RESUMO
El dicloruro de radio-223 es un radiofármaco emisor alfa que prolonga la supervivencia global en pacientes con cáncer de próstata resistente a la castración y metástasis óseas sintomáticas. Presentamos un análisis retrospectivo de 68 pacientes tratados. MÉTODO: Se evaluó la incidencia de eventos adversos hematológicos, gastrointestinales y otros, incluidos aquellos que llevaron a la interrupción o el retraso del tratamiento. Se determinó la mejoría o empeoramiento del dolor óseo, los niveles de antígeno prostático específico y de fosfatasa alcalina sérica. Se valoró la gammagrafía ósea pre- y postratamiento y se correlacionó con la evolución clínica. RESULTADOS: Fueron incluidos 68 pacientes. La media del número de inyecciones de radio-223 fue de 5 (rango 1-6), el 69% de los pacientes recibieron 5 o 6 inyecciones. Los efectos secundarios más comunes fueron alteraciones digestivas en 24 pacientes, anemia en 7 y trombocitopenia en 5. Se observaron claras tendencias a la baja en la fosfatasa alcalina sérica. La fosfatasa alcalina sérica media disminuyó desde el inicio en el 77% de los pacientes y el antígeno prostático específico en menos del 40%. La mayoría de los pacientes (62) experimentaron una mejoría en la intensidad o estabilidad del dolor. No se observó ningún fenómeno de llamarada de antígeno prostático específico. CONCLUSIONES: El radio-223 fue generalmente bien tolerado y no hubo problemas de seguridad. Los eventos adversos fueron leves y manejables. Fue más común una disminución en la fosfatasa alcalina sérica que del antígeno prostático específico. La monitorización de la dinámica de la fosfatasa alcalina sérica puede ser útil
PURPUSE: Radium-223 is an alpha-emitting radiopharmaceutical that significantly prolongs overall survival in patients with castration-resistant prostate cancer and symptomatic bone metastases. We report a retrospective analysis of our clinical experience with Radium-223 in the first 68 patients treated. METHODS: The incidence of hematologic, gastrointestinal, and other adverse events was identified, including events that led to treatment discontinuation or delay. Alterations in bone pain and prostate-specific antigen and serum alkaline phosphatase levels were evaluated. Bone scan changes were identified and correlated with the clinical course. RESULTS: Sixty-eight patients were included in the study. The median number of radium-223 injections was 5 (range 1-6), with 69% of patients receiving 5 to 6 injections. The most common side effects were digestive alterations in 24 patients, anemia in 7 patients, and thrombocytopenia in 5 patients. Clear downward trends in serum alkaline phosphatase were seen, that were less clear in prostate-specific antigen. Mean serum alkaline phosphatase decreased from baseline in 77% of the patients, and prostate-specific antigen in less than 40%. The majority of patients (62) experienced an improvement in bone pain intensity or no increase in bone pain intensity. No prostate-specific antigen flare phenomenon was noted. CONCLUSIONS: Radium-223 was generally well tolerated and there were no safety concerns. The adverse events were mild and manageable. A decline in serum alkaline phosphatase was more common than a decline in prostate-specific antigen. Monitoring changes in serum alkaline phosphatase dynamics may be useful
Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Fosfatase Alcalina/sangue , Calicreínas/sangue , Antígeno Prostático Específico/sangue , Neoplasias de Próstata Resistentes à Castração/sangue , Neoplasias de Próstata Resistentes à Castração/radioterapia , Compostos Radiofarmacêuticos/uso terapêutico , Rádio (Elemento)/uso terapêutico , Estudos Retrospectivos , Fatores de TempoRESUMO
PURPOSE: Radium-223 is an alpha-emitting radiopharmaceutical that significantly prolongs overall survival in patients with castration-resistant prostate cancer and symptomatic bone metastases. We report a retrospective analysis of our clinical experience with Radium-223 in the first 68 patients treated. METHODS: The incidence of hematologic, gastrointestinal, and other adverse events was identified, including events that led to treatment discontinuation or delay. Alterations in bone pain and prostate-specific antigen and serum alkaline phosphatase levels were evaluated. Bone scan changes were identified and correlated with the clinical course. RESULTS: Sixty-eight patients were included in the study. The median number of radium-223 injections was 5 (range 1-6), with 69% of patients receiving 5 to 6 injections. The most common side effects were digestive alterations in 24 patients, anemia in 7 patients, and thrombocytopenia in 5 patients. Clear downward trends in serum alkaline phosphatase were seen, that were less clear in prostate-specific antigen. Mean serum alkaline phosphatase decreased from baseline in 77% of the patients, and prostate-specific antigen in less than 40%. The majority of patients (62) experienced an improvement in bone pain intensity or no increase in bone pain intensity. No prostate-specific antigen flare phenomenon was noted. CONCLUSIONS: Radium-223 was generally well tolerated and there were no safety concerns. The adverse events were mild and manageable. A decline in serum alkaline phosphatase was more common than a decline in prostate-specific antigen. Monitoring changes in serum alkaline phosphatase dynamics may be useful.
