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Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study

BACKGROUND: Radium-223 and enzalutamide are approved agents for patients with metastatic castration-resistant prostate cancer (mCRPC). Combining radium-223 and enzalutamide to improve outcomes is of clinical interest due to their differing modes of action and non-overlapping toxicity profiles. METHO...

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Autores principales: McDermott, Raymond S., Greene, John, McCaffrey, John, Parker, Imelda, Helanova, Sylva, Baird, Anne-Marie, Teiserskiene, Ausra, Lim, Marvin, Matthews, Helen, Deignan, Olwyn, Feeney, John, Thirion, Pierre G., Finn, Stephen P., Kelly, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427915/
https://www.ncbi.nlm.nih.gov/pubmed/34512801
http://dx.doi.org/10.1177/17588359211042691
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author McDermott, Raymond S.
Greene, John
McCaffrey, John
Parker, Imelda
Helanova, Sylva
Baird, Anne-Marie
Teiserskiene, Ausra
Lim, Marvin
Matthews, Helen
Deignan, Olwyn
Feeney, John
Thirion, Pierre G.
Finn, Stephen P.
Kelly, Paul J.
author_facet McDermott, Raymond S.
Greene, John
McCaffrey, John
Parker, Imelda
Helanova, Sylva
Baird, Anne-Marie
Teiserskiene, Ausra
Lim, Marvin
Matthews, Helen
Deignan, Olwyn
Feeney, John
Thirion, Pierre G.
Finn, Stephen P.
Kelly, Paul J.
author_sort McDermott, Raymond S.
collection PubMed
description BACKGROUND: Radium-223 and enzalutamide are approved agents for patients with metastatic castration-resistant prostate cancer (mCRPC). Combining radium-223 and enzalutamide to improve outcomes is of clinical interest due to their differing modes of action and non-overlapping toxicity profiles. METHODS: This phase II study enrolled patients with mCRPC and bone metastases. Patients received six cycles of radium-223 in combination with enzalutamide, followed by enzalutamide alone. The primary endpoint was safety for the combination; secondary endpoints included radiographic/clinical progression-free survival (PFS), PSA PFS, overall survival (OS), change in alkaline phosphatase, patient-reported pain outcomes and skeletal related events. RESULTS: Forty-five patients received the combination treatment: 42 patients (93.3%) received all six cycles. Fourteen patients (31.1%) developed grade 3 or 4 toxicities, most commonly fatigue and neutropaenia. Fractures during the combination period occurred in four patients (8.9%). A further 13 patients (28.9%) developed fractures after completing combination treatment, giving a total of 17 patients (37.8%) who developed a fracture at any time on study. The median time to fracture was greater than 17.2 months [95% confidence interval (CI), 17.2–not estimable]. The median time to PSA progression was 18.1 months (95% CI, 12.68–22.60) and the median time to radiological/clinical progression was 28.0 months (95% CI, 22.54–not reached). At the primary analysis, 19 (42.2%) out of 45 patients had died with a median OS not reached (mean 34.8 months, standard error 1.4). CONCLUSION: In men with progressive mCRPC and bone metastases, the combination of radium-223 and enzalutamide was tolerable with the majority of patients completing the combination treatment. Bone fractures during the combination period were uncommon; however, we did identify a higher incidence of fractures occurring in patients after completing combination treatment. Bone health agents should be administered and bone health should be closely monitored following treatment with radium-223 and enzalutamide.
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spelling pubmed-84279152021-09-10 Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study McDermott, Raymond S. Greene, John McCaffrey, John Parker, Imelda Helanova, Sylva Baird, Anne-Marie Teiserskiene, Ausra Lim, Marvin Matthews, Helen Deignan, Olwyn Feeney, John Thirion, Pierre G. Finn, Stephen P. Kelly, Paul J. Ther Adv Med Oncol Original Research BACKGROUND: Radium-223 and enzalutamide are approved agents for patients with metastatic castration-resistant prostate cancer (mCRPC). Combining radium-223 and enzalutamide to improve outcomes is of clinical interest due to their differing modes of action and non-overlapping toxicity profiles. METHODS: This phase II study enrolled patients with mCRPC and bone metastases. Patients received six cycles of radium-223 in combination with enzalutamide, followed by enzalutamide alone. The primary endpoint was safety for the combination; secondary endpoints included radiographic/clinical progression-free survival (PFS), PSA PFS, overall survival (OS), change in alkaline phosphatase, patient-reported pain outcomes and skeletal related events. RESULTS: Forty-five patients received the combination treatment: 42 patients (93.3%) received all six cycles. Fourteen patients (31.1%) developed grade 3 or 4 toxicities, most commonly fatigue and neutropaenia. Fractures during the combination period occurred in four patients (8.9%). A further 13 patients (28.9%) developed fractures after completing combination treatment, giving a total of 17 patients (37.8%) who developed a fracture at any time on study. The median time to fracture was greater than 17.2 months [95% confidence interval (CI), 17.2–not estimable]. The median time to PSA progression was 18.1 months (95% CI, 12.68–22.60) and the median time to radiological/clinical progression was 28.0 months (95% CI, 22.54–not reached). At the primary analysis, 19 (42.2%) out of 45 patients had died with a median OS not reached (mean 34.8 months, standard error 1.4). CONCLUSION: In men with progressive mCRPC and bone metastases, the combination of radium-223 and enzalutamide was tolerable with the majority of patients completing the combination treatment. Bone fractures during the combination period were uncommon; however, we did identify a higher incidence of fractures occurring in patients after completing combination treatment. Bone health agents should be administered and bone health should be closely monitored following treatment with radium-223 and enzalutamide. SAGE Publications 2021-09-06 /pmc/articles/PMC8427915/ /pubmed/34512801 http://dx.doi.org/10.1177/17588359211042691 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
McDermott, Raymond S.
Greene, John
McCaffrey, John
Parker, Imelda
Helanova, Sylva
Baird, Anne-Marie
Teiserskiene, Ausra
Lim, Marvin
Matthews, Helen
Deignan, Olwyn
Feeney, John
Thirion, Pierre G.
Finn, Stephen P.
Kelly, Paul J.
Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study
title Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study
title_full Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study
title_fullStr Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study
title_full_unstemmed Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study
title_short Radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase II open-label study
title_sort radium-223 in combination with enzalutamide in metastatic castration-resistant prostate cancer: a multi-centre, phase ii open-label study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427915/
https://www.ncbi.nlm.nih.gov/pubmed/34512801
http://dx.doi.org/10.1177/17588359211042691
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