Department of Medical Laboratory Sciences, Jordan University of Science and Technology, P.O.Box 3030, Irbid, 22110, Jordan.
Department of Special Surgery, King Hussein Cancer Center, Amman, 11941, Jordan.
Med Mol Morphol. 2024 Jun;57(2):136-146. doi: 10.1007/s00795-024-00383-2. Epub 2024 Mar 9.
The purpose of this study was to assess the clinicopathological features of oropharyngeal cancer patients in Jordan based on their HPV status. Sixty-nine biopsies from two hospitals were included. Tissue microarrays were prepared from formalin-fixed paraffin-embedded (FFPE) specimens and stained with antibodies for CDKN2A/P16, EGFR, PI3K, PTEN, AKT, pS473AKT, PS2mTOR, and TIMAP. The cohort was divided according to P16 expression. Chi-square test and survival analyses were employed to evaluate the variations among the study variables and determine the prognostic factors, respectively. P16 expression was found in 55.1% of patients; however, there was no significant association between P16 expression and the patients' clinicopathological features. The Kaplan-Meier test revealed that smoking in P16-positive group and younger age (< 58 years) negatively impacted disease-free survival (DFS) (P = 0.04 and P = 0.003, respectively). Multivariate Cox regression test indicated that smoking, age, PI3K, and AKT were negative predictors of DFS (P = 0.021, P = 0.002, P = 0.021, and P = 0.009, respectively), while TIMAP was a positive predictor (P = 0.045). Elevated P16 expression is found in more than half of the patients' specimens. DFS is negatively affected by younger age and the combined effect of smoking and P16 overexpression. TIMAP is overexpressed in P16-positive oropharyngeal cancer, and it is a favorable predictor of DFS.
本研究旨在根据 HPV 状态评估约旦口咽癌患者的临床病理特征。纳入来自两家医院的 69 份活检组织。使用针对 CDKN2A/P16、EGFR、PI3K、PTEN、AKT、pS473AKT、PS2mTOR 和 TIMAP 的抗体对福尔马林固定石蜡包埋(FFPE)标本制备组织微阵列并进行染色。根据 P16 表达将队列分组。采用卡方检验和生存分析分别评估研究变量之间的差异和确定预后因素。在 55.1%的患者中发现了 P16 表达;然而,P16 表达与患者的临床病理特征之间没有显著关联。Kaplan-Meier 检验显示,P16 阳性组的吸烟和年龄较小(<58 岁)对无病生存期(DFS)产生负面影响(P=0.04 和 P=0.003)。多变量 Cox 回归检验表明,吸烟、年龄、PI3K 和 AKT 是 DFS 的负预测因子(P=0.021、P=0.002、P=0.021 和 P=0.009),而 TIMAP 是正预测因子(P=0.045)。超过一半的患者标本中发现 P16 表达升高。DFS 受年龄较小和吸烟与 P16 过表达的联合影响而受到负面影响。TIMAP 在 P16 阳性的口咽癌中过表达,并且是 DFS 的有利预测因子。