光免疫疗法的监管批准:诱导免疫原性细胞死亡的光动力疗法。
Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death.
作者信息
Gomes-da-Silva Lígia C, Kepp Oliver, Kroemer Guido
机构信息
CQC, Coimbra Chemistry Center, University of Coimbra, Coimbra, Portugal.
Metabolomics and Cell Biology Platforms, Gustave Roussy Comprehensive Cancer Institute, Villejuif, France.
出版信息
Oncoimmunology. 2020 Oct 27;9(1):1841393. doi: 10.1080/2162402X.2020.1841393.
In September 2020, the Japanese government approved cetuximab saratolacan (previously known as RM-1929, commercial name: Akalux) for the treatment of unresectable locally advanced or recurrent head and neck cancer. Cetuximab saratolacan is a chemical conjugate of the photosensitizer IR700 with cetuximab, which targets EGFR. The treatment consists in the intravenous injection of cetuximab saratolacan, which binds to head and neck cancer cells expressing high levels of EGFR, followed by illumination of the tumor with red light (690 nm) for photodynamic therapy. This approach causes immunogenic cell death in malignant tissues, thus triggering a potent anticancer immune response.
2020年9月,日本政府批准西妥昔单抗萨拉托拉坎(先前称为RM - 1929,商品名:Akalux)用于治疗不可切除的局部晚期或复发性头颈癌。西妥昔单抗萨拉托拉坎是光敏剂IR700与靶向表皮生长因子受体(EGFR)的西妥昔单抗的化学偶联物。治疗方法是静脉注射西妥昔单抗萨拉托拉坎,其与表达高水平EGFR的头颈癌细胞结合,然后用红光(690纳米)照射肿瘤进行光动力疗法。这种方法会导致恶性组织发生免疫原性细胞死亡,从而引发强大的抗癌免疫反应。
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