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. 2020 Mar 6;10(1):4240.
doi: 10.1038/s41598-020-61235-4.

Second-line Hormonal Therapy for the Management of Metastatic Castration-resistant Prostate Cancer: a Real-World Data Study Using a Claims Database

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Second-line Hormonal Therapy for the Management of Metastatic Castration-resistant Prostate Cancer: a Real-World Data Study Using a Claims Database

Jui-Ming Liu et al. Sci Rep. .

Abstract

We evaluated the efficacy of second-line hormonal therapy for treatment of metastatic castration-resistant prostate cancer (mCRPC) in a real-world retrospective study. We conducted a population-based real-world cohort study of 258 mCRPC patients between 2014 and 2018 using the Chang Gung Research Database (CGRD) of Taiwan. The second-line hormonal therapy included abiraterone acetate and enzalutamide. The clinical efficacy outcomes were overall survival (OS) and prostate-specific antigen (PSA) doubling time. The median PSA level was also assessed. In total, 223 mCRPC patients who underwent second-line hormonal therapy met all of the inclusion and exclusion criteria for this study. Among them, 65 (29.1%) patients were in the PSA response group and 158 (70.9%) were in the non-response group. The median age was 72.9 years. The median OS was 12.3 months (range: 9.9-19.9 months) and 9.6 months (range: 5.3-15.9 months) in the response and non-response groups, respectively, and the respective PSA doubling times were 9.0 months (range: 4.4-11.6 months) and 3.9 months (range: 2.2-9.1 months), with a median follow-up period of 10.5 months. A significantly longer median OS was seen in the PSA response group. This real-world database study demonstrated that clinical outcomes of second-line hormonal therapy were better in patients with a PSA response. Further studies are warranted to achieve a better understanding of second-line hormonal therapy for mCRPC in Asian populations.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Patient selection.
Figure 2
Figure 2
The median PSA levels in response and non-response groups of mCRPC patients with second-line hormonal therapy. mCRPC: metastatic castration-resistant prostate cancer.
Figure 3
Figure 3
The cumulative survival calculated by the Kaplan-Meier analysis of mCRPC patients with second-line hormonal therapy. mCRPC: metastatic castration-resistant prostate cancer.

References

    1. Huggins C, Hodges CV. Studies on prostatic cancer. I. The effect of castration, of estrogen and androgen injection on serum phosphatases in metastatic carcinoma of the prostate. CA Cancer J. Clin. 1972;22:232–240. doi: 10.3322/canjclin.22.4.232. - DOI - PubMed
    1. de Bono JS, et al. Abiraterone and increased survival in metastatic prostate cancer. N. Engl. J. Med. 2011;364:1995–2005. doi: 10.1056/NEJMoa1014618. - DOI - PMC - PubMed
    1. Scher HI, et al. Increased survival with enzalutamide in prostate cancer after chemotherapy. N. Engl. J. Med. 2012;367:1187–1197. doi: 10.1056/NEJMoa1207506. - DOI - PubMed
    1. Ryan CJ, et al. Abiraterone in metastatic prostate cancer without previous chemotherapy. N. Engl. J. Med. 2013;368:138–148. doi: 10.1056/NEJMoa1209096. - DOI - PMC - PubMed
    1. Beer TM, et al. Enzalutamide in metastatic prostate cancer before chemotherapy. N. Engl. J. Med. 2014;371:424–433. doi: 10.1056/NEJMoa1405095. - DOI - PMC - PubMed

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