Quality of Life in Men With Prostate Cancer Randomly Allocated to Receive Docetaxel or Abiraterone in the STAMPEDE Trial

Author:

Rush Hannah L.1ORCID,Murphy Laura1,Morgans Alicia K.2ORCID,Clarke Noel W.3,Cook Adrian D.1,Attard Gerhardt4ORCID,Macnair Archie15,Dearnaley David P.6ORCID,Parker Christopher C.6,Russell J. Martin7ORCID,Gillessen Silke8ORCID,Matheson David9ORCID,Millman Robin1,Brawley Christopher D.1,Pugh Cheryl1ORCID,Tanguay Jacob S.10,Jones Robert J.7ORCID,Wagstaff John10ORCID,Rudman Sarah5,O'Sullivan Joe M.11ORCID,Gale Joanna12ORCID,Birtle Alison1314ORCID,Protheroe Andrew15ORCID,Gray Emma16,Perna Carla17,Tolan Shaun18,McPhail Neil19,Malik Zaf I.18,Vengalil Salil20,Fackrell David21,Hoskin Peter1422ORCID,Sydes Matthew R.1ORCID,Chowdhury Simon5,Gilbert Duncan C.1ORCID,Parmar Mahesh K. B.1ORCID,James Nicholas D.6ORCID,Langley Ruth E.1ORCID

Affiliation:

1. MRC Clinical Trials Units at University College London, London, United Kingdom

2. Northwestern University, Chicago, IL

3. The Christie and Salford Royal NHS Foundation Trusts, Manchester, United Kingdom

4. UCL Cancer Institute, London, United Kingdom

5. Guys and St Thomas' NHS Foundation Trust, London, United Kingdom

6. Royal Marsden NHS Foundation Trust and the Institute of Cancer Research, London, United Kingdom

7. Institute of Cancer Sciences, University of Glasgow, Beatson West of Scotland Cancer Centre, Glasgow, Scotland

8. Oncology Institute of Southern Switzerland, Bellinzona, Switzerland

9. University of Wolverhampton, Wolverhampton, United Kingdom

10. Velindre Cancer Centre, Cardiff, Wales

11. Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, United Kingdom

12. Portsmouth Hospital University Trust, Portsmouth, United Kingdom

13. Rosemere Cancer Centre, Lancs Teaching Hospitals, Preston, United Kingdom

14. University of Manchester, Manchester, United Kingdom

15. Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom

16. Musgrove Park Hospital, Taunton, United Kingdom

17. Royal Surrey Hospital Foundation Trust, Guildford, United Kingdom

18. The Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool, United Kingdom

19. Raigmore Hospital, Inverness, Scotland

20. University Hospital North Midlands NHS Trust, Stoke-on-Trent, United Kingdom

21. University Hospital Birmingham, Birmingham, United Kingdom

22. Mount Vernon Cancer Centre and University of Manchester, Manchester, United Kingdom

Abstract

PURPOSE Docetaxel and abiraterone acetate plus prednisone or prednisolone (AAP) both improve survival when commenced alongside standard of care (SOC) androgen deprivation therapy in locally advanced or metastatic hormone-sensitive prostate cancer. Thus, patient-reported quality of life (QOL) data may guide treatment choices. METHODS A group of patients within the STAMPEDE trial were contemporaneously enrolled with the possibility of being randomly allocated to receive either docetaxel + SOC or AAP + SOC. A mixed-model assessed QOL in those who had completed at least one QLQ-C30 + PR25 questionnaire. The primary outcome measure was difference in global-QOL (QLQ-C30 Q29&30) between patients allocated to docetaxel + SOC or AAP + SOC over the 2 years after random assignment, with a predefined criterion for clinically meaningful difference of > 4.0 points. Secondary outcome measures included longitudinal comparison of functional domains, pain, and fatigue, plus global-QOL at defined timepoints. RESULTS Five hundred fifteen patients (173 docetaxel + SOC and 342 AAP + SOC) were included. Baseline characteristics, proportion of missing data, and mean baseline global-QOL scores (docetaxel + SOC 77.8 and AAP + SOC 78.0) were similar. Over the 2 years following random assignment, the mean modeled global-QOL score was +3.9 points (95% CI, +0.5 to +7.2; P = .022) higher in patients allocated to AAP + SOC. Global-QOL was higher for patients allocated to AAP + SOC over the first year (+5.7 points, 95% CI, +3.0 to +8.5; P < .001), particularly at 12 (+7.0 points, 95% CI, +3.0 to +11.0; P = .001) and 24 weeks (+8.3 points, 95% CI, +4.0 to +12.6; P < .001). CONCLUSION Patient-reported QOL was superior for patients allocated to receive AAP + SOC, compared with docetaxel + SOC over a 2-year period, narrowly missing the predefined value for clinical significance. Patients receiving AAP + SOC reported clinically meaningful higher global-QOL scores throughout the first year following random assignment.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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