Department of Digestive Surgery, St Antoine Hospital (AP-HP), Sorbonne Université, Paris, France.
Centre for Colorectal Disease, St Vincent's University Hospital, Dublin, Ireland.
Colorectal Dis. 2018 Sep;20(9):O248-O255. doi: 10.1111/codi.14289. Epub 2018 Jun 30.
The presence of tumour deposits (TDs) in colorectal cancer (CRC) is associated with poor prognosis. The seventh edition of TNM subclassified a new nodal stage, N1c, characterized by the presence of TDs without any concurrent positive lymph node (LN). It is not clear if the N1c category is or is not equal to LN metastasis. We aimed to examine the prevalence, characteristics and prognostic significance of this new subcategory.
Consecutive patients who underwent surgery for CRC in two centres (2011-2014) were analysed. N1 cM0 patients were matched against non-N1 cM0 (N0, N1a and N1b) patients for 3-year overall survival (OS) and disease-free survival (DFS).
We identified 1122 patients with 648 (57.8%) colonic cancers. In 57 patients (5.1%), N1c status was associated with rectal cancers [rectum = 33/57 (57.9%) vs colon = 24/57 (42.1%); P = 0.029], a higher pathological tumour stage [pT3-T4 N1c = 55/843 (6.5% vspT3-T4 non-N1c = 2/279 (0.7%); P < 0.0001] and vascular emboli [n = 35 (61.4%) vs n = 552 (51.8%); P = 0.0305]. Synchronous metastasis was observed in 23 cases (40%). After a mean follow-up of 31 months, 3-year OS for M0 patients, was 89.4%, 89.1%, 86.6% and 81.8% for N0, N1a, N1b and N1c tumours, respectively. DFS was significantly worse for N1c than for N0 (P = 0.0169), with N1c status having a significant effect on DFS in colonic cancers (P = 0.014). The presence of more than one TD was associated with a significantly worse DFS (P = 0.021).
Our results indicate that N1c CRC patients should be included among high-risk patients for whom it is widely accepted that adjuvant chemotherapy should be considered.
结直肠癌(CRC)中肿瘤沉积物(TDs)的存在与预后不良有关。第七版 TNM 将新的淋巴结分期 N1c 分类为特征为存在 TD 而无任何伴行阳性淋巴结(LN)的情况。目前尚不清楚 N1c 分类是否等同于 LN 转移。我们旨在检查这一新亚类的患病率、特征和预后意义。
对两个中心(2011-2014 年)接受 CRC 手术的连续患者进行分析。N1 cM0 患者与非 N1 cM0(N0、N1a 和 N1b)患者进行 3 年总生存(OS)和无病生存(DFS)匹配。
我们确定了 1122 例患者,其中 648 例(57.8%)为结肠癌症。在 57 例患者(5.1%)中,N1c 状态与直肠癌相关[直肠=33/57(57.9%)比结肠=24/57(42.1%);P=0.029],更高的病理肿瘤分期[pT3-T4 N1c=55/843(6.5%)比 pT3-T4 非-N1c=2/279(0.7%);P<0.0001]和血管内血栓[n=35(61.4%)比 n=552(51.8%);P=0.0305]。23 例(40%)观察到同步转移。平均随访 31 个月后,M0 患者的 3 年 OS 分别为 N0、N1a、N1b 和 N1c 肿瘤的 89.4%、89.1%、86.6%和 81.8%。与 N0 相比,N1c 的 DFS 明显更差(P=0.0169),并且 N1c 状态对结肠癌的 DFS 有显著影响(P=0.014)。存在多个 TD 与 DFS 显著恶化相关(P=0.021)。
我们的结果表明,N1c CRC 患者应被纳入高危患者,广泛认为应考虑辅助化疗。