Renal involvement in solid cancers: epidemiological, clinical and histological characteristics study of 154 onconephrology patients.


Journal

BMC nephrology
ISSN: 1471-2369
Titre abrégé: BMC Nephrol
Pays: England
ID NLM: 100967793

Informations de publication

Date de publication:
19 Oct 2024
Historique:
received: 01 07 2024
accepted: 09 10 2024
medline: 20 10 2024
pubmed: 20 10 2024
entrez: 19 10 2024
Statut: epublish

Résumé

Onconephrology is a growing discipline that aims to improve the management of patients with cancer and kidney disease. If kidney histology is an essential key, the anatomopathological data remain weak although essential to this complex management. Patients with active cancer who had a kidney biopsy (KB) between 2014 and 2020 were included, and their clinicobiological and histological data were analyzed retrospectively. Our cohort consisted of 154 patients (83 women) with a mean age of 58 years. One hundred twelve patients presented with proteinuria, 95 with acute kidney injury, and 59 with arterial hypertension. Histologically, interstitial fibrosis was found in 74% of KBs, tubular atrophy in 55.1%, arteriolar hyalinosis in 58.4%, and fibrous endarteritis in 54.4%. Regarding the main acute lesions, thrombotic microangiopathy (TMA) was found in 29.9% of biopsies, acute tubular necrosis (ATN) in 51.3%, and acute interstitial nephritis in 24.8%. The etiological diagnosis most often made was the nephrotoxicity of anticancer drugs (87 patients), followed by a pre-renal (15 patients) and kidney disease unrelated to cancer (13 patients). Sixty-seven patients presented with at least 2 associated diagnoses reflecting the complexity of kidney damage in cancer. Different clusters were found, highlighting that immunotherapy and anti-VEGF were the most commonly involved drugs. During onconephrology practice, kidney toxicity of treatments is the most common etiology. Several mechanisms can be involved, underscoring the importance of kidney biopsy and the complexity of its management. Chronic histological lesions were very common.

Sections du résumé

BACKGROUND BACKGROUND
Onconephrology is a growing discipline that aims to improve the management of patients with cancer and kidney disease. If kidney histology is an essential key, the anatomopathological data remain weak although essential to this complex management.
METHODS METHODS
Patients with active cancer who had a kidney biopsy (KB) between 2014 and 2020 were included, and their clinicobiological and histological data were analyzed retrospectively.
RESULTS RESULTS
Our cohort consisted of 154 patients (83 women) with a mean age of 58 years. One hundred twelve patients presented with proteinuria, 95 with acute kidney injury, and 59 with arterial hypertension. Histologically, interstitial fibrosis was found in 74% of KBs, tubular atrophy in 55.1%, arteriolar hyalinosis in 58.4%, and fibrous endarteritis in 54.4%. Regarding the main acute lesions, thrombotic microangiopathy (TMA) was found in 29.9% of biopsies, acute tubular necrosis (ATN) in 51.3%, and acute interstitial nephritis in 24.8%. The etiological diagnosis most often made was the nephrotoxicity of anticancer drugs (87 patients), followed by a pre-renal (15 patients) and kidney disease unrelated to cancer (13 patients). Sixty-seven patients presented with at least 2 associated diagnoses reflecting the complexity of kidney damage in cancer. Different clusters were found, highlighting that immunotherapy and anti-VEGF were the most commonly involved drugs.
CONCLUSIONS CONCLUSIONS
During onconephrology practice, kidney toxicity of treatments is the most common etiology. Several mechanisms can be involved, underscoring the importance of kidney biopsy and the complexity of its management. Chronic histological lesions were very common.

Identifiants

pubmed: 39427142
doi: 10.1186/s12882-024-03812-7
pii: 10.1186/s12882-024-03812-7
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

367

Informations de copyright

© 2024. The Author(s).

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Auteurs

Victor Gueutin (V)

Service de néphrologie-dialyse-transplantation CHU de CAEN, Côte de Nacre, Caen, France. gueutin-v@chu-caen.fr.
Service de néphrologie-dialyse, hôpital Jacques-Monod, Rue Eugène-Garnier, Flers, France. gueutin-v@chu-caen.fr.

Aurore Cardineau (A)

Service de néphrologie-dialyse CH Mémorial France Etats-Unis, 715 rue Henri Dunant, Saint Lô, France.

Alexis Mathian (A)

Assistance Publique-Hôpitaux de Paris (AP-HP), Groupement Hospitalier Pitié- Salpêtrière, Centre de Référence pour le Lupus, le Syndrome des anti-phospholipides et autres maladies auto-immunes rares, Service de Médecine Interne 2, Institut E3M, Paris, France.

Antoine Lanot (A)

Service de néphrologie-dialyse-transplantation CHU de CAEN, Côte de Nacre, Caen, France.
Service de néphrologie-dialyse, hôpital Jacques-Monod, Rue Eugène-Garnier, Flers, France.

François Comoz (F)

Service d'Anatomie et Cytologie Pathologiques, CHU Côte de Nacre, Caen, France.

Isabelle Brocheriou (I)

Service d'Anatomie et Cytologie Pathologiques, La Pitié Salpêtrière, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, Paris, France.
UMRS 1155, Institut National de la Santé et de la Recherche Médicale, Hôpital Tenon, Sorbonne Université, Paris, France.

Hassan Izzedine (H)

Department of Nephrology, Peupliers Private Hospital, Paris, France.

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