Imaging of heart and lung changes after childhood cancer treatment in ALL or lymphoma
Official title: "MaximALL" More Than Just X-Rays - Imaging of Chemotherapy-induced Morphological and Functional Cardiovascular and Lung Changes After Childhood ALL and Other Cancers - a Monocentric Late Effects Study (MaximALL)
Run by University of Erlangen-Nürnberg Medical School · NCT07705178 · Data updated 2026-11-12
This study tests whether MRI, MSOT, and echocardiography can detect lasting heart and lung changes in adults who were treated for ALL or lymphoma in childhood, compared with healthy controls.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 3 Years and up |
| Sex | All |
| Enrollment | 180 (estimated) |
| Sponsor | University of Erlangen-Nürnberg Medical School Academic / other |
| Locations | 1 site (Erlangen) |
| Status | Recruiting |
| Started | July 1, 2026 |
| Main results expected | May 31, 2028 |
| Study ends | October 31, 2028 |
| Registry record updated | October 30, 2026 |
| Trial ID | NCT07705178 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults (18+ years) who completed ALL or lymphoma treatment in childhood and are currently in long-term follow-up.
✕Probably not a fit
Patients without a history of childhood cancer treatment or who do not undergo the imaging procedures may not directly benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Researchers will compare survivors of childhood ALL or lymphoma who are now long-term patients with healthy controls. They will use low-field MRI, multispectral optoacoustic tomography, spirometry, DLCO, echocardiography with strain analysis, and ECG, along with questionnaires about physical and mental health. The goal is to validate and expand findings on ventilation and perfusion defects and reduced aerobic capacity, and to characterize long-term cardiopulmonary effects after childhood cancer treatment. This multicenter follow-up study will focus on individuals at least 5 years post-treatment and will assess structural and functional changes in the lungs and heart. Safety and feasibility of the imaging approaches in this population will also be evaluated.
Why it matters
Potential benefit: If successful, the study could improve understanding of late effects after childhood cancer treatment and inform monitoring and management for survivors.
How similar studies have gone: Prior data suggest detectable cardiopulmonary changes in this population, but larger validation in a multicenter setting is needed.
Who can join: the full rules
Show full inclusion / exclusion criteria
Control Group: Inclusion Criteria: * no cancer diagnosis * no lung diseases * no vascular diseases * No subjective reduction in physical performance * age \>/= 18 years Exclusion Criteria: * Pregnancy, Lactation * Known pleural or pericardial effusion * Critical condition (requiring respiratory support, ventilation, oxygen, shock, symptomatic heart failure) * Marked thoracic deformities/malformations * Previous lung surgery * Injuries that do not allow physical stress diagnostics * Rejection of MRI imaging * General contraindications for MRI examinations (e.g. electrical implants such as cardiac pacemakers or perfusion pumps, copper IUD etc.) Survivors of ALL: Inclusion Criteria: * Completed therapy for ALL * age \>/= 3 years Exclusion Criteria: * Pregnancy, Lactation * Known pleural or pericardial effusion * Critical condition (requiring respiratory support, ventilation, oxygen, shock, symptomatic heart failure) * Marked thoracic deformities/malformations * Previous lung surgery * Injuries that do not allow physical stress diagnostics * Rejection of MRI imaging * General contraindications for MRI examinations (e.g. electrical implants such as cardiac pacemakers or perfusion pumps, copper IUD etc.) Survivors of Lymphoma: Inclusion Criteria: * Completed therapy for lymphoma * age \>/= 3 years Exclusion Criteria: * Pregnancy, Lactation * Known pleural or pericardial effusion * Critical condition (requiring respiratory support, ventilation, oxygen, shock, symptomatic heart failure) * Marked thoracic deformities/malformations * Previous lung surgery * Injuries that do not allow physical stress diagnostics * Rejection of MRI imaging * General contraindications for MRI examinations (e.g. electrical implants such as cardiac pacemakers or perfusion pumps, copper IUD etc.)
Where it's running
-
Department of Pediatrics and Adolescent Medicine
Erlangen, Germany Recruiting
Study contacts
- Study coordinator: Axel Karow, PD. Dr. med.
- Email: axel.karow@uk-erlangen.de
- Phone: 09131 8533118
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.