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I 期临床试验:一种 I 型抗孕激素药物——onapristone,在既往治疗后复发或转移性孕激素受体阳性的女性癌症患者中的应用。

Phase I study of onapristone, a type I antiprogestin, in female patients with previously treated recurrent or metastatic progesterone receptor-expressing cancers.

机构信息

Department of Medical Oncology, Institut Curie, Paris, France.

Department of Medical Oncology, Centre Oscar Lambret, Lille, France.

出版信息

PLoS One. 2018 Oct 10;13(10):e0204973. doi: 10.1371/journal.pone.0204973. eCollection 2018.

Abstract

INTRODUCTION

Onapristone is a type I progesterone receptor (PR) antagonist, which prevents PR- mediated DNA transcription. Onapristone is active in multiple preclinical models and two prior studies demonstrated promising activity in patients with breast cancer. We conducted a study of extended release (ER) Onapristone to determine a recommended dose and explore the role of transcriptionally-activated PR (APR), detected as an aggregated subnuclear distribution pattern, as a predictive biomarker.

METHODS

An open-label, multicenter, randomized, parallel-group, phase 1 study (target n = 60; NCT02052128) included female patients ≥18 years with PRpos tumors. APR analysis was performed on archival tumor tissue. Patients were randomized to five cohorts of extended release (ER) onapristone tablets 10, 20, 30, 40 or 50 mg BID, or immediate release 100 mg QD until progressive disease or intolerability. Primary endpoint was to identify the recommended phase 2 dose. Secondary endpoints included safety, clinical benefit and pharmacokinetics.

RESULTS

The phase 1 dose escalation component of the study is complete (n = 52). Tumor diagnosis included: endometrial carcinoma 12; breast cancer 20; ovarian cancer 13; other 7. Median age was 64 (36-84). No dose limiting toxicity was observed with reported liver function test elevation related only to liver metastases. The RP2D was 50 mg ER BID. Median therapy duration was 8 weeks (range 2-44), and 9 patients had clinical benefit ≥24 weeks, including 2 patients with APRpos endometrial carcinoma.

CONCLUSION

Clinical benefit with excellent tolerance was seen in heavily pretreated patients with endometrial, ovarian and breast cancer. The data support the development of Onapristone in endometrial endometrioid cancer. Onapristone should also be evaluated in ovarian and breast cancers along with APR immunohistochemistry validation.

摘要

简介

Onapristone 是一种 I 型孕激素受体(PR)拮抗剂,可阻止 PR 介导的 DNA 转录。Onapristone 在多种临床前模型中具有活性,并且两项先前的研究表明其在乳腺癌患者中具有有前景的活性。我们进行了一项延长释放(ER)Onapristone 的研究,以确定推荐剂量并探索转录激活的 PR(APR)作为预测生物标志物的作用,APR 表现为聚集的亚核分布模式。

方法

一项开放标签、多中心、随机、平行组、I 期研究(目标 n = 60;NCT02052128)纳入了年龄≥18 岁且 PR 阳性肿瘤的女性患者。对存档的肿瘤组织进行 APR 分析。患者被随机分配到五个延长释放(ER)Onapristone 片剂 10、20、30、40 或 50 mg BID 或立即释放 100 mg QD 组,直至疾病进展或不耐受。主要终点是确定 II 期推荐剂量。次要终点包括安全性、临床获益和药代动力学。

结果

该研究的 I 期剂量递增部分已完成(n = 52)。肿瘤诊断包括:子宫内膜癌 12 例;乳腺癌 20 例;卵巢癌 13 例;其他 7 例。中位年龄为 64 岁(36-84 岁)。未观察到剂量限制毒性,仅报告的肝功能试验升高与肝转移有关。RP2D 为 50 mg ER BID。中位治疗持续时间为 8 周(范围 2-44 周),9 例患者的临床获益≥24 周,包括 2 例 APR 阳性子宫内膜癌患者。

结论

在接受过大量预处理的子宫内膜癌、卵巢癌和乳腺癌患者中观察到了良好耐受性的临床获益。数据支持 Onapristone 在子宫内膜子宫内膜样癌中的开发。还应评估 Onapristone 在卵巢癌和乳腺癌中的应用,同时进行 APR 免疫组织化学验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/825b/6179222/c4040a556b8c/pone.0204973.g001.jpg

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