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Treatment beyond progression with anti-PD-1/PD-L1 based regimens in advanced solid tumors: a systematic review

机译:在高级实体瘤中的基于抗PD-1 / PD-L1的进展之外的治疗:系统评价

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Treatment beyond progression with immunotherapy may be appropriate in selected patients based on the potential for late responses. The aim of this systematic review was to explore the impact of treatment beyond progression in patients receiving an anti-PD-1/PD-L1 based regimen for an advanced solid tumor. A systematic literature search was performed to identify prospective clinical trials reporting data on overall response rate by immune-related criteria and/or the number of patients treated beyond conventional criteria-defined PD and/or the number of patients achieving a clinical benefit after an initial PD with regimens including an anti-PD-1/PD-L1 agent which received the FDA approval for the treatment of an advanced solid tumor. 254 (4.6%) responses after an initial RECIST-defined progressive disease were observed among 5588 patients, based on 35 trials included in our analysis reporting this information. The overall rate of patients receiving treatment beyond progressive disease was 30.2%, based on data on 5334 patients enrolled in 36 trials, and the rate of patients who achieved an unconventional response among those treated beyond progressive disease was 19.7% (based on 25 trials for a total of 853 patients). The results of our systematic review support the clinical relevance of unconventional responses to anti-PD-1/PD-L1-based regimens; however, most publications provided only partial information regarding immune-related clinical activity, or did not provide any information at all, highlighting the need of a more comprehensive report of such data in trials investigating immunotherapy for the treatment of patients with advanced tumors.
机译:基于晚期反应的潜力,在选定的患者中可能适用于免疫疗法的进展。这种系统审查的目的是探讨接受基于抗PD-1 / PD-L1的患者的进展的治疗的影响,该治疗基于抗PD-1 / PD-L1为先进的实体瘤。进行系统文献搜索以确定通过免疫相关标准和/或根据常规标准定义的PD治疗的患者数量和/或在初始临床效益的患者数量上进行过临床临床试验PD与包括抗PD-1 / PD-L1剂的方案,该试剂接受了用于治疗先进实体瘤的FDA认证。在5588名患者中观察到初始重新定义的渐进性疾病后,应对55例患者进行初始定义的渐进疾病,根据我们的分析报告此信息,在5588名患者中观察到。根据36项试验的5334名患者的数据,基于5334名患者的数据,接受渐进疾病的患者的总体速率为30.2%,患者在逐步疾病患者患者中取得了非常规应对的患者的速度为19.7%(基于25项审判共有853名患者)。我们的系统评价结果支持对基于抗PD-1 / PD-L1的非传统反应的临床相关性;然而,大多数出版物仅提供了关于免疫相关临床活动的部分信息,或者根本没有提供任何信息,突出了需要更全面的报告在调查免疫治疗治疗晚期肿瘤患者的免疫疗法中的更全面的报告。

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