Sergi Consolato M, Burnett Mervin, Jantuan Eugeniu, Hakoum Mariam, Beug Shawn T, Leng Roger, Shen Fan
Division of Anatomic Pathology, Department of Laboratory Medicine, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON K1H 8L1, Canada.
Department of Laboratory Medicine, Stollery Children's Hospital, University of Alberta, Edmonton, AB T6G 2R3, Canada.
Biomedicines. 2025 Mar 8;13(3):664. doi: 10.3390/biomedicines13030664.
Osteosarcoma (OS) is the predominant mesenchymal primary malignant bone tumor in oncology and pathology, impacting a wide age range from adolescents to older adults. It frequently advances to lung metastasis, ultimately resulting in the mortality of OS patients. The precise pathological pathways responsible for OS progression and dissemination are not fully understood due to its heterogeneity. The integration of surgery with neoadjuvant and postoperative chemotherapy has significantly increased the 5-year survival rate to more than 70% for patients with localized OS tumors. However, about 30% of patients experience local recurrence and/or metastasis. Hence, there is a requirement for innovative therapeutic approaches to address the limitations of traditional treatments. Immunotherapy has garnered increasing attention as a promising avenue for tumors resistant to standard therapies, including OS, despite the underlying mechanisms of disease progression and dissemination remaining not well elucidated. Immunotherapy may not have been suitable for use in patients with OS because of the tumor's immunosuppressive microenvironment and limited immunogenicity. Nevertheless, there are immune-based treatments now being developed for clinical use, such as bispecific antibodies, chimeric antigen receptor T cells, and immune checkpoint inhibitors. Also, additional immunotherapy techniques including cytokines, vaccines, and modified-Natural Killer (NK) cells/macrophages are in the early phases of research but will certainly be popular subjects in the nearest future. Our goal in writing this review was to spark new lines of inquiry into OS immunotherapy by summarizing the findings from both preclinical and current clinical studies examining different approaches.
骨肉瘤(OS)是肿瘤学和病理学中主要的间充质原发性恶性骨肿瘤,影响从青少年到老年人的广泛年龄范围。它经常进展为肺转移,最终导致骨肉瘤患者死亡。由于其异质性,导致骨肉瘤进展和扩散的确切病理途径尚未完全了解。手术与新辅助化疗和术后化疗相结合,已使局限性骨肉瘤肿瘤患者的5年生存率显著提高至70%以上。然而,约30%的患者会出现局部复发和/或转移。因此,需要创新的治疗方法来解决传统治疗的局限性。免疫疗法作为一种治疗对包括骨肉瘤在内的标准疗法耐药的肿瘤的有前景的途径,已受到越来越多的关注,尽管疾病进展和扩散的潜在机制仍未得到充分阐明。由于肿瘤的免疫抑制微环境和有限的免疫原性,免疫疗法可能不适用于骨肉瘤患者。尽管如此,目前正在开发基于免疫的临床治疗方法,如双特异性抗体、嵌合抗原受体T细胞和免疫检查点抑制剂。此外,包括细胞因子、疫苗和经修饰的自然杀伤(NK)细胞/巨噬细胞在内的其他免疫治疗技术正处于研究的早期阶段,但肯定会在不久的将来成为热门研究对象。我们撰写这篇综述的目的是通过总结临床前和当前临床研究中关于不同方法的研究结果,激发对骨肉瘤免疫治疗的新研究方向。