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NCT06605833Enrolling by invitation

CARDiac Toxicity Following ImmunOtherapy Treatment for Melanoma

CARD-IO - CARDiac Toxicity Following ImmunOtherapy Treatment for Melanoma

Source: ClinicalTrials.gov · Last updated 1 Oct 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

People who develop a type of skin cancer known as 'melanoma' are often treated with immunotherapy. The type of immunotherapy used for patients with melanoma is known as Immune Checkpoint Inhibitors (ICI). While ICI is very successful, it can lead to negative side effects that are known as 'immune related adverse events' (irAEs). These irAEs can affect any part of the body and can range in severity from mild symptoms to death. There has been a lot of research on irAEs that occur during ICI, but less is known about how irAEs can affect people in the long-term. Although irAEs are common from ICI, acute irAEs affecting the heart (cardiac irAEs) are uncommon. However, as they relate to the heart, they are often serious and have a higher rate of death compared to other types of irAEs. Little is known regarding the long-term effects of ICI on the heart. However, there is some evidence to suggest that ICI may also cause long-term cardiac irAEs such as accelerating a build-up of fatty materials in the arteries known as 'atherosclerosis' and inflammation of plaque in the heart. This can lead to an increased risk of heart attack. Although there are guidelines for patients on ICI treatment to receive investigations to look for irAEs, including cardiac irAEs, there are no guidelines for monitoring long-term survivors. The aim of the CARD-IO study is to establish if it is possible to investigate in long-term follow-up cardiac side-effects in patients who received ICI for melanoma. The data for this study would be used to support a larger study in the same patient population. Potentially, this could lead to a change in guidelines and long-term follow-up care for melanoma patients who have received ICI.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
60 (estimated)
First submitted
18 Sept 2024
Start date
26 Sept 2025
Primary completion date
30 Sept 2026
Lead sponsor
Royal Marsden NHS Foundation Trust
Diseases
Melanoma
NCT number
NCT06605833

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 26 Sept 2025 to the primary completion date, 30 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Known contraindications to MRI, such as claustrophobia, pregnancy, or indwelling metallic implant which is not MR conditional
  • Current active treatment with systemic therapy for any malignancy.
  • Active treatment with systemic therapy for any malignancy started after the completion of immunotherapy for melanoma.
  • Planned participation in a drug trial receiving investigational agents.

Other illness

  • Medical or psychological condition that would preclude informed consent.

Other

  • Subjects unable to comply with the study or sample schedule.

Who the study is looking for

  • Written informed consent
  • Age 18 years or older
  • Confirmed diagnosis of melanoma
  • Stage IIB or IIC or stage III or stage IV melanoma
  • Previous immunotherapy with immune-checkpoint inhibitors (anti PD-(L)1 +/- anti CTLA-4) for melanoma
  • On standard of care surveillance, at 2 to 10+ years following the completion of immunotherapy treatment

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Royal Marsden NHS Foundation Trust
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.