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 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 1619-7070 1619-7089 |
DOI: | 10.1007/s00259-020-04796-w |