TY - JOUR
T1 - Clinicopathologic predictors of renal outcomes in light chain cast nephropathy
T2 - A multicenter retrospective study
AU - the International Kidney and Monoclonal Gammopathy Research Group
AU - Royal, Virginie
AU - Leung, Nelson
AU - Troyanov, Stéphan
AU - Nasr, Samih H.
AU - Écotière, Laure
AU - LeBlanc, Richard
AU - Adam, Benjamin A.
AU - Angioi, Andrea
AU - Alexander, Mariam P.
AU - Asunis, Anna Maria
AU - Barreca, Antonella
AU - Bianco, Paola
AU - Cohen, Camille
AU - Drosou, Maria E.
AU - Fatima, Huma
AU - Fenoglio, Roberta
AU - Gougeon, François
AU - Goujon, Jean Michel
AU - Herrera, Guillermo A.
AU - Knebelmann, Bertrand
AU - Lepori, Nicola
AU - Maletta, Francesca
AU - Manso, Rita
AU - Motwani, Shveta S.
AU - Pani, Antonello
AU - Rabant, Marion
AU - Rennke, Helmut G.
AU - Rocatello, Dario
AU - Rosenblum, Frida
AU - Sanders, Paul W.
AU - Santos, Afonso
AU - Soto, Karina
AU - Sis, Banu
AU - Touchard, Guy
AU - Venner, Christopher P.
AU - Bridoux, Frank
N1 - Funding Information:
P.W.S. is supported by a Merit Award (2 I01 CX001326) from the US Department of Veterans Affairs Clinical Sciences R&D (CSRD) Service and a National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases George M. O’Brien Kidney and Urological Research Centers Program grant (5 P30 DK079337).
Funding Information:
The authors thank their colleagues from the participating centers who provided insight and expertise that greatly assisted the research: CHU Poitiers (Poitiers, France), Mayo Clinic (Rochester, MN), University of Alabama at Birmingham (Birmingham, AL), Hôpital Necker-Enfants Malades (Paris, France), Hospital Fernando Fonseca (Lisbon, Portugal), University of Alberta (Edmonton, AB, Canada), Brigham and Women's Hospital (Boston, MA), St. Giovanni Bosco Hospital (Turin, Italy), Azienda Ospedaliera G. Brotzu (Cagliari, Italy) and Hôpital Maisonneuve-Rosemont (Montréal, QC, Canada). P.W.S. is supported by a Merit Award (2 I01 CX001326) from the US Department of Veterans Affairs Clinical Sciences R&D (CSRD) Service and a National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases George M. O'Brien Kidney and Urological Research Centers Program grant (5 P30 DK079337).
Publisher Copyright:
© 2020 American Society of Hematology. All rights reserved.
PY - 2020/5/21
Y1 - 2020/5/21
N2 - 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 6 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 6 30 mL/min/1.73 m2. Age, b2microglobulin, 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.
AB - 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 6 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 6 30 mL/min/1.73 m2. Age, b2microglobulin, 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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U2 - 10.1182/blood.2019003807
DO - 10.1182/blood.2019003807
M3 - Article
C2 - 32160635
AN - SCOPUS:85085263789
SN - 0006-4971
VL - 135
SP - 1833
EP - 1846
JO - Blood
JF - Blood
IS - 21
ER -