PURPOSETo identify the criteria for hematologic and cardiac response to treatment in immunoglobulin light chain (AL) amyloidosis based on survival analysis of a large patient population. PATIENTS AND METHODSWe gathered for analysis 816 patients with AL amyloidosis from seven referral centers in the European Union and the United States. A different cohort of 374 patients prospectively evaluated at the Pavia Amyloidosis Research and Treatment Center was used for validation. Data was available for all patients before and 3 and/or 6 months after initiation of first-line therapy. The prognostic relevance of different criteria for hematologic and cardiac response was assessed. RESULTS: amyloid complete response (normal FLC ratio and negative seru...
Organ response correlates with overall survival in patients with immunoglobulin light chain amyloido...
Introduction: Cardiac involvement in immunoglobulin light chain amyloidosis (AL) is the major determ...
Amyloidosis is a term for diseases with extracellular deposition of insoluble beta-fibrillar protein...
PURPOSETo identify the criteria for hematologic and cardiac response to treatment in immunoglobulin ...
International audiencePURPOSE: To identify the criteria for hematologic and cardiac response to trea...
PURPOSE: Binary cardiac response assessment using cardiac biomarkers is prognostic in light chain am...
Purpose: Immunoglobulin M (IgM)-related light chain (AL) amyloidosis, which accounts for 6% to 10% o...
Amyloid light-chain (AL) amyloidosis is a rare disease characterized by amyloid fibril deposits made...
Immunoglobulin light chain amyloidosis is a rare, multisystemic, phenotypically heterogenous disease...
Purpose: Immunoglobulin M (IgM)–related light chain (AL) amyloidosis, which accounts for 6% to 10% ...
Data are presented as medians (25th, 75th quartiles) or as percentages, as appropriate. ^ Kumar S, D...
Treatment outcomes of patients with cardiac stage III light chain (AL) amyloidosis remain poorly stu...
In AL amyloidosis complete response (aCR) is defined as negative serum and urine immunofixation with...
The validated criteria of hematologic response in light-chain (AL) amyloidosis are based on the meas...
N-terminal natriuretic peptide type B (NT-proBNP) is a marker of cardiac dysfunction in light chain ...
Organ response correlates with overall survival in patients with immunoglobulin light chain amyloido...
Introduction: Cardiac involvement in immunoglobulin light chain amyloidosis (AL) is the major determ...
Amyloidosis is a term for diseases with extracellular deposition of insoluble beta-fibrillar protein...
PURPOSETo identify the criteria for hematologic and cardiac response to treatment in immunoglobulin ...
International audiencePURPOSE: To identify the criteria for hematologic and cardiac response to trea...
PURPOSE: Binary cardiac response assessment using cardiac biomarkers is prognostic in light chain am...
Purpose: Immunoglobulin M (IgM)-related light chain (AL) amyloidosis, which accounts for 6% to 10% o...
Amyloid light-chain (AL) amyloidosis is a rare disease characterized by amyloid fibril deposits made...
Immunoglobulin light chain amyloidosis is a rare, multisystemic, phenotypically heterogenous disease...
Purpose: Immunoglobulin M (IgM)–related light chain (AL) amyloidosis, which accounts for 6% to 10% ...
Data are presented as medians (25th, 75th quartiles) or as percentages, as appropriate. ^ Kumar S, D...
Treatment outcomes of patients with cardiac stage III light chain (AL) amyloidosis remain poorly stu...
In AL amyloidosis complete response (aCR) is defined as negative serum and urine immunofixation with...
The validated criteria of hematologic response in light-chain (AL) amyloidosis are based on the meas...
N-terminal natriuretic peptide type B (NT-proBNP) is a marker of cardiac dysfunction in light chain ...
Organ response correlates with overall survival in patients with immunoglobulin light chain amyloido...
Introduction: Cardiac involvement in immunoglobulin light chain amyloidosis (AL) is the major determ...
Amyloidosis is a term for diseases with extracellular deposition of insoluble beta-fibrillar protein...