival after neoadjuvant therapy is developed.
Seven hundred and fifteen patients with oesophageal squamous cell (SCC) or adenocarcinoma (AC) undergoing NT and esophagectomy were analysed. Histopathologic response was classified according to percentage of vital residual tumour cells (VRTC): complete response (CR) without VRTC, major response with <10% VRTC, minor response with >10% VRTC. Nodal stage was classified as ypN0 and ypN+. Kaplan-Meier and Cox regression were used for survival analysis.
Survival analysis identified three groups with significantly different mortality risks: (1) low-risk group for CR (ypT0N0) with 72% 5-year overall survival (5y-OS), (2) intermediate-risk group for minor/major responders and ypN0 with 59% 5y-OS, and (3) high-risk group for minor/major responders and ypN+ with 20% 5y-OS (p < 0.001). Median survival in AC and SCC cohorts were comparable (3.8 (CI 95%: 3.1, 5.3) vs. 4.6 years (CI 95%: 3.3, not reached), p = 0.3).
Histopathologic regression and nodal status should be combined for estimating AC and SCC prognosis. Poor survival in the high-risk group highlights need for adjuvant therapy.
新辅助治疗(NT)后食管鳞癌(SCC)和腺癌(AC)的组织病理学消退是生存的预后因素,但不考虑淋巴结状态。在此,开发了一种结合两者的评分,以提高新辅助治疗后生存预测的准确性。
分析了 715 例接受 NT 和食管切除术的食管 SCC 或 AC 患者。根据存活肿瘤细胞的百分比(VRTC)将组织病理学反应分为完全缓解(CR)无 VRTC、主要缓解(<10% VRTC)、次要缓解(>10% VRTC)。淋巴结分期分为 ypN0 和 ypN+。使用 Kaplan-Meier 和 Cox 回归进行生存分析。
生存分析确定了三组死亡率风险显著不同:(1)CR(ypT0N0)的低危组,5 年总生存率(5y-OS)为 72%,(2)ypN0 伴有微小/主要反应的中危组,5y-OS 为 59%,(3)ypN+伴有微小/主要反应的高危组,5y-OS 为 20%(p<0.001)。AC 和 SCC 队列的中位生存时间相当(3.8(95%CI:3.1,5.3)vs. 4.6 年(95%CI:3.3,未达到),p=0.3)。
组织病理学消退和淋巴结状态应结合起来估计 AC 和 SCC 的预后。高危组的生存状况较差,突出了辅助治疗的必要性。