Clinicopathologic predictors of renal outcomes in light chain cast nephropathy: a multicenter retrospective study

Virginie Royal(Hôpital Maisonneuve-Rosemont), Nelson Leung(Mayo Clinic), Stéphan Troyanov(Hôpital du Sacré-Cœur de Montréal), Samih H. Nasr(Mayo Clinic in Arizona), Laure Écotière(Centre National de la Recherche Scientifique), Richard LeBlanc(Hôpital Maisonneuve-Rosemont), Benjamin Adam(University of Alberta), Andrea Angioi(Azienda Ospedaliera G. Brotzu), Mariam P. Alexander(Mayo Clinic in Arizona), Anna Maria Asunis(Azienda Ospedaliera G. Brotzu), Antonella Barreca(Azienda Ospedaliera Citta' della Salute e della Scienza di Torino), Paola Del Bianco(Azienda Ospedaliera G. Brotzu), Camille Cohen(Hôpital Necker-Enfants Malades), Maria Eleni Drosou(Mayo Clinic), Huma Fatima(University of Alabama at Birmingham), Roberta Fenoglio(Ospedale San Giovanni Bosco), F. Gougeon(Centre Hospitalier de l’Université de Montréal), Jean‐Michel Goujon(Centre Hospitalier Universitaire de Poitiers), Guillermo A. Herrera(University of South Alabama), Bertrand Knebelmann(Hôpital Necker-Enfants Malades), Nicola Lepori(Azienda Ospedaliera G. Brotzu), Francesca Maletta(Azienda Ospedaliera Citta' della Salute e della Scienza di Torino), Rita Manso(Hospital Prof. Dr. Fernando Fonseca), Shveta S. Motwani(Brigham and Women's Hospital), Antonello Pani(Azienda Ospedaliera G. Brotzu), Marion Rabant(Hôpital Necker-Enfants Malades), Helmut G. Rennke(Brigham and Women's Hospital), Dario Rocatello(Ospedale San Giovanni Bosco), Frida Rosenblum(University of Alabama at Birmingham), Paul W. Sanders(University of Alabama at Birmingham), Afonso Santos(Hospital Prof. Dr. Fernando Fonseca), Karina Soto(Hospital Prof. Dr. Fernando Fonseca), B. Sis(University of Alberta), Guy Touchard(Centre National de la Recherche Scientifique), Christopher P. Venner(University of Alberta), Frank Bridoux(Centre National de la Recherche Scientifique)
Blood
March 11, 2020
Cited by 90Open Access
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Abstract

Light chain cast nephropathy (LCCN) in multiple myeloma often leads to severe and poorly reversible acute kidney injury. Severe renal impairment influences the allocation of chemotherapy and its tolerability; it also affects patient survival. Whether renal biopsy findings add to the clinical assessment in predicting renal and patient outcomes in LCCN is uncertain. We retrospectively reviewed clinical presentation, chemotherapy regimens, hematologic response, and renal and patient outcomes in 178 patients with biopsy-proven LCCN from 10 centers in Europe and North America. A detailed pathology review, including assessment of the extent of cast formation, was performed to study correlations with initial presentation and outcomes. Patients presented with a mean estimated glomerular filtration rate (eGFR) of 13 ± 11 mL/min/1.73 m2, and 82% had stage 3 acute kidney injury. The mean number of casts was 3.2/mm2 in the cortex. Tubulointerstitial lesions were frequent: acute tubular injury (94%), tubulitis (82%), tubular rupture (62%), giant cell reaction (60%), and cortical and medullary inflammation (95% and 75%, respectively). Medullary inflammation, giant cell reaction, and the extent of cast formation correlated with eGFR value at LCCN diagnosis. During a median follow-up of 22 months, mean eGFR increased to 43 ± 30 mL/min/1.73 m2. Age, β2-microglobulin, best hematologic response, number of cortical casts per square millimeter, and degree of interstitial fibrosis/tubular atrophy (IFTA) were independently associated with a higher eGFR during follow-up. This eGFR value correlated with overall survival, independently of the hematologic response. This study shows that extent of cast formation and IFTA in LCCN predicts the quality of renal response, which, in turn, is associated with overall survival.


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