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Sequencing Life-Prolonging Agents in Castration-Resistant Prostate Cancer Patients: Comparison of Sequences With and Without 223 Ra.

Authors :
Caffo O
Frantellizzi V
Monari F
Galli L
Costa RP
Pinto C
Tucci M
Baldari S
Facchini G
Bortolus R
Alongi F
Alongi P
Donner D
Fanti S
Sbrana A
Morabito A
Masini C
Zichi C
Pignata S
Borsatti E
Salgarello M
Spada M
De Giorgi U
Lo Re G
Cortesi E
De Vincentis G
Source :
Cancer biotherapy & radiopharmaceuticals [Cancer Biother Radiopharm] 2021 Jun; Vol. 36 (5), pp. 391-396. Date of Electronic Publication: 2021 Mar 25.
Publication Year :
2021

Abstract

Background: The retrospective studies that have so far described the outcomes of the sequential use of life-prolonging agents (LPAs) did not include metastatic castration-resistant prostate cancer (mCRPC) patients who received radium-223 ( <superscript>223</superscript> Ra) as part of their treatment. Consequently, it is not known whether including <superscript>223</superscript> Ra in the therapeutic sequence has an impact on cumulative survival. The aim of this study was to evaluate this impact by comparing the cumulative overall survival (OS) in two series of mCRPC patients sequentially treated with two or three LPAs after first-line docetaxel (DOC), including <superscript>223</superscript> Ra and not. Materials and Methods: The authors retrospectively reviewed the records of mCRPC patients with bone involvement alone who received two or three LPAs (including <superscript>223</superscript> Ra) after first-line DOC. The control group was a contemporary series of mCRPC patients with bone involvement alone treated with sequences of two or three LPAs other than <superscript>223</superscript> Ra after first-line DOC. Results: Median cumulative OS was 40.6 months in the <superscript>223</superscript> Ra group of 78 patients and 36.2 months in the non- <superscript>223</superscript> Ra group of 186 patients ( p  = 0.08). OS outcomes were significantly influenced by the number of treatment lines, and baseline Eastern Cooperative Oncology Group performance status (PS) and prostate-specific antigen levels. Conclusions: To the best of the authors' knowledge, this is the first study designed to evaluate the impact of introducing <superscript>223</superscript> Ra in the treatment sequences for mCRPC patients, and the results show that its use does not negatively affect cumulative OS.

Details

Language :
English
ISSN :
1557-8852
Volume :
36
Issue :
5
Database :
MEDLINE
Journal :
Cancer biotherapy & radiopharmaceuticals
Publication Type :
Academic Journal
Accession number :
33769088
Full Text :
https://doi.org/10.1089/cbr.2020.4442