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REmote iSchemic condItioning in Lymphoma PatIents REceiving ANthraCyclinEs

REmote iSchemic condItioning in Lymphoma PatIents REceiving ANthraCyclinEs

Recruiting
18-99 years
All
Phase N/A

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Overview

Multinational, prospective, proof of concept phase II, double-blinded, sham-controlled, randomized clinical trial (RCT) to evaluate the efficacy and safety of Remote Ischaemic PreConditioning (RIPC) in Lymphoma patients receiving anthracyclines.

Description

Multinational, prospective, proof of concept phase II, double-blinded, sham-controlled, randomized clinical trial (RCT) to evaluate the efficacy and safety of Remote Ischaemic PreConditioning (RIPC) in lymphoma patients receiving anthracyclines. Patients scheduled to undergo ≥5 chemotherapy cycles will be eligible. Patients fulfilling all inclusion and no exclusion criteria will be enrolled and undergo baseline Cardiac Magnetic Baseline (CMR), and high sensitivity troponin (hsTn) and NT-proBNP blood test. Patients with confirmed LVEF >40% by CMR will be randomized 1:1 to RIPC vs simulated RIPC (Sham). After the third chemotherapy cycle, a second CMR+ hsTn/ NT-proBNP will be performed for the validation of the early marker of cardiotoxicity. A third hsTn/ NT-proBNP blood test will be performed in the last chemotherapy cycle. Nine weeks after finishing chemotherapy, a last CMR+ hsTn/ NT-proBNP will be performed. Patients will be followed-up for clinical events at 6, 12, 18, 30 and 42 months until the last patient undergoes the final CMR. When the last patient undergoes the third CMR, the follow-up will be closed. The median follow-up estimation for clinical endpoints is 24 months (range: 6 to 42 months).

Eligibility

Inclusion Criteria:

        ≥18 years old First Lymphoma diagnosis Scheduled to undergo ≥5 chemotherapy cycles
        including anthracyclines. Pre-chemo LVEF >40% on screening echocardiography.
        Presence of ≥1 of the following risk factors for developing cardiotoxicity:
        Previous coronary artery disease (any of the following):
        Previous coronary revascularisation (PCI or CABG) or Medical history of previous
        significant nonrevascularized coronary stenosis Previous Acute Coronary Syndrome / Acute
        Myocardial Infarction with a LVEF > 40 LVEF 41-54% Age ≥ 65 years old Previous diagnosis of
        arterial hypertension (with or without treatment) Chronic kidney disease (estimated
        glomerular filtration rate <60ml/min/1.73m2) Current or former smoker. Obesity (BMI≥30
        kg/m2) LVH on screening echocardiography (LV thickness ≥12mm). High alcohol intake (≥21
        alcoholic beverages per week) Sinus rhythm on screening ECG Previous diagnosis of diabetes
        (except those treated with sulfonylureas or those with neuropathy) Previous
        non-anthracycline-based chemotherapy Signed Informed Consent Form (ICF)
        Exclusion Criteria:
          -  History of any of the following diseases:
               -  Any cancer who received anthracyclines treatment before the index episode.
               -  Previous clinical diagnosis of heart failure.
               -  Permanent atrial fibrillation (AF).
               -  Severe valvular or sub-valvular heart disease.
               -  Severe peripheral arterial disease in the upper extremities or arteriovenous (AV)
                  shunt in the arm selected for RIPC.
          -  Clinical diagnosis of diabetes neuropathy
          -  Contraindication for CMR:
               -  Severe claustrophobia.
               -  Any device which is known to threaten or pose hazard in all MR environments
                  (http://www.mrisafety.com/).
               -  Patients with implanted biomedical cardiac devices: pacemakers, ICDs or CRT.
          -  Severe thrombocytopenia (platelets <50,000/µL) on any blood test within the previous 3
             months.
          -  Patients participating in other clinical trials.
          -  Impossibility to consent or undergo study follow-ups.

Study details
    Anthracycline-induced Cardiac Toxicity
    Lymphoma

NCT05223413

Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III

27 January 2024

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