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局限性前列腺癌患者不同风险组的前列腺癌特异性死亡率负担:对研究和临床试验重点的影响。

Prostate cancer-specific mortality burden by risk group among men with localized disease: Implications for research and clinical trial priorities.

机构信息

Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Harvard Medical School, Boston, Massachusetts.

出版信息

Prostate. 2020 Sep;80(13):1128-1133. doi: 10.1002/pros.24041. Epub 2020 Jul 13.

Abstract

OBJECTIVE

To estimate contemporary population-based patterns of the relative burden of prostate cancer-specific mortality (PCSM) attributable to each N0M0 prostate cancer risk-group, that may guide prioritization in research, trial design, and clinical practice.

METHODS

We categorized 2004-2015 Surveillance, Epidemiology, and End Results database patients by risk group (low, favorable intermediate, unfavorable intermediate, high, and very highrisk). Using the Fine-Gray method, we calculated the relative burden of 10-year PCSM attributable to each risk group.

RESULTS

Among N = 337 162 men (6.8-year median follow-up; median age 65 years), the relative proportion of low-, favorable intermediate-, unfavorable intermediate-, high-, and very high-risk diagnoses were 29.9% (N = 100 969), 31.1% (N = 104 696), 17.9% (N = 60 360), 18.1% (N = 61 023), and 3.0% (N = 10 114). Within 10 years of diagnosis, among patients who died of prostate cancer (N = 15 064), 5.0% (N = 746) had low-risk, 13.7% (N = 2060) had favorable intermediate-risk, 16.1% (N = 2429) had unfavorable intermediate-risk, 47.8% (N = 7196) had high-risk, and 17.5% (N = 2633) had very high-risk disease at diagnosis. Patients aged 65 and older accounted for 51.9% of all diagnoses and 72.3% of 10-year PCSM. Although black patients accounted for 15.0% of low-risk diagnoses, they accounted for 20.6% of 10-year PCSM. White patients accounted for 80.3% of low-risk diagnoses and 75.7% of 10-year PCSM.

CONCLUSION

Although high-risk and very high-risk disease account for one-fifth of diagnoses, they account for two-thirds of 10-year PCSM. Older patients and black patients with low-risk disease accounted for a disproportionately large proportion of deaths. These findings support targeting research toward high-risk disease and ensuring adequate representation of older and black men in clinical trials.

摘要

目的

评估基于人群的前列腺癌特异性死亡率(PCSM)归因于每个 N0M0 前列腺癌风险组的相对负担,以指导研究、试验设计和临床实践中的优先级排序。

方法

我们通过风险组(低、中有利、中不利、高和非常高风险)对 2004-2015 年监测、流行病学和最终结果数据库中的患者进行分类。使用 Fine-Gray 方法,我们计算了每个风险组 10 年 PCSM 的归因相对负担。

结果

在 337162 名男性患者中(中位随访 6.8 年;中位年龄 65 岁),低、中有利、中不利、高和非常高风险诊断的相对比例分别为 29.9%(N=100969)、31.1%(N=104696)、17.9%(N=60360)、18.1%(N=61023)和 3.0%(N=10114)。在诊断后 10 年内,死于前列腺癌的患者(N=15064)中,5.0%(N=746)为低风险,13.7%(N=2060)为中有利风险,16.1%(N=2429)为中不利风险,47.8%(N=7196)为高风险,17.5%(N=2633)为非常高风险。65 岁及以上的患者占所有诊断的 51.9%,占 10 年 PCSM 的 72.3%。尽管黑人患者占低风险诊断的 15.0%,但他们占 10 年 PCSM 的 20.6%。白人患者占低风险诊断的 80.3%和 10 年 PCSM 的 75.7%。

结论

尽管高风险和非常高风险疾病占诊断的五分之一,但占 10 年 PCSM 的三分之二。年龄较大的患者和患有低风险疾病的黑人患者占死亡人数的比例不成比例地较大。这些发现支持将研究重点放在高危疾病上,并确保在临床试验中充分代表老年和黑人男性。

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