TY - JOUR
T1 - Early-onset prostate cancer is associated with increased risks of disease progression and cancer-specific mortality
AU - Shih, Hung Jen
AU - Fang, Su Chen
AU - An, Lu
AU - Shao, Yu Hsuan J.
N1 - Funding Information:
We would like to thank the Health and Welfare Data Science Center Data of Taiwan for providing data. This study was supported by the Ministry of Science and Technology, Taiwan, under grant MOST‐108‐2314‐B‐038‐091 and Taipei Medical University–Wan Fang Hospital under grant 108TMU‐WFH‐09.
Publisher Copyright:
© 2020 Wiley Periodicals LLC
PY - 2021/2
Y1 - 2021/2
N2 - Objective: Prostate cancer (PCa) incidence has stabilized but not in patients at a young age. We assessed patient characteristics and disease progression in early-onset PCa. Methods: A retrospective cohort of 28,039 newly diagnosed PCa patients aged ≥35 years was constructed using the Taiwan Cancer Registry in 2008–2016. Patients were categorized by age at diagnosis (≤54, 55–59, 60–69, 70–74, and ≥75 years). The clinical stage at diagnosis, Gleason score, prostate-specific antigen level at diagnosis, Charlson's comorbidity index, and primary and secondary treatments for PCa were included in the analysis. All-cause mortality and prostate cancer-specific mortality (PCSM) were reported. Hazard ratios (HRs) and 95% confidence intervals (CIs) estimating the risks of death and of receiving secondary cancer treatment were generated by Cox hazard models. Results: In patients aged ≤54, 55–59, and 60–69 years, about 60% of them in each group were classified into the high-risk, very high-risk, or metastatic group. However, young patients ≤54 years had a higher risk of PCSM than patients aged 60–69 years (HR = 1.22; 95% CI = 1.10–1.49). This trend of an increased risk in PCSM remained for high-risk, very high-risk, or metastatic patients (HR = 1.24; 95% CI = 1.01–1.51), but not in low- or intermediate-risk patients. Besides, young patients diagnosed with high-risk diseases had the highest risk of receiving secondary cancer treatment within 180 days after completing primary treatment among all age groups (HR = 1.32; 95% CI = 1.07–1.63). Conclusions: PCa arising in young patients ≤54 years of age, especially those with a high risk or metastatic form, might be more aggressive than that in other age groups.
AB - Objective: Prostate cancer (PCa) incidence has stabilized but not in patients at a young age. We assessed patient characteristics and disease progression in early-onset PCa. Methods: A retrospective cohort of 28,039 newly diagnosed PCa patients aged ≥35 years was constructed using the Taiwan Cancer Registry in 2008–2016. Patients were categorized by age at diagnosis (≤54, 55–59, 60–69, 70–74, and ≥75 years). The clinical stage at diagnosis, Gleason score, prostate-specific antigen level at diagnosis, Charlson's comorbidity index, and primary and secondary treatments for PCa were included in the analysis. All-cause mortality and prostate cancer-specific mortality (PCSM) were reported. Hazard ratios (HRs) and 95% confidence intervals (CIs) estimating the risks of death and of receiving secondary cancer treatment were generated by Cox hazard models. Results: In patients aged ≤54, 55–59, and 60–69 years, about 60% of them in each group were classified into the high-risk, very high-risk, or metastatic group. However, young patients ≤54 years had a higher risk of PCSM than patients aged 60–69 years (HR = 1.22; 95% CI = 1.10–1.49). This trend of an increased risk in PCSM remained for high-risk, very high-risk, or metastatic patients (HR = 1.24; 95% CI = 1.01–1.51), but not in low- or intermediate-risk patients. Besides, young patients diagnosed with high-risk diseases had the highest risk of receiving secondary cancer treatment within 180 days after completing primary treatment among all age groups (HR = 1.32; 95% CI = 1.07–1.63). Conclusions: PCa arising in young patients ≤54 years of age, especially those with a high risk or metastatic form, might be more aggressive than that in other age groups.
KW - early-onset
KW - prostate cancer
KW - prostate cancer-specific mortality
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U2 - 10.1002/pros.24087
DO - 10.1002/pros.24087
M3 - Article
C2 - 33152137
AN - SCOPUS:85096702802
SN - 0270-4137
VL - 81
SP - 118
EP - 126
JO - Prostate
JF - Prostate
IS - 2
ER -