Pryor David, Bressel Mathias, Lawrentschuk Nathan, Tran Ben, Mooi Jennifer, Lewin Jeremy, Azad Arun, Colyer Duncan, Neha Nitika, Shaw Mark, Chander Sarat, Neeson Paul, Moon Daniel, Cuff Katharine, Wood Simon, Murphy Declan G, Sandhu Shahneen, Loi Sherene, Siva Shankar
Princess Alexandra Hospital, Brisbane, Australia.
University of Queensland, Brisbane, Australia.
Contemp Clin Trials Commun. 2021 Jan 6;21:100703. doi: 10.1016/j.conctc.2021.100703. eCollection 2021 Mar.
The management of oligometastatic clear cell renal cell carcinoma (ccRCC) varies widely, ranging from observation to resection or systemic therapies. Prolonged survival has been observed following resection or stereotactic ablative body radiotherapy (SABR). Immunotherapy combinations have shown survival benefits, however, toxicity is higher than that for monotherapy and complete response rates remain less than 10%. The combination of effective local therapies in conjunction with immunotherapy may provide more durable control and pre-clinical models have suggested a synergistic immune-priming effect of SABR.
and Methods: RAPPORT is a prospective, single arm, phase I/II study assessing the safety, efficacy and biological effects of single fraction SABR followed by pembrolizumab for oligometastatic ccRCC. The study will include 30 patients with histological confirmed ccRCC and 1-5 oligometastases, one or more of which must be suitable for SABR. Patients can have received prior systemic therapy but not prior immunotherapy. A single 20Gy of SABR is followed 5 days later by 8 cycles of 200 mg pembrolizumab, every 3 weeks. Adverse events are recorded using CTCAE V4.03 and tumour response evaluated by Response Evaluation Criteria in Solid Tumours version 1.1 (RECIST 1.1). Tumour tissue and peripheral blood samples will be collected pre-, during and post-treatment to assess longitudinal changes in immune subsets.
The RAPPORT study will provide important safety and early efficacy data on the combination of SABR and pembrolizumab in oligometastatic ccRCC and will provide an insight into the underlying biological effects of combination therapy.
clinicaltrials.gov ID NCT02855203.
寡转移透明细胞肾细胞癌(ccRCC)的治疗方法差异很大,从观察等待到手术切除或全身治疗。手术切除或立体定向消融体部放疗(SABR)后可观察到生存期延长。免疫治疗联合方案已显示出生存获益,然而,毒性高于单药治疗,完全缓解率仍低于10%。有效的局部治疗与免疫治疗联合应用可能提供更持久的控制,临床前模型提示SABR具有协同免疫启动作用。
RAPPORT是一项前瞻性、单臂、I/II期研究,评估单次分割SABR序贯帕博利珠单抗治疗寡转移ccRCC的安全性、疗效和生物学效应。该研究将纳入30例经组织学确诊为ccRCC且有1 - 5个寡转移灶的患者,其中一个或多个寡转移灶必须适合SABR治疗。患者可以接受过既往全身治疗,但未接受过免疫治疗。单次20Gy的SABR治疗5天后,每3周给予8个周期的200mg帕博利珠单抗。使用CTCAE V4.03记录不良事件,采用实体瘤疗效评价标准1.1版(RECIST 1.1)评估肿瘤反应。在治疗前、治疗期间和治疗后收集肿瘤组织和外周血样本,以评估免疫亚群的纵向变化。
RAPPORT研究将提供关于SABR与帕博利珠单抗联合治疗寡转移ccRCC的重要安全性和早期疗效数据,并将深入了解联合治疗的潜在生物学效应。
clinicaltrials.gov标识符NCT02855203。