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聚乙二醇化精氨酸脱亚氨酶、顺铂和培美曲塞用于精氨琥珀酸合成酶1缺乏的胸段癌症患者的1期剂量递增研究。

Phase 1 Dose-Escalation Study of Pegylated Arginine Deiminase, Cisplatin, and Pemetrexed in Patients With Argininosuccinate Synthetase 1-Deficient Thoracic Cancers.

作者信息

Beddowes Emma, Spicer James, Chan Pui Ying, Khadeir Ramsay, Corbacho Javier Garcia, Repana Dimitra, Steele Jeremy P, Schmid Peter, Szyszko Teresa, Cook Gary, Diaz Monica, Feng Xiaoxing, Johnston Amanda, Thomson Jim, Sheaff Michael, Wu Bor-Wen, Bomalaski John, Pacey Simon, Szlosarek Peter W

机构信息

Emma Beddowes, Javier Garcia Corbacho, and Simon Pacey, University of Cambridge, Cambridge; James Spicer, Dimitra Repana, Teresa Szyszko, and Gary Cook, King's College London; Pui Ying Chan, Jeremy P. Steele, Peter Schmid, Michael Sheaff, and Peter W. Szlosarek, St Bartholomew's Hospital; Ramsay Khadeir, Peter Schmid, and Peter W. Szlosarek, Queen Mary University of London, London, United Kindgom; and Monica Diaz, Xiaoxing Feng, Amanda Johnston, Jim Thomson, Bor-Wen Wu, and John Bomalaski, Polaris Pharmaceuticals, San Diego, CA.

出版信息

J Clin Oncol. 2017 Jun 1;35(16):1778-1785. doi: 10.1200/JCO.2016.71.3230. Epub 2017 Apr 7.

Abstract

Purpose Pegylated arginine deiminase (ADI-PEG 20) depletes essential amino acid levels in argininosuccinate synthetase 1 (ASS1) -negative tumors by converting arginine to citrulline and ammonia. The main aim of this study was to determine the recommended dose, safety, and tolerability of ADI-PEG 20, cisplatin, and pemetrexed in patients with ASS1-deficient malignant pleural mesothelioma (MPM) or non-small-cell lung cancer (NSCLC). Patients and Methods Using a 3 + 3 + 3 dose-escalation study, nine chemotherapy-naïve patients (five MPM, four NSCLC) received weekly ADI-PEG 20 doses of 18 mg/m, 27 mg/m, or 36 mg/m, together with pemetrexed 500 mg/m and cisplatin 75 mg/m which were given every three weeks (maximum of six cycles). Patients achieving stable disease or better could continue ADI-PEG 20 monotherapy until disease progression or withdrawal. Adverse events were assessed by Common Terminology Criteria for Adverse Events version 4.03, and pharmacodynamics and immunogenicity were also evaluated. Tumor response was assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 for NSCLC and by modified RECIST criteria for MPM. Results No dose-limiting toxicities were reported; nine of 38 reported adverse events (all grade 1 or 2) were related to ADI-PEG 20. Circulating arginine concentrations declined rapidly, and citrulline levels increased; both changes persisted at 18 weeks. Partial responses were observed in seven of nine patients (78%), including three with either sarcomatoid or biphasic MPM. Conclusion Target engagement with depletion of arginine was maintained throughout treatment with no dose-limiting toxicities. In this biomarker-selected group of patients with ASS1-deficient cancers, clinical activity was observed in patients with poor-prognosis tumors. Therefore, we recommend a dose for future studies of weekly ADI-PEG 20 36 mg/m plus three-weekly cisplatin 75 mg/m and pemetrexed 500 mg/m.

摘要

目的 聚乙二醇化精氨酸脱亚氨酶(ADI-PEG 20)通过将精氨酸转化为瓜氨酸和氨来降低精氨酸琥珀酸合成酶1(ASS1)阴性肿瘤中的必需氨基酸水平。本研究的主要目的是确定ADI-PEG 20、顺铂和培美曲塞在ASS1缺陷型恶性胸膜间皮瘤(MPM)或非小细胞肺癌(NSCLC)患者中的推荐剂量、安全性和耐受性。患者与方法 使用3+3+3剂量递增研究,9例未接受过化疗的患者(5例MPM,4例NSCLC)接受每周18mg/m²、27mg/m²或36mg/m²的ADI-PEG 20剂量,同时每三周给予培美曲塞500mg/m²和顺铂75mg/m²(最多六个周期)。病情稳定或改善的患者可继续接受ADI-PEG 20单药治疗,直至疾病进展或停药。不良事件采用《不良事件通用术语标准》第4.03版进行评估,同时还评估了药效学和免疫原性。肿瘤反应采用实体瘤疗效评价标准(RECIST)第1.1版对NSCLC进行评估,采用改良RECIST标准对MPM进行评估。结果 未报告剂量限制性毒性;38例报告的不良事件中有9例(均为1级或2级)与ADI-PEG 20相关。循环精氨酸浓度迅速下降,瓜氨酸水平升高;这两种变化在18周时持续存在。9例患者中有7例(78%)观察到部分缓解,包括3例肉瘤样或双相MPM患者。结论 在整个治疗过程中,精氨酸的靶向作用得以维持,且无剂量限制性毒性。在这一经过生物标志物选择的ASS1缺陷型癌症患者组中,预后不良的肿瘤患者观察到了临床活性。因此,我们推荐在未来研究中使用每周36mg/m²的ADI-PEG 20加每三周75mg/m²的顺铂和500mg/m²的培美曲塞的剂量。

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