转移性葡萄膜黑色素瘤该如何治疗?FDA授予tebentafusp“突破性疗法称号”

2021-02-20 Allan MedSci原创

tebentafusp能够显著延长患者总生存率(OS),且优于其他免疫疗法,因此该试验达到了主要终点。

葡萄膜黑色素瘤是最常见的眼内肿瘤,在中国,其发病率则仅次于视网膜母细胞瘤,居眼内肿瘤的第二位。Immunocore是一家晚期生物技术公司,致力于开发新型T细胞受体(TCR)双特异性免疫疗法,Immunocore今日宣布,美国食品药品监督管理局(FDA)已授予tebentafusp(IMCgp100)“突破性疗法称号”(BTD),以治疗不可切除或转移性葡萄膜黑色素瘤(mUM)成年患者。

 

在对先前未经治疗的转移性葡萄膜黑色素瘤患者进行的一项随机III期临床试验(IMCgp100-202研究)中,中期分析表明,tebentafusp能够显著延长患者总生存率(OS),且优于其他免疫疗法,因此该试验达到了主要终点。

此前,Tebentafusp还获得了FDA的“快速通道资格”和“孤儿药称号”,以及英国早期药物计划下的“有前途的创新药物称号”。Immunocore将与FDA合作,以促进tebentafusp的上市。如果获得批准,Immunocore相信tebentafusp将是40年来治疗转移性葡萄膜黑色素瘤的一种新疗法。

Immunocore首席执行官Bahija Jallal表示:“我们很高兴FDA根据我们2020年11月宣布的III期临床试验的生存获益,授予替tebentafusp突破性疗法称号。患者迫切需要批准的治疗方法来治疗这种罕见且具有侵略性的黑色素瘤”。

 

原始出处:

https://www.firstwordpharma.com/node/1802311?tsid=4

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    2021-03-22 sunylz
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  5. 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  6. 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  7. 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    2021-02-20 ms1000000987981057

    学到了

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背景:葡萄膜黑色素瘤的特点是GNAQ和GNA11突变,导致Ras /Raf/ MEK / ERK通路激活。司美替尼(AZD6244,ARRY-142886)MEK1/2抑制剂,其对葡萄膜黑色素瘤的临床前模型研究中有抗肿瘤效应。针对转移性葡萄膜黑色素瘤的患者以司美替尼单药治疗对比替莫唑胺或达卡巴嗪化疗,随机II期临床试验表明有改善的无进展生存期(PFS)和反应率(RR)。临床前,司美替尼联合烷基化试

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NEJM:转移性葡萄膜黑色素瘤采用Tebentafusp治疗的总生存获益

与对照治疗相比,Tebentafusp治疗延长了既往未治疗过的转移性葡萄膜黑色素瘤患者的总生存期

NEJM:Tebentafusp治疗可改善转移性葡萄膜黑色素瘤患者总生存期

对于先前未经治疗的转移性葡萄膜黑色素瘤患者,Tebentafusp治疗方案在延长患者总生存期,提高无进展生存率方面优于现有治疗方案

Immunocore的tebentafusp治疗转移性葡萄膜黑色素瘤被FDA授予快速通道指定

T细胞受体(TCR)生物技术公司Immunocore的候选药物tebentafusp(IMCgp100)获得FDA快速通道指定治疗转移性葡萄膜黑色素瘤(mUM)。

Lancet Oncology:细胞疗法用于治疗转移性葡萄膜黑色素瘤

自体TIL过继转移介导用于治疗转移性葡萄膜黑色素瘤的首次报道,为转移性葡萄膜黑色素瘤的治疗带来新的希望

BMC Cancer:司美替尼联合达卡巴嗪用于转移性葡萄膜黑色素瘤的临床研究

背景:葡萄膜黑色素瘤的特点是GNAQ和GNA11突变,导致Ras /Raf/ MEK / ERK通路激活。司美替尼(AZD6244,ARRY-142886)MEK1/2抑制剂,其对葡萄膜黑色素瘤的临床前模型研究中有抗肿瘤效应。针对转移性葡萄膜黑色素瘤的患者以司美替尼单药治疗对比替莫唑胺或达卡巴嗪化疗,随机II期临床试验表明有改善的无进展生存期(PFS)和反应率(RR)。临床前,司美替尼联合烷基化试