Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA.
Division of Research, Kaiser Permanente Northern California, Oakland, CA.
Ethn Dis. 2018 Oct 18;28(4):565-574. doi: 10.18865/ed.28.4.565. eCollection 2018 Fall.
It is unknown how subsequent breast cancer outcomes vary by biologic subtype and race/ethnicity in a diverse cohort of breast cancer survivors.
We conducted a prospective cohort study of 6,154 insured breast cancer survivors (AJCC TNM stages 0-IV) diagnosed between 1996-2007 and followed them through 1/1/2010 for subsequent breast cancer events (recurrence, contralateral breast cancer, metastasis, mortality). We compared subsequent breast cancer rates by race/ethnicity groups and biologic subtype (luminal A, luminal B, HER2-enriched, and triple negative). We calculated hazard ratios (HRs) with 95% CIs using multivariable Cox proportional hazards models, adjusted for sociodemographics, cancer treatments, and tumor characteristics.
The cohort was diverse: 62.4% non-Hispanic White, 13.2% Hispanic, 14.9% African American, and 9.5% Asian. We identified 1,456 subsequent breast cancer events over 22,830 person-years. Although certain Asian women had higher crude subsequent breast cancer rates compared with Whites, within each biologic subtype category, these disparities disappeared in the multivariable analyses. After accounting for race/ethnicity, compared with women with luminal A tumors (reference), women with luminal B (adjusted HR=3.65, 95% CI: 3.08-4.32), HER2-enriched (adjusted HR=2.81, 95% CI: 2.25-3.51) and triple negative (adjusted HR=1.25, 95% CI: 1.01-1.54) tumors had statistically increased risks of subsequent breast cancer. Factors that were statistically significantly associated with increased risk included higher stage, larger tumor size, positive lymph nodes, and no adjuvant endocrine or chemotherapy (all P<.025).
Our data suggest that disparities in subsequent breast cancer outcomes were more strongly associated with tumor characteristics and non-use of adjuvant treatments than race/ethnicity.
在一个多样化的乳腺癌幸存者队列中,我们尚不清楚生物亚型和种族/民族如何影响后续乳腺癌的结局。
我们进行了一项前瞻性队列研究,纳入了 6154 名 1996-2007 年间确诊的、AJCC TNM 分期为 0-IV 期的有保险的乳腺癌幸存者,并随访至 2010 年 1 月 1 日,以观察后续的乳腺癌事件(复发、对侧乳腺癌、转移、死亡)。我们比较了不同种族/民族组和生物亚型(管腔 A 型、管腔 B 型、HER2 富集型和三阴性型)的后续乳腺癌发生率。我们使用多变量 Cox 比例风险模型计算了风险比(HR)及其 95%置信区间,调整了社会人口统计学、癌症治疗和肿瘤特征因素。
该队列的种族构成多样,其中非西班牙裔白人占 62.4%,西班牙裔占 13.2%,非裔美国人占 14.9%,亚裔美国人占 9.5%。我们在 22830 人年中发现了 1456 例后续乳腺癌事件。尽管某些亚裔女性的后续乳腺癌粗发生率高于白人,但在每个生物亚型类别中,这些差异在多变量分析中消失了。在考虑了种族/民族因素后,与管腔 A 型肿瘤的女性(参考)相比,管腔 B 型(调整后的 HR=3.65,95%CI:3.08-4.32)、HER2 富集型(调整后的 HR=2.81,95%CI:2.25-3.51)和三阴性型(调整后的 HR=1.25,95%CI:1.01-1.54)肿瘤的女性有统计学上更高的后续乳腺癌风险。与风险增加相关的统计学显著因素包括更高的分期、更大的肿瘤大小、阳性淋巴结和未接受辅助内分泌或化疗(均 P<.025)。
我们的数据表明,后续乳腺癌结局的差异与肿瘤特征和不使用辅助治疗的关系比种族/民族更为密切。