Improving outcomes for patients with osteosarcoma
ICONIC: Improving Outcomes Through Collaboration in OsteosarComa
This study is trying to gather information and samples from people with osteosarcoma to better understand the disease and find ways to improve treatment and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 300 (estimated) |
| Sex | All |
| Sponsor | University College, London Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 22 sites (London, Greater London and 21 other locations) |
| Trial ID | NCT04132895 on ClinicalTrials.gov |
What this trial studies
This project aims to collect high-quality clinical data and biological samples from patients diagnosed with osteosarcoma, a common bone cancer. By gathering information on disease characteristics, treatment responses, and patient demographics, the study seeks to enhance understanding of osteosarcoma biology. The collected blood and tissue samples will be analyzed in research laboratories to identify potential tumor markers and improve treatment strategies. The ultimate goal is to improve patient outcomes through better-informed clinical decisions.
Who should consider this trial
Good fit: Ideal candidates include patients of all ages with a new histological diagnosis of osteosarcoma or those with supportive imaging findings.
Not a fit: Patients diagnosed with osteosarcoma more than four months prior to registration may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies and outcomes for patients with osteosarcoma.
How similar studies have performed: While there have been few recent trials for osteosarcoma, this study's approach of comprehensive data collection and analysis is novel and aims to fill existing knowledge gaps.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * New histological diagnosis of osteosarcoma or in the absence of osteoid seen on biopsy, pathology and imaging supportive of a diagnosis of osteosarcoma. (It is well recognised that some patients may present with features suggestive of osteosarcoma (under 40 years, radiological abnormality compatible) but in whom no osteoid is detected in needle biopsy. Although categorised as spindle cell tumour of bone, such patients are usually treated in an identical approach to osteosarcoma. A definite diagnosis of osteosarcoma is then often possible after surgery when the entire resection specimen is available.) * Written informed consent of patient and/or parent/legal guardian. Exclusion Criteria: • Diagnosis more than four months prior to registration.
Where this trial is running
London, Greater London and 21 other locations
- University College Hospitals London NHS Foundation Trust — London, Greater London, United Kingdom (Recruiting)
- NHS Grampian Health Board — Aberdeen, United Kingdom (Recruiting)
- Birmingham Women's and Childrens NHS Foundation Trust — Birmingham, United Kingdom (Recruiting)
- The Royal Orthopaedic Hospital NHS Foundation Trust — Birmingham, United Kingdom (Recruiting)
- University Hospitals Birmingham NHS Foundation Trust — Birmingham, United Kingdom (Recruiting)
- Cambridge University Hospitals NHS Foundation Trust — Cambridge, United Kingdom (Recruiting)
- Cardiff and Vale University LHB — Cardiff, United Kingdom (Recruiting)
- NHS Lothian Health Board — Edinburgh, United Kingdom (Recruiting)
- NHS Greater Glasgow and Clyde Health Board — Glasgow, United Kingdom (Recruiting)
- Leeds Teaching Hospitals NHS Trust — Leeds, United Kingdom (Recruiting)
- University Hospitals of Leicester NHS Trust — Leicester, United Kingdom (Recruiting)
- Alder Hey Children's NHS Foundation Trust — Liverpool, United Kingdom (Recruiting)
- The Clatterbridge Cancer Centre NHS Foundation Trust — Liverpool, United Kingdom (Recruiting)
- Manchester University NHS Foundation Trust — Manchester, United Kingdom (Recruiting)
- The Christie NHS Foundation Trust — Manchester, United Kingdom (Recruiting)
- The Newcastle upon Tyne Hospitals NHS Foundation Trust — Newcastle, United Kingdom (Recruiting)
- Nottingham University Hospitals NHS Trust — Nottingham, United Kingdom (Recruiting)
- The Robert Jones and Agnes Hunt Orthopaedic Hospital NHS Foundation Trust — Oswestry, United Kingdom (Recruiting)
- Oxford University Hospitals NHS Foundation Trust — Oxford, United Kingdom (Recruiting)
- Sheffield Children's NHS Foundation Trust — Sheffield, United Kingdom (Recruiting)
- Sheffield Teaching Hospitals NHS Foundation Trust — Sheffield, United Kingdom (Recruiting)
- University Hospital Southampton NHS Foundation Trust — Southampton, United Kingdom (Recruiting)
Study contacts
- Principal investigator: Sandra Strauss, MD — University College Hospitals London
- Study coordinator: Krystyna Reczko
- Email: ctc.iconic@ucl.ac.uk
- Phone: 020 7679 9878
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.