Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously in association with improvement of survival in AL

Author:

Palladini Giovanni1,Lavatelli Francesca1,Russo Paola1,Perlini Stefano1,Perfetti Vittorio1,Bosoni Tiziana1,Obici Laura1,Bradwell Arthur R.1,D'Eril GianVico Melzi1,Fogari Roberto1,Moratti Remigio1,Merlini Giampaolo1

Affiliation:

1. From the Center for Amyloidosis, Biotechnology Research Laboratories and Department of Biochemistry, the Department of Internal Medicine, the Clinical Chemistry Laboratory, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) San Matteo, and the University of Pavia, Pavia, Italy; the Binding Site Ltd and the Medical School, University of Birmingham, Birmingham, United Kingdom; and the Department of Medicine and Surgery, University of Milan, Milan, Italy.

Abstract

N-terminal natriuretic peptide type B (NT-proBNP) is a marker of cardiac dysfunction in light chain amyloidosis (AL) and a powerful prognostic determinant. Serum NT-proBNP and circulating free light chains (FLCs) were measured at enrollment and after 3 cycles of chemotherapy in 51 patients with cardiac AL. In patients (n = 22, 43%) in whom FLCs decreased by more than 50% (hematologic response), NT-proBNP concentration decreased by a median of 48%, whereas in the remaining patients it increased by 47% (P = .01). The reduction of NT-proBNP was greater in patients (n = 9) in whom amyloidogenic FLCs disappeared at immunofixation (median 53%), than in the remaining responding patients (median 31%, P = .04). Left ventricular wall thickness decreased by at least 2 mm in 3 of 20 patients in whom NT-proBNP improved. Fifteen patients died. Thirteen of them, in whom NT-proBNP and FLCs did not improve, died after a median of 1.8 months. The decrease of FLCs translates into a simultaneous decrease of NT-proBNP and improved survival. Patients in whom chemotherapy fails to induce such a decrease are at risk of early death. Cardiac function in AL can rapidly improve due to a reduction of the circulating amyloidogenic precursor, despite the amount of cardiac amyloid deposits remaining apparently unaltered, as measured by echocardiography.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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