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Clinical Outcome and Prognostic Variables of Second-line Therapy for Patients With Castration-resistant Prostate Cancer After Failure of First-line Androgen Receptor Axis-targeted Therapy.
Fujiwara, Motohiro; Fujiwara, Ryo; Oguchi, Tomohiko; Komai, Yoshinobu; Numao, Noboru; Yamamoto, Shinya; Yonese, Junji; Yuasa, Takeshi.
Affiliation
  • Fujiwara M; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan motohiro.fujiwara@gmail.com.
  • Fujiwara R; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Oguchi T; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Komai Y; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Numao N; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Yamamoto S; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Yonese J; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Yuasa T; Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Anticancer Res ; 42(4): 2123-2130, 2022 Apr.
Article in En | MEDLINE | ID: mdl-35347036
ABSTRACT

BACKGROUND:

Despite the rapid introduction of androgen receptor-targeted agents (ARTA) into clinical practice for castration-resistant prostate cancer (CRPC), the optimal treatment strategy after first-line ARTA remains unclear. The object of this study was to clarify clinical outcomes of second-line therapy for CRPC after first-line ARTA. PATIENTS AND

METHODS:

The medical records of 130 consecutive patients with CRPC with disease progression during first-line ARTA and who started second-line therapy at our Institution between 2014 and 2020 were analyzed.

RESULTS:

A total of 130 patients with CRPC were identified. Ninety patients underwent ARTA-ARTA treatment, and 40 patients underwent ARTA-docetaxel treatment. The median observation period after second-line ARTA or docetaxel administration was 14.2 months. The prostate-specific antigen response rates overall, and after second-line ARTA, and docetaxel were 26.8%, 24.7%, and 31.6%, respectively. The median progression-free survival (PFS) and 1- and 2-year PFS rates of second-line therapy were 7.9 months and 34.6% and 15.4%, respectively. The median overall survival (OS) and 1- and 2-year OS rates were 27.4 months and 81.8%, and 54.9%, respectively. Multivariate analyses for OS disclosed that a C-reactive protein over the upper limit of normal and time from first-line ARTA to progression under 12 months were associated with shorter OS. Prostate-specific antigen response, PFS and OS of second-line therapy were not significantly different between second-line ARTA and docetaxel.

CONCLUSION:

There was no significant difference in OS between ARTA-ARTA and ARTA-docetaxel groups in the present study, suggesting that second-line ARTA might be the preferred treatment after initial failure of ARTA.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Androgen Receptor Antagonists / Prostatic Neoplasms, Castration-Resistant Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Anticancer Res Year: 2022 Document type: Article Affiliation country: Japan Publication country: GR / GRECIA / GREECE / GRÉCIA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Androgen Receptor Antagonists / Prostatic Neoplasms, Castration-Resistant Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Anticancer Res Year: 2022 Document type: Article Affiliation country: Japan Publication country: GR / GRECIA / GREECE / GRÉCIA