{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,31]],"date-time":"2026-10-31T09:10:50Z","timestamp":1793437850044,"version":"4.5.0"},"reference-count":32,"publisher":"American Medical Association (AMA)","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA"],"abstract":"<jats:sec>\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Diagnosing cardiac amyloidosis remains challenging because current imaging approaches are limited to transthyretin amyloidosis. A noninvasive test capable of directly imaging cardiac amyloidosis from various amyloid types and in multiple organs could address an important unmet diagnostic need.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      To evaluate the sensitivity and specificity of\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide positron emission tomography (PET)\/computed tomography (CT) for diagnosing cardiac amyloidosis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>\n                      Prospective, multicenter (18 US centers), single-group study evaluating the efficacy of\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide to diagnose cardiac amyloidosis. This study was conducted from January 14, 2025, to March 12, 2026, including a 60-day follow-up period. Three physicians with cardiac PET\/CT experience independently reviewed PET\/CT images for visual cardiac\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide uptake while blinded to clinical data. Three expert clinical amyloidosis physicians, blinded to PET\/CT data, independently adjudicated the diagnosis based on the standard-of-care diagnostic algorithm. A total of 195 adults suspected of having cardiac amyloidosis were enrolled when they presented for diagnostic evaluation at participating institutions, excluding patients with an established diagnosis of cardiac or systemic amyloidosis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interventions<\/jats:title>\n                    <jats:p>\n                      PET\/CT scans were obtained 3 to 5 hours after intravenous administration of 1 mCi of\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide. Potassium iodide (130 mg) was given orally for 3 days starting at least 30 minutes prior to\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide injection.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>\n                      Coprimary end points of this study were to assess the sensitivity and specificity of\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide for the diagnosis of cardiac amyloidosis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Overall, 170 patients were included (median [IQR] age, 72 [64-79] years; 75.3% male, 19.2% Black, 79.0% White). Median N-terminal pro\u2013brain natriuretic peptide was 471 pg\/mL and 61.7% had New York Heart Association class II or III heart failure symptoms. The overall sensitivity was 94% (95% CI, 85%-98%;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001); specificity, 86% (95% CI, 77%-92%;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001); positive predictive value, 85% (95% CI, 75%-92%); and negative predictive value, 94% (95% CI, 87%-98%).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide PET\/CT is highly sensitive and specific for diagnosing cardiac amyloidosis with an acceptable safety profile. These results support\n                      <jats:sup>124<\/jats:sup>\n                      I-evuzamitide PET\/CT as a diagnostic test to evaluate patients with suspected cardiac amyloidosis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Trial Registration<\/jats:title>\n                    <jats:p>\n                      ClinicalTrials.gov Identifier:\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/clinicaltrials.gov\/study\/NCT06788535\">NCT06788535<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jama.2026.17361","type":"journal-article","created":{"date-parts":[[2026,8,30]],"date-time":"2026-08-30T12:30:20Z","timestamp":1788093020000},"source":"Crossref","is-referenced-by-count":3,"title":["<sup>124<\/sup>\n                    I-Evuzamitide Positron Emission Tomography\/Computed Tomography for Diagnosing Cardiac Amyloidosis"],"prefix":"10.1001","author":[{"given":"Sharmila","family":"Dorbala","sequence":"first","affiliation":[{"name":"Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Brigham and Women\u2019s Hospital, Boston, Massachusetts"},{"name":"Cardiac Amyloidosis Program, Brigham and Women\u2019s Hospital, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mathew S.","family":"Maurer","sequence":"additional","affiliation":[{"name":"Columbia University, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarah A. 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