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Prognostic biomarkers in the use of radium-223 in patients with metastatic castration-resistent prostate cancer.
Vidal, M; Cárdenas-Perilla, R; Delgado, A; Morón, S; Londoño Blair, J L; Vega, I; Correa Ochoa, J J; Rojas, J.
Afiliação
  • Vidal M; Departamento de Medicina Nuclear, Hospital Pablo Tobón Uribe, Medellín, Colombia. Electronic address: mvidal@hptu.org.co.
  • Cárdenas-Perilla R; Departamento de Medicina Nuclear, Clínica Imbanaco-Grupo Quironsalud, Cali, Colombia; Grupo de Investigaciones y Educación, Clínica de Occidente, Cali, Colombia.
  • Delgado A; Departamento de Medicina Nuclear, Hospital Pablo Tobón Uribe, Medellín, Colombia.
  • Morón S; Departamento de Medicina Nuclear, Medicina Nuclear SAS, Valledupar, Colombia.
  • Londoño Blair JL; Departamento de Medicina Nuclear, Hospital Universitario San Vicente Fundación, Medellín, Colombia.
  • Vega I; Departamento de Medicina Nuclear, Clínica Las Américas AUNA, Medellín, Colombia.
  • Correa Ochoa JJ; Departamento de Urología, Hospital Pablo Tobón Uribe, Medellín, Colombia.
  • Rojas J; Departamento de Medicina Nuclear, Instituto Nacional de Cancerología, Bogotá, Colombia.
Article em En | MEDLINE | ID: mdl-37419250
ABSTRACT

OBJECTIVES:

This study aimed to establish basal biomarkers in patients with bone metastatic castration-resistant prostate cancer (mCRPC) treated with 223Ra to predict better overall survival (OS), and assess hematologic toxicity and treatment response. MATERIALS AND

METHODS:

This was a retrospective multicenter study including 151 patients with mCRPC between 2013 and 2020. OS was assessed according to basal hemoglobin (Hb), prostate-specific antigen (PSA), and alkaline phosphatase (AP) values, the World Health Organization pain scale, the Eastern Cooperative Oncology Group (ECOG) performance status scale, the number of metastatic lesions on bone scintigraphy (BS), and the use of protective bone agents and the dose received. The grade of hematological toxicities was evaluated as well as treatment response based on changes in AP and pre- and post-treatment pain.

RESULTS:

The median OS was 24 months (95% confidence interval 16.5-31). The OS in 70% of patients who received complete (5-6 doses) versus incomplete (1-4 doses) 223Ra treatment was 34.9 vs. 5.8 months, respectively, being longer in patients with lower PSA and AP values, Hb >13 g/dl, lesser bone metastasis on bone scan and with an ECOG 0-1. 52/151 patients (34%) died during follow-up. Pain reduced in nearly 70% of patients and 66% presented a reduction in AP values. Half of the patients presented mild and 5 % severe hematological adverse effects.

CONCLUSIONS:

mCRPC patients treated with 223Ra with Hb values >13 g/mL, an ECOG 0-1, low AP values, PSA < 20 ng/mL and lesser bone metastasis on BS presented a better OS with an adequate safety profile.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans / Male Idioma: En Revista: Rev Esp Med Nucl Imagen Mol (Engl Ed) Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans / Male Idioma: En Revista: Rev Esp Med Nucl Imagen Mol (Engl Ed) Ano de publicação: 2023 Tipo de documento: Article