Rates for breast cancer characteristics by estrogen and progesterone receptor status in the major racial/ethnic groups

Rates for breast cancer characteristics by estrogen and progesterone receptor status in the major racial/ethnic groups
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DOI:
10.1023/a:1016361932220
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发表时间:
2002-08-01
影响因子:
3.8
通讯作者:
Anderson, WF
Anderson, WF
中科院分区:
医学2区
文献类型:
--
作者:
Chu, KC;Anderson, WF

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据报道,年龄特异性乳腺癌发病率因雌激素受体和孕激素受体状态而异。我们报告了六个主要种族/民族的乳腺癌发病率,包括诊断年龄、诊断阶段、组织学分级和雌激素(ER)和孕激素(PgR)受体状态的类型。雌激素受体阳性(ER+)、ER-、孕激素受体阳性(PgR(+))、PgR(-)、ER(+)PgR(+)、ER(+)PgR(-)、ER(+)PgR(-)、ER(-)PgR(+)、ER(-)PgR(+)和ER(-)PgR(-)乳腺癌的平均年年龄调整率来自11个监测、流行病学和最终结果(SEER)癌症登记处1992年至1998年诊断的123,732例已知ER状态的乳腺癌。对于每个种族/民族,他们的ER+ (ER(+)PgR(+)和ER(+)PgR(-))年龄特异性率随着年龄的增长而增加(但在50-54岁之后速度较慢),而ER- (ER- PgR(+)和ER(-)PgR(-))年龄特异性率在50-54岁之后没有增加。不同的ER/PgR状态,不同种族/族裔群体的发病率排序不同。除了ER-和ER(-)PgR(-)癌症外,ER/PgR组的I期发病率高于II期发病率。ER+癌的2级(中分化)率高于3级和4级(低分化和未分化)率,但ER-癌的2级(中分化)率不高。这些结果提示,尽管乳腺癌是一种具有巨大异质性的疾病,但多种类型的乳腺癌可以通过其ER状态,甚至ER/PgR状态划分为不同的亚群,其癌症特征可能对理解乳腺癌的多重性具有重要意义。
It has been reported that age-specific breast cancer rates vary by estrogen receptor and progesterone receptor status. We report breast cancer rates for age-at-diagnosis, stage-at-diagnosis, histological grade and type by estrogen (ER) and progesterone (PgR) receptor status in six major racial/ethnic groups. The average annual age-adjusted rates for breast cancers with estrogen receptor positive (ER+), ER-, progesterone receptor positive (PgR(+)), PgR(-), ER(+)PgR(+), ER(+)PgR(-), ER(-)PgR(+) and ER(-)PgR(-) are determined from 123,732 breast cancers with known ER status, diagnosed from 1992 to 1998 from 11 Surveillance, Epidemiology, and End Results (SEER) cancer registries. For each racial/ethnic group, their ER+ (ER(+)PgR(+) and ER(+)PgR(-)) age-specific rates increased with age (but at a slower pace after ages 50-54) while their ER- (ER- PgR(+) and ER(-)PgR(-)) age-specific rates did not increase after ages 50-54. The rank orders of the rates among the racial/ethnic groups varied by ER/PgR status. The stage I rates were greater than the stage II rates for the ER/PgR groups except for ER- and ER(-)PgR(-) cancers. The grade 2 (moderately differentiated) rates were greater than the grades 3 and 4 (poorly differentiated and undifferentiated cancers) rates for ER+ cancers, but not for ER- cancers. These results suggest that although breast cancer is a disease with enormous heterogeneity, the multiple types of breast cancer can be separated into distinct subgroups by their ER status, and perhaps by their ER/PgR status, and their cancer characteristics may be important in understanding the multiple nature of breast cancer.