Ludwig Center for Cancer Immunotherapy and Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Clin Cancer Res. 2009 Dec 1;15(23):7412-20. doi: 10.1158/1078-0432.CCR-09-1624. Epub 2009 Nov 24.
Immunotherapeutic agents produce antitumor effects by inducing cancer-specific immune responses or by modifying native immune processes. Resulting clinical response patterns extend beyond those of cytotoxic agents and can manifest after an initial increase in tumor burden or the appearance of new lesions (progressive disease). Response Evaluation Criteria in Solid Tumors or WHO criteria, designed to detect early effects of cytotoxic agents, may not provide a complete assessment of immunotherapeutic agents. Novel criteria for the evaluation of antitumor responses with immunotherapeutic agents are required.
The phase II clinical trial program with ipilimumab, an antibody that blocks CTL antigen-4, represents the most comprehensive data set available to date for an immunotherapeutic agent. Novel immune therapy response criteria proposed, based on the shared experience from community workshops and several investigators, were evaluated using data from ipilimumab phase II clinical trials in patients with advanced melanoma.
Ipilimumab monotherapy resulted in four distinct response patterns: (a) shrinkage in baseline lesions, without new lesions; (b) durable stable disease (in some patients followed by a slow, steady decline in total tumor burden); (c) response after an increase in total tumor burden; and (d) response in the presence of new lesions. All patterns were associated with favorable survival.
Systematic criteria, designated immune-related response criteria, were defined in an attempt to capture additional response patterns observed with immune therapy in advanced melanoma beyond those described by Response Evaluation Criteria in Solid Tumors or WHO criteria. Further prospective evaluations of the immune-related response criteria, particularly their association with overall survival, are warranted.
免疫治疗药物通过诱导肿瘤特异性免疫反应或改变固有免疫过程来产生抗肿瘤作用。由此产生的临床反应模式超出了细胞毒性药物的范围,并且可以在肿瘤负荷最初增加或出现新病变(进展性疾病)后表现出来。旨在检测细胞毒性药物早期作用的实体瘤反应评估标准或世卫组织标准,可能无法对免疫治疗药物进行完整评估。需要针对免疫治疗药物评估抗肿瘤反应制定新的标准。
ipilimumab 的 II 期临床试验计划是迄今为止针对免疫治疗药物提供的最全面的数据集,该药物是一种阻断 CTL 抗原-4 的抗体。根据来自社区研讨会和几位研究人员的共同经验提出的新免疫治疗反应标准,使用晚期黑色素瘤患者的 ipilimumab II 期临床试验数据进行了评估。
ipilimumab 单药治疗导致了四种不同的反应模式:(a)基线病变缩小,无新病变;(b)持久稳定的疾病(在一些患者中,随后总肿瘤负担缓慢而稳定下降);(c)总肿瘤负担增加后的反应;(d)存在新病变时的反应。所有模式都与良好的生存相关。
为了试图捕捉晚期黑色素瘤免疫治疗中观察到的除实体瘤反应评估标准或世卫组织标准描述之外的其他反应模式,系统地定义了指定的免疫相关反应标准。需要进一步前瞻性评估免疫相关反应标准,特别是它们与总生存的关联。