Heller Danielle R, Chiu Alexander S, Farrell Kaitlin, Killelea Brigid K, Lannin Donald R
Department of Surgery, Yale School of Medicine, New Haven, CT 06520, USA.
The Breast Center/Section of Surgical Oncology, Department of Surgery, Yale School of Medicine, New Haven, CT 06520, USA.
Cancers (Basel). 2019 Apr 8;11(4):500. doi: 10.3390/cancers11040500.
: Despite screening mammography, the incidence of Stage IV breast cancer (BC) at diagnosis has not decreased over the past four decades. We previously found that many BCs are small due to favorable biology rather than early detection. This study compared the biology of Stage IV cancers with that of small cancers typically found by screening. : Trends in the incidence of localized, regional, and distant female BC were compared using SEERStat. The National Cancer Database (NCDB) was then queried for invasive cancers from 2010 to 2015, and patient/disease variables were compared across stages. Biological variables including estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (Her2), grade, and lymphovascular invasion were sorted into 48 combinations, from which three biological subtypes emerged: indolent, intermediate, and aggressive. The distributions of the subtypes were compared across disease stages. Multivariable regression assessed the association between Stage IV disease and biology. : SEERStat confirmed that the incidence of distant BC increased between 1973 and 2015 (annual percent change [APC] = 0.46). NCDB data on roughly 993,000 individuals showed that Stage IV disease at presentation is more common in young, black, uninsured women with low income/education and large, biologically aggressive tumors. The distribution of tumor biology varied by stage, with Stage IV disease including 37.6% aggressive and 6.0% indolent tumors, versus sub-centimeter Stage I disease that included 5.1% aggressive and 40.6% indolent tumors ( < 0.001). The odds of Stage IV disease presentation more than tripled for patients with aggressive tumors (OR3.2, 95% CI 3.0⁻3.5). : Stage I and Stage IV breast cancers represent very different populations of biologic tumor types. This may explain why the incidence of Stage IV cancer has not decreased with screening.
尽管进行了乳腺钼靶筛查,但在过去四十年中,IV期乳腺癌(BC)在诊断时的发病率并未下降。我们之前发现,许多乳腺癌体积较小是由于生物学特性良好,而非早期发现。本研究比较了IV期癌症与筛查中通常发现的小癌症的生物学特性。:使用SEERStat比较了局限性、区域性和远处性女性乳腺癌的发病率趋势。随后查询了国家癌症数据库(NCDB)中2010年至2015年的浸润性癌症,并比较了各阶段的患者/疾病变量。将包括雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2(Her2)、分级和淋巴管浸润在内的生物学变量分为48种组合,从中出现了三种生物学亚型:惰性、中间型和侵袭性。比较了各疾病阶段亚型的分布情况。多变量回归评估了IV期疾病与生物学特性之间的关联。:SEERStat证实,1973年至2015年间远处乳腺癌的发病率有所上升(年度百分比变化[APC]=0.46)。NCDB关于约993,000人的数据显示,初诊时IV期疾病在年轻、黑人、未参保、低收入/低教育水平且患有生物学侵袭性大肿瘤的女性中更为常见。肿瘤生物学特性的分布因阶段而异,IV期疾病包括37.6%的侵袭性肿瘤和6.0%的惰性肿瘤,而I期亚厘米疾病包括5.1%的侵袭性肿瘤和40.6%的惰性肿瘤(<0.001)。侵袭性肿瘤患者出现IV期疾病的几率增加了两倍多(OR 3.2,95%CI 3.0⁻3.5)。:I期和IV期乳腺癌代表了生物学肿瘤类型非常不同的群体。这可能解释了为什么IV期癌症的发病率并未因筛查而下降。