Understanding disparities in endometrial cancer

  • Research type

    Research Study

  • Full title

    Understanding disparities in endometrial cancer.

  • IRAS ID

    362169

  • Contact name

    Aleksandra Gentry-Maharaj

  • Contact email

    a.gentry-maharaj@ucl.ac.uk

  • Sponsor organisation

    University College London

  • Clinicaltrials.gov Identifier

    Z6364106 2025 09 46, UCL Data Protection Registration Number

  • Duration of Study in the UK

    9 years, 8 months, 30 days

  • Research summary

    In the UK, endometrial cancer (EC), a cancer that develops in the lining of the womb, is the most common gynaecological cancer, with approximately 9,828 new cases diagnosed each year (Cancer Research UK, 2015). Since 1990, the incidence of endometrial cancer in the UK has risen by nearly 58% (Cancer Research UK, 2015). Black women have a lower incidence of EC compared to White women, but their outcomes are much worse. They are also twice as likely to die from the disease (ONS 2012; Moss et al 2023). This disparity in mortality is partly attributed to differences in EC histology and advanced stage at diagnosis. Black women are more likely to be diagnosed with aggressive histological subtypes such as high-grade serous carcinomas and uterine sarcomas (Javadian et al., 2021). Compared with other ethnic groups, Black women are also more likely to be diagnosed with an advanced disease stage (Doll et al., 2020) and more likely to have higher mortality (Moss et al., 2023).

    Given the higher mortality rates and later-stage diagnoses of EC among economically deprived and Black women, understanding the barriers they face in accessing timely care is crucial for improving outcomes. Previous research highlights disparities in symptom recognition, healthcare access, diagnosis, and treatment. Previous studies have primarily focused on epidemiological data and physiological differences, yet we lack a clear understanding of how patients and healthcare providers understand and experience these disparities. This research takes a patient-centred approach to uncover systemic and experiential factors contributing to inequalities. This study has been identified as valuable in addressing gaps in culturally sensitive awareness, diagnostic pathways, and treatment equity through consultation with patient groups.

    The proposed study aims to understand disparities across the endometrial cancer continuum by conducting a national audit of EC treatment and outcomes and exploratory qualitative research with poorly served women, health care providers, and community groups.

  • REC name

    West Midlands - Solihull Research Ethics Committee

  • REC reference

    26/WM/0005

  • Date of REC Opinion

    21 Jan 2026

  • REC opinion

    Unfavourable Opinion