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

Author:

Royal Virginie1ORCID,Leung Nelson2ORCID,Troyanov Stéphan3,Nasr Samih H.4,Écotière Laure5,LeBlanc Richard6ORCID,Adam Benjamin A.7ORCID,Angioi Andrea8ORCID,Alexander Mariam P.4,Asunis Anna Maria9,Barreca Antonella10,Bianco Paola9,Cohen Camille11,Drosou Maria E.2,Fatima Huma12,Fenoglio Roberta13,Gougeon François14,Goujon Jean-Michel15,Herrera Guillermo A.16,Knebelmann Bertrand11,Lepori Nicola8,Maletta Francesca10,Manso Rita17,Motwani Shveta S.18ORCID,Pani Antonello8ORCID,Rabant Marion19,Rennke Helmut G.20,Rocatello Dario13,Rosenblum Frida12ORCID,Sanders Paul W.2122,Santos Afonso23,Soto Karina23ORCID,Sis Banu7,Touchard Guy515,Venner Christopher P.24,Bridoux Frank5ORCID

Affiliation:

1. Division of Pathology, Hôpital Maisonneuve-Rosemont, Université de Montréal, Montréal, QC, Canada;

2. Division of Nephrology and Hypertension and Division of Hematology, Mayo Clinic, Rochester, Minnesota;

3. Department of Medicine, Hôpital du Sacré-Cœur de Montréal, Université de Montréal, Montréal, QC, Canada;

4. Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN;

5. Department of Nephrology and Renal Transplantation, CIC INSERM 1402, Centre Hospitalier Universitaire, Université de Poitiers, Poitiers, CNRS UMR 7276, Limoges, and French Reference Centre for AL Amyloidosis, Poitiers, France;

6. Division of Hemato-Oncology, Hôpital Maisonneuve-Rosemont, Université de Montréal, Montréal, QC, Canada;

7. Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada;

8. Divisione di Nefrologia e Dialisi, Azienda Ospedaliera G. Brotzu, Cagliari, Italy;

9. Department of Pathology, Azienda Ospedaliera G. Brotzu, Cagliari, Italy;

10. Division of Pathology, Città della Salute e della Scienza Hospital, Turin, Italy;

11. Department of Nephrology, Hôpital Necker-Enfants Malades, AP-HP, Centre-Université de Paris, Paris, France;

12. Department of Pathology, University of Alabama at Birmingham, Birmingham, AL;

13. Nephrology and Dialysis Unit, S. Giovanni Bosco Hospital and University of Turin, Turin, Italy;

14. Division of Pathology, Centre Hospitalier de l’Université de Montréal, Montréal, QC, Canada;

15. Department of Pathology and Ultrastructural Pathology, Centre Hospitalier Universitaire de Poitiers, Poitiers, France;

16. Department of Pathology, College of Medicine, University of South Alabama, Mobile, AL;

17. Department of Pathology, Hospital Fernando Fonseca, Lisbon, Portugal;

18. Dana-Farber Cancer Institute and Division of Nephrology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA;

19. Department of Pathology, Hôpital Necker-Enfants Malades, AP-HP, Centre-Université de Paris, Paris, France;

20. Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA;

21. Department of Medicine, University of Alabama at Birmingham, Birmingham, AL;

22. Department of Veterans Affairs Medical Center, Birmingham, AL;

23. Department of Nephrology, Hospital Fernando Fonseca, Lisbon, Portugal; and

24. Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada

Abstract

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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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