Richter Maximilian, Doll Christian, Mrosk Friedrich, Hofmann Elena, Koerdt Steffen, Heiland Max, Neumann Konrad, Beck Marcus, Dommerich Steffen, Jöhrens Korinna, Raguse Jan-Dirk
Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Oral and Maxillofacial Surgery, Berlin, Germany.
Berlin Institute of Health at Charité - Universitätsmedizin Berlin, BIH Biomedical Innovation Academy, BIH Charité Junior Clinician Scientist Program, Berlin, Germany.
Front Oncol. 2024 Nov 27;14:1493281. doi: 10.3389/fonc.2024.1493281. eCollection 2024.
Despite numerous studies addressing the impact of p16 in oral squamous cell carcinoma (OSCC), consistent data regarding survival and tumor proliferation behavior are lacking. Although some authors investigate both p16 and Mib/Ki-67 in their cohorts, direct correlations are consistently missing. The aim of this study was to investigate the combined influence of p16 and Mib/Ki-67 status on prognosis in OSCC.
Clinical data of all patients diagnosed with OSCC and treated curatively between 2005 and 2011 were collected retrospectively. Tissue microarrays of formalin-fixed paraffin-embedded specimens were stained for p16 and Mib/Ki-67 using the CINtec Histology V-Kit or MIB-1 antibody and correlated with the clinical outcome.
A total of 316 patients, with a mean age of 61.7 years were included. Tumor tissues that were tested p16 positive with low Mib/Ki-67 expression demonstrated a remarkable 5-year survival rate of 83% with an improved RFS compared to all other subgroups (p=0.034; p=0.017; p=0.026) and an improved OS compared to those with high Mib/Ki-67 expression (p=0.026; p=0.020). Cox regression identified the combined p16 and Mib/Ki-67 status as a risk factor on OS (HR 6.25; CI1.26-31.0; p=0.025) and RFS (HR 5.88; CI1.19-29.20; p=0.030).
These results underscore the importance of a combined assessment of p16 and Mib/Ki-67 in evaluating the prognosis of OSCC, leading to the identification of distinct subgroups that may serve as risk factors for treatment stratification.
尽管有大量研究探讨了p16在口腔鳞状细胞癌(OSCC)中的作用,但关于生存率和肿瘤增殖行为的一致数据仍然缺乏。虽然一些作者在其队列研究中同时检测了p16和Mib/Ki-67,但一直缺少直接的相关性分析。本研究的目的是探讨p16和Mib/Ki-67状态对OSCC预后的综合影响。
回顾性收集2005年至2011年间所有诊断为OSCC并接受根治性治疗的患者的临床资料。使用CINtec Histology V-Kit或MIB-1抗体对福尔马林固定石蜡包埋标本的组织微阵列进行p16和Mib/Ki-67染色,并与临床结果进行相关性分析。
共纳入316例患者,平均年龄61.7岁。p16检测为阳性且Mib/Ki-67表达较低的肿瘤组织显示出显著的5年生存率,为83%,与所有其他亚组相比,无复发生存期(RFS)得到改善(p=0.034;p=0.017;p=0.026),与Mib/Ki-67高表达的患者相比,总生存期(OS)也得到改善(p=0.026;p=0.020)。Cox回归分析确定p16和Mib/Ki-67的联合状态是OS(风险比[HR]6.25;95%置信区间[CI]1.26-31.0;p=0.025)和RFS(HR 5.88;CI 1.19-29.20;p=0.030)的危险因素。
这些结果强调了联合评估p16和Mib/Ki-67在评估OSCC预后中的重要性,从而确定了可能作为治疗分层危险因素的不同亚组。