Abstract 817P
Background
Emerging evidence suggests pharmacogenomic differences between ethnic groups contributes to disparate treatment effects in cancer patients treated with systemic anti-cancer therapies (SACT). It is important to understand the representation of ethnic minority groups in research, and how this relates to patient outcomes. This systematic review compared participation of ethnic minority groups in contemporary gynae-oncology RCTs of SACT, and described the global distribution of research sites.
Methods
Medline, Embase and ClinicalTrials.gov databases were systematically searched. Phase II & III RCTs of SACT for ovarian, cervical, endometrial, vaginal and vulvar cancers of any stage, published 01/11/2012-01/11/2022 and reporting ethnicity were included. SACT licensed at time of search were eligible. Studies of non-systemic agents, vaccines, radiotherapy or surgery alone were excluded. Outcomes were recruitment by ethnicity and location of research sites. Recruitment by ethnicity was extracted, participation calculated for each group and compared by indication, trial phase and publication period, as well as to incidence in real-world populations. PRISMA guidance was used to report results.
Results
26 RCTs met inclusion criteria. 17,041 patients participated; 79.8% (13,595) were “Caucasian”, 9,1% (1552) “Asian”, 3.7% (630) “Black/African American”, and 6.1% (1,031) “Other/Unknown”. The remaining 1.3% (233) comprised other groups. “Caucasian” patients were over-represented in RCTs for each disease indication, and recruited at a higher rate to phase II than phase III RCTs. “Black/African American” patients recruited at a lower rate to phase III than phase II RCTs.Of 26 studies, 20 were conducted in multiple countries, 5 only in the US, and 1 only in Italy. Of 5478 sites, 4,390 (80.1%) were located in North America or Europe, 187 (3.4%) in East Asia, and 901 (16.5%) in other regions. Notably, no sites were located in Africa or South Asia.
Conclusions
Ethnic minorities are under-represented in contemporary gynae-oncology RCTs. Efforts must be made to include ethnic minority patients to ensure findings are generalisable to real-world populations.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
K. Man: Financial Interests, Institutional, Research Funding: UK National Institute for Health and Care Research, Hong Kong Research Grant Council, CW Maplethorpe Fellowship, European Commission Framework Horizon 2020 , Innovation and Technology Commission of the Government of the Hong Kong Special Administrative Region; Financial Interests, Personal, Funding: IQVIA Ltd. S. Nicum: Financial Interests, Personal, Advisory Board: GSK, AstraZeneca; Financial Interests, Personal, Invited Speaker: GSK, AstraZeneca, Clovis; Financial Interests, Personal, Other: GSK; Financial Interests, Personal, Stocks/Shares: GSK; Financial Interests, Institutional, Funding: AstraZeneca. All other authors have declared no conflicts of interest.
Resources from the same session
800P - Response to chemotherapy following PARP inhibition in UK ovarian cancer (OC) patients
Presenter: Sarah Howlett
Session: Poster session 11
802P - Real-world data of olaparib maintenance therapy in patients with BRCA-mutated platinum-sensitive relapsed ovarian cancer: Final results of the C-PATROL study
Presenter: Frederik Marmé
Session: Poster session 11
803P - Pre-treatment systemic inflammatory markers predict survival in endometrial cancer cases: A Japanese gynaecologic oncology group 2043 exploratory data analysis
Presenter: Shin Nishio
Session: Poster session 11
805P - Tumor-informed ctDNA detection as a predictive marker for postoperative residual disease in epithelial ovarian cancer: A feasibility study
Presenter: Christoph Grimm
Session: Poster session 11
806P - Pilot ambulatory malignant bowel obstruction (MBO) electronic monitoring program in patients with gynecologic cancers
Presenter: Ainhoa Madariaga Urrutia
Session: Poster session 11
807P - Predicting surgical outcomes in patients with advanced ovarian cancer through MRI based preoperative evaluation
Presenter: Shujuan Liu
Session: Poster session 11
808P - Cell-free human papillomavirus (HPV) DNA is a sensitive biomarker for monitoring treatment response and for detecting relapse in locally advanced cervical cancer
Presenter: Lars Sivars
Session: Poster session 11
809P - Mental and socioeconomic burden in endometrial and cervical cancer patients: A Swedish population-based study of survivorship
Presenter: jiangrong wang
Session: Poster session 11
810P - The influence of preoperative conization (pc) to patient’s (pts) outcome and tumor biology of cervical cancer (CC)
Presenter: Dimitra Trantaki
Session: Poster session 11