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LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial

BACKGROUND: Although the benefit of androgen deprivation therapy (ADT) continuation in metastatic castration-resistant prostate cancer (mCRPC) remains controversial, clinical evidence is lacking. Recent results indicated that treatment with abiraterone acetate (AA) plus prednisone (P) further suppre...

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Autores principales: Ohlmann, Carsten-Henning, Jäschke, Michelle, Jaehnig, Peter, Krege, Susanne, Gschwend, Jürgen, Rexer, Heidrun, Junker, Kerstin, Zillmann, Roger, Rüssel, Christoph, Hellmis, Eva, Suttmann, Henrik, Janssen, Martin, Marin, Jan, Hübner, Andreas, Mathers, Michael, Gleißner, Jochen, Scheffler, Michael, Feyerabend, Susan, Telle, Jens, Klier, Jörg, Stöckle, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705242/
https://www.ncbi.nlm.nih.gov/pubmed/35430584
http://dx.doi.org/10.1038/s41391-022-00533-6
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author Ohlmann, Carsten-Henning
Jäschke, Michelle
Jaehnig, Peter
Krege, Susanne
Gschwend, Jürgen
Rexer, Heidrun
Junker, Kerstin
Zillmann, Roger
Rüssel, Christoph
Hellmis, Eva
Suttmann, Henrik
Janssen, Martin
Marin, Jan
Hübner, Andreas
Mathers, Michael
Gleißner, Jochen
Scheffler, Michael
Feyerabend, Susan
Telle, Jens
Klier, Jörg
Stöckle, Michael
author_facet Ohlmann, Carsten-Henning
Jäschke, Michelle
Jaehnig, Peter
Krege, Susanne
Gschwend, Jürgen
Rexer, Heidrun
Junker, Kerstin
Zillmann, Roger
Rüssel, Christoph
Hellmis, Eva
Suttmann, Henrik
Janssen, Martin
Marin, Jan
Hübner, Andreas
Mathers, Michael
Gleißner, Jochen
Scheffler, Michael
Feyerabend, Susan
Telle, Jens
Klier, Jörg
Stöckle, Michael
author_sort Ohlmann, Carsten-Henning
collection PubMed
description BACKGROUND: Although the benefit of androgen deprivation therapy (ADT) continuation in metastatic castration-resistant prostate cancer (mCRPC) remains controversial, clinical evidence is lacking. Recent results indicated that treatment with abiraterone acetate (AA) plus prednisone (P) further suppresses serum testosterone levels over ADT alone, suggesting that continuation of ADT in the treatment of mCRPC may not be necessary. METHODS: In this exploratory phase 2 study, mCRPC patients were randomized with a 1:1 ratio to receive either continued ADT plus AA + P (Arm A) or AA + P alone (Arm B). The primary endpoint was the rate of radiographic progression-free survival (rPFS) at month 12. Secondary endpoints included PSA-response rate, objective response, time to PSA progression and safety. RESULTS: A total of 68 patients were equally randomized between the two study arms. Median testosterone-levels remained below castrate-levels throughout treatment in all patients. According to the intention-to-treat analysis the rPFS rate was 0.84 in Arm A and 0.89 in Arm B. Moderate and severe treatment-emergent adverse events were reported for 72% of the patients in Arm A and for 85% of the patients in Arm B. CONCLUSIONS: AA + P treatment without ADT may be effective in mCRPC patients and ADT may not be necessary in patients receiving AA + P.
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spelling pubmed-97052422022-11-30 LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial Ohlmann, Carsten-Henning Jäschke, Michelle Jaehnig, Peter Krege, Susanne Gschwend, Jürgen Rexer, Heidrun Junker, Kerstin Zillmann, Roger Rüssel, Christoph Hellmis, Eva Suttmann, Henrik Janssen, Martin Marin, Jan Hübner, Andreas Mathers, Michael Gleißner, Jochen Scheffler, Michael Feyerabend, Susan Telle, Jens Klier, Jörg Stöckle, Michael Prostate Cancer Prostatic Dis Article BACKGROUND: Although the benefit of androgen deprivation therapy (ADT) continuation in metastatic castration-resistant prostate cancer (mCRPC) remains controversial, clinical evidence is lacking. Recent results indicated that treatment with abiraterone acetate (AA) plus prednisone (P) further suppresses serum testosterone levels over ADT alone, suggesting that continuation of ADT in the treatment of mCRPC may not be necessary. METHODS: In this exploratory phase 2 study, mCRPC patients were randomized with a 1:1 ratio to receive either continued ADT plus AA + P (Arm A) or AA + P alone (Arm B). The primary endpoint was the rate of radiographic progression-free survival (rPFS) at month 12. Secondary endpoints included PSA-response rate, objective response, time to PSA progression and safety. RESULTS: A total of 68 patients were equally randomized between the two study arms. Median testosterone-levels remained below castrate-levels throughout treatment in all patients. According to the intention-to-treat analysis the rPFS rate was 0.84 in Arm A and 0.89 in Arm B. Moderate and severe treatment-emergent adverse events were reported for 72% of the patients in Arm A and for 85% of the patients in Arm B. CONCLUSIONS: AA + P treatment without ADT may be effective in mCRPC patients and ADT may not be necessary in patients receiving AA + P. Nature Publishing Group UK 2022-04-16 2022 /pmc/articles/PMC9705242/ /pubmed/35430584 http://dx.doi.org/10.1038/s41391-022-00533-6 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ohlmann, Carsten-Henning
Jäschke, Michelle
Jaehnig, Peter
Krege, Susanne
Gschwend, Jürgen
Rexer, Heidrun
Junker, Kerstin
Zillmann, Roger
Rüssel, Christoph
Hellmis, Eva
Suttmann, Henrik
Janssen, Martin
Marin, Jan
Hübner, Andreas
Mathers, Michael
Gleißner, Jochen
Scheffler, Michael
Feyerabend, Susan
Telle, Jens
Klier, Jörg
Stöckle, Michael
LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial
title LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial
title_full LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial
title_fullStr LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial
title_full_unstemmed LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial
title_short LHRH sparing therapy in patients with chemotherapy-naïve, mCRPC treated with abiraterone acetate plus prednisone: results of the randomized phase II SPARE trial
title_sort lhrh sparing therapy in patients with chemotherapy-naïve, mcrpc treated with abiraterone acetate plus prednisone: results of the randomized phase ii spare trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705242/
https://www.ncbi.nlm.nih.gov/pubmed/35430584
http://dx.doi.org/10.1038/s41391-022-00533-6
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