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Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial

PURPOSE: Systemic Therapy for Advanced or Metastatic Prostate Cancer: Evaluation of Drug Efficacy is a randomized controlled trial using a multiarm, multistage, platform design. It recruits men with high-risk, locally advanced or metastatic prostate cancer who were initiating long-term hormone thera...

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Autores principales: Mason, Malcolm D., Clarke, Noel W., James, Nicholas D., Dearnaley, David P., Spears, Melissa R., Ritchie, Alastair W.S., Attard, Gerhardt, Cross, William, Jones, Rob J., Parker, Christopher C., Russell, J. Martin, Thalmann, George N., Schiavone, Francesca, Cassoly, Estelle, Matheson, David, Millman, Robin, Rentsch, Cyrill A., Barber, Jim, Gilson, Clare, Ibrahim, Azman, Logue, John, Lydon, Anna, Nikapota, Ashok D., O’Sullivan, Joe M., Porfiri, Emilio, Protheroe, Andrew, Srihari, Narayanan Nair, Tsang, David, Wagstaff, John, Wallace, Jan, Walmsley, Catherine, Parmar, Mahesh K.B., Sydes, Matthew R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Clinical Oncology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455701/
https://www.ncbi.nlm.nih.gov/pubmed/28300506
http://dx.doi.org/10.1200/JCO.2016.69.0677
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author Mason, Malcolm D.
Clarke, Noel W.
James, Nicholas D.
Dearnaley, David P.
Spears, Melissa R.
Ritchie, Alastair W.S.
Attard, Gerhardt
Cross, William
Jones, Rob J.
Parker, Christopher C.
Russell, J. Martin
Thalmann, George N.
Schiavone, Francesca
Cassoly, Estelle
Matheson, David
Millman, Robin
Rentsch, Cyrill A.
Barber, Jim
Gilson, Clare
Ibrahim, Azman
Logue, John
Lydon, Anna
Nikapota, Ashok D.
O’Sullivan, Joe M.
Porfiri, Emilio
Protheroe, Andrew
Srihari, Narayanan Nair
Tsang, David
Wagstaff, John
Wallace, Jan
Walmsley, Catherine
Parmar, Mahesh K.B.
Sydes, Matthew R.
author_facet Mason, Malcolm D.
Clarke, Noel W.
James, Nicholas D.
Dearnaley, David P.
Spears, Melissa R.
Ritchie, Alastair W.S.
Attard, Gerhardt
Cross, William
Jones, Rob J.
Parker, Christopher C.
Russell, J. Martin
Thalmann, George N.
Schiavone, Francesca
Cassoly, Estelle
Matheson, David
Millman, Robin
Rentsch, Cyrill A.
Barber, Jim
Gilson, Clare
Ibrahim, Azman
Logue, John
Lydon, Anna
Nikapota, Ashok D.
O’Sullivan, Joe M.
Porfiri, Emilio
Protheroe, Andrew
Srihari, Narayanan Nair
Tsang, David
Wagstaff, John
Wallace, Jan
Walmsley, Catherine
Parmar, Mahesh K.B.
Sydes, Matthew R.
author_sort Mason, Malcolm D.
collection PubMed
description PURPOSE: Systemic Therapy for Advanced or Metastatic Prostate Cancer: Evaluation of Drug Efficacy is a randomized controlled trial using a multiarm, multistage, platform design. It recruits men with high-risk, locally advanced or metastatic prostate cancer who were initiating long-term hormone therapy. We report survival data for two celecoxib (Cel)-containing comparisons, which stopped accrual early at interim analysis on the basis of failure-free survival. PATIENTS AND METHODS: Standard of care (SOC) was hormone therapy continuously (metastatic) or for ≥ 2 years (nonmetastatic); prostate (± pelvic node) radiotherapy was encouraged for men without metastases. Cel 400 mg was administered twice a day for 1 year. Zoledronic acid (ZA) 4 mg was administered for six 3-weekly cycles, then 4-weekly for 2 years. Stratified random assignment allocated patients 2:1:1 to SOC (control), SOC + Cel, or SOC + ZA + Cel. The primary outcome measure was all-cause mortality. Results were analyzed with Cox proportional hazards and flexible parametric models adjusted for stratification factors. RESULTS: A total of 1,245 men were randomly assigned (Oct 2005 to April 2011). Groups were balanced: median age, 65 years; 61% metastatic, 14% N+/X M0, 25% N0M0; 94% newly diagnosed; median prostate-specific antigen, 66 ng/mL. Median follow-up was 69 months. Grade 3 to 5 adverse events were seen in 36% SOC-only, 33% SOC + Cel, and 32% SOC + ZA + Cel patients. There were 303 control arm deaths (83% prostate cancer), and median survival was 66 months. Compared with SOC, the adjusted hazard ratio was 0.98 (95% CI, 0.80 to 1.20; P = .847; median survival, 70 months) for SOC + Cel and 0.86 (95% CI, 0.70 to 1.05; P =.130; median survival, 76 months) for SOC + ZA + Cel. Preplanned subgroup analyses in men with metastatic disease showed a hazard ratio of 0.78 (95% CI, 0.62 to 0.98; P = .033) for SOC + ZA + Cel. CONCLUSION: These data show no overall evidence of improved survival with Cel. Preplanned subgroup analyses provide hypotheses for future studies.
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spelling pubmed-54557012018-03-16 Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial Mason, Malcolm D. Clarke, Noel W. James, Nicholas D. Dearnaley, David P. Spears, Melissa R. Ritchie, Alastair W.S. Attard, Gerhardt Cross, William Jones, Rob J. Parker, Christopher C. Russell, J. Martin Thalmann, George N. Schiavone, Francesca Cassoly, Estelle Matheson, David Millman, Robin Rentsch, Cyrill A. Barber, Jim Gilson, Clare Ibrahim, Azman Logue, John Lydon, Anna Nikapota, Ashok D. O’Sullivan, Joe M. Porfiri, Emilio Protheroe, Andrew Srihari, Narayanan Nair Tsang, David Wagstaff, John Wallace, Jan Walmsley, Catherine Parmar, Mahesh K.B. Sydes, Matthew R. J Clin Oncol ORIGINAL REPORTS PURPOSE: Systemic Therapy for Advanced or Metastatic Prostate Cancer: Evaluation of Drug Efficacy is a randomized controlled trial using a multiarm, multistage, platform design. It recruits men with high-risk, locally advanced or metastatic prostate cancer who were initiating long-term hormone therapy. We report survival data for two celecoxib (Cel)-containing comparisons, which stopped accrual early at interim analysis on the basis of failure-free survival. PATIENTS AND METHODS: Standard of care (SOC) was hormone therapy continuously (metastatic) or for ≥ 2 years (nonmetastatic); prostate (± pelvic node) radiotherapy was encouraged for men without metastases. Cel 400 mg was administered twice a day for 1 year. Zoledronic acid (ZA) 4 mg was administered for six 3-weekly cycles, then 4-weekly for 2 years. Stratified random assignment allocated patients 2:1:1 to SOC (control), SOC + Cel, or SOC + ZA + Cel. The primary outcome measure was all-cause mortality. Results were analyzed with Cox proportional hazards and flexible parametric models adjusted for stratification factors. RESULTS: A total of 1,245 men were randomly assigned (Oct 2005 to April 2011). Groups were balanced: median age, 65 years; 61% metastatic, 14% N+/X M0, 25% N0M0; 94% newly diagnosed; median prostate-specific antigen, 66 ng/mL. Median follow-up was 69 months. Grade 3 to 5 adverse events were seen in 36% SOC-only, 33% SOC + Cel, and 32% SOC + ZA + Cel patients. There were 303 control arm deaths (83% prostate cancer), and median survival was 66 months. Compared with SOC, the adjusted hazard ratio was 0.98 (95% CI, 0.80 to 1.20; P = .847; median survival, 70 months) for SOC + Cel and 0.86 (95% CI, 0.70 to 1.05; P =.130; median survival, 76 months) for SOC + ZA + Cel. Preplanned subgroup analyses in men with metastatic disease showed a hazard ratio of 0.78 (95% CI, 0.62 to 0.98; P = .033) for SOC + ZA + Cel. CONCLUSION: These data show no overall evidence of improved survival with Cel. Preplanned subgroup analyses provide hypotheses for future studies. American Society of Clinical Oncology 2017-05-10 2017-03-13 /pmc/articles/PMC5455701/ /pubmed/28300506 http://dx.doi.org/10.1200/JCO.2016.69.0677 Text en © 2017 by American Society of Clinical Oncology http://creativecommons.org/licenses/by/4.0/ Licensed under the Creative Commons Attribution 4.0 License: http://creativecommons.org/licenses/by/4.0/
spellingShingle ORIGINAL REPORTS
Mason, Malcolm D.
Clarke, Noel W.
James, Nicholas D.
Dearnaley, David P.
Spears, Melissa R.
Ritchie, Alastair W.S.
Attard, Gerhardt
Cross, William
Jones, Rob J.
Parker, Christopher C.
Russell, J. Martin
Thalmann, George N.
Schiavone, Francesca
Cassoly, Estelle
Matheson, David
Millman, Robin
Rentsch, Cyrill A.
Barber, Jim
Gilson, Clare
Ibrahim, Azman
Logue, John
Lydon, Anna
Nikapota, Ashok D.
O’Sullivan, Joe M.
Porfiri, Emilio
Protheroe, Andrew
Srihari, Narayanan Nair
Tsang, David
Wagstaff, John
Wallace, Jan
Walmsley, Catherine
Parmar, Mahesh K.B.
Sydes, Matthew R.
Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial
title Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial
title_full Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial
title_fullStr Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial
title_full_unstemmed Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial
title_short Adding Celecoxib With or Without Zoledronic Acid for Hormone-Naïve Prostate Cancer: Long-Term Survival Results From an Adaptive, Multiarm, Multistage, Platform, Randomized Controlled Trial
title_sort adding celecoxib with or without zoledronic acid for hormone-naïve prostate cancer: long-term survival results from an adaptive, multiarm, multistage, platform, randomized controlled trial
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455701/
https://www.ncbi.nlm.nih.gov/pubmed/28300506
http://dx.doi.org/10.1200/JCO.2016.69.0677
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