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Quality of Life in Men With Prostate Cancer Randomly Allocated to Receive Docetaxel or Abiraterone in the STAMPEDE Trial.
Rush, Hannah L; Murphy, Laura; Morgans, Alicia K; Clarke, Noel W; Cook, Adrian D; Attard, Gerhardt; Macnair, Archie; Dearnaley, David P; Parker, Christopher C; Russell, J Martin; Gillessen, Silke; Matheson, David; Millman, Robin; Brawley, Christopher D; Pugh, Cheryl; Tanguay, Jacob S; Jones, Robert J; Wagstaff, John; Rudman, Sarah; O'Sullivan, Joe M; Gale, Joanna; Birtle, Alison; Protheroe, Andrew; Gray, Emma; Perna, Carla; Tolan, Shaun; McPhail, Neil; Malik, Zaf I; Vengalil, Salil; Fackrell, David; Hoskin, Peter; Sydes, Matthew R; Chowdhury, Simon; Gilbert, Duncan C; Parmar, Mahesh K B; James, Nicholas D; Langley, Ruth E.
Afiliación
  • Rush HL; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • Murphy L; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • Morgans AK; Northwestern University, Chicago, IL.
  • Clarke NW; The Christie and Salford Royal NHS Foundation Trusts, Manchester, United Kingdom.
  • Cook AD; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • Attard G; UCL Cancer Institute, London, United Kingdom.
  • Macnair A; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • Dearnaley DP; Guys and St Thomas' NHS Foundation Trust, London, United Kingdom.
  • Parker CC; Royal Marsden NHS Foundation Trust and the Institute of Cancer Research, London, United Kingdom.
  • Russell JM; Royal Marsden NHS Foundation Trust and the Institute of Cancer Research, London, United Kingdom.
  • Gillessen S; Institute of Cancer Sciences, University of Glasgow, Beatson West of Scotland Cancer Centre, Glasgow, Scotland.
  • Matheson D; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Millman R; University of Wolverhampton, Wolverhampton, United Kingdom.
  • Brawley CD; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • Pugh C; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • Tanguay JS; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • Jones RJ; Velindre Cancer Centre, Cardiff, Wales.
  • Wagstaff J; Institute of Cancer Sciences, University of Glasgow, Beatson West of Scotland Cancer Centre, Glasgow, Scotland.
  • Rudman S; Velindre Cancer Centre, Cardiff, Wales.
  • O'Sullivan JM; Guys and St Thomas' NHS Foundation Trust, London, United Kingdom.
  • Gale J; Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, United Kingdom.
  • Birtle A; Portsmouth Hospital University Trust, Portsmouth, United Kingdom.
  • Protheroe A; Rosemere Cancer Centre, Lancs Teaching Hospitals, Preston, United Kingdom.
  • Gray E; University of Manchester, Manchester, United Kingdom.
  • Perna C; Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Tolan S; Musgrove Park Hospital, Taunton, United Kingdom.
  • McPhail N; Royal Surrey Hospital Foundation Trust, Guildford, United Kingdom.
  • Malik ZI; The Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool, United Kingdom.
  • Vengalil S; Raigmore Hospital, Inverness, Scotland.
  • Fackrell D; The Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool, United Kingdom.
  • Hoskin P; University Hospital North Midlands NHS Trust, Stoke-on-Trent, United Kingdom.
  • Sydes MR; University Hospital Birmingham, Birmingham, United Kingdom.
  • Chowdhury S; University of Manchester, Manchester, United Kingdom.
  • Gilbert DC; Mount Vernon Cancer Centre and University of Manchester, Manchester, United Kingdom.
  • Parmar MKB; MRC Clinical Trials Units at University College London, London, United Kingdom.
  • James ND; Guys and St Thomas' NHS Foundation Trust, London, United Kingdom.
  • Langley RE; MRC Clinical Trials Units at University College London, London, United Kingdom.
J Clin Oncol ; 40(8): 825-836, 2022 03 10.
Article en En | MEDLINE | ID: mdl-34757812
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Calidad de Vida Tipo de estudio: Clinical_trials / Prognostic_studies / Qualitative_research Límite: Humans / Male Idioma: En Revista: J Clin Oncol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Calidad de Vida Tipo de estudio: Clinical_trials / Prognostic_studies / Qualitative_research Límite: Humans / Male Idioma: En Revista: J Clin Oncol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido