Redefining Cardiac Involvement and Targets of Treatment in Systemic Immunoglobulin AL Amyloidosis

Author:

Porcari Aldostefano123,Masi Ambra1,Martinez-Naharro Ana1,Razvi Yousuf1,Patel Rishi1,Ioannou Adam1,Rauf Muhammad U.1,Sinigiani Giulio4,Wisniowski Brendan1,Filisetti Stefano56,Currie-Cathey Jasmine1,O’Beara Sophie1,Kotecha Tushar1,Knight Dan1,Moon James C.78,Sinagra Gianfranco23,Virsinskaite Ruta1,Gilbertson Janet1,Venneri Lucia1,Petrie Aviva1,Lachmann Helen1,Whelan Carol1,Kellman Peter9,Ravichandran Sriram1,Cohen Oliver1,Mahmood Shameem1,Manisty Charlotte10,Hawkins Philip N.1,Gillmore Julian D.1,Wechalekar Ashutosh D.1,Fontana Marianna1

Affiliation:

1. National Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, United Kingdom

2. Centre for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina (ASUGI), University of Trieste, Trieste, Italy

3. European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-HEART), Trieste, Italy

4. Department of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua, Padua, Italy

5. Cardiology University Department, Heart Failure Unit, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy

6. Faculty of Medicine, University of Milano, Milan, Italy

7. Institute of Cardiovascular Science, University College London, London, United Kingdom

8. Barts Heart Centre, West Smithfield, London, United Kingdom

9. National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland

10. St Bartholomew’s Hospital, London, United Kingdom

Abstract

ImportanceCardiac amyloid infiltration is the key determinant of survival in systemic light-chain (AL) amyloidosis. Current guidelines recommend early switching therapy in patients with a nonoptimal or suboptimal response regardless of the extent of cardiac amyloid infiltration.ObjectiveTo assess the differences between serum biomarkers, echocardiography, and cardiovascular magnetic resonance (CMR) with extracellular volume (ECV) mapping in characterizing cardiac amyloid, the independent prognostic role of these approaches, and the role of ECV mapping to guide treatment strategies.Design, Setting, and ParticipantsConsecutive patients newly diagnosed with systemic AL amyloidosis (2015-2021) underwent echocardiography, cardiac biomarkers, and CMR with ECV mapping at diagnosis. Data were analyzed from January to June 2024.Main Outcomes and MeasuresThe primary outcomes of the study were all-cause mortality and hematological response as defined according to validated criteria: no response (NR), partial response (PR), very good partial response (VGPR), and complete response (CR). Secondary outcomes were the depth and speed of hematological response and overall survival according to ECV.ResultsOf 560 patients with AL amyloidosis, the median (IQR) age was 68 years (59-74 years); 346 patients were male (61.8%) and 214 female (38.2%). Over a median (IQR) 40.5 months 9-58 months), ECV was independently associated with mortality. In the landmark analysis at 1 month, long-term survival was independent of the achieved hematological response in ECV less than 0.30% and ECV of 0.31% to 0.40%, while it was dependent on the depth of the hematological response in ECV greater than 0.40%. In the landmark analysis at 6 months, survival was independent of the achieved hematological response in ECV less than 0.30% and dependent on achieving at least PR in ECV of 0.31% to 0.40%. Survival was dependent on achieving CR in ECV of 0.41% to 0.50% and ECV greater than 0.50%. Achieving a deep hematological response at 1 month was associated with better survival compared with 6 months in patients with ECV greater than 0.40% but not with ECV less than 0.40%.Conclusions and RelevanceThis study found that ECV mapping, in systemic AL amyloidosis, is an independent predictor of prognosis, can help define the hematological response associated with better long-term outcomes for each patient and potentially inform treatment strategies.

Publisher

American Medical Association (AMA)

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