Francoeur Alex A, Liao Cheng-I, Johnson Caitlin R, Argueta Chris, Tian Chunqiao, Darcy Kathleen M, Kapp Daniel S, Bristow Robert E, Chan John K
Department of Obstetrics and Gynecology, University of California, Irvine, Orange, CA, USA.
Division of Obstetrics and Gynecology, Pingtung Veterans General Hospital, Pingtung, Taiwan.
Int J Gynecol Cancer. 2025 Jan;35(1):100013. doi: 10.1016/j.ijgc.2024.100013. Epub 2024 Dec 18.
The aim of this study was to examine disparities in 20-year incidence trends and mutations in advanced-stage uterine cancer in the United States, given poor survival rates.
Data were obtained from the United States Cancer Statistics for patients from 2001 to 2019 with International Federation of Gynecology and Obstetrics 2009 stage IVA and IVB uterine cancer. SEER∗Stat 8.3.9.2 and Joinpoint Regression Program 4.9.0.0 were used to calculate cancer incidence per 100,000 women, annual percentages, and average annual percent change (AAPC). The mutational landscape of advanced uterine cancer was explored using data from the Genomic Data Commons.
In United States Cancer Statistics, 75,450 patients with advanced uterine cancer were identified with an annual percentage increase of 2.63% between 2001 and 2019 and significantly higher rates in Black, Hispanic, and Asian patients compared with White patients (AAPC Black: 3.56%, AAPC Hispanic: 3.12%, and AAPC Asian 3.06% vs AAPC White: 2.07%, each p < .001). AAPC in patients with serous carcinomas increased by 6.32% in Black vs 3.91% in White patients (p < .001). Furthermore, AAPC was 3.0% for Black patients vs 0.7% for White patients with leiomyosarcoma (p < .001). In the Genomic Data Commons, TP53 mutations were more common, and PTEN was less common in Black vs White patients, older vs younger patients, advanced vs early stage, or high- vs low-risk histologic subtypes (p < .05). Mutations in BRCA1, BRCA2, POLE, and PMS2 were less common in high- vs low-risk histologic subtypes (p < .05).
Advanced-stage uterine cancer rates are rising in the United States, particularly affecting Black and Hispanic women. Molecular differences exist by age, race, stage, and histology.
鉴于晚期子宫癌生存率较低,本研究旨在调查美国晚期子宫癌20年发病率趋势及突变情况的差异。
数据来源于美国癌症统计,研究对象为2001年至2019年患有国际妇产科联盟2009年分期IVA和IVB期子宫癌的患者。使用SEER∗Stat 8.3.9.2和Joinpoint回归程序4.9.0.0计算每10万名女性的癌症发病率、年度百分比和平均年度百分比变化(AAPC)。利用基因组数据共享库的数据探索晚期子宫癌的突变图谱。
在美国癌症统计中,共识别出75450例晚期子宫癌患者,2001年至2019年间年增长率为2.63%,与白人患者相比,黑人、西班牙裔和亚裔患者的发病率显著更高(AAPC黑人:3.56%,AAPC西班牙裔:3.12%,AAPC亚裔:3.06%,而AAPC白人:2.07%,各p <.001)。浆液性癌患者中,黑人的AAPC增加了6.32%,而白人患者为3.91%(p <.001)。此外,平滑肌肉瘤患者中,黑人的AAPC为3.0%,而白人患者为0.7%(p <.001)。在基因组数据共享库中,TP53突变在黑人患者中比白人患者更常见,PTEN突变在黑人患者中比白人患者、老年患者比年轻患者、晚期患者比早期患者、高风险组织学亚型比低风险组织学亚型中更少见(p <.05)。BRCA1、BRCA2、POLE和PMS2突变在高风险组织学亚型比低风险组织学亚型中更少见(p <.05)。
美国晚期子宫癌发病率正在上升,尤其影响黑人及西班牙裔女性。在年龄、种族、分期和组织学方面存在分子差异。