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本文引用的文献

1
Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers.对携带BRCA突变的肿瘤中聚(ADP - 核糖)聚合酶的抑制作用。
N Engl J Med. 2009 Jul 9;361(2):123-34. doi: 10.1056/NEJMoa0900212. Epub 2009 Jun 24.
2
Intraepithelial T cells and prognosis in ovarian carcinoma: novel associations with stage, tumor type, and BRCA1 loss.上皮内T细胞与卵巢癌预后:与分期、肿瘤类型及BRCA1缺失的新关联
Mod Pathol. 2009 Mar;22(3):393-402. doi: 10.1038/modpathol.2008.191. Epub 2008 Dec 5.
3
"BRCAness" syndrome in ovarian cancer: a case-control study describing the clinical features and outcome of patients with epithelial ovarian cancer associated with BRCA1 and BRCA2 mutations.卵巢癌中的“BRCA样”综合征:一项病例对照研究,描述与BRCA1和BRCA2突变相关的上皮性卵巢癌患者的临床特征和预后。
J Clin Oncol. 2008 Dec 1;26(34):5530-6. doi: 10.1200/JCO.2008.16.1703. Epub 2008 Oct 27.
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Cancer statistics, 2008.2008年癌症统计数据。
CA Cancer J Clin. 2008 Mar-Apr;58(2):71-96. doi: 10.3322/CA.2007.0010. Epub 2008 Feb 20.
5
Platinum resistance and impaired survival in patients with advanced primary peritoneal carcinoma: matched-case comparison with patients with epithelial ovarian carcinoma.晚期原发性腹膜癌患者的铂耐药与生存受损:与上皮性卵巢癌患者的配对病例对照研究
Am J Obstet Gynecol. 2008 Feb;198(2):213.e1-7. doi: 10.1016/j.ajog.2007.07.003.
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Effect of BRCA1/2 mutations on long-term survival of patients with invasive ovarian cancer: the national Israeli study of ovarian cancer.BRCA1/2基因突变对侵袭性卵巢癌患者长期生存的影响:以色列全国卵巢癌研究
J Clin Oncol. 2008 Jan 1;26(1):20-5. doi: 10.1200/JCO.2007.11.6905.
7
Is It time to stratify for BRCA mutation status in therapeutic trials in ovarian cancer?是时候在卵巢癌治疗试验中根据BRCA突变状态进行分层了吗?
J Clin Oncol. 2008 Jan 1;26(1):9-10. doi: 10.1200/JCO.2007.14.0244.
8
KRAS wild-type state predicts survival and is associated to early radiological response in metastatic colorectal cancer treated with cetuximab.KRAS野生型状态可预测转移性结直肠癌患者接受西妥昔单抗治疗后的生存期,并与早期放射学反应相关。
Ann Oncol. 2008 Mar;19(3):508-15. doi: 10.1093/annonc/mdm496. Epub 2007 Nov 12.
9
Prognostic factors for stage III epithelial ovarian cancer: a Gynecologic Oncology Group Study.Ⅲ期上皮性卵巢癌的预后因素:一项妇科肿瘤学组研究
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PIEPOC: a new prognostic index for advanced epithelial ovarian cancer--Japan Multinational Trial Organization OC01-01.PIEPOC:晚期上皮性卵巢癌的一种新预后指数——日本多中心试验组织OC01-01
J Clin Oncol. 2007 Aug 1;25(22):3302-6. doi: 10.1200/JCO.2007.11.0114.

上皮性卵巢癌的生存:包含 BRCA 突变状态和铂类敏感性的多变量分析。

Survival in epithelial ovarian cancer: a multivariate analysis incorporating BRCA mutation status and platinum sensitivity.

机构信息

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.

出版信息

Ann Oncol. 2011 May;22(5):1127-1132. doi: 10.1093/annonc/mdq577. Epub 2010 Nov 17.

DOI:10.1093/annonc/mdq577
PMID:21084428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6267858/
Abstract

BACKGROUND

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.

PATIENTS AND METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

背景

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。

患者和方法

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。

结果

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)。

结论

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。