Time to castration resistance is a novel prognostic factor of cancer-specific survival in patients with nonmetastatic castration-resistant prostate cancer

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作者
Yuji Hakozaki
Yuta Yamada
Taketo Kawai
Masaki Nakamura
Yuta Takeshima
Takuya Iwaki
Taro Teshima
Yoshitaka Kinoshita
Yoichi Fujii
Yoshiyuki Akiyama
Yusuke Sato
Daisuke Yamada
Motofumi Suzuki
Mayu Kashiwagi-Hakozaki
Tetsuo Ushiku
Haruki Kume
机构
[1] The University of Tokyo Graduate School of Medicine,Department of Urology
[2] NTT Medical Center,Department of Urology
[3] The University of Tokyo,Department of Urology, The Institute of Medical Science
[4] Chiba Tokushukai Hospital,Department of Urology
[5] Tokyo Metropolitan Bokutoh Hospital,Department of Urology
[6] The University of Tokyo,Department of Pathology, Graduate School of Medicine
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摘要
We aimed to identify prognostic factors of cancer-specific survival (CSS) in non-metastatic castration-resistant prostate cancer (M0CRPC) patients. The final analysis of this retrospective cohort included 82 patients who were diagnosed as M0CRPC between 1998 and 2018 at the University of Tokyo Hospital. CRPC was defined as prostate-specific antigen (PSA) progression (increased PSA ≥ 25% and ≥ 2 ng/mL above the nadir or detection of a metastatic lesion). The median value of age and PSA at the time of CRPC were 76 (range 55–94) years and 2.84 (range 2.04–22.5) ng/mL, respectively. The median follow-up time from CRPC diagnosis was 38 (range 3–188) months. The prognostic factors of CSS were ‘PSA doubling time (PSADT) ≤ 3 months’, ‘time to CRPC diagnosis from the start of androgen deprivation therapy (TTCRPC) ≤ 12 months’, of which TTCRPC was a novel risk factor of CSS. In the multivariate analysis, ‘PSADT ≤ 3 months’ and TTCRPC ≤ 12 months’ remained as statistically significant predictors of CSS. Novel risk stratification was developed based on the number of these risk factors. The high-risk group showed a hazard ratio of 4.416 (95% confidence interval 1.701–11.47, C-index = 0.727).
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