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Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center

BACKGROUND: Guidelines for optimal sequencing of radium-223 and chemotherapy for metastatic castration resistant prostate cancer (mCRPC) do not exist. This study evaluated treatment patterns and overall survival (OS) among patients with mCRPC treated with radium-223 in an academic clinical setting....

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Autores principales: McKay, Rana R., Silver, Rebecca, Bhak, Rachel H., Korves, Caroline, Cheng, Mu, Appukkuttan, Sreevalsa, Simmons, Stacey J., Duh, Mei Sheng, Taplin, Mary-Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012208/
https://www.ncbi.nlm.nih.gov/pubmed/32814846
http://dx.doi.org/10.1038/s41391-020-00271-7
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author McKay, Rana R.
Silver, Rebecca
Bhak, Rachel H.
Korves, Caroline
Cheng, Mu
Appukkuttan, Sreevalsa
Simmons, Stacey J.
Duh, Mei Sheng
Taplin, Mary-Ellen
author_facet McKay, Rana R.
Silver, Rebecca
Bhak, Rachel H.
Korves, Caroline
Cheng, Mu
Appukkuttan, Sreevalsa
Simmons, Stacey J.
Duh, Mei Sheng
Taplin, Mary-Ellen
author_sort McKay, Rana R.
collection PubMed
description BACKGROUND: Guidelines for optimal sequencing of radium-223 and chemotherapy for metastatic castration resistant prostate cancer (mCRPC) do not exist. This study evaluated treatment patterns and overall survival (OS) among patients with mCRPC treated with radium-223 in an academic clinical setting. METHODS: A retrospective study was conducted of bone metastases-predominant mCRPC patients treated with radium-223. Treatment patterns from 2013 to 2018 were evaluated in patients treated with radium-223 pre- vs. post-chemotherapy. OS was examined using Kaplan–Meier medians and 95% confidence intervals. RESULTS: In total, 220 patients were treated with radium-223 (64 pre-chemotherapy, 83 post-chemotherapy, 73 no chemotherapy). Mean radium-223 injections per patient was 5.3 and 4.3 in the pre- vs. post-chemotherapy cohorts, respectively (p < 0.001). The number of chemotherapy cycles was similar for chemotherapy given pre- or post-radium-223. Mean line of mCRPC therapy of radium-223 was 3rd and 5th when given pre- and post-chemotherapy, respectively (p < 0.001). 41.8% patients were treated with radium-223 in combination with another mCRPC therapy, commonly abiraterone acetate (43.5%) or enzalutamide (52.2%). The majority received combination therapy for the duration of radium-223 treatment; 20.7% started another agent after radium-223 initiation; 20.7% initiated radium-223 while on established therapy. Median OS from first mCRPC treatment was 39.4 months (95% CI 33.0, 48.8) for patients with radium-223 pre-chemotherapy vs. 37.4 months (95% CI 32.0, 43.5) post-chemotherapy (and 35.2 months [95% CI 27.9, 43.3] vs. 32.0 months [95% CI 26.9, 36.0] for patients with radium-223 combination vs. monotherapy). CONCLUSIONS: This retrospective analysis of patients treated with radium-223 demonstrates that administration of radium-223 pre-chemotherapy increased likelihood of completion of radium-223 treatment. Radium-223 given pre- or post-chemotherapy and with or without combination therapy did not result in significant differences in OS. Additional studies are needed to determine the optimal sequencing strategy of mCRPC in the modern era.
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spelling pubmed-80122082021-04-16 Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center McKay, Rana R. Silver, Rebecca Bhak, Rachel H. Korves, Caroline Cheng, Mu Appukkuttan, Sreevalsa Simmons, Stacey J. Duh, Mei Sheng Taplin, Mary-Ellen Prostate Cancer Prostatic Dis Article BACKGROUND: Guidelines for optimal sequencing of radium-223 and chemotherapy for metastatic castration resistant prostate cancer (mCRPC) do not exist. This study evaluated treatment patterns and overall survival (OS) among patients with mCRPC treated with radium-223 in an academic clinical setting. METHODS: A retrospective study was conducted of bone metastases-predominant mCRPC patients treated with radium-223. Treatment patterns from 2013 to 2018 were evaluated in patients treated with radium-223 pre- vs. post-chemotherapy. OS was examined using Kaplan–Meier medians and 95% confidence intervals. RESULTS: In total, 220 patients were treated with radium-223 (64 pre-chemotherapy, 83 post-chemotherapy, 73 no chemotherapy). Mean radium-223 injections per patient was 5.3 and 4.3 in the pre- vs. post-chemotherapy cohorts, respectively (p < 0.001). The number of chemotherapy cycles was similar for chemotherapy given pre- or post-radium-223. Mean line of mCRPC therapy of radium-223 was 3rd and 5th when given pre- and post-chemotherapy, respectively (p < 0.001). 41.8% patients were treated with radium-223 in combination with another mCRPC therapy, commonly abiraterone acetate (43.5%) or enzalutamide (52.2%). The majority received combination therapy for the duration of radium-223 treatment; 20.7% started another agent after radium-223 initiation; 20.7% initiated radium-223 while on established therapy. Median OS from first mCRPC treatment was 39.4 months (95% CI 33.0, 48.8) for patients with radium-223 pre-chemotherapy vs. 37.4 months (95% CI 32.0, 43.5) post-chemotherapy (and 35.2 months [95% CI 27.9, 43.3] vs. 32.0 months [95% CI 26.9, 36.0] for patients with radium-223 combination vs. monotherapy). CONCLUSIONS: This retrospective analysis of patients treated with radium-223 demonstrates that administration of radium-223 pre-chemotherapy increased likelihood of completion of radium-223 treatment. Radium-223 given pre- or post-chemotherapy and with or without combination therapy did not result in significant differences in OS. Additional studies are needed to determine the optimal sequencing strategy of mCRPC in the modern era. Nature Publishing Group UK 2020-08-19 2021 /pmc/articles/PMC8012208/ /pubmed/32814846 http://dx.doi.org/10.1038/s41391-020-00271-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
McKay, Rana R.
Silver, Rebecca
Bhak, Rachel H.
Korves, Caroline
Cheng, Mu
Appukkuttan, Sreevalsa
Simmons, Stacey J.
Duh, Mei Sheng
Taplin, Mary-Ellen
Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center
title Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center
title_full Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center
title_fullStr Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center
title_full_unstemmed Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center
title_short Treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a US tertiary oncology center
title_sort treatment of metastatic castration resistant prostate cancer with radium-223: a retrospective study at a us tertiary oncology center
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012208/
https://www.ncbi.nlm.nih.gov/pubmed/32814846
http://dx.doi.org/10.1038/s41391-020-00271-7
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