Kroemer Guido, Galluzzi Lorenzo
INSERM ; U1138; Paris, France ; Université Paris Descartes/Paris V; Sorbonne Paris Cité ; Paris, France ; Université Pierre et Marie Curie/Paris VI ; Paris, France ; Equipe 11 labellisée Ligue contre le Cancer; Center de Recherche des Cordeliers ; Paris, France ; Metabolomics and Cell Biology Platforms; Gustave Roussy Comprehensive Cancer Institute ; Villejuif, France ; Pôle de Biologie, Hôpital Européen Georges Pompidou; AP-HP ; Paris, France.
INSERM ; U1138; Paris, France ; Université Paris Descartes/Paris V; Sorbonne Paris Cité ; Paris, France ; Université Pierre et Marie Curie/Paris VI ; Paris, France ; Equipe 11 labellisée Ligue contre le Cancer; Center de Recherche des Cordeliers ; Paris, France ; Gustave Roussy Comprehensive Cancer Institute ; Villejuif, France.
Oncoimmunology. 2015 Jun 3;4(7):e1058037. doi: 10.1080/2162402X.2015.1058037. eCollection 2015 Jul.
Results from recent clinical trials demonstrate that a combinatorial immunotherapeutic regimen based on 2 distinct checkpoint blockers, namely, the CTLA4-targeting agent ipilimumab and the PD-1-specific molecule nivolumab, causes objective responses in a majority of subjects with advanced melanoma. These findings revolutionize the treatment of a neoplasm that was considered incurable until recently. Nonetheless, announcing the defeat of melanoma appears premature. Indeed, a sizeable fraction of patients does not respond to ipilimumab plus nivolumab, and the long-term efficacy of this immunotherapeutic regimen has not yet been investigated. Moreover, many patients experience severe side effects, calling for the development of strategies that uncouple the efficacy of ipilimumab plus nivolumab from their toxicity.
近期临床试验结果表明,一种基于两种不同检查点阻断剂的联合免疫治疗方案,即靶向CTLA4的药物伊匹单抗和PD-1特异性分子纳武单抗,可使大多数晚期黑色素瘤患者产生客观反应。这些发现彻底改变了一种直到最近还被认为无法治愈的肿瘤的治疗方法。尽管如此,宣称战胜黑色素瘤似乎还为时过早。事实上,相当一部分患者对伊匹单抗加纳武单抗没有反应,而且这种免疫治疗方案的长期疗效尚未得到研究。此外,许多患者会出现严重的副作用,这就需要开发一些策略,将伊匹单抗加纳武单抗的疗效与其毒性分离开来。