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Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study)

BACKGROUND: Despite most metastatic castration-resistant prostate cancer (mCRPC) patients benefit from abiraterone acetate plus prednisone 5 mg bid (AA + P), resistance eventually occurs. Long-term use of prednisone has been suggested as one of the mechanisms driving resistance, which may be reverse...

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Autores principales: Romero-Laorden, Nuria, Lozano, Rebeca, Jayaram, Anuradha, López-Campos, Fernando, Saez, Maria I., Montesa, Alvaro, Gutierrez-Pecharoman, Ana, Villatoro, Rosa, Herrera, Bernardo, Correa, Raquel, Rosero, Adriana, Pacheco, María I., Garcés, Teresa, Cendón, Ylenia, Nombela, Ma Paz, Van de Poll, Floortje, Grau, Gala, Rivera, Leticia, López, Pedro P., Cruz, Juan-Jesús, Lorente, David, Attard, Gerhardt, Castro, Elena, Olmos, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219494/
https://www.ncbi.nlm.nih.gov/pubmed/30131546
http://dx.doi.org/10.1038/s41416-018-0123-9
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author Romero-Laorden, Nuria
Lozano, Rebeca
Jayaram, Anuradha
López-Campos, Fernando
Saez, Maria I.
Montesa, Alvaro
Gutierrez-Pecharoman, Ana
Villatoro, Rosa
Herrera, Bernardo
Correa, Raquel
Rosero, Adriana
Pacheco, María I.
Garcés, Teresa
Cendón, Ylenia
Nombela, Ma Paz
Van de Poll, Floortje
Grau, Gala
Rivera, Leticia
López, Pedro P.
Cruz, Juan-Jesús
Lorente, David
Attard, Gerhardt
Castro, Elena
Olmos, David
author_facet Romero-Laorden, Nuria
Lozano, Rebeca
Jayaram, Anuradha
López-Campos, Fernando
Saez, Maria I.
Montesa, Alvaro
Gutierrez-Pecharoman, Ana
Villatoro, Rosa
Herrera, Bernardo
Correa, Raquel
Rosero, Adriana
Pacheco, María I.
Garcés, Teresa
Cendón, Ylenia
Nombela, Ma Paz
Van de Poll, Floortje
Grau, Gala
Rivera, Leticia
López, Pedro P.
Cruz, Juan-Jesús
Lorente, David
Attard, Gerhardt
Castro, Elena
Olmos, David
author_sort Romero-Laorden, Nuria
collection PubMed
description BACKGROUND: Despite most metastatic castration-resistant prostate cancer (mCRPC) patients benefit from abiraterone acetate plus prednisone 5 mg bid (AA + P), resistance eventually occurs. Long-term use of prednisone has been suggested as one of the mechanisms driving resistance, which may be reversed by switching to another steroid. METHODS: SWITCH was a single-arm, open-label, single-stage phase II study. The primary objective was to evaluate the antitumour activity of abiraterone acetate plus dexamethasone 0.5 mg daily (AA + D) in mCRPC patients progressing to AA + P. Clinically stable mCRPC patients who had prostate-specific antigen (PSA) and/or limited radiographic progression after at least 12 weeks on AA + P, were eligible. The primary endpoint was measured as the proportion of patients achieving a PSA decline of  ≥ 30% (PSA30) from baseline after 6 weeks on AA + D. Secondary endpoints included: PSA50 response rate at 12 weeks, time to biochemical and radiological progression, overall survival, safety profile evaluation, benefit from subsequent treatment lines and the identification of biomarkers of response (AR copy number, TMPRSS2-ERG status and PTEN expression). RESULTS: Twenty-six patients were enrolled. PSA30 and PSA50 were 46.2% and 34.6%, respectively. Median time to biochemical and radiological progression were 5.3 and 11.8 months, respectively. Two radiological responses were observed. Median overall survival was 20.9 months. Patients with AR gain detected in plasma circulating tumour DNA did not respond to switch, whereas patients with AR normal status benefited the most. No significant toxicities were observed and PSA50 response rate to subsequent taxane was 50%. CONCLUSIONS: In selected clinical stable mCRPC patients with limited disease progression on AA + P, a steroid switch from prednisone to dexamethasone can lead to PSA and radiological responses.
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spelling pubmed-62194942019-09-05 Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study) Romero-Laorden, Nuria Lozano, Rebeca Jayaram, Anuradha López-Campos, Fernando Saez, Maria I. Montesa, Alvaro Gutierrez-Pecharoman, Ana Villatoro, Rosa Herrera, Bernardo Correa, Raquel Rosero, Adriana Pacheco, María I. Garcés, Teresa Cendón, Ylenia Nombela, Ma Paz Van de Poll, Floortje Grau, Gala Rivera, Leticia López, Pedro P. Cruz, Juan-Jesús Lorente, David Attard, Gerhardt Castro, Elena Olmos, David Br J Cancer Article BACKGROUND: Despite most metastatic castration-resistant prostate cancer (mCRPC) patients benefit from abiraterone acetate plus prednisone 5 mg bid (AA + P), resistance eventually occurs. Long-term use of prednisone has been suggested as one of the mechanisms driving resistance, which may be reversed by switching to another steroid. METHODS: SWITCH was a single-arm, open-label, single-stage phase II study. The primary objective was to evaluate the antitumour activity of abiraterone acetate plus dexamethasone 0.5 mg daily (AA + D) in mCRPC patients progressing to AA + P. Clinically stable mCRPC patients who had prostate-specific antigen (PSA) and/or limited radiographic progression after at least 12 weeks on AA + P, were eligible. The primary endpoint was measured as the proportion of patients achieving a PSA decline of  ≥ 30% (PSA30) from baseline after 6 weeks on AA + D. Secondary endpoints included: PSA50 response rate at 12 weeks, time to biochemical and radiological progression, overall survival, safety profile evaluation, benefit from subsequent treatment lines and the identification of biomarkers of response (AR copy number, TMPRSS2-ERG status and PTEN expression). RESULTS: Twenty-six patients were enrolled. PSA30 and PSA50 were 46.2% and 34.6%, respectively. Median time to biochemical and radiological progression were 5.3 and 11.8 months, respectively. Two radiological responses were observed. Median overall survival was 20.9 months. Patients with AR gain detected in plasma circulating tumour DNA did not respond to switch, whereas patients with AR normal status benefited the most. No significant toxicities were observed and PSA50 response rate to subsequent taxane was 50%. CONCLUSIONS: In selected clinical stable mCRPC patients with limited disease progression on AA + P, a steroid switch from prednisone to dexamethasone can lead to PSA and radiological responses. Nature Publishing Group UK 2018-08-21 2018-10-30 /pmc/articles/PMC6219494/ /pubmed/30131546 http://dx.doi.org/10.1038/s41416-018-0123-9 Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by/4.0/Note: This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Romero-Laorden, Nuria
Lozano, Rebeca
Jayaram, Anuradha
López-Campos, Fernando
Saez, Maria I.
Montesa, Alvaro
Gutierrez-Pecharoman, Ana
Villatoro, Rosa
Herrera, Bernardo
Correa, Raquel
Rosero, Adriana
Pacheco, María I.
Garcés, Teresa
Cendón, Ylenia
Nombela, Ma Paz
Van de Poll, Floortje
Grau, Gala
Rivera, Leticia
López, Pedro P.
Cruz, Juan-Jesús
Lorente, David
Attard, Gerhardt
Castro, Elena
Olmos, David
Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study)
title Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study)
title_full Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study)
title_fullStr Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study)
title_full_unstemmed Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study)
title_short Phase II pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mCRPC) patients with limited progression on abiraterone plus prednisone (SWITCH study)
title_sort phase ii pilot study of the prednisone to dexamethasone switch in metastatic castration-resistant prostate cancer (mcrpc) patients with limited progression on abiraterone plus prednisone (switch study)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219494/
https://www.ncbi.nlm.nih.gov/pubmed/30131546
http://dx.doi.org/10.1038/s41416-018-0123-9
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