Department of Surgery, Boston Medical Center, Boston University School of Medicine, Boston, MA, USA.
Department of Surgical Oncology, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
J Gastrointest Surg. 2021 Jun;25(6):1363-1369. doi: 10.1007/s11605-021-04993-4. Epub 2021 Apr 12.
Clinical staging guides decisions about optimal treatment sequence in patients with gastric cancer, although the preoperative accuracy is not strongly established. This study investigates concordance of clinical and pathologic stage as well as its impact on the survival of patients with gastric adenocarcinoma.
Patients with clinical stage T2-4, N0, M0 gastric adenocarcinoma who underwent surgery without neoadjuvant therapy were identified from the National Cancer Database (2010-2015). The primary outcome was up-staging, defined as cT < pT, pN1-3, and/or pM1 (AJCC 7 edition). Multivariable logistic regression analysis was performed to predict up-staging. Survival analysis was performed using the Kaplan-Meier method.
In total, 2254 patients were identified. cTNM staging was discordant with pTNM staging in 65.6% of cases, with 50.4% up-staged and 15.2% down-staged. On multivariable logistic regression, younger age (OR 0.991, 95% CI 0.984-0.999, p=0.0188), male sex (versus female; OR 1.392, 95% CI 1.158-1.673, p=0.0004), poor or undifferentiated tumor grade (versus well differentiated or moderately differentiated; OR 2.399, 95% CI 1.987-2.896; p<0.0001), positive margin status (versus negative; OR 4.575, 95% CI 3.360-6.230; p<0.0001), and days from diagnosis to surgery (15-32 days versus ≤ 14 days; OR 1.411, 95% CI 1.098-1.814, p=0.0072) were predictive of up-staging. Patients who were up-staged had a decreased survival compared to patients who were accurately staged (median survival 27.9 months versus 67.6 months; log-rank p<0.0001).
This study found a substantial discordance between clinical and pathologic staging of resectable locally advanced gastric adenocarcinoma. These data support that patients may have more advanced disease at presentation than reflected in clinical staging and may benefit from improved diagnostic modalities and neoadjuvant chemotherapy.
临床分期指导胃癌患者最佳治疗顺序的决策,尽管术前准确性尚未得到充分证实。本研究旨在探讨临床分期与病理分期的一致性及其对胃腺癌患者生存的影响。
从国家癌症数据库(2010-2015 年)中筛选出接受无新辅助治疗的临床分期 T2-4、N0、M0 胃腺癌手术的患者。主要结局为 cT < pT、pN1-3 和/或 pM1(AJCC 第 7 版)定义的升级分期。采用多变量逻辑回归分析预测升级分期。采用 Kaplan-Meier 方法进行生存分析。
共纳入 2254 例患者。cTNM 分期与 pTNM 分期不符的比例为 65.6%,其中 50.4%为升级分期,15.2%为降级分期。多变量逻辑回归分析显示,年龄较小(OR 0.991,95%CI 0.984-0.999,p=0.0188)、男性(与女性相比;OR 1.392,95%CI 1.158-1.673,p=0.0004)、肿瘤分化程度差或未分化(与分化程度好或中分化相比;OR 2.399,95%CI 1.987-2.896;p<0.0001)、切缘阳性(与阴性相比;OR 4.575,95%CI 3.360-6.230;p<0.0001)和诊断至手术的天数(15-32 天与≤14 天;OR 1.411,95%CI 1.098-1.814,p=0.0072)与升级分期相关。与准确分期的患者相比,升级分期的患者生存时间缩短(中位生存时间 27.9 个月与 67.6 个月;log-rank p<0.0001)。
本研究发现可切除局部晚期胃腺癌的临床分期与病理分期存在显著差异。这些数据支持患者在就诊时可能比临床分期所反映的疾病更为晚期,可能受益于改进的诊断方法和新辅助化疗。