Abiraterone in patients with recurrent epithelial ovarian cancer: principal results of the phase II Cancer of the Ovary Abiraterone (CORAL) trial (CRUK – A16037)

Author:

Banerjee Susana12,Tovey Holly3,Bowen Rebecca4,Folkerd Elizabeth2,Kilburn Lucy3,McLachlan Jennifer5,Hall Marcia6,Tunariu Nina7,Attygalle Ayoma8,Lima Joao Paulo Da Silveira Nogueira9,Perry Sophie3,Chatfield Peter3,Hills Margaret10,Kaye Stan11,Attard Gert12,Dowsett Mitch13,Bliss Judith M.3

Affiliation:

1. Gynaecology Unit, The Royal Marsden NHS Foundation Trust, Downs Road, Sutton, SM2 5PT, UK

2. The Institute of Cancer Research, London, UK

3. Clinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK

4. Royal United Hospitals Bath NHS Foundation Trust, Bath, UK

5. Department of Medical Oncology, Christchurch Hospital, Christchurch, New Zealand

6. Medical Oncology, Mount Vernon Cancer Centre, Northwood, UK

7. Radiology, The Royal Marsden Hospital NHS Foundation Trust, London, UK

8. Histopathology, The Royal Marsden Hospital NHS Foundation Trust, London, UK

9. A.C. Camargo Cancer Center, Oncologia Clinica, São Paulo, Brazil

10. The Royal Marsden Hospital NHS Foundation Trust, London, UK

11. Gynaecology Unit, The Royal Marsden NHS Foundation Trust, London, UK

12. UCL Cancer Institute, University College London, London, UK

13. The Royal Marsden NHS Foundation Trust, Sutton, UK

Abstract

Background: Recurrent epithelial ovarian cancer (EOC) remains difficult to treat, with an urgent need for more therapy options. Androgens bind to the androgen receptor (AR), commonly expressed in EOC. CYP17 inhibitor abiraterone irreversibly inhibits androgen biosynthesis. The Cancer of the Ovary Abiraterone (CORAL) trial was designed to evaluate the clinical activity of abiraterone in EOC. Patients & Methods: CORAL was a multi-centre, open-label, non-randomised, 2-stage phase II clinical trial. Eligible patients had progression within 12 months of last systemic therapy and no prior hormonal anti-cancer agents. Patients received abiraterone 1000 mg daily plus 5 mg prednisone until progression. The primary endpoint was objective response rate (ORR) according to combined Response Evaluation Criteria in Solid Tumours/Gynaecological Cancer Intergroup (RECIST/GCIG) criteria at 12 weeks. Secondary endpoints included clinical benefit rate (CBR) at 12 weeks. Results: A total of 42 patients were recruited; median age 65 (range 34–85) years; 37 (88.1%) had high-grade serous tumours; 20 (48%) had at least three prior lines of therapy; 29/40 (72.5%) were AR+. In stage 1, 1/26 response was observed (in an AR+, low-grade serous EOC); response lasted 47 weeks. Overall, 12 week ORR was 1/42 (2%), CBR was 11/42 (26%) (8/29 (28%) in AR+ patients). Disease control was ⩾6 months for 4/29 (14%). One patient (AR+, low-grade serous) had a RECIST response at 82 weeks. Four (10%) had grade ⩾3 hypokalaemia; 11 (26%) had dose delays. Conclusions: CORAL represents the first trial of an AR targeted agent in ovarian cancer. While responses were rare, a subset of patients achieved sustained clinical benefit. Targeting AR in EOC including low-grade serous cancer warrants further investigation. Trial registration: CORAL is registered on the ISRCTN registry: ISRCTN63407050; http://www.isrctn.com/ISRCTN63407050

Funder

Janssen-Cilag Ltd

Cancer Research UK

The Royal Marsden NHS Foundation Trust & The Institute of Cancer Research

National Institute for Health Research Clinical Research Network

The Gynaecological Cancer Fund

Publisher

SAGE Publications

Subject

Oncology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3