The multicentric retrospective BIO-Ra study combined inflammatory indices from peripheral blood and clinical factors in a composite prognostic score for metastatic castration-resistant prostate cancer patients receiving Radium-223 (Ra-223). In the present study, we evaluated (i) the prognostic power of the BIO-Ra score in the framework of the restricted use of Ra-223 promoted by the European Medicines Agency in 2018; (ii) the treatment completion prediction of the BIO-Ra score. Four hundred ninety-four patients from the BIO-Ra cohort were divided into three risk classes accord-ing to the BIO-Ra score to predict the treatment completion rate (p < 0.001 among all the three groups). Patients receiving Ra-223 after restriction (89/494) were at later stages of the disease compared with the pre-restriction cohort (405/494), as a higher percentage of BIO-Ra high-risk classes (46.1% vs. 34.6%) and lower median Overall survival (12.4 vs. 23.7 months, p < 0.001) was observed. Despite this clinically relevant difference, BIO-Ra classes still predicted divergent treatment completion rates in the post-restriction subgroup (72%, 52.2%, and 46.3% of patients belonging to low-, intermediate-, and high-risk classes, respectively). Although the restricted use has increased patients at higher risk with unfavourable outcome after Ra-223 treatment, the BIO-Ra score maintains its prognostic value.

Prognostic Value of the BIO-Ra Score in Metastatic Castration-Resistant Prostate Cancer Patients Treated with Radium-223 after the European Medicines Agency Restricted Use: Secondary Investigations of the Multicentric BIO-Ra Study / Bauckneht, M.; Rebuzzi, S. E.; Ponzano, M.; Borea, R.; Signori, A.; Frantellizzi, V.; Rizzini, E. L.; Mascia, M.; Lavelli, V.; Miceli, A.; De Feo, M. S.; Pisani, A. R.; Nuvoli, S.; Tripoli, V.; Morganti, A. G.; Mammucci, P.; Caponnetto, S.; Mantica, G.; Di Nicola, A. D.; Villano, C.; Cindolo, L.; Morbelli, S.; Sambuceti, G.; Fanti, S.; Costa, R. P.; Spanu, A.; Rubini, G.; Monari, F.; De Vincentis, G.; Fornarini, G.. - In: CANCERS. - ISSN 2072-6694. - 14:7(2022), p. 1744. [10.3390/cancers14071744]

Prognostic Value of the BIO-Ra Score in Metastatic Castration-Resistant Prostate Cancer Patients Treated with Radium-223 after the European Medicines Agency Restricted Use: Secondary Investigations of the Multicentric BIO-Ra Study

Nuvoli S.;Spanu A.;
2022-01-01

Abstract

The multicentric retrospective BIO-Ra study combined inflammatory indices from peripheral blood and clinical factors in a composite prognostic score for metastatic castration-resistant prostate cancer patients receiving Radium-223 (Ra-223). In the present study, we evaluated (i) the prognostic power of the BIO-Ra score in the framework of the restricted use of Ra-223 promoted by the European Medicines Agency in 2018; (ii) the treatment completion prediction of the BIO-Ra score. Four hundred ninety-four patients from the BIO-Ra cohort were divided into three risk classes accord-ing to the BIO-Ra score to predict the treatment completion rate (p < 0.001 among all the three groups). Patients receiving Ra-223 after restriction (89/494) were at later stages of the disease compared with the pre-restriction cohort (405/494), as a higher percentage of BIO-Ra high-risk classes (46.1% vs. 34.6%) and lower median Overall survival (12.4 vs. 23.7 months, p < 0.001) was observed. Despite this clinically relevant difference, BIO-Ra classes still predicted divergent treatment completion rates in the post-restriction subgroup (72%, 52.2%, and 46.3% of patients belonging to low-, intermediate-, and high-risk classes, respectively). Although the restricted use has increased patients at higher risk with unfavourable outcome after Ra-223 treatment, the BIO-Ra score maintains its prognostic value.
2022
Prognostic Value of the BIO-Ra Score in Metastatic Castration-Resistant Prostate Cancer Patients Treated with Radium-223 after the European Medicines Agency Restricted Use: Secondary Investigations of the Multicentric BIO-Ra Study / Bauckneht, M.; Rebuzzi, S. E.; Ponzano, M.; Borea, R.; Signori, A.; Frantellizzi, V.; Rizzini, E. L.; Mascia, M.; Lavelli, V.; Miceli, A.; De Feo, M. S.; Pisani, A. R.; Nuvoli, S.; Tripoli, V.; Morganti, A. G.; Mammucci, P.; Caponnetto, S.; Mantica, G.; Di Nicola, A. D.; Villano, C.; Cindolo, L.; Morbelli, S.; Sambuceti, G.; Fanti, S.; Costa, R. P.; Spanu, A.; Rubini, G.; Monari, F.; De Vincentis, G.; Fornarini, G.. - In: CANCERS. - ISSN 2072-6694. - 14:7(2022), p. 1744. [10.3390/cancers14071744]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/279468
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