Bello Jibril Oyekunle
Department of Surgery, University of Ilorin Teaching Hospital, Ilorin, Nigeria.
BMC Urol. 2017 May 30;17(1):39. doi: 10.1186/s12894-017-0228-0.
Though it is well established that black men are at higher risk of prostate cancer (PCa) very little is known about the disease in native sub Saharan black men. Newly diagnosed metastatic PCa patients treated with primary androgen deprivation therapy were identified and predictors of progression-free survival (PFS) assessed.
Patients diagnosed with metastatic PCa between 2010 and 2015 in a sub Saharan black population were included in the study. Primary outcome measure was PFS defined as time from primary androgen deprivation therapy to clinical progression or death. Demographic, clinical and PSA kinetic variables were evaluated for their prognostic power using Cox proportional hazard regression models.
Seventy-nine patients met the eligibility criteria and were analyzed. Median age, median overall survival and PFS was 69 years, 40 months and 27 months respectively. A PSA nadir >4 ng/mL was found to predict an earlier clinical progression. Median PFS was shorter in those with PSA nadir >4 ng/mL (15 months) compared to those with PSA nadir ≤4 ng/mL (29 months); log rank p value = 0.003.
The PSA nadir achieved following primary androgen deprivation therapy predicts progression-free survival in sub Saharan black men newly diagnosed with metastatic PCa. PSA nadir >4 ng/mL was found to be associated with a more rapid clinical progression.
尽管已有充分证据表明黑人男性患前列腺癌(PCa)的风险更高,但对于撒哈拉以南非洲本土黑人男性的这种疾病却知之甚少。我们识别了接受一线雄激素剥夺治疗的新诊断转移性PCa患者,并评估了无进展生存期(PFS)的预测因素。
本研究纳入了2010年至2015年间在撒哈拉以南黑人人群中诊断为转移性PCa的患者。主要结局指标为PFS,定义为从一线雄激素剥夺治疗至临床进展或死亡的时间。使用Cox比例风险回归模型评估人口统计学、临床和PSA动力学变量的预后能力。
79例患者符合纳入标准并进行了分析。中位年龄、中位总生存期和PFS分别为69岁、40个月和27个月。发现PSA最低点>4 ng/mL可预测更早的临床进展。PSA最低点>4 ng/mL的患者中位PFS(15个月)短于PSA最低点≤4 ng/mL的患者(29个月);对数秩检验p值=0.003。
一线雄激素剥夺治疗后达到的PSA最低点可预测新诊断为转移性PCa的撒哈拉以南黑人男性的无进展生存期。发现PSA最低点>4 ng/mL与更快的临床进展相关。