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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01505829
Other study ID # 11/LO/1598 CCR3694
Secondary ID C1353/A12762
Status Completed
Phase
First received
Last updated
Start date August 2012
Est. completion date October 13, 2018

Study information

Verified date January 2020
Source Institute of Cancer Research, United Kingdom
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This project seeks to develop a quantitative imaging biomarker for evaluating and monitoring treatment response in ovarian cancer metastases and assess its potential in monitoring treatment response. This will involve standardising DW-MRI for the abdomen and pelvis across multiple centres and platforms, assessing reproducibility of the measurement in patients planned for neoadjuvant chemotherapy and assessing its utility as an early response biomarker in patients with platinum-sensitive relapse due to receive therapy with carboplatin. Scanning measurements will be correlated with histopathological markers in tumour samples in order to link the biomarker with response mechanisms.


Recruitment information / eligibility

Status Completed
Enrollment 134
Est. completion date October 13, 2018
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Histologically confirmed ovarian, primary peritoneal or fallopian tube cancer stage III or IV

- Scheduled to receive neoadjuvant chemotherapy (carboplatin/cisplatin)with planned debulking surgery.

Exclusion Criteria:

- Life expectancy of less than 6 months

- MRI contraindications

- Low grade or heavily calcified disease

Study Design


Locations

Country Name City State
United Kingdom Addenbrookes Hospital, Cambridge University Hospitals NHS Foundation Trust Cambridge Cambridgeshire
United Kingdom Imperial College Healthcare NHS Trust London
United Kingdom Queen Elizabeth Hospital Newcastle Gateshead
United Kingdom Mount Vernon Cancer Centre Northwood Middlesex
United Kingdom The Institute of Cancer Research and Royal Marsden NHS Foundation Trust Sutton Surrey
United Kingdom Singleton Hospital Swansea Wales

Sponsors (7)

Lead Sponsor Collaborator
Institute of Cancer Research, United Kingdom Cambridge University Hospitals NHS Foundation Trust, Cancer Research UK, East and North Hertfordshire NHS Trust, Imperial College Healthcare NHS Trust, Northumbria Healthcare NHS Foundation Trust, Royal Marsden NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Development of a Quantitative Imaging Biomarker for Evaluating Ovarian Cancer Metastases and Assessment of its Potential in Monitoring Treatment Response. Diffusion-weighted magnetic resonance imaging (DW-MRI) for visualising peritoneal metastases will be developed.Reproducibility will be assessed in a multi-centre setting across multiple vendor platforms and field strengths by comparing 2 baseline scans per person and plotting absolute difference in ADC against mean of the 2 measurements.Biological validation will be achieved by correlating scan data (ADC change) following chemotherapy with histology of the tumour(amount of cell death) at surgery. 4.0 years
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