Abstract 600P
Background
Ethnicity and deprivation affect cancer outcomes. We sought to determine whether the ovarian cancer (OC) trial population was representative of the general OC population in terms of ethnicity and socio-economic status (SES), across two London tertiary cancer centres.
Methods
All OC patients treated between 2017 and 2022 were included. Any patients participating in a clinical trial during this period were included in the trial population (TP) and the remainder classified as the non-trial population (NTP). Demographic and treatment data were collected from electronic patient records. Ethnicity was classified using NHS coding, based on the UK 2021 Census. The UK Indices of Multiple Deprivation (IMD) was calculated based upon postcode, grouped into quintiles. Pearson’s chi-square test was used to evaluate differences between TP and NTP.
Results
215 TP and 680 NTP were included. In the TP; 88, 104 and 23 entered phase II, phase III or observational trials, respectively. 11 (5.1%) TP were non-English speaking. There was a statistically significant difference in SES (p=0.0260) and ethnicity (p<0.0001) between TP and NTP cohorts (Table). Table: 600P
TP (n=215; %) | NTP (n=680; %) | P value | ||
Socio-Economic Status: Indices of Multiple Deprivation (Quintiles) | Q1 Most Deprived | 30 (13.9) | 107 (15.7) | P = 0.0260 |
Q2 | 50 (23.3) | 234 (34.4) | ||
Q3 | 51 (23.7) | 128 (18.8) | ||
Q4 | 35 (16.3) | 106 (15.6) | ||
Q5 Least Deprived | 43 (20.0) | 104 (15.3) | ||
Unclassified | 6 (2.8) | 1 (0.2) | ||
Ethnicity | Asian or Asian British | 14 (6.5) | 86 (12.6) | P <0.0001 |
Black (African, Black British, Black Caribbean, Black Other) | 11 (5.1) | 65 (9.6) | ||
Other ethnic group | 11 (5.1) | 53 (7.8) | ||
Mixed/Multiple Ethnic Groups | 8 (3.7) | 7 (1.0) | ||
White (British, Irish, Other) | 157 (73.0) | 381 (56.0) | ||
Unclassified | 14 (6.5) | 88 (12.9) |
The odds ratio for clinical trial enrolment was 0.69 (95% confidence interval (CI): 0.50 - 0.94; p=0.018) and 0.51 (95% CI: 0.35 - 0.74; p=0.003) for those more vs less deprived and in non-white vs white patients, respectively.
Conclusions
Patients with higher levels of deprivation and non-white ethnicity were under-represented in clinical trials at our centres, which may worsen health disparities. Further research is required to understand the systematic, clinician-focused and patient-focused barriers to trial recruitment in such groups.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.