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Impact of timing of radium­223 administration on the survival of patients with bone metastatic castration­resistant prostate cancer.
Makita, Kenji; Hamamoto, Yasushi; Kanzaki, Hiromitsu; Yamashita, Natsumi; Nagasaki, Kei; Kido, Teruhito; Miura, Noriyoshi; Saika, Takashi; Hashine, Katsuyoshi.
Afiliación
  • Makita K; Department of Radiation Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Ehime 791-0280, Japan.
  • Hamamoto Y; Department of Radiology, Ehime University Graduate School of Medicine, Toon, Ehime 791-0295, Japan.
  • Kanzaki H; Department of Radiology, Ehime Prefectural Central Hospital, Matsuyama, Ehime 790-0024, Japan.
  • Yamashita N; Department of Radiation Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Ehime 791-0280, Japan.
  • Nagasaki K; Department of Radiation Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Ehime 791-0280, Japan.
  • Kido T; Division of Clinical Biostatistics, Section of Cancer Prevention and Epidemiology, Clinical Research Center, National Hospital Organization Shikoku Cancer Center, Matsuyama, Ehime 791-0280, Japan.
  • Miura N; Department of Radiation Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Ehime 791-0280, Japan.
  • Saika T; Department of Radiology, Ehime University Graduate School of Medicine, Toon, Ehime 791-0295, Japan.
  • Hashine K; Department of Urology, Ehime University Graduate School of Medicine, Toon, Ehime 791-0295, Japan.
Med Int (Lond) ; 3(4): 38, 2023.
Article en En | MEDLINE | ID: mdl-37533801
ABSTRACT
The present study aimed to evaluate the optimal timing of radium-223 chloride (Ra-223) administration among patients with bone metastasis from castration-resistant prostate cancer (BmCRPC). Patients, who were diagnosed with BmCRPC and treated with Ra-223 therapy between October, 2016 and January, 2022, were reviewed. The survival time was calculated from the initiation of Ra-223 administration. The time from the diagnosis of BmCRPC to the initiation of Ra-223 administration was identified as a potential prognostic factor. A total of 51 patients were examined in the present study. Ra-223 was administered as the first- and second-line therapy (earlier Ra-223 administration) in 32 patients and as the third- to fifth-line therapy (later Ra-223 administration) in 19 patients. In the multivariate analysis, which considered the potential prognosis, the difference in survival times between patients who received early and late Ra-223 administration was not significant [hazard ratio (HR), 2.67; 95% confidence interval (CI), 0.79-9.07; P=0.11]. By contrast, an incomplete Ra-223 administration (HR, 128.03; 95% CI, 10.59-1548.42; P<0.01) and higher levels of prostate-specific antigen prior to Ra-223 administration (HR, 7.86; 95% CI, 2.7-27.24; P<0.01) were independent factors, significantly associated with a poorer prognosis. The timing of Ra-223 administration did not significantly affect the survival of patients from the initiation of treatment. Further studies are thus required to determine the optimal timing for Ra-223 administration.
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Med Int (Lond) Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Med Int (Lond) Año: 2023 Tipo del documento: Article País de afiliación: Japón