Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
J Ovarian Res. 2013 Feb 13;6(1):14. doi: 10.1186/1757-2215-6-14.
There is no consensus regarding the management of ovarian cancer patients, who have shown complete clinical response (CCR) to primary therapy and have rising cancer antigen CA-125 levels but have no symptoms of recurrent disease. The present study aims to determine whether follow-up CA-125 levels can be used to identify the need for imaging studies and secondary cytoreductive surgery (CRS).
We identified 410 ovarian cancer patients treated at The University of Texas MD Anderson Cancer Center between 1984 and 2011. These patients had shown CCR to primary therapy. Follow-up was conducted based on the surveillance protocol of the MD Anderson Cancer Center. We used the Cox proportional hazards model and log-rank test to assess the associations between the follow-up CA-125 levels and secondary CRS and survival duration.
The CA-125 level of 1.68 × nadir was defined as the indicator of recurrent disease (p < 0.001). The specificity and sensitivity of this criterion were 82.9% and 85.6%, respectively, and the median lead-time of the CA-125 biochemical progression prior to clinically-defined relapse was 31 days (ranging from 1 to 391 days). The median number of the negative imaging studies for the clinical relapse findings in patients with a CA-125 level of < 1.68 × nadir was 3 (ranging from 0 to 24 times). The increase of CA-125 level at relapse was an independent predictor of overall and progression free survival in patients who had shown CCR to primary therapy (p = 0.04 and 0.02 respectively). The overall and progression free survival durations in patients with a CA-125 level ≤ 1.68 × nadir at relapse (69.4 and 13.8 months) were longer than those with a CA-125 level > 1.68 × nadir at relapse (55.7 and 10.4 months; p = 0.04 and 0.01, respectively). The overall and progression free survival duration of patients with asymptomatic relapse and underwent a secondary CRS was longer than that of patients with symptomatic relapse (p = 0.02 and 0.04 respectively).
The increase of serum CA-125 levels is an early warning of clinical relapse in ovarian cancer. Using CA-125 levels in guiding the treatment of patients with asymptomatic recurrent ovarian cancer, who have shown CCR to primary therapy, can facilitate optimal secondary CRS and extend the survival duration of the patients.
对于已经对初始治疗表现出完全临床缓解(CCR)且癌抗原 CA-125 水平升高但无复发病症的卵巢癌患者,目前尚无明确的管理方法。本研究旨在确定随访 CA-125 水平是否可用于确定是否需要进行影像学检查和二次细胞减灭术(CRS)。
我们在 1984 年至 2011 年间,共确定了 410 名在德克萨斯大学 MD 安德森癌症中心接受治疗的卵巢癌患者。这些患者在初始治疗中表现出 CCR。根据 MD 安德森癌症中心的监测方案进行随访。我们使用 Cox 比例风险模型和对数秩检验来评估随访 CA-125 水平与二次 CRS 和生存时间之间的关系。
将 CA-125 水平 1.68× 基线定义为疾病复发的指标(p<0.001)。该标准的特异性和敏感性分别为 82.9%和 85.6%,CA-125 生化进展到临床定义的复发之前的中位领先时间为 31 天(范围为 1 至 391 天)。在 CA-125 水平<1.68×基线的患者中,临床复发发现的阴性影像学检查次数中位数为 3(范围为 0 至 24 次)。在对初始治疗有 CCR 的患者中,CA-125 水平升高是总生存期和无进展生存期的独立预测因子(p=0.04 和 0.02)。在复发时 CA-125 水平≤1.68×基线的患者中(69.4 和 13.8 个月)的总生存期和无进展生存期长于 CA-125 水平>1.68×基线的患者(55.7 和 10.4 个月;p=0.04 和 0.01)。无症状复发并接受二次 CRS 的患者的总生存期和无进展生存期长于有症状复发的患者(p=0.02 和 0.04)。
血清 CA-125 水平升高是卵巢癌临床复发的早期预警。在指导对初始治疗有 CCR 且无症状复发性卵巢癌患者的治疗中,使用 CA-125 水平可以促进最佳的二次 CRS,并延长患者的生存时间。