通过靶向肿瘤相关巨噬细胞的嵌合受体工程化溶瘤病毒重振内源性抗肿瘤免疫
Rejuvenating endogenous antitumor immunity via a chimeric receptor-engineered oncolytic virus targeting tumor-associated macrophages.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The treatment of advanced melanoma: a review of systemic and local therapies in combination with immune checkpoint inhibitors in phase 1 and 2 clinical trials.
The treatment of advanced melanoma: a review of systemic and local therapies in combination with immune checkpoint inhibitors in phase 1 and 2 clinical trials.
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本文讨论的药物组合似乎是晚期黑色素瘤有前景的治疗方案。对免疫检查点抑制剂原发性、适应性和获得性耐药机制的深入理解,可能指导未来联合方案的开发。
尽管黑色素瘤的发病率持续上升,但该病的死亡率似乎已趋于稳定。这可能部分归因于免疫检查点抑制剂作为晚期黑色素瘤标准治疗的发展和临床应用。然而,许多患者对这些疗法单独使用并无应答。将免疫检查点抑制剂与其他类别的治疗药物联合使用,似乎是改善晚期黑色素瘤应答和生存的一个有前景的方向。涵盖领域:本文旨在讨论评估免疫检查点抑制剂联合治疗用于治疗晚期、不可切除黑色素瘤的1期和2期临床试验。具体而言,这些方案包括各种激酶抑制剂、TIL、toll样受体激动剂、细胞因子和溶瘤病毒疗法。所讨论的联合方案包括全身治疗以及全身/局部联合治疗。
INTRODUCTION: While the incidence of melanoma continues to rise, the mortality of the disease appears to have stabilized. This may, in part, be due to the development and application of immune checkpoint inhibitors as standard of care in advanced melanoma.
However, many patients do not respond to these therapies alone. Combining immune checkpoint inhibitors with other classes of therapeutics appears to be a promising direction to improve response and survival in advanced melanoma. AREAS COVERED: This review article aims to discuss phase 1 and 2 clinical trials examining immune checkpoint inhibitors in combination therapy for the treatment of advanced, unresectable melanoma.
In particular, these regimens include various kinase inhibitors, tumor-infiltrating lymphocytes, toll-like receptor agonists, cytokines, and oncolytic viral therapies. The combinations under discussion include both systemic and combination systemic/local therapies. EXPERT OPINION: Drug combinations discussed here appear to be promising therapeutic regimens for advanced melanoma. Improved understanding of the mechanisms of primary, adaptive, and acquired resistance to immune checkpoint inhibitors may guide the development of future combination regimens.
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