Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Melanoma Institute of Australia, The University of Sydney, Sydney, NSW, Australia; Department of Medical Oncology, Royal North Shore Hospital, Sydney, NSW, Australia; Department of Medical Oncology, Mater Hospital Sydney, Sydney, NSW, Australia.
Lancet Oncol. 2019 Jul;20(7):e378-e389. doi: 10.1016/S1470-2045(19)30332-8.
Advances in the treatment of metastatic melanoma have improved responses and survival. However, many patients continue to experience resistance or toxicity to treatment, highlighting a crucial need to identify biomarkers and understand mechanisms of response and toxicity. Neoadjuvant therapy for regional metastases might improve operability and clinical outcomes over upfront surgery and adjuvant therapy, and has become an established role for drug development and biomarker discovery in other cancers (including locally advanced breast cancer, head and neck squamous cell carcinomas, gastroesophageal cancer, and anal cancer). Patients with clinically detectable stage III melanoma are ideal candidates for neoadjuvant therapy, because they represent a high-risk patient population with poor outcomes when treated with upfront surgery alone. Neoadjuvant therapy is now an active area of research for melanoma with numerous completed and ongoing trials (since 2014) with disparate designs, endpoints, and analyses under investigation. We have, therefore, established the International Neoadjuvant Melanoma Consortium with experts in medical oncology, surgical oncology, pathology, radiation oncology, radiology, and translational research to develop recommendations for investigating neoadjuvant therapy in melanoma to align future trial designs and correlative analyses. Alignment and consistency of neoadjuvant trials will facilitate optimal data organisation for future regulatory review and strengthen translational research across the melanoma disease continuum.
转移性黑色素瘤治疗的进展改善了反应和生存。然而,许多患者继续对治疗产生耐药性或毒性,这突出表明需要确定生物标志物并了解反应和毒性的机制。局部转移的新辅助治疗可能会提高手术的可操作性和临床结果,优于直接手术和辅助治疗,并且已经成为其他癌症(包括局部晚期乳腺癌、头颈部鳞状细胞癌、胃食管交界处癌和肛门癌)药物开发和生物标志物发现的既定作用。具有临床可检测的 III 期黑色素瘤的患者是新辅助治疗的理想候选者,因为他们是高风险患者人群,仅用直接手术治疗,预后较差。新辅助治疗现已成为黑色素瘤的一个活跃研究领域,有许多已完成和正在进行的试验(自 2014 年以来),这些试验具有不同的设计、终点和分析方法。因此,我们建立了国际新辅助黑色素瘤联盟,该联盟汇集了肿瘤内科、肿瘤外科、病理学、放射肿瘤学、放射学和转化研究方面的专家,以制定新辅助治疗黑色素瘤的研究建议,使未来的试验设计和相关分析保持一致。新辅助试验的一致性和一致性将有助于为未来的监管审查优化数据组织,并加强黑色素瘤疾病连续体的转化研究。