Lee Ji-Ae, Park Hye Eun, Jin Hye-Yeong, Jin Lingyan, Yoo Seung Yeon, Cho Nam-Yun, Bae Jeong Mo, Kim Jung Ho, Kang Gyeong Hoon
Department of Pathology, Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Pathology, Seoul National University Boramae Hospital, Seoul, Korea.
J Pathol Transl Med. 2025 Jan;59(1):50-59. doi: 10.4132/jptm.2024.09.26. Epub 2024 Oct 24.
Colorectal carcinomas (CRCs) with caudal-type homeobox 2 (CDX2) loss are recognized to pursue an aggressive behavior but tend to be accompanied by a high density of tumor-infiltrating lymphocytes (TILs). However, little is known about whether there is an interplay between CDX2 loss and TIL density in the survival of patients with CRC.
Stage III CRC tissues were assessed for CDX2 loss using immunohistochemistry and analyzed for their densities of CD8 TILs in both intraepithelial (iTILs) and stromal areas using a machine learning-based analytic method.
CDX2 loss was significantly associated with a higher density of CD8 TILs in both intraepithelial and stromal areas. Both CDX2 loss and a high CD8 iTIL density were found to be prognostic parameters and showed hazard ratios of 2.314 (1.050-5.100) and 0.378 (0.175-0.817), respectively, for cancer-specific survival. A subset of CRCs with retained CDX2 expression and a high density of CD8 iTILs showed the best clinical outcome (hazard ratio of 0.138 [0.023-0.826]), whereas a subset with CDX2 loss and a high density of CD8 iTILs exhibited the worst clinical outcome (15.781 [3.939-63.230]).
Altogether, a high density of CD8 iTILs did not make a difference in the survival of patients with CRC with CDX2 loss. The combination of CDX2 expression and intraepithelial CD8 TIL density was an independent prognostic marker in adjuvant chemotherapy-treated patients with stage III CRC.
尾型同源盒2(CDX2)缺失的结直肠癌(CRC)具有侵袭性行为,但往往伴有高密度的肿瘤浸润淋巴细胞(TILs)。然而,关于CDX2缺失与TIL密度在CRC患者生存中的相互作用知之甚少。
采用免疫组织化学方法评估III期CRC组织中CDX2缺失情况,并使用基于机器学习的分析方法分析其上皮内(iTILs)和基质区域中CD8 TILs的密度。
CDX2缺失与上皮内和基质区域中较高密度的CD8 TILs显著相关。CDX2缺失和高CD8 iTIL密度均被发现是预后参数,癌症特异性生存的风险比分别为2.314(1.050 - 5.100)和0.378(0.175 - 0.817)。一部分CDX2表达保留且CD8 iTIL密度高的CRC患者显示出最佳临床结局(风险比为0.138 [0.023 - 0.826]),而一部分CDX2缺失且CD8 iTIL密度高的患者则表现出最差的临床结局(15.781 [3.939 - 63.230])。
总之,高密度的CD8 iTILs对CDX2缺失的CRC患者生存没有影响。CDX2表达与上皮内CD8 TIL密度的组合是接受辅助化疗的III期CRC患者的独立预后标志物。