Park J H, van Wyk H, Roxburgh C S D, Horgan P G, Edwards J, McMillan D C
Academic Unit of Surgery, School of Medicine, Dentistry &Nursing, University of Glasgow, Glasgow Royal Infirmary, Glasgow G31 2ER, UK.
Unit of Experimental Therapeutics, Institute of Cancer Sciences, University of Glasgow, Garscube Estate, Glasgow G61 1BD, UK.
Br J Cancer. 2017 May 23;116(11):1444-1450. doi: 10.1038/bjc.2017.108. Epub 2017 Apr 20.
The present study aimed to examine the relationship between tumour invasiveness (T stage), the local and systemic environment and cancer-specific survival (CSS) of patients with primary operable colorectal cancer.
The tumour microenvironment was examined using measures of the inflammatory infiltrate (Klintrup-Makinen (KM) grade and Immunoscore), tumour stroma percentage (TSP) and tumour budding. The systemic inflammatory environment was examined using modified Glasgow Prognostic Score (mGPS) and neutrophil:lymphocyte ratio (NLR). A 5-year CSS was examined.
A total of 331 patients were included. Increasing T stage was associated with colonic primary, N stage, poor differentiation, margin involvement and venous invasion (P<0.05). T stage was significantly associated with KM grade (P=0.001), Immunoscore (P=0.016), TSP (P=0.006), tumour budding (P<0.001), and elevated mGPS and NLR (both P<0.05). In patients with T3 cancer, N stage stratified survival from 88 to 64%, whereas Immunoscore and budding stratified survival from 100 to 70% and from 91 to 56%, respectively. The Glasgow Microenvironment Score, a score based on KM grade and TSP, stratified survival from 93 to 58%.
Although associated with increasing T stage, local and systemic tumour environment characteristics, and in particular Immunoscore, budding, TSP and mGPS, are stage-independent determinants of survival and may be utilised in the staging of patients with primary operable colorectal cancer.
本研究旨在探讨原发性可手术切除的结直肠癌患者的肿瘤侵袭性(T分期)、局部和全身环境与癌症特异性生存(CSS)之间的关系。
采用炎症浸润指标(克林特鲁普-马基宁(KM)分级和免疫评分)、肿瘤间质百分比(TSP)和肿瘤芽生情况来检测肿瘤微环境。采用改良格拉斯哥预后评分(mGPS)和中性粒细胞与淋巴细胞比值(NLR)来检测全身炎症环境。对5年CSS进行检测。
共纳入331例患者。T分期增加与结肠原发、N分期、低分化、切缘受累和静脉侵犯相关(P<0.05)。T分期与KM分级(P=0.001)、免疫评分(P=0.016)、TSP(P=0.006)、肿瘤芽生(P<0.001)以及mGPS和NLR升高均显著相关(P均<0.05)。在T3期癌症患者中,N分期将生存率从88%分层至64%,而免疫评分和芽生分别将生存率从100%分层至70%和从91%分层至56%。基于KM分级和TSP的格拉斯哥微环境评分将生存率从93%分层至58%。
虽然与T分期增加相关,但局部和全身肿瘤环境特征,尤其是免疫评分、芽生、TSP和mGPS,是生存的分期独立决定因素,可用于原发性可手术切除的结直肠癌患者的分期。