Optimising Cardiovascular Health in Endometrial Cancer Survivors (OPTIMUS)

Women successfully treated for endometrial cancer remain at higher risk of dying than women without a history of the disease, predominately due to an excess risk of cardiovascular disease. Our previous work has shown that endometrial cancer survivors are more likely to have undiagnosed and undertreated cardiovascular risk factors than the general population, despite being seen regularly by medical professionals. This study aims to determine the impact of optimising modifiable cardiovascular risk factors in endometrial cancer survivors on their quality of life and to identify barriers to lifestyle modifications.

Study Overview

• Status: Active, not recruiting
• Conditions: Cardiovascular Diseases; Endometrial Cancer
• Intervention / Treatment: Behavioral: Lifestyle modification; Drug: Cardiovascular Agents, Other; Other: QRISK 3 Score

Detailed Description

A comprehensive cardiovascular risk assessment will be performed as part of clinical care on women previously treated for endometrial cancer at the study site. This will include a focused interview, examination to determine body mass index (BMI) and waist circumference, blood pressure, blood tests and a urine sample.

The blood tests will screen for diabetes and non-diabetic hyperglycaemia (HbA1c), renal impairment (full blood count- FBC, urea and electrolytes- U&E), non-alcoholic fatty liver disease and contraindication to statin therapy (liver function tests- LFT), hypercholesterolaemia (total, HDL and LDL cholesterol) and hypothyroidism (thyroid function tests- TFT). Urine samples will be used to screen for renal impairment using dipstick testing for microscopic haematuria and determination of albumin: creatinine ratio (ACR).

An individualised cardiovascular risk assessment will be undertaken using the QRISK3 score, which is assessed by virtue of the presence or absence of individual cardiovascular risk factors.

Based on these findings, an individualised management plan will be generated and appropriate treatment for any modifiable risk factors commenced in accordance with NICE (National Institute for Health and Care Excellence) and local guidelines. This will include advice and support with lifestyle modification, commencing medication if needed and referral to community or specialist clinics. This will be carried with close communication and in conjunction with the patient's general practitioner (GP).

Women will be followed up over a one year period to monitor their response and compliance to treatment and the impact this has on their quality of life.

The quality of life assessments will be undertaken by a member of the research team using the generic 36-Item Short Form Survey [SF-36] and cancer-specific Quality of Life in Adult Cancer Survivors [QLACS] questionnaires. A subset of approximately twenty women, purposively sampled to include maximal variation in age, body mass index and time from diagnosis, will be selected to participate in a qualitative study of the barriers to the implementation and adherence of lifestyle interventions.

Study visits will be timed to coincide with routine follow-up appointments or be carried out remotely by telephone or Zoom to minimise the risk of COVID-19 exposure. Follow-up visits will consist of a focused interview and quality of life questionnaires, with a repeat of the comprehensive cardiovascular risk assessment at 12 months.

• Study Type: Observational
• Enrollment (Actual): 80

Contacts and Locations

Study Locations

• United Kingdom
  • Manchester, United Kingdom, M13 9WL
    • St Mary's Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 110 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

Women who have had endometrial cancer treated within the last 4 years.

Description

Inclusion Criteria:

• Previous treatment for endometrial cancer within the last four years
• Able to consent to participation in the study

Exclusion Criteria:

• Currently undergoing treatment for endometrial cancer recurrence
• Anticipated life expectancy <12 months
• To cease routine surveillance in next 12 months
• Not registered with a General Practitioner (GP)

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort

Intervention / Treatment

Endometrial cancer survivors

Behavioral: Lifestyle modification; Could include all/some of the following: weight loss, increased physical activity, smoking cessation and reduction in alcohol intake; Drug: Cardiovascular Agents, Other; Could include all/some of the following: statins, antihypertensives, diabetic medication, levothyroxine; Other: QRISK 3 Score; Could include a combination of lifestyle measures and/or cardiovascular agents as described above

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
To assess the change in quality of life in endometrial cancer survivors by treating modifiable cardiovascular risk factors over a period of 12 months.	The generic 36-Item Short Form Survey (SF-36) questionnaire focused on general wellbeing and quality of life. A variety of responses are used in this questionnaire. Some use numeric indicators, with a lower overall score meaning a worse outcome and a higher score meaning a better outcome.	Baseline, 3 months, 6 months and 12 months.
To assess the change in quality of life in endometrial cancer survivors by treating modifiable cardiovascular risk factors over a period of 12 months.	The cancer-specific Quality of Life in Adult Cancer Survivors (QLACS) questionnaire focused on general well-being and quality of life. This questionnaire uses numeric indicators from 1 to 7, with a lower overall score meaning a worse outcome and a higher score meaning a better outcome.	Baseline, 3 months, 6 months and 12 months.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
To identify barriers to the implementation of lifestyle changes in endometrial cancer survivors.	A subset of approximately twenty women, will take part in semi-structured interviews to discuss barriers to implementation and adherence to lifestyle interventions. Questioning will focus on the motivations, opportunities and capability of individuals to change their behaviour and will be thematically analysed, with particular attention paid to features of the Behavioural Change Wheel.	Between 3 and 9 months.

Collaborators and Investigators

• Sponsor: University of Manchester
• Investigators: Principal Investigator: Emma Crosbie, University Of Manchester

Study record dates

Study Major Dates

• Study Start (Actual): February 9, 2022
• Primary Completion (Anticipated): April 1, 2024
• Study Completion (Anticipated): October 1, 2024

Study Registration Dates

• First Submitted: January 4, 2022
• First Submitted That Met QC Criteria: January 31, 2022
• First Posted (Actual): February 1, 2022

Study Record Updates

• Last Update Posted (Actual): May 16, 2023
• Last Update Submitted That Met QC Criteria: May 13, 2023
• Last Verified: May 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms; Urogenital Neoplasms; Neoplasms by Site; Uterine Neoplasms; Genital Neoplasms, Female; Uterine Diseases; Cardiovascular Diseases; Endometrial Neoplasms
• Other Study ID Numbers: IRAS 298610

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No