Real-world outcomes of radium-223 dichloride for metastatic castration resistant prostate cancer

Timing of radium-223 (Ra-223) in metastatic castration-resistant prostate cancer (mCRPC) remains challenging due to alternative options and short window of opportunity. : Ra-223 treated patients in the CAPRI-registry were included. Outcomes were evaluated based on treatment line of Ra-223. Out of 28...

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Veröffentlicht in:Future oncology (London, England) England), 2020-07, Vol.16 (19), p.1371-1384
Hauptverfasser: Kuppen, Malou Cp, Westgeest, Hans M, van der Doelen, Maarten J, van den Eertwegh, Alphonsus Jm, Coenen, Jules Llm, Aben, Katja Kh, van den Bergh, Alphons Cm, Bergman, Andries M, den Bosch, Joan van, Celik, Filiz, Hendriks, Mathijs P, Lavalaye, Jules, der Meer, Saskia van, Polee, Marco B, Somford, Diederik M, van Oort, Inge M, Uyl-de Groot, Carin A, Gerritsen, Winald R
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Sprache:eng
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Zusammenfassung:Timing of radium-223 (Ra-223) in metastatic castration-resistant prostate cancer (mCRPC) remains challenging due to alternative options and short window of opportunity. : Ra-223 treated patients in the CAPRI-registry were included. Outcomes were evaluated based on treatment line of Ra-223. Out of 285 patients, 49% received Ra-223 in line ≥3. 51% completed six Ra-223 injections and 34% had a symptomatic skeletal event after first Ra-223 without differences between subgroups. After correction of known prognostic factors Ra-223 in line ≥3 (HR: 3.267; 95% CI: 1.689–6.317; p < 0.01) remained associated with worse OS. : In the Netherlands, Ra-223 was mainly started as second or third mCRPC-treatment in 2014–2018. Later timing of Ra-223 did affect OS, but not treatment completion and occurrence of symptomatic skeletal events.
ISSN:1479-6694
1744-8301
DOI:10.2217/fon-2020-0039