Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine; Clinical Genetics Service, Division of Solid Tumor Oncology, Department of Medicine.
Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine.
Ann Oncol. 2011 May;22(5):1127-1132. doi: 10.1093/annonc/mdq577. Epub 2010 Nov 17.
Patients with BRCA-associated ovarian cancer (OC) have a survival advantage over those with sporadic OC. To further explore this, we examined the impact of prognostic factors on disease-free survival (DFS) and overall survival (OS) in patients with known BRCA mutation status.
We reviewed stage III-IV OC patients treated at our institution between 1 December 1996 and 30 September 2006 and also tested on protocol for BRCA mutations. Impact on DFS and OS was determined by Kaplan-Meier analysis and a Cox proportional hazards model.
Of the 110 patients, 36 had deleterious BRCA mutations [BRCA (+)] and 74 were BRCA wild type [BRCA(-)]. Thirty-one of 36 (86%) BRCA (+) and 60 of 74 (81%) BRCA (-) patients were platinum sensitive (P = 0.60). Median OS was longer for BRCA (+) patients (not reached versus 67.8 months; P = 0.02), but DFS was similar (26.9 versus 24.0, P = 0.3). On multivariate analysis, OS correlated with primary platinum sensitivity [HR = 0.15; 95% CI (confidence interval) 0.06-0.34] and BRCA (+) mutation status (HR = 0.33; 95% CI 0.12-0.86).
BRCA mutation status predicted OS independent of primary platinum sensitivity, suggesting that underlying tumor biology contributes to disease outcome and may be worthy of consideration in future clinical trial design.
与散发型卵巢癌(OC)相比,携带 BRCA 相关卵巢癌(OC)的患者具有生存优势。为了进一步探讨这一点,我们研究了已知 BRCA 突变状态的患者的预后因素对无病生存(DFS)和总生存(OS)的影响。
我们回顾了 1996 年 12 月 1 日至 2006 年 9 月 30 日在我们机构治疗的 III-IV 期 OC 患者,并按方案进行了 BRCA 突变检测。通过 Kaplan-Meier 分析和 Cox 比例风险模型确定 DFS 和 OS 的影响。
在 110 名患者中,36 名患者存在有害 BRCA 突变[BRCA(+)],74 名患者为 BRCA 野生型[BRCA(-)]。36 名 BRCA(+)患者中有 31 名(86%)和 74 名 BRCA(-)患者中有 60 名(81%)为铂类敏感(P=0.60)。BRCA(+)患者的中位 OS 更长(未达到 vs. 67.8 个月;P=0.02),但 DFS 相似(26.9 vs. 24.0,P=0.3)。多变量分析显示,OS 与原发性铂类敏感性相关[HR=0.15;95%置信区间(CI)0.06-0.34]和 BRCA(+)突变状态(HR=0.33;95%CI 0.12-0.86)。
BRCA 突变状态独立于原发性铂类敏感性预测 OS,表明潜在的肿瘤生物学有助于疾病结局,可能值得在未来的临床试验设计中考虑。