Sand Freja Lærke, Lindquist Sofie, Aalborg Gitte Lerche, Kjaer Susanne K
Unit of Virus, Lifestyle and Genes, Danish Cancer Institute, Strandboulevarden, Copenhagen, Denmark.
Unit of Statistics and Data Analysis, Danish Cancer Institute, Strandboulevarden, Copenhagen, Denmark.
Pathology. 2025 Apr;57(3):276-284. doi: 10.1016/j.pathol.2024.11.006. Epub 2025 Jan 17.
This meta-analysis aimed to explore penile cancer survival based on p53 and Ki-67 status. A systematic literature search identified studies assessing overall and cancer-specific survival after penile cancer with p53 or Ki-67 expression. Pooled hazard ratios (HRs) and restricted mean survival time (RMST) differences were calculated using a random-effects model. The analysis included 930 and 391 men for p53 expression in overall survival (OS) and cancer-specific survival (CSS), respectively. Those with the p53 mutant pattern exhibited significantly worse OS and CSS compared to the p53 wild-type pattern (HR=2.42, 95% CI 1.75-3.34; HR=4.18, 95% CI 1.87-9.35). The 5-year RMST difference for OS, according to p53 status, was -10.62 months (95% CI -16.20 to -5.03). We included 202 men with penile cancer tested for Ki-67 expression and found an HR of CSS of 1.96 (95% CI 1.15-3.32). In conclusion, men with the p53 mutant pattern penile cancer have worse OS and CSS than men with p53 wild-type pattern penile cancer. Evidence regarding Ki-67 status was sparse, but the pooled estimate indicated that penile cancers with high Ki-67 expression may have a slightly worse CSS than those with low Ki-67 expression. These findings may inform clinicians when planning the best management and follow-up strategy for penile cancer patients.
本荟萃分析旨在基于p53和Ki-67状态探讨阴茎癌的生存率。系统的文献检索确定了评估阴茎癌伴p53或Ki-67表达后的总生存率和癌症特异性生存率的研究。使用随机效应模型计算合并风险比(HRs)和受限平均生存时间(RMST)差异。该分析分别纳入了930名和391名男性,以评估p53表达在总生存(OS)和癌症特异性生存(CSS)中的情况。与p53野生型模式相比,具有p53突变模式的患者的OS和CSS明显更差(HR=2.42,95%CI 1.75-3.34;HR=4.18,95%CI 1.87-9.35)。根据p53状态,OS的5年RMST差异为-10.62个月(95%CI -16.20至-5.03)。我们纳入了202名检测Ki-67表达的阴茎癌男性,发现CSS的HR为1.96(95%CI 1.15-3.32)。总之,患有p53突变模式阴茎癌的男性的OS和CSS比患有p53野生型模式阴茎癌的男性更差。关于Ki-67状态的证据很少,但汇总估计表明,Ki-67高表达的阴茎癌的CSS可能比Ki-67低表达的阴茎癌略差。这些发现可能为临床医生规划阴茎癌患者的最佳管理和随访策略提供参考。