Cutaneous Oncology and Immunology, H. Lee Moffitt Cancer Center and Research Institute, University of South Florida Morsani College of Medicine, Tampa, Florida, USA
Medicine, University of Pennsylvania Abramson Cancer Center, Philadelphia, Pennsylvania, USA.
J Immunother Cancer. 2022 Aug;10(8). doi: 10.1136/jitc-2022-005036.
Definitive management of locoregionally advanced solid tumors presents a major challenge and often consists of a combination of surgical, radiotherapeutic and systemic therapy approaches. Upfront surgical treatment with or without adjuvant radiotherapy carries the risks of significant morbidities and potential complications that could be lasting. In addition, these patients continue to have a high risk of local or distant disease relapse despite the use of standard adjuvant therapy. Preoperative neoadjuvant systemic therapy has the potential to significantly improve clinical outcomes, particularly in this era of expanding immunotherapeutic agents that have transformed the care of patients with metastatic/unresectable malignancies. Tremendous progress has been made with neoadjuvant immunotherapy in the treatment of several locoregionally advanced resectable solid tumors leading to ongoing phase 3 trials and change in clinical practice. The promise of neoadjuvant immunotherapy has been supported by the high pathologic tumor response rates in early trials as well as the durability of these responses making cure a more achievable potential outcome compared with other forms of systemic therapy. Furthermore, neoadjuvant studies allow the assessment of radiologic and pathological responses and the access to biospecimens before and during systemic therapy. Pathological responses may guide future treatment decisions, and biospecimens allow the conduct of mechanistic and biomarker studies that may guide future drug development. On behalf of the National Cancer Institute Early Drug Development Neoadjuvant Immunotherapy Working Group, this article summarizes the current state of neoadjuvant immunotherapy of solid tumors focusing primarily on locoregionally advanced melanoma, gynecologic malignancies, gastrointestinal malignancies, non-small cell lung cancer and head and neck cancer including recent advances and our expert recommendations related to future neoadjuvant trial designs and associated clinical and translational research questions.
局部晚期实体瘤的确定性治疗是一个主要挑战,通常包括手术、放射治疗和系统治疗方法的组合。术前治疗(包括或不包括辅助放疗)会带来显著的发病率和潜在并发症风险,这些风险可能是持久的。此外,尽管使用了标准辅助治疗,这些患者仍有很高的局部或远处疾病复发风险。新辅助全身治疗有可能显著改善临床结果,特别是在免疫治疗药物不断扩展的时代,这些药物改变了转移性/不可切除恶性肿瘤患者的治疗方式。新辅助免疫疗法在治疗几种局部晚期可切除实体瘤方面取得了巨大进展,正在进行 3 期临床试验,并改变了临床实践。新辅助免疫疗法的前景得到了早期试验中高病理肿瘤缓解率以及这些缓解的持久性的支持,与其他形式的全身治疗相比,治愈的可能性更大。此外,新辅助研究允许在全身治疗之前和期间评估影像学和病理学反应,并获得生物样本。病理学反应可以指导未来的治疗决策,而生物样本允许进行机制和生物标志物研究,从而可能指导未来的药物开发。代表美国国立癌症研究所早期药物开发新辅助免疫治疗工作组,本文总结了目前实体瘤新辅助免疫治疗的现状,主要集中在局部晚期黑色素瘤、妇科恶性肿瘤、胃肠道恶性肿瘤、非小细胞肺癌和头颈部癌症,包括最近的进展和我们关于未来新辅助试验设计和相关临床和转化研究问题的专家建议。