Dana-Farber Cancer Institute, Harvard Medical School, 450 Brookline Avenue, Dana540C, Boston, MA 02215 USA.
Rutgers Cancer Institute of New Jersey, 195 Little Albany Street, New Brunswick, NJ 08901 USA.
J Immunother Cancer. 2017 Feb 21;5:16. doi: 10.1186/s40425-017-0218-5. eCollection 2017.
Cancer immunotherapy and in particular monoclonal antibodies blocking the inhibitory programed cell death 1 pathway (PD-1/PD-L1) have made a significant impact on the treatment of cancer patients in recent years. However, despite the remarkable clinical efficacy of these agents in a number of malignancies, it has become clear that they are not sufficiently active for many patients. Initial evidence, for example with combined inhibition of PD-1 and CTLA-4 in melanoma and non-small cell lung cancer (NSCLC), has highlighted the potential to further enhance the clinical benefits of monotherapies by combining agents with synergistic mechanisms of action. In order to address the current progress and consider challenges associated with these novel approaches, the Society for Immunotherapy of Cancer (SITC) convened a Combination Immunotherapy Task Force. This Task Force was charged with identifying and prioritizing the most promising prospects for combinatorial approaches as well as addressing the challenges associated with developing these strategies. As a result of the extensive clinical benefit and tolerable side effects demonstrated with agents inhibiting the PD-1 pathway, an overview of current evidence to support its promising potential for use as a backbone in combination strategies is presented. In addition, key issues in the development of these strategies including preclinical modeling, patient safety and toxicity considerations, clinical trial design, and endpoints are also discussed. Overall, the goal of this manuscript is to provide a summary of the current status and potential challenges associated with the development and clinical implementation of these strategies.
近年来,癌症免疫疗法,特别是阻断抑制性程序性细胞死亡 1 途径(PD-1/PD-L1)的单克隆抗体,对癌症患者的治疗产生了重大影响。然而,尽管这些药物在许多恶性肿瘤中具有显著的临床疗效,但很明显,它们对许多患者的活性并不足够。例如,在黑色素瘤和非小细胞肺癌(NSCLC)中联合抑制 PD-1 和 CTLA-4 的初步证据,强调了通过联合具有协同作用机制的药物来进一步提高单药治疗的临床获益的潜力。为了评估这些新方法的当前进展和考虑相关挑战,癌症免疫治疗学会(SITC)召集了一个联合免疫治疗工作组。该工作组的任务是确定和优先考虑最有前途的联合方法,并解决与开发这些策略相关的挑战。由于抑制 PD-1 途径的药物表现出广泛的临床益处和可耐受的副作用,本文对目前支持其作为联合策略骨干的有前途的潜力的证据进行了概述。此外,还讨论了开发这些策略时的关键问题,包括临床前模型、患者安全性和毒性考虑、临床试验设计和终点。总体而言,本文的目的是总结这些策略的开发和临床实施所涉及的当前状况和潜在挑战。