Chahoud Jad, Pickering Curtis R, Pettaway Curtis A
Department of Cancer Medicine.
Department of Head and Neck Surgery.
Curr Opin Urol. 2019 Jul;29(4):364-370. doi: 10.1097/MOU.0000000000000640.
We summarize the recent developments in the molecular landscape of penile squamous cell carcinoma (PSCC).
Recent genomic studies have demonstrated a molecular convergence of PSCC with other squamous cell carcinomas (SCCs) from different organ sites. Similarly, human papillomavirus (HPV)-related PSCCs appear to have epigenetic and genomic similarities with other HPV-related cancers. This could have implications on future HPV-related cancer trial design. Growing efforts to characterize recurrent gene alterations in PSCC have expanded our understanding over the past years, showing a predominance of tumor suppressor gene alterations such as TP53 and NOTCH1. In addition, these studies have demonstrated that at least 30% of PSCC cases have targetable gene alterations. Further, the similar tumor mutational burden with other SCCs and the relatively high rates of programmed death-1 (PD-1) positive expression in PSCC constitute the rationale for investigation of PD-1 inhibition in ongoing clinical trials. Multiple studies have identified potential epigenetic and RNA signatures predictive of metastasis or survival, but these still require validation in larger cohorts.
PSCC appears to be genomicaly similar to other SCCs and HPV-related cancers. This provides the rationale and opportunity to include a rare tumor like PSCC in future 'basket type' trials using novel agents targeting multiple SCCs that may exhibit similar biology.
我们总结阴茎鳞状细胞癌(PSCC)分子格局的最新进展。
近期的基因组研究表明,PSCC与来自不同器官部位的其他鳞状细胞癌(SCC)在分子层面存在趋同现象。同样,人乳头瘤病毒(HPV)相关的PSCC似乎在表观遗传学和基因组方面与其他HPV相关癌症具有相似性。这可能会对未来HPV相关癌症的试验设计产生影响。在过去几年中,对PSCC中复发性基因改变进行特征描述的工作不断增加,这扩展了我们的认识,显示出诸如TP53和NOTCH1等肿瘤抑制基因改变占主导地位。此外,这些研究表明,至少30%的PSCC病例具有可靶向的基因改变。此外,PSCC与其他SCC相似的肿瘤突变负担以及相对较高的程序性死亡-1(PD-1)阳性表达率,构成了在正在进行的临床试验中研究PD-1抑制作用的理论依据。多项研究已经确定了预测转移或生存的潜在表观遗传学和RNA特征,但这些仍需要在更大的队列中进行验证。
PSCC在基因组上似乎与其他SCC和HPV相关癌症相似。这为在未来使用针对多种可能具有相似生物学特性的SCC的新型药物进行“篮子型”试验中纳入像PSCC这样的罕见肿瘤提供了理论依据和机会。