Why the study?
During anthracycline cancer treatment, there is a lack of cardiotoxicity biomarkers besides cardiac dysfunction.
Does [123I]MIBG imaging detect doxorubicin-induced cardiotoxicity earlier than [18F]FDG imaging in a rat model?
Does [123I]MIBG imaging detect doxorubicin-induced cardiotoxicity earlier than [18F]FDG imaging in a rat model?
Cardiac innervation imaging with [123I]MIBG detects anthracycline-induced cardiotoxicity earlier than [18F]FDG PET or cardiac MRI in a preclinical model.
[123I]MIBG detects doxorubicin cardiotoxicity earlier than FDG or MRI in rats; leaves open translation to clinical monitoring.
Background During anthracycline treatment of cancer, there is a lack for biomarkers of cardiotoxicity besides the cardiac dysfunction. The objective of the present study was to compare [ 18 F]FDG and [ 123 I]MIBG (metaiodobenzylguanidine) in a longitudinal study in a doxorubicin-induced cardiotoxicity rat model. Methods Male Wistar Han rats were intravenously administered 3 times at 10 days’ interval with saline or doxorubicin (5 mg/kg). [ 123 I]MIBG SPECT/CT (single photon emission computed tomography-computed tomography) and simultaneous [ 18 F]FDG PET (positron emission tomography)/7 Tesla cardiac MR (magnetic resonance) imaging acquisitions were performed at 24 h interval before first doxorubicin / saline injection and every 2 weeks during 6 weeks. At 6 weeks, the heart tissue was collected for histomorphometry measurements. Results At week 4, left ventricle (LV) end-diastolic volume was significantly reduced in the doxorubicin group. At week 6, the decreased LV end-diastolic volume was maintained, and LV end-systolic volume was increased resulting in a significant reduction of LV ejection fraction (47 ± 6% vs. 70 ± 3%). At weeks 4 and 6, but not at week 2, myocardial [ 18 F]FDG uptake was decreased compared with the control group (respectively, 4.2 ± 0.5%ID/g and 9.2 ± 0.8%ID/g at week 6). Moreover, [ 18 F]FDG cardiac uptake correlated with cardiac function impairment. In contrast, from week 2, a significant decrease of myocardial [ 123 I]MIBG heart to mediastinum ratio was detected in the doxorubicin group and was maintained at weeks 4 and 6 with a 45.6% decrease at week 6. Conclusion This longitudinal study precises that after doxorubicin treatment, cardiac [ 123 I]MIBG uptake is significantly reduced as early as 2 weeks followed by the decrease of the LV end-diastolic volume and [ 18 F]FDG uptake at 4 weeks and finally by the increase of LV end-systolic volume and decrease of LV ejection fraction at 6 weeks. Cardiac innervation imaging should thus be considered as an early key feature of anthracycline cardiac toxicity.
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Oudot et al. (2021) studied this question.
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