下一代肿瘤不可知靶点即将出现
Next-generation tumor-agnostic targets on the horizon.
肿瘤不可知药物开发将肿瘤学重新聚焦于共享的分子依赖性而非组织来源,从而能够针对跨肿瘤的罕见可操作驱动因素进行高效开发。
英文原题:Treatment at Relapse for Synovial Sarcoma of Children, Adolescents and Young Adults: From the State of Art to Future Clinical Perspectives.
尽管初诊为局限性滑膜肉瘤的儿童、青少年和年轻患者总体预后通常相当令人满意,但复发后患者的结局仍然很差。
儿童、青少年及年轻成人首次诊断为局限性滑膜肉瘤时总体预后通常较好,但复发患者的结局仍然较差。与一线标准化治疗不同,复发患者通常采用个体化治疗,目前仍缺乏标准治疗方案的共识。复发性滑膜肉瘤研究已发现影响复发后生存的一些预后变量,可用于制定风险适配的挽救治疗方案。治疗方案须考虑既往一线治疗、潜在毒性,以及通过再次手术和/或再程放疗实现充分局部治疗的可能性。亟需有效的二线药物治疗。值得注意的是,过继工程化TCR-T细胞免疫治疗等实验性疗法在成人中显示出前景,目前也正在儿童患者中进行验证。
While the overall prognosis is generally quite satisfactory in children, adolescents and young adults with localised synovial sarcoma at first diagnosis, the outcome remains poor for patients after relapse. Conversely to the front-line standardised treatment options, patients with relapse generally have an individualised approach and to date, there is still a lack of consensus regarding standard treatment approaches. Studies on relapsed synovial sarcoma were able to identify some prognostic variables that influence post-relapse survival, in order to plan risk-adapted salvage protocols. Treatment proposals must consider previous first-line treatments, potential toxicities, and the possibility of achieving an adequate local treatment by new surgery and/or re-irradiation. Effective second-line drug therapies are urgently needed. Notably, experimental treatments such as adoptive engineered TCR-T cell immunotherapy seem promising in adults and are currently under validation also in paediatric patients.
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