Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223

ABSTRACT Objective Radium-223(223Ra) is indicated for patients (p) with metastatic castration resistant prostate cancer (mCRCP). Objectives The aim of this study was to evaluate the role of baseline clinical variables associated with overall survival (OS) and toxicity of 223Ra. Its purpose was to identify the factors that can predict a better response to treatment and provide information regarding the most appropriate time for the application of 223Ra. Materials and Methods Prospective study in 40p with mCRPC treated with 223Ra. End points were OS, progression-free survival and time to progression. The follow-up parameters were: doses received, hemoglobin (Hb), absolute neutrophil count (ANC), platelet count (PC), prostate specific antigen (PSA), alkaline phosphatase (ALP), Visual Analogue Scale for pain, Eastern Cooperative Oncology Group (ECOG) and WHO’s Cancer Pain Ladder. The use of other treatments was also evaluated. Results Median OS was 17.1 months(mo) (CI95%6.5-27.7); 26/40p received complete treatment of 223Ra, without reaching a median OS and 14p received incomplete treatment with a median OS 13.6mo(CI95%1.6-25.6). Median follow-up was 11.2mo (range:1.3-45.2). The univariate analysis showed that factors as VAS, ECOG, Hb and ALP values were independently associated with OS. First line treatment with 223Ra was started in 11/40p, while 19p had been heavily pre-treated and 13p received concomitant treatment. Conclusions 223Ra therapy require an adequate selection of patients to obtain the greatest clinical benefit. Low basal Hb, hight basal ALP, bone marrow involvement and an altered ECOG were the main factors that decreased OS in our patients. 223Ra should be considered relatively early in the course of treatment.

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Main Authors: Vidal,Monica, Delgado,Alejandro, Martinez,Carlos, Correa,José Jaime, Durango,Isabel Cristina
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Urologia 2020
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382020000400599
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spelling oai:scielo:S1677-553820200004005992020-05-28Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223Vidal,MonicaDelgado,AlejandroMartinez,CarlosCorrea,José JaimeDurango,Isabel Cristina Radium-223 [Supplementary Concept] Castration Prostatic Neoplasms ABSTRACT Objective Radium-223(223Ra) is indicated for patients (p) with metastatic castration resistant prostate cancer (mCRCP). Objectives The aim of this study was to evaluate the role of baseline clinical variables associated with overall survival (OS) and toxicity of 223Ra. Its purpose was to identify the factors that can predict a better response to treatment and provide information regarding the most appropriate time for the application of 223Ra. Materials and Methods Prospective study in 40p with mCRPC treated with 223Ra. End points were OS, progression-free survival and time to progression. The follow-up parameters were: doses received, hemoglobin (Hb), absolute neutrophil count (ANC), platelet count (PC), prostate specific antigen (PSA), alkaline phosphatase (ALP), Visual Analogue Scale for pain, Eastern Cooperative Oncology Group (ECOG) and WHO’s Cancer Pain Ladder. The use of other treatments was also evaluated. Results Median OS was 17.1 months(mo) (CI95%6.5-27.7); 26/40p received complete treatment of 223Ra, without reaching a median OS and 14p received incomplete treatment with a median OS 13.6mo(CI95%1.6-25.6). Median follow-up was 11.2mo (range:1.3-45.2). The univariate analysis showed that factors as VAS, ECOG, Hb and ALP values were independently associated with OS. First line treatment with 223Ra was started in 11/40p, while 19p had been heavily pre-treated and 13p received concomitant treatment. Conclusions 223Ra therapy require an adequate selection of patients to obtain the greatest clinical benefit. Low basal Hb, hight basal ALP, bone marrow involvement and an altered ECOG were the main factors that decreased OS in our patients. 223Ra should be considered relatively early in the course of treatment.info:eu-repo/semantics/openAccessSociedade Brasileira de UrologiaInternational braz j urol v.46 n.4 20202020-08-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382020000400599en10.1590/s1677-5538.ibju.2019.0343
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countrycode BR
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libraryname SciELO
language English
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author Vidal,Monica
Delgado,Alejandro
Martinez,Carlos
Correa,José Jaime
Durango,Isabel Cristina
spellingShingle Vidal,Monica
Delgado,Alejandro
Martinez,Carlos
Correa,José Jaime
Durango,Isabel Cristina
Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223
author_facet Vidal,Monica
Delgado,Alejandro
Martinez,Carlos
Correa,José Jaime
Durango,Isabel Cristina
author_sort Vidal,Monica
title Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223
title_short Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223
title_full Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223
title_fullStr Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223
title_full_unstemmed Overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223
title_sort overall survival prediction in metastatic castration-resistant prostate cancer treated with radium-223
description ABSTRACT Objective Radium-223(223Ra) is indicated for patients (p) with metastatic castration resistant prostate cancer (mCRCP). Objectives The aim of this study was to evaluate the role of baseline clinical variables associated with overall survival (OS) and toxicity of 223Ra. Its purpose was to identify the factors that can predict a better response to treatment and provide information regarding the most appropriate time for the application of 223Ra. Materials and Methods Prospective study in 40p with mCRPC treated with 223Ra. End points were OS, progression-free survival and time to progression. The follow-up parameters were: doses received, hemoglobin (Hb), absolute neutrophil count (ANC), platelet count (PC), prostate specific antigen (PSA), alkaline phosphatase (ALP), Visual Analogue Scale for pain, Eastern Cooperative Oncology Group (ECOG) and WHO’s Cancer Pain Ladder. The use of other treatments was also evaluated. Results Median OS was 17.1 months(mo) (CI95%6.5-27.7); 26/40p received complete treatment of 223Ra, without reaching a median OS and 14p received incomplete treatment with a median OS 13.6mo(CI95%1.6-25.6). Median follow-up was 11.2mo (range:1.3-45.2). The univariate analysis showed that factors as VAS, ECOG, Hb and ALP values were independently associated with OS. First line treatment with 223Ra was started in 11/40p, while 19p had been heavily pre-treated and 13p received concomitant treatment. Conclusions 223Ra therapy require an adequate selection of patients to obtain the greatest clinical benefit. Low basal Hb, hight basal ALP, bone marrow involvement and an altered ECOG were the main factors that decreased OS in our patients. 223Ra should be considered relatively early in the course of treatment.
publisher Sociedade Brasileira de Urologia
publishDate 2020
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382020000400599
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