外阴癌生物学和管理的进展。

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-10-31 DOI:10.1200/JCO.24.01071
Rania Chehade, Katarzyna J Jerzak, Farideh Tavanger, Anna Plotkin, Lilian T Gien, Eric Leung, Helen Mackay
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引用次数: 0

摘要

目的:外阴鳞状细胞癌(VSCC)是一种罕见的妇科恶性肿瘤,发病率呈上升趋势。根据人乳头状瘤病毒(HPV)和肿瘤蛋白 53(p53)状态进行的分子分类确定了三种临床上截然不同的亚型,但我们对所有 VSCC 的治疗方法仍然相同。在此,我们回顾了VSCC的分子分类,概述了治疗情况,并强调了晚期VSCC靶向治疗的潜力:设计:我们对晚期VSCC的治疗文献进行了全面回顾,尤其关注基于HPV和p53状态的分子分层对晚期VSCC治疗前景的影响:结果:将HPV和p53状态纳入局部治疗决策有可能为(去)升级策略提供建议。免疫疗法的作用,无论是单独使用还是联合使用,都需要进一步探讨,尤其是在疾病的早期阶段。在晚期阶段,VSCC 的潜在靶向疗法包括血管内皮生长因子、内皮生长因子受体、细胞周期和 DNA 损伤反应抑制剂,尤其是在 HPV 阴性(HPV-)VSCC 中。靶向磷酸肌酸 3 激酶/哺乳动物雷帕霉素靶点通路对 HPV 阳性和 HPV-/p53 野生型 VSCC 颇具吸引力。应考虑结合抗体药物共轭物(如滋养层细胞表面抗原 2、人表皮生长因子受体 2)进行试验,并应在会阴鳞状细胞癌中进行一篮子试验。临床前模型有限,应加以扩展,为试验设计提供依据:结论:与其他罕见癌症一样,外阴癌在精准医疗策略的识别和优化方面落后于其他癌症。我们迫切需要基于分子的临床前模型和合理设计的临床试验,其中包括高质量的转化研究。这些试验将需要国际合作,以确保可行性并改善确诊为该疾病的妇女的治疗效果。
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Advances in Vulvar Cancer Biology and Management.

Purpose: Vulvar squamous cell carcinoma (VSCC), a rare gynecologic malignancy, has been rising in incidence. Molecular classification on the basis of human papilloma virus (HPV) and tumor protein 53 (p53) status has identified three clinically distinct subtypes, but we still treat all VSCCs the same. Here, we review molecular classification of VSCC, outline treatment landscape, and highlight potential for targeted therapies in advanced VSCC.

Design: We conducted a comprehensive review of the literature on treatment of advanced VSCC with particular focus on the implications of molecular stratification on the basis of HPV and p53 status on the treatment landscape of advanced VSCC.

Results: Incorporation of HPV and p53 status in locoregional treatment decision making has the potential to advise (de)escalation strategies. The role of immunotherapy, alone and in combination, requires further exploration particularly earlier in the course of the disease. In advanced stages, potential for targeted therapies in VSCCs include inhibitors of vascular endothelial growth factor, endothelial growth factor receptor, cell cycle, and DNA damage response, particularly in HPV-negative (HPV-) VSCCs. Targeting the phosphoinositide 3 kinase/mammalian target of rapamycin pathway is attractive in HPV-positive and HPV-/p53 wildtype VSCCs. Trials incorporating antibody-drug conjugates (eg, trophoblast cell-surface antigen 2, human epidermal growth factor receptor 2) should be considered, and basket trials in perineal squamous cell cancers are warranted. Preclinical models are limited and should be expanded to inform trial design.

Conclusion: Like other rare cancers, vulvar cancer lags behind in the identification and optimization of precision medicine strategies. Molecular-based preclinical models and rationally designed clinical trials, incorporating high-quality translational studies, are urgently required. These trials will require international collaboration to ensure feasibility and improvement of outcomes for women diagnosed with this disease.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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