Division of Hematology/Medical Oncology, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Sanofi US, Bridgewater, NJ, USA.
Med Oncol. 2017 Aug 10;34(9):160. doi: 10.1007/s12032-017-1014-2.
It is unclear how treatment sequencing for metastatic castration-resistant prostate cancer (mCRPC) affects real-world patient outcomes. We assessed treatment sequences, patient characteristics and overall survival (OS) in post-docetaxel mCRPC patients. mCRPC patients receiving second-line cabazitaxel or androgen receptor-targeted therapy (ART; abiraterone/enzalutamide) post-docetaxel were identified using electronic medical records. OS was assessed from second-line therapy initiation using Cox regressions adjusting for: metastases; prostate-specific antigen (PSA); hemoglobin; alkaline phosphatase (ALP); albumin; second-line therapy initiation year. Following docetaxel (n = 629), 123 (19.6%) and 506 (80.4%) patients received cabazitaxel and ART, respectively. One hundred and ninety-five patients received additional treatments thereafter (54 following cabazitaxel; 141 following ART). Although patients receiving second-line cabazitaxel versus ART had similar disease characteristics at first-line therapy initiation, at second-line therapy initiation they had higher mean PSA (386.6 vs. 233.9 ng/mL) and ALP (182.0 vs. 167.3 u/L), lower mean hemoglobin (10.8 vs. 11.5 g/dL), and more frequently had intermediate/high-risk Halabi scores (61.8 vs. 48.4%); all p < 0.05. Overall, crude survival was not significantly different. Among Halabi high-risk patients, adjusted median OS was significantly longer in patients receiving cabazitaxel versus ART (HR 0.48; 95% CI 0.24-0.93; p = 0.030). Low albumin and hemoglobin led to similar findings (HR 0.43; 95% CI 0.23-0.80; p = 0.0077; HR 0.60; 95% CI 0.40-0.90; p = 0.014). Most post-docetaxel patients received second-line ART. Patients receiving second-line cabazitaxel had more high-risk features; however, second-line cabazitaxel administered after docetaxel may improve OS in patients with Halabi high-risk scores or low albumin/hemoglobin.
转移性去势抵抗性前列腺癌(mCRPC)的治疗顺序如何影响真实世界患者的结局尚不清楚。我们评估了接受多西他赛后的 mCRPC 患者的治疗顺序、患者特征和总生存期(OS)。使用电子病历确定接受多西他赛二线卡巴他赛或雄激素受体靶向治疗(abiraterone/enzalutamide,ART)的 mCRPC 患者。使用 Cox 回归分析从二线治疗开始评估 OS,调整因素包括转移、前列腺特异性抗原(PSA)、血红蛋白、碱性磷酸酶(ALP)、白蛋白、二线治疗开始年份。在多西他赛治疗后(n=629),分别有 123(19.6%)和 506(80.4%)例患者接受卡巴他赛和 ART。此后有 195 例患者接受了额外的治疗(卡巴他赛后 54 例,ART 后 141 例)。尽管二线接受卡巴他赛与 ART 的患者在一线治疗开始时具有相似的疾病特征,但在二线治疗开始时,他们的 PSA(386.6 与 233.9ng/mL)和 ALP(182.0 与 167.3u/L)更高,血红蛋白(10.8 与 11.5g/dL)更低,且更常具有中高危 Halabi 评分(61.8%与 48.4%);所有差异均有统计学意义(均 P<0.05)。总体而言,未观察到两组的生存差异。在 Halabi 高危患者中,与接受 ART 相比,接受卡巴他赛的患者中位 OS 显著延长(HR 0.48;95%CI 0.24-0.93;P=0.030)。低白蛋白和低血红蛋白也有类似的发现(HR 0.43;95%CI 0.23-0.80;P=0.0077;HR 0.60;95%CI 0.40-0.90;P=0.014)。大多数接受多西他赛治疗后的患者接受了二线 ART。接受二线卡巴他赛的患者具有更多高危特征;然而,多西他赛治疗后给予二线卡巴他赛可能会改善 Halabi 高危评分或低白蛋白/血红蛋白患者的 OS。