Gaspar Nathalie, Marques da Costa Maria Eugenia, Fromigue Olivia, Droit Robin, Berlanga Pablo, Marchais Antonin
Department of Oncology for Child and adolescent, Gustave Roussy cancer campus. France.
National Institute for Health and Medical Research (INSERM) U1015, Gustave Roussy, France.
Fac Rev. 2020 Nov 26;9:18. doi: 10.12703/r/9-18. eCollection 2020.
Osteosarcoma is the most common bone cancer in adolescents and young adults, but it is a rare cancer with no improvement in patient survival in the last four decades. The main problem of this bone tumor is its evolution toward lung metastatic disease, despite the current treatment strategy (chemotherapy and surgery). To further improve survival, there is a strong need for new therapies that control osteosarcoma cells with metastatic potential and their favoring tumor microenvironment (ME) from the diagnosis. However, the complexity and heterogeneity of those tumor cell genomic/epigenetic and biology, the diversity of tumor ME where it develops, the sparsity of appropriate preclinical models, and the heterogeneity of therapeutic trials have rendered the task difficult. No tumor- or ME-targeted drugs are routinely available in front-line treatment. This article presents up-to-date information from preclinical and clinical studies that were recently published or presented in recent meetings which we hope might help change the osteosarcoma treatment landscape and patient survival in the near future.
骨肉瘤是青少年和年轻成年人中最常见的骨癌,但它是一种罕见癌症,在过去四十年中患者生存率并无改善。尽管目前有治疗策略(化疗和手术),但这种骨肿瘤的主要问题是其会发展为肺转移性疾病。为进一步提高生存率,迫切需要从诊断开始就采用新疗法来控制具有转移潜能的骨肉瘤细胞及其有利的肿瘤微环境(ME)。然而,这些肿瘤细胞基因组/表观基因组和生物学的复杂性与异质性、肿瘤发生部位肿瘤微环境的多样性、合适临床前模型的稀缺性以及治疗试验的异质性,使得这项任务变得困难。一线治疗中尚无常规可用的针对肿瘤或肿瘤微环境的药物。本文介绍了最近发表或在近期会议上展示的临床前和临床研究的最新信息,我们希望这些信息可能有助于在不久的将来改变骨肉瘤的治疗格局并提高患者生存率。