Fracture risk and survival outcomes in metastatic castration-resistant prostate cancer patients sequentially treated with abiraterone acetate and RADIUM-223

Purpose To evaluate the fracture risk and survival outcomes in patients with metastatic castration-resistant prostate cancer (mCRPC) who received sequentially abiraterone acetate (AA) and radium 223 [223Ra]RaCl 2 in the daily clinical practice. Materials We retrospectively reviewed the records of mC...

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Veröffentlicht in:European journal of nuclear medicine and molecular imaging 2020-10, Vol.47 (11), p.2633-2638
Hauptverfasser: Caffo, Orazio, Frantellizzi, Viviana, Tucci, Marcello, Galli, Luca, Monari, Fabio, Baldari, Sergio, Masini, Cristina, Bortolus, Roberto, Facchini, Gaetano, Alongi, Pierpaolo, Agostini, Stefania, Zichi, Clizia, Biasco, Elisa, Fanti, Stefano, Pignata, Salvatore, Filice, Angelina, Borsatti, Eugenio, Rossetti, Sabrina, Spada, Massimiliano, Cortesi, Enrico, De Vincentis, Giuseppe
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container_issue 11
container_start_page 2633
container_title European journal of nuclear medicine and molecular imaging
container_volume 47
creator Caffo, Orazio
Frantellizzi, Viviana
Tucci, Marcello
Galli, Luca
Monari, Fabio
Baldari, Sergio
Masini, Cristina
Bortolus, Roberto
Facchini, Gaetano
Alongi, Pierpaolo
Agostini, Stefania
Zichi, Clizia
Biasco, Elisa
Fanti, Stefano
Pignata, Salvatore
Filice, Angelina
Borsatti, Eugenio
Rossetti, Sabrina
Spada, Massimiliano
Cortesi, Enrico
De Vincentis, Giuseppe
description Purpose To evaluate the fracture risk and survival outcomes in patients with metastatic castration-resistant prostate cancer (mCRPC) who received sequentially abiraterone acetate (AA) and radium 223 [223Ra]RaCl 2 in the daily clinical practice. Materials We retrospectively reviewed the records of mCRPC patients who received [223Ra]RaCl 2 immediately after progressing during an AA treatment line in everyday clinical practice. Results We reviewed data of a consecutive series of 94 mCRPC patients. Most of the patients (85.1%) received [223Ra]RaCl 2 as second- or third-line treatment. [223Ra]RaCl 2 treatment was well-tolerated; there were only four cases of grade 3 anaemia, two cases of grade 3 leukopenia and one case of grade 3 neutropenia. The overall fracture rate is 2.1%; one fracture was recorded during the course of [223Ra]RaCl 2 treatment, and one was recorded 1 month after its end. The fractures both occurred at metastatic sites. Median OS from [223Ra]RaCl 2 start was more than 14 months regardless of the treatment line when [223Ra]RaCl 2 was administered. Conclusion The findings of this study show that the treatment with [223Ra]RaCl 2 immediately after AA was active and safe with a very low risk of a fracture. Thus, the present observational report makes a valuable contribution to the current debate concerning the risks and benefits of including [223Ra]RaCl 2 in the therapeutic algorithm.
doi_str_mv 10.1007/s00259-020-04796-w
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Materials We retrospectively reviewed the records of mCRPC patients who received [223Ra]RaCl 2 immediately after progressing during an AA treatment line in everyday clinical practice. Results We reviewed data of a consecutive series of 94 mCRPC patients. Most of the patients (85.1%) received [223Ra]RaCl 2 as second- or third-line treatment. [223Ra]RaCl 2 treatment was well-tolerated; there were only four cases of grade 3 anaemia, two cases of grade 3 leukopenia and one case of grade 3 neutropenia. The overall fracture rate is 2.1%; one fracture was recorded during the course of [223Ra]RaCl 2 treatment, and one was recorded 1 month after its end. The fractures both occurred at metastatic sites. Median OS from [223Ra]RaCl 2 start was more than 14 months regardless of the treatment line when [223Ra]RaCl 2 was administered. Conclusion The findings of this study show that the treatment with [223Ra]RaCl 2 immediately after AA was active and safe with a very low risk of a fracture. 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Materials We retrospectively reviewed the records of mCRPC patients who received [223Ra]RaCl 2 immediately after progressing during an AA treatment line in everyday clinical practice. Results We reviewed data of a consecutive series of 94 mCRPC patients. Most of the patients (85.1%) received [223Ra]RaCl 2 as second- or third-line treatment. [223Ra]RaCl 2 treatment was well-tolerated; there were only four cases of grade 3 anaemia, two cases of grade 3 leukopenia and one case of grade 3 neutropenia. The overall fracture rate is 2.1%; one fracture was recorded during the course of [223Ra]RaCl 2 treatment, and one was recorded 1 month after its end. The fractures both occurred at metastatic sites. Median OS from [223Ra]RaCl 2 start was more than 14 months regardless of the treatment line when [223Ra]RaCl 2 was administered. Conclusion The findings of this study show that the treatment with [223Ra]RaCl 2 immediately after AA was active and safe with a very low risk of a fracture. 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Materials We retrospectively reviewed the records of mCRPC patients who received [223Ra]RaCl 2 immediately after progressing during an AA treatment line in everyday clinical practice. Results We reviewed data of a consecutive series of 94 mCRPC patients. Most of the patients (85.1%) received [223Ra]RaCl 2 as second- or third-line treatment. [223Ra]RaCl 2 treatment was well-tolerated; there were only four cases of grade 3 anaemia, two cases of grade 3 leukopenia and one case of grade 3 neutropenia. The overall fracture rate is 2.1%; one fracture was recorded during the course of [223Ra]RaCl 2 treatment, and one was recorded 1 month after its end. The fractures both occurred at metastatic sites. Median OS from [223Ra]RaCl 2 start was more than 14 months regardless of the treatment line when [223Ra]RaCl 2 was administered. Conclusion The findings of this study show that the treatment with [223Ra]RaCl 2 immediately after AA was active and safe with a very low risk of a fracture. Thus, the present observational report makes a valuable contribution to the current debate concerning the risks and benefits of including [223Ra]RaCl 2 in the therapeutic algorithm.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32249345</pmid><doi>10.1007/s00259-020-04796-w</doi><tpages>6</tpages></addata></record>
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subjects Abiraterone Acetate - adverse effects
Bone Neoplasms - drug therapy
Cardiology
Humans
Imaging
Male
Medicine
Medicine & Public Health
Nuclear Medicine
Oncology
Oncology – Genitourinary
Original Article
Orthopedics
Prostatic Neoplasms, Castration-Resistant - drug therapy
Radiology
Radium - adverse effects
Retrospective Studies
Treatment Outcome
title Fracture risk and survival outcomes in metastatic castration-resistant prostate cancer patients sequentially treated with abiraterone acetate and RADIUM-223
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