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不同族裔背景的转移性去势抵抗性前列腺癌男性患者的临床结局。

Clinical outcomes in men of diverse ethnic backgrounds with metastatic castration-resistant prostate cancer.

机构信息

Duke University Medical Center and Duke University, Durham, USA.

Old Dominion University, Norfolk, USA.

出版信息

Ann Oncol. 2020 Jul;31(7):930-941. doi: 10.1016/j.annonc.2020.03.309. Epub 2020 Apr 11.

Abstract

BACKGROUND

We have shown previously in multivariable analysis that black men had 19% lower risk of death than white men with metastatic castration-resistant prostate cancer (mCRPC) treated with a docetaxel and prednisone (DP)-based regimen. The primary goal of this analysis was to compare progression-free survival (PFS), biochemical PFS, ≥50% decline in prostate-specific antigen (PSA) from baseline and objective response rate (ORR) in white, black and Asian men with mCRPC treated with a DP-based regimen.

PATIENTS AND METHODS

Individual patient data from 8820 mCRPC men randomized on nine phase III trials to a DP-containing regimen were combined. Race used in the analysis was based on self-report. End points were PFS, biochemical PSA, ≥50% decline in PSA from baseline and ORR. The proportional hazards and the logistic regression models were employed to assess the prognostic importance of race in predicting outcomes adjusting for established prognostic factors.

RESULTS

Of 8820 patients, 7528 (85%) were white, 500 (6%) were black, 424 were Asian (5%) and 368 (4%) had race unspecified. Median PFS were 8.3 [95% confidence interval (CI) 8.2-8.5], 8.2 (95% CI 7.4-8.8) and 8.3 (95% CI 7.6-8.8) months in white, black and Asian men, respectively. Median PSA PFS were 9.9 (95% CI 9.7-10.4), 8.5 (95% CI 8.0-10.3) and 11.1 (95% CI 9.9-12.5) months in white, black and Asian men, respectively.

CONCLUSIONS

We observed no differences in clinical outcomes by race and ethnic groups in men with mCRPC enrolled on these phase III clinical trials with DP.

摘要

背景

我们之前的多变量分析表明,接受多西他赛和泼尼松(DP)方案治疗的转移性去势抵抗性前列腺癌(mCRPC)的黑人男性死亡风险比白人男性低 19%。本分析的主要目的是比较 DP 方案治疗的 mCRPC 白种人、黑人和亚洲男性的无进展生存期(PFS)、生化无进展生存期(bPFS)、前列腺特异性抗原(PSA)基线下降≥50%和客观缓解率(ORR)。

方法

对 9 项 III 期临床试验中 8820 例 mCRPC 男性患者的个体患者数据进行了合并,分析中使用的种族是基于自我报告。终点是 PFS、bPFS、PSA 基线下降≥50%和 ORR。采用比例风险和逻辑回归模型评估种族对预测结果的预后重要性,同时调整了既定的预后因素。

结果

在 8820 例患者中,7528 例(85%)为白人,500 例(6%)为黑人,424 例(5%)为亚洲人,368 例(4%)种族不详。白人、黑人、亚洲男性的中位 PFS 分别为 8.3 [95%置信区间(CI)8.2-8.5]、8.2(95% CI 7.4-8.8)和 8.3(95% CI 7.6-8.8)个月。白人、黑人、亚洲男性的中位 bPFS 分别为 9.9(95% CI 9.7-10.4)、8.5(95% CI 8.0-10.3)和 11.1(95% CI 9.9-12.5)个月。

结论

在这些 DP 方案 III 期临床试验中,我们没有观察到 mCRPC 患者种族和族裔群体之间的临床结局存在差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1012/7580036/42e8319beb26/nihms-1629458-f0001.jpg

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