Department of Surgery, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Upper Gastrointestinal/Soft Tissue Unit, Princess Alexandra Hospital, Brisbane, QLD, Australia.
Ann Surg Oncol. 2019 Aug;26(8):2375-2384. doi: 10.1245/s10434-019-07322-x. Epub 2019 Apr 2.
Little is known about the association between signet ring cell (SRC) differentiation and response to neoadjuvant chemotherapy (nCT) or neoadjuvant chemoradiotherapy (nCRT) in patients with esophageal and junctional adenocarcinoma (EAC). We aimed to assess if SRC differentiation is associated with survival and response to nCT or nCRT in patients with EAC.
Patients who underwent nCT and nCRT followed by surgery for EAC from 2000 until 2016 were identified from two institutional prospectively maintained databases. The pretreatment biopsy report or surgical resection specimen was used to differentiate patients into an SRC or non-SRC group.
Overall, 129 (19%) of 689 patients included had SRCs (nCT: n = 64; nCRT: n = 65). The SRC group had a more advanced ypT stage (p = 0.003), a higher number of positive lymph nodes in the resection specimen {median (interquartile range [IQR]) 2 [0-5] vs. 1 [0-3]; p = 0.002} and a higher rate of R1/R2 resections (19.4% vs. 12%; p = 0.026). SRC differentiation was not an independent prognostic factor for overall survival (OS) or disease-free survival (DFS). Following nCT, the SRC group had significantly shorter DFS (median [IQR] 12 [5-50] vs. 23 [8-164]; p = 0.013), but not OS, compared with the non-SRC group. In contrast, no differences according to SRC status for OS or DFS were found in patients who underwent nCRT.
SRC differentiation was not independently associated with worse OS in patients with EAC who underwent neoadjuvant therapy and surgery. However, nCRT was associated with greater tumor downstaging and better DFS.
对于食管胃结合部腺癌(EAC)患者,尚不清楚印戒细胞(SRC)分化与新辅助化疗(nCT)或新辅助放化疗(nCRT)反应之间的关系。我们旨在评估 SRC 分化是否与 EAC 患者的 nCT 或 nCRT 反应相关。
从两个机构前瞻性维护的数据库中确定了 2000 年至 2016 年间接受 nCT 和 nCRT 治疗后接受手术的 EAC 患者。根据预处理活检报告或手术切除标本将患者分为 SRC 或非-SRC 组。
在 689 例患者中,共有 129 例(19%)患者存在 SRC(nCT:n=64;nCRT:n=65)。SRC 组患者的 ypT 分期更晚(p=0.003),切除标本中阳性淋巴结数量更多(中位数(四分位距[IQR])2 [0-5] vs. 1 [0-3];p=0.002),R1/R2 切除率更高(19.4% vs. 12%;p=0.026)。SRC 分化不是总生存(OS)或无病生存(DFS)的独立预后因素。在 nCT 后,SRC 组的 DFS 明显更短(中位数(IQR)12 [5-50] vs. 23 [8-164];p=0.013),但 OS 无差异。相比之下,在接受 nCRT 的患者中,SRC 状态与 OS 或 DFS 均无差异。
对于接受新辅助治疗和手术的 EAC 患者,SRC 分化与 OS 无显著相关性。然而,nCRT 与更大的肿瘤降期和更好的 DFS 相关。