Division of Urology, Department of Surgery, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Duke Cancer Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Cancer. 2020 Jul 15;126(14):3274-3280. doi: 10.1002/cncr.32933. Epub 2020 May 6.
The impact of race on prostate cancer skeletal-related events (SREs) remains understudied. In the current study, the authors tested the impact of race on time to SREs and overall survival in men with newly diagnosed, bone metastatic castration-resistant prostate cancer (mCRPC).
The authors performed a retrospective study of patients from 8 Veterans Affairs hospitals who were newly diagnosed with bone mCRPC in the year 2000 or later. SREs comprised pathologic fracture, spinal cord compression, radiotherapy to the bone, or surgery to the bone. Time from diagnosis of bone mCRPC to SREs and overall mortality was estimated using the Kaplan-Meier method. Cox models tested the association between race and SREs and overall mortality.
Of 837 patients with bone mCRPC, 232 patients (28%) were black and 605 (72%) were nonblack. At the time of diagnosis of bone mCRPC, black men were found to be more likely to have more bone metastases compared with nonblack men (29% vs 19% with ≥10 bone metastases; P = .021) and to have higher prostate-specific antigen (41.7 ng/mL vs 29.2 ng/mL; P = .005) and a longer time from the diagnosis of CRPC to metastasis (17.9 months vs 14.3 months; P < .01). On multivariable analysis, there were no differences noted with regard to SRE risk (hazard ratio [HR], 0.80; 95% CI, 0.59-1.07) or overall mortality (HR, 0.87; 95% CI, 0.73-1.04) between black and nonblack people, although the HRs were <1, which suggested the possibility of better outcomes.
No significant association between black race and risk of SREs and overall mortality was observed in the current study. These data have suggested that efforts to understand the basis for the excess risk of aggressive prostate cancer in black men should focus on cancer development and progression in individuals with early-stage disease.
种族对前列腺癌骨骼相关事件(SREs)的影响仍研究不足。在本研究中,作者检测了种族对新诊断为骨转移去势抵抗性前列腺癌(mCRPC)男性的 SREs 发生时间和总生存的影响。
作者对 8 家退伍军人事务医院在 2000 年或之后新诊断为骨 mCRPC 的患者进行了回顾性研究。SREs 包括病理性骨折、脊髓压迫、骨放疗或骨手术。使用 Kaplan-Meier 方法估计从诊断为骨 mCRPC 到 SREs 和总死亡率的时间。Cox 模型检测种族与 SREs 和总死亡率之间的关联。
在 837 例骨 mCRPC 患者中,232 例(28%)为黑人,605 例(72%)为非黑人。在诊断为骨 mCRPC 时,与非黑人相比,黑人男性更有可能有更多的骨转移(29%比 19%有≥10 处骨转移;P=0.021),且前列腺特异性抗原水平更高(41.7ng/mL 比 29.2ng/mL;P=0.005),从 CRPC 诊断到转移的时间更长(17.9 个月比 14.3 个月;P<0.01)。多变量分析显示,黑人与非黑人之间 SRE 风险(危险比[HR],0.80;95%置信区间,0.59-1.07)或总死亡率(HR,0.87;95%置信区间,0.73-1.04)无差异,尽管 HR<1,这表明黑人可能有更好的结局。
在本研究中,未观察到黑种人与 SREs 发生风险和总死亡率之间存在显著关联。这些数据表明,为了解释黑人男性中侵袭性前列腺癌风险增加的原因,应该集中研究个体在疾病早期的癌症发展和进展。