PSA Doubling Time 4.65 months as an Optimal Cut-off of Japanese Nonmetastatic Castration-Resistant Prostate Cancer: Multi-institutional Study of Japanese Urological Oncology Group (JUOG)

Author:

Sakamoto Shinichi1,Sato Kodai1,Kimura Takahiro2,Matsui Yoshiyuki3,Shiraishi Yusuke4,Hashimoto Kohei5,Miyake Hideaki6,Narita Shintaro7,Miki Jun8,Matsumoto Ryuji9,Kato Takuma10,Saito Toshihiro11,Tomida Ryotaro12,Shiota Masaki13,Akira Joraku14,Terada Naoki15,Shigetaka Suekane16,Kaneko Tomoyuki17,Tatarano Shuichi18,Nishiyama Naotaka19,Kawakami Eiryo1,Ichikawa Tomohiko1,Kitamura Hiroshi19,Yoshio Yuko20,Yoshino Takayuki21

Affiliation:

1. Chiba University Graduate School of Medicine

2. Jikei University School of Medicine

3. National Cancer Center

4. Shizuoka General Hospital

5. Sapporo Medical University

6. Hamamatsu University School of Medicine

7. Akita University

8. The Jikei University School of Medicine, Kashiwa Hospital

9. Hokkaido University

10. Kagawa University

11. Niigata Cancer Center Hospital

12. Shikoku Cancer Center

13. Kyushu University

14. Ibaraki Prefectural Hospital, Ibaraki Cancer Center

15. University of Fukui

16. Kurume University

17. Teikyo University

18. Kagoshima University

19. University of Toyama

20. Mie University

21. University of Tsukuba

Abstract

Abstract A multicenter study of nonmetastatic castration-resistant prostate cancer (nmCRPC) was conducted to examine the prognostic to identify the optimal cut-off value of prostate-specific antigen (PSA) doubling time (PSADT) in Japanese nmCRPC. Of the 515 patients diagnosed and treated for nmCRPC at 25 participating Japanese Urological Oncology Group centers, 450 patients with complete clinical information were included. The prognostic values of clinical factors were evaluated with respect to prostate specific antigen progression-free (PFS), cancer-specific survival (CSS), and overall survival (OS). The optimal cutoff value of PSADT was identified using survival tree analysis by Python. The Median PSA and PSADT at diagnosis of nmCRPC were 3.3 ng/ml, and 5.2 months, respectively. Patients treated with novel hormonal therapy (NHT) showed significantly longer PFS (HR: Hazard Ratio 0.38, p < .0001) and PFS2 (HR 0.45, p < .0001) than those treated with vintage nonsteroidal antiandrogen agent (Vintage). The survival tree identified 4.65 months as the most prognostic PSADT cutoff point. Among the clinical and pathological factors PSADT of < 4.65 months remained an independent prognostic factor for OS (HR 2.96, p = .0003) and CSS (HR 3.66, p < .0001). Current data represented optimal cut-off of PSADT 4.65 months for a Japanese nmCRPC.

Publisher

Research Square Platform LLC

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