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

Importance Cardiac 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. Objective To 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 Participants Consecutive 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 Measures The 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. Results Of 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 Relevance This 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.

[1]  Tracking Treatment Response in Cardiac Light-Chain Amyloidosis With Native T1 Mapping , 2023, JAMA cardiology.

[2]  M. Liedtke,et al.  AL Amyloidosis for Cardiologists , 2022, JACC. CardioOncology.

[3]  P. Kellman,et al.  Multi-Imaging Characterization of Cardiac Phenotype in Different Types of Amyloidosis. , 2022, JACC. Cardiovascular imaging.

[4]  P. Kellman,et al.  Cardiovascular magnetic resonance in light-chain amyloidosis to guide treatment , 2022, European heart journal.

[5]  P. Hawkins,et al.  A UK consensus algorithm for early treatment modification in newly diagnosed systemic light‐chain amyloidosis , 2022, British journal of haematology.

[6]  R. Falk,et al.  Longitudinal strain is an independent predictor of survival and response to therapy in patients with systemic AL amyloidosis. , 2021, European heart journal.

[7]  P. Hawkins,et al.  Impact of early response on outcomes in AL amyloidosis following treatment with frontline Bortezomib , 2021, Blood Cancer Journal.

[8]  P. Milani,et al.  Clarification on the definition of complete haematologic response in light-chain (AL) amyloidosis , 2021, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

[9]  J. Weinberg,et al.  Patient outcomes in light chain (AL) amyloidosis: The clock is ticking from symptoms to diagnosis , 2020, European journal of haematology.

[10]  G. Pontone,et al.  Noncontrast Magnetic Resonance for the Diagnosis of Cardiac Amyloidosis. , 2020, JACC. Cardiovascular imaging.

[11]  G. Pontone,et al.  Multiparametric Echocardiography Scores for the Diagnosis of Cardiac Amyloidosis. , 2019, JACC. Cardiovascular imaging.

[12]  H. Goldschmidt,et al.  AL amyloidosis patients with low amyloidogenic free light chain levels at first diagnosis have an excellent prognosis. , 2017, Blood.

[13]  A. Dispenzieri,et al.  Immunoglobulin Light-Chain Amyloidosis: From Basics to New Developments in Diagnosis, Prognosis and Therapy , 2016, Acta Haematologica.

[14]  A. Foli,et al.  Patients with light-chain amyloidosis and low free light-chain burden have distinct clinical features and outcome. , 2015, Blood.

[15]  J. Cavenagh,et al.  Guidelines on the management of AL amyloidosis , 2015, British journal of haematology.

[16]  P. Kellman,et al.  T1-mapping in the heart: accuracy and precision , 2014, Journal of Cardiovascular Magnetic Resonance.

[17]  M. Dimopoulos,et al.  A European collaborative study of treatment outcomes in 346 patients with cardiac stage III AL amyloidosis. , 2013, Blood.

[18]  Andrew S Flett,et al.  Comparison of T1 mapping techniques for ECV quantification. Histological validation and reproducibility of ShMOLLI versus multibreath-hold T1 quantification equilibrium contrast CMR , 2012, Journal of Cardiovascular Magnetic Resonance.

[19]  M. Dimopoulos,et al.  New criteria for response to treatment in immunoglobulin light chain amyloidosis based on free light chain measurement and cardiac biomarkers: impact on survival outcomes. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[20]  A. Balduini,et al.  Serum N-Terminal Pro–Brain Natriuretic Peptide Is a Sensitive Marker of Myocardial Dysfunction in AL Amyloidosis , 2003, Circulation.

[21]  D. Dingli,et al.  Recent improvements in survival in primary systemic amyloidosis and the importance of an early mortality risk score. , 2011, Mayo Clinic proceedings.

[22]  It Istituto Superiore di Sanit,et al.  Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from th 10th International Symposium on Amyloid an Amyloidosis, Tours, France, 18-22 April 2004 , 2005 .