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Submitted
Abstract
Frequency and clinical significance of CDK12 mutation in Metastatic Hormone-sensitive Prostate Cancer
Non-Moderated Poster Abstract
Meta Analysis / Systematic Review
Oncology: Prostate
Author's Information
4
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China
SHUN ZHANG explorershun@126.com Nanjing Drum Tower Hospital Department of Urology NAN JING China *
JUNLONG ZHUANG zhuangjl-2008@163.com Nanjing Drum Tower Hospital Department of Urology NAN JING China -
xuefeng_qiu@nju.edu.cn Nanjing Drum Tower Hospital Department of Urology NAN JING China -
HONGQIAN GUO dr.ghq@163.com Nanjing Drum Tower Hospital Department of Urology NAN JING China -
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Abstract Content
To investigate the frequency and prognostic significance of CDK12 mutation in Metastatic Hormone-sensitive Prostate(mHSPC).
The frequency of CDK12 mutation of 91 patients with mHSPC were detected by Next Generation Sequencing(NGS). The clinical information of patients was collected. The prognostic significance of CDK12 mutation was analyzed by time to castration resistance.
We detected CDK12 mutation in 11 of 91(12.09%)patients. There was a significant difference between CDK12 mutation and time to castration resistance(χ2=6.278,P=0.012). Logistic regression analysis showed that CDK12 mutation significantly increased the risk of mHSPC patients progressing to mCRPC stage within 12 months(OR=5.86, 95% CI:1.46-23.49, P=0.013). Also, the ISUP subgroup was an independent risk factor(OR=2.92, 95% CI:1.23-6.92, P=0.015).
The frequency of CDK12 mutation in Chinese population is much higher than that in Caucasian. CDK12 is an important indicator of poor prognostic, which can be used as an effective biomarker to predict the prognosis of patients with mHSPC.
Prostate cancer; Metastatic Hormone-sensitive Prostate Cancer; CDK12; Prognostic
https://storage.unitedwebnetwork.com/files/1237/55201fb63c2dea0df150126204760318.png
Mutation Profiles of 91 Patients with Metastatic Hormone-Sensitive Prostate Cancer (mHSPC)
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Clinical Characteristics of 91 mHSPC Patients
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Logistic Regression Analysis of Factors Associated with Progression to mCRPC
 
 
 
 
2059
 
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