Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, UK.
University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
J Pathol Clin Res. 2020 Apr;6(2):146-153. doi: 10.1002/cjp2.155. Epub 2020 Feb 5.
Multifocal (MF)/multicentric (MC) breast cancer is generally considered to be where two or more breast tumours are present within the same breast, and is seen in ~10% of breast cancer cases. This study investigates the prevalence of multifocality/multicentricity in a cohort of BRCA1/2 mutation carriers with breast cancer from Northern Ireland via cross-sectional analysis. Data from 211 women with BRCA1/2 mutations (BRCA1-91, BRCA2-120) and breast cancer were collected including age, tumour focality, size, type, grade and receptor profile. The prevalence of multifocality/multicentricity within this group was 25% but, within subgroups, prevalence amongst BRCA2 carriers was more than double that of BRCA1 carriers (p = 0.001). Women affected by MF/MC tumours had proportionately higher oestrogen receptor positivity (p = 0.001) and lower triple negativity (p = 0.004). These observations are likely to be driven by the higher BRCA2 mutation prevalence observed within this cohort. The odds of a BRCA2 carrier developing MF/MC cancer were almost four-fold higher than a BRCA1 carrier (odds ratio: 3.71, CI: 1.77-7.78, p = 0.001). These findings were subsequently validated in a second, large independent cohort of patients with BRCA-associated breast cancers from a UK-wide multicentre study. This confirmed a significantly higher prevalence of MF/MC tumours amongst BRCA2 mutation carriers compared with BRCA1 mutation carriers. This has important implications for clinicians involved in the treatment of BRCA2-associated breast cancer, both in the diagnostic process, in ensuring that tumour focality is adequately assessed to facilitate treatment decision-making, and for breast surgeons, particularly if breast conserving surgery is being considered as a treatment option for these patients.
多灶性(MF)/多中心性(MC)乳腺癌通常被认为是同一乳房内存在两个或多个肿瘤,约占乳腺癌病例的 10%。本研究通过横断面分析,调查了北爱尔兰 BRCA1/2 突变携带者乳腺癌患者中多灶性/多中心性的患病率。该研究收集了 211 名携带 BRCA1/2 突变(BRCA1-91、BRCA2-120)和乳腺癌的女性的数据,包括年龄、肿瘤灶数、大小、类型、分级和受体谱。该组多灶性/多中心性的患病率为 25%,但在亚组中,BRCA2 携带者的患病率是 BRCA1 携带者的两倍多(p=0.001)。患有 MF/MC 肿瘤的女性雌激素受体阳性比例较高(p=0.001),三阴性比例较低(p=0.004)。这些观察结果可能是由于该队列中 BRCA2 突变的高患病率所驱动的。BRCA2 携带者发生 MF/MC 癌症的几率是 BRCA1 携带者的近四倍(比值比:3.71,95%置信区间:1.77-7.78,p=0.001)。这些发现随后在英国范围内一项多中心研究的第二个大型独立 BRCA 相关乳腺癌患者队列中得到了验证。这证实了 BRCA2 突变携带者中 MF/MC 肿瘤的患病率明显高于 BRCA1 突变携带者。这对参与 BRCA2 相关乳腺癌治疗的临床医生具有重要意义,无论是在诊断过程中,确保充分评估肿瘤灶以促进治疗决策,还是对乳腺外科医生,特别是如果考虑对这些患者进行保乳手术作为治疗选择时。