Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/237894
Type: Artigo de periódico
Title: Factors Affecting 223ra Therapy: Clinical Experience After 532 Cycles From A Single Institution
Abstract: Purpose: The aim of this study was to identify baseline features that predict outcome in 223Ra therapy. Methods: We retrospectively reviewed 110 patients with metastatic castration-resistant prostate cancer treated with 223Ra. End points were overall survival (OS), progression-free survival (PFS), bone event-free survival (BeFS), and bone marrow failure (BMF). The following parameters were evaluated prior to the first 223Ra cycle: serum levels of hemoglobin (Hb), prostate-specific antigen (PSA), alkaline phosphatase (ALP), Eastern Cooperative Oncology Group (ECOG) status, pain score, use of chemotherapy, and external beam radiation therapy (EBRT). During/after 223Ra we evaluated: the total number of radium cycles (RaTot), the PSA doubling time (PSADT), and the use of chemotherapy, EBRT, abiraterone, and enzalutamide. Results: A significant reduction of ALP (p < 0.001) and pain score (p = 0.041) occurred throughout the 223 Ra cycles. The risk of progression was associated with declining ECOG status [hazard ratio (HR) = 3.79; p < 0.001] and decrease in PSADT (HR = 8.22; p < 0.001). RaTot, ALP, initial ECOG status, initial pain score, and use of abiraterone were associated with OS (p ≤ 0.008), PFS (p ≤ 0.003), and BeFS (p ≤ 0.020). RaTot, ALP, initial ECOG status, and initial pain score were significantly associated with BMF (p ≤ 0.001) as well as Hb (p < 0.001) and EBRT (p = 0.009). On multivariable analysis, only RaTot and abiraterone remained significantly associated with OS (p < 0.001; p = 0.033, respectively), PFS (p < 0.001; p = 0.041, respectively), and BeFS (p < 0.001; p = 0.019, respectively). Additionally, RaTot (p = 0.027) and EBRT (p = 0.013) remained significantly associated with BMF. Conclusion: Concomitant use of abiraterone and 223Ra seems to have a beneficial effect, while the EBRT may increase the risk of BMF. © 2015, Springer-Verlag Berlin Heidelberg.
Editor: springer berlin
Citation: European Journal Of Nuclear Medicine And Molecular Imaging. Springer Berlin, v. 43, n. 1, p. 8 - 20, 2016.
Rights: fechado
Identifier DOI: 10.1007/s00259-015-3185-4
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-84951906696&partnerID=40&md5=66e6f357e36011cb7ca66ddd1a97a82c
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

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