Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsN/A

ICONIC: Improving Outcomes Through Collaboration in OsteosarComa

Sponsor: University College, London

NCT ID: NCT04132895

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
observational only, no interventions are prescribed in protocol. (other)
How long the study runs
Study runs about 87 months (dates as stated)
About the drug or intervention
observational only, no interventions are prescribed in protocol. — other: * Treatment will be given as per usual standard of care.
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
Not specified
Who
All
Number of participants
300
Started
2019-10-25
Last checked
2024-07

Plain English Summary

What is this study?

  • • Testing a new treatment for osteosarcoma
  • • Clinical study - 300 participants
  • • There has been little improvement in outcome for patients with osteosarcoma (OS) over the last 20 years

Who can take part?

  • • Adults
  • • Diagnosed with osteosarcoma

Where?

  • • London - University College Hospitals London NHS Foundation Trust
  • • Aberdeen - NHS Grampian Health Board
  • • Birmingham - Birmingham Women's and Childrens NHS Foundation Trust
  • • Birmingham - The Royal Orthopaedic Hospital NHS Foundation Trust
  • • +18 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

There has been little improvement in outcome for patients with osteosarcoma (OS) over the last 20 years. There have been only a few clinical trials of new treatments and no major new therapies introduced recently. This is in part because there is no good understanding of the biology of osteosarcoma, but also trials have only included subgroups of patients. The more that is understood about how and why osteosarcoma arises and grows the better clinicians will be able to decide what treatments are most likely to work best. The purpose of this project is to collect high quality clinical data about patients of all ages with osteosarcoma, such as information about the size of the disease, how it was diagnosed and where it is at diagnosis, what treatments were given and how the disease responded the treatments. Blood and tissue samples will also be collected for analysis in research laboratories. By looking at the results of the laboratory findings and the clinical data together, the questions will start to be answered about why osteosarcomas arise and grow, what makes it spread, and why some patients respond to treatment better than others. As time goes on, this information is planned to be used to develop clinical trials of new treatments. Alongside this, the aim is to find out more about how osteosarcoma and its treatments affect the lives of those living with this disease. This information will help provide the most appropriate care and support that will meet the needs of each patient. Ultimately, the aim is to improve the care and treatment of osteosarcoma patients so that they may live longer and better lives.

More detail

Osteosarcoma is the most common bone sarcoma, accounting for approximately 30% of all bone sarcoma diagnoses. In England, it accounts for approximately 130 cases per year across all ages. Generally osteosarcoma has an early peak in adolescent patients, with a second peak in patients over 60 years of age. There are differing treatments, including chemotherapy with more than one drug and surgery to the primary site - and for metastases where these occur. Outcome, however, has improved little over the past 25 years with the proportion of patients surviving to 5 years remaining at about 42% for all ages and stages in the UK. Patients under 40 years of age (52%) are more likely to survive for 5 years than patients over 40 years (25%). Survival also depends on the primary site of the osteosarcoma. It is poor for patients with tumours that are not in the limbs, at 36% for patients under the age of 40 years and as low as 6% for patients over 40 years. Also patients with metastatic disease at diagnosis still have a poor outcome. The use of chemotherapy and surgery depends on factors such as age, the site of the osteosarcoma, how far spread it is and how well the patient is generally, with approximately two thirds of patients currently receiving chemotherapy, radiotherapy and surgery in England each year. The most recent randomised trial for osteosarcoma, EURAMOS-1 \[A randomized trial of the European and American Osteosarcoma Study Group to optimize treatment strategies for resectable osteosarcoma based on histological response to pre-operative chemotherapy\], was an excellent example of an international effort to seek improved treatments for a rare cancer. Despite the participation of over 2000 patients, there were no changes to the standard of care for osteosarcoma. There is still an unmet need to find new approaches, including biomarkers and new, targeted patient specific therapeutic approaches to improve outcomes for this group. This includes searching for improved systemic treatments and better approaches to management of the osteosarcoma. The ICONIC Study will provide a dataset for translational research into osteosarcoma. Osteosarcoma clinical trials to date have focussed on a limited number of outcomes, usually in the younger patients with a tumour in a limb. So addressing complex inter-related questions has not been possible and several subpopulations of patients have not been studied. This limits opportunities to improve the standard of care. These groups include: * patients with widely spread (metastatic) disease; * patients with tumours in the less common locations such as the pelvis, spine and skull; * patients with osteosarcoma with a background of skeletal abnormalities or an underlying genetic predisposition; * the 50% of osteosarcoma arising in patients over 40 years. Little is currently known about factors influencing treatment decisions in these groups and how consistently a standard of care is applied. The effect of treatments on quality of life, patient reported outcomes and other performance assessments is also not well described or understood. As osteosarcoma is quite rare it can be difficult for General Practitioners (GPs) to identify symptoms and patients often wait a long time before tests for osteosarcoma are carried out. How this affects outcomes is not known. Overall, there is a need to broaden the ambition and scope of osteosarcoma research while improving access for all patients.

Osteosarcoma

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: Not specified
  • Who can join: All genders

What the study is looking for

  • ✓Written agreement to take part of patient and/or parent/legal guardian.

Who cannot take part

  • ✗Diagnosis more than four months prior to registration.
See the full 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 Is This Study? (22 UK sites)

University College Hospitals London NHS Foundation Trust

London NW1 2BU, United Kingdom

Recruiting
Site contact (verified)
The Chief Investigatorctc.iconic@ucl.ac.uk

NHS Grampian Health Board

Aberdeen, United Kingdom

Recruiting
Hospital R&D contact (matched)

Fiona Brebner

gram.randd@nhs.scot01224 551121

Birmingham Women's and Childrens NHS Foundation Trust

Birmingham, United Kingdom

Recruiting
Hospital R&D contact (matched)

Sarah Hadfield

bwc.research@nhs.net0121 333 8751

The Royal Orthopaedic Hospital NHS Foundation Trust

Birmingham, United Kingdom

Recruiting
Hospital R&D contact (matched)

Gareth Stephens

roh-tr.research@nhs.net0121 685 4316

University Hospitals Birmingham NHS Foundation Trust

Birmingham, United Kingdom

Recruiting
Hospital R&D contact (matched)

Sarah Pountain Head of Research Governance

R&D@uhb.nhs.uk0121 371 4185

Cambridge University Hospitals NHS Foundation Trust

Cambridge, United Kingdom

Recruiting
Hospital R&D contact (matched)

Stephen Kelleher

cuh.research@nhs.net01223 348490

Cardiff and Vale University LHB

Cardiff, United Kingdom

Recruiting
Hospital R&D contact (matched)

Sarah Martin

research.development@wales.nhs.uk029 2074 6986

NHS Lothian Health Board

Edinburgh, United Kingdom

Recruiting
Hospital R&D contact (matched)

Accord Office

enquiries@accord.scot0131 242 3330

NHS Greater Glasgow and Clyde Health Board

Glasgow, United Kingdom

Recruiting
Hospital R&D contact (matched)

Radek Penar

radoslaw.penar@nhs.scotn/a

Leeds Teaching Hospitals NHS Trust

Leeds, United Kingdom

Recruiting
Hospital R&D contact (matched)

R&I Team

leedsth-tr.researchfacilitation@nhs.net0113 2060469

University Hospitals of Leicester NHS Trust

Leicester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Carolyn Maloney

uhl-tr.researchandinnovationadminmailbox@nhs.net0116 258 8351

Alder Hey Children's NHS Foundation Trust

Liverpool, United Kingdom

Recruiting
Hospital R&D contact (matched)

Kelly Davies

research@alderhey.nhs.uk0151 2525570

The Clatterbridge Cancer Centre NHS Foundation Trust

Liverpool, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Maria Maguire

maria.maguire2@nhs.net0151 556 5321

Manchester University NHS Foundation Trust

Manchester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Elizabeth Mainwaring

R&D.applications@mft.nhs.uk0161 276 3340

The Christie NHS Foundation Trust

Manchester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Innovation Office

the-christie.ri@nhs.net---

The Newcastle upon Tyne Hospitals NHS Foundation Trust

Newcastle, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Development

nuth.genericqueries@nhs.net0191 282 4926

Nottingham University Hospitals NHS Trust

Nottingham, United Kingdom

Recruiting
Hospital R&D contact (matched)

Alison Lloyd

nuhnt.researchsponsor@nhs.net0115 9249924

The Robert Jones and Agnes Hunt Orthopaedic Hospital NHS Foundation Trust

Oswestry, United Kingdom

Recruiting
Hospital R&D contact (matched)

Teresa Jones

rjah.researchoffice@nhs.net01691 404143

Oxford University Hospitals NHS Foundation Trust

Oxford, United Kingdom

Recruiting
Hospital R&D contact (matched)

Shahista Hussain

ouhtma@ouh.nhs.uk---

Sheffield Children's NHS Foundation Trust

Sheffield, United Kingdom

Recruiting
Hospital R&D contact (matched)

Sarah Flude

scn-tr.research.governance@nhs.net0114 226 7980

Sheffield Teaching Hospitals NHS Foundation Trust

Sheffield, United Kingdom

Recruiting
Hospital R&D contact (matched)

Alessia Dunn

STH.ResearchAdministration@nhs.net0114 2712550

University Hospital Southampton NHS Foundation Trust

Southampton, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Mikayala King

researchmanagement@uhs.nhs.uk023 81208215

How to Get in Touch

Krystyna Reczko

Sponsor contact

CONTACT

020 7679 9878 ctc.iconic@ucl.ac.uk

Rubina Begum

Sponsor contact

CONTACT

020 7679 9514 ctc.iconic@ucl.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-07