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Is the breast-conserving treatment with radiotherapy appropriate in BRCA1/2 mutation carriers? Long-term results and review of the literature

机译:BRCA1 / 2突变携带者是否适合采用放射治疗保乳?长期结果和文献复习

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As tumours in BRCA1/2 mutation carriers might be more sensitive to radiation, we investigated after long-term follow-up whether mutation status influenced the rate of ipsilateral and contralateral breast cancers after breast-conserving treatment (BCT). BRCA1 and BRCA2 genes were screened for germline mutations in 131 patients with a family history of breast and/or ovarian cancer who had undergone BCT and radiotherapy. Patients were matched to 261 controls with sporadic breast cancer according to age at diagnosis and year of treatment. Controls were followed up for at least as long as the interval between diagnosis and genetic screening in familial cases. Rates of ipsilateral and contralateral cancer between groups were compared by the log-rank test. The BRCA1/2 mutations occurred in 20.6% of tested patients. Tumours in mutation carriers were more likely to be grade III (P < 10−4) and oestrogen receptor negative (P = 0.005) than in non-carriers and controls. Overall median follow-up was 161 months. There was no significant difference in ipsilateral tumours between mutation carriers, non-carriers and controls (P = 0.13). On multivariate analysis, age was the most significant predictor for ipsilateral recurrence (P < 10−3). The rate of contralateral cancer was significantly higher in familial cases: 40.7% (mutation carriers), 20% (non-carriers), and 11% (controls) (P < 10−4). After 13.4 years of follow-up, the rate of ipsilateral tumours was no higher in mutation carriers than in non-carriers or controls. As tumours in BRCA1/2 mutation carriers might be more sensitive to radiation, BCT is a possible treatment option. Keywords BRCA1/2 mutations - Breast-conserving treatment - Radiotherapy - Recurrence This article was presented at Breast Cancer Symposium in October 2009, San Francisco, USA.
机译:由于BRCA1 / 2突变携带者中的肿瘤可能对放射线更敏感,因此,在长期随访之后,我们调查了突变状态是否影响保乳治疗(BCT)后同侧和对侧乳腺癌的发生率。在接受过BCT和放疗的131例有乳腺癌和/或卵巢癌家族病史的患者中,筛选了BRCA1和BRCA2基因的生殖系突变。根据诊断时的年龄和治疗年份将患者与261名散发性乳腺癌对照进行匹配。在家族病例中,对对照的随访时间至少要长于诊断和基因筛查之间的间隔。通过对数秩检验比较两组之间同侧和对侧癌症的发生率。 BRCA1 / 2突变发生在20.6%的测试患者中。与非携带者和对照组相比,突变携带者中的肿瘤更可能为III级(P <10 -4 )和雌激素受体阴性(P = 0.005)。总体中位随访时间为161个月。突变携带者,非携带者和对照之间的同侧肿瘤无显着差异(P = 0.13)。在多变量分析中,年龄是同侧复发的最重要预测因子(P <10 -3 )。在家族性病例中,对侧癌的发生率明显更高:分别为40.7%(突变携带者),20%(非携带者)和11%(对照)(P <10 -4 )。经过13.4年的随访,突变携带者的同侧肿瘤发生率不高于非携带者或对照者。由于BRCA1 / 2突变携带者中的肿瘤可能对放射线更为敏感,因此BCT是一种可能的治疗选择。关键词BRCA1 / 2突变-保乳治疗-放疗-复发本文在2009年10月于美国旧金山举行的乳腺癌研讨会上发表。

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