Griffin Kagan, Csizmadi Ilona, Howard Lauren E, Pomann Gina-Maria, Aronson William J, Kane Christopher J, Amling Christopher L, Cooperberg Matthew R, Terris Martha K, Beebe-Dimmer Jennifer, Freedland Stephen J
Urology Section, Department of Surgery, Veterans Affairs Medical Centers, Durham, NC, USA.
Division of Urology, Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Cancer Causes Control. 2019 Mar;30(3):259-269. doi: 10.1007/s10552-019-1133-5. Epub 2019 Jan 30.
We aimed to study the associations between androgen-deprivation therapy (ADT)-induced weight changes and prostate cancer (PC) progression and mortality in men who had undergone radical prostatectomy (RP).
Data from the Shared Equal Access Regional Cancer Hospital (SEARCH) cohort were used to study the associations between weight change approximately 1-year post-ADT initiation and metastases, castration-resistant prostate cancer (CRPC), all-cause mortality (ACM), and PC-specific mortality (PCSM) in 357 patients who had undergone RP between 1988 and 2014. We estimated hazard ratios (HR) and 95% confidence intervals (95% CI) using covariate-adjusted Cox regression models for associations between weight loss, and weight gains of 2.3 kg or more, and PC progression and mortality post-ADT.
During a median (IQR) follow-up of 81 (46-119) months, 55 men were diagnosed with metastases, 61 with CRPC, 36 died of PC, and 122 died of any cause. In multivariable analysis, weight loss was associated with increases in risks of metastases (HR 3.13; 95% CI 1.40-6.97), PCSM (HR 4.73; 95% CI 1.59-14.0), and ACM (HR 2.16; 95% CI 1.25-3.74) compared with mild weight gains of ≤ 2.2. Results were slightly attenuated but remained statistically significant in analyses that accounted for competing risks of non-PC death. Estimates for the associations between weight gains of ≥ 2.3 kg and metastases (HR 1.58; 95% CI 0.73-3.42), CRPC (HR 1.33; 95% CI 0.66-2.66), and PCSM (HR 2.44; 95% CI 0.84-7.11) were elevated, but not statistically significant.
Our results suggest that weight loss following ADT initiation in men who have undergone RP is a poor prognostic sign. If confirmed in future studies, testing ways to mitigate weight loss post-ADT may be warranted.
我们旨在研究雄激素剥夺治疗(ADT)引起的体重变化与接受根治性前列腺切除术(RP)的男性前列腺癌(PC)进展及死亡率之间的关联。
利用共享平等获取区域癌症医院(SEARCH)队列的数据,研究1988年至2014年间接受RP的357例患者在ADT开始后约1年时体重变化与转移、去势抵抗性前列腺癌(CRPC)、全因死亡率(ACM)和PC特异性死亡率(PCSM)之间的关联。我们使用协变量调整的Cox回归模型估计风险比(HR)和95%置信区间(95%CI),以分析体重减轻以及体重增加2.3千克或更多与ADT后PC进展和死亡率之间的关联。
在中位(四分位间距)81(46 - 119)个月的随访期间,55名男性被诊断为转移,61名患有CRPC,36名死于PC,122名死于任何原因。在多变量分析中,与轻度体重增加(≤2.2千克)相比,体重减轻与转移风险增加(HR 3.13;95%CI 1.40 - 6.97)、PCSM(HR 4.73;95%CI 1.59 - 14.0)和ACM(HR 2.16;95%CI 1.25 - 3.74)相关。在考虑非PC死亡竞争风险的分析中,结果略有减弱但仍具有统计学意义。体重增加≥2.3千克与转移(HR 1.58;95%CI 0.73 - 3.42)、CRPC(HR 1.33;95%CI 0.66 - 2.66)和PCSM(HR 2.44;95%CI 0.84 - 7.11)之间关联的估计值升高,但无统计学意义。
我们的结果表明,接受RP的男性在ADT开始后体重减轻是预后不良的迹象。如果在未来研究中得到证实,可能有必要探索减轻ADT后体重减轻的方法。