# Next-generation Bruton’s tyrosine kinase inhibitors for chronic lymphocytic leukemia-associated membranoproliferative glomerulonephritis: a case report

**Authors:** Li Chen, Yuting Huang, Jing Xu, Sinian Huang, Qianying Zhang, Fanli Hua, Xiaoxia Pan, Jian-Qing Mi

PMC · DOI: 10.1007/s00277-026-06730-w · 2026-01-30

## TL;DR

Two patients with chronic lymphocytic leukemia and kidney disease improved after treatment with new Bruton’s tyrosine kinase inhibitors.

## Contribution

Demonstrates successful treatment of CLL-associated MPGN using next-generation BTK inhibitors with favorable renal and hematologic outcomes.

## Key findings

- Two patients with CLL-associated MPGN achieved remission with next-generation BTK inhibitors.
- Orelabrutinib and zanubrutinib showed good tolerability and clinical improvement in renal and hematologic parameters.
- Kidney biopsy was critical for confirming diagnosis and guiding treatment decisions.

## Abstract

Renal involvement in chronic lymphocytic leukemia (CLL) is uncommon but can lead to significant morbidity. Membranoproliferative glomerulonephritis (MPGN) is among the most frequently reported glomerular lesions associated with CLL and may presents with nephrotic syndrome. Early recognition of the association between renal lesions and CLL is crucial for guiding treatment and improving both renal and hematologic outcomes. We report two biopsy-proven cases of CLL-associated MPGN successfully treated with next-generation Bruton’s tyrosine kinase inhibitors (BTKis). Both patients presented with nephrotic-range proteinuria. In Case 1, the patient exhibited monoclonal IgG-κ gammopathy and isolated low serum C3, suggestive of complement-mediated injury without direct immunoglobulin deposition. He achieved sustained hematologic and renal remission with orelabrutinib following early discontinuation of rituximab–chlorambucil due to infection. In Case 2, renal biopsy showed interstitial infiltration by CLL cells and immune complex deposition, supporting a leukemic infiltration and immune-complex mediated mechanism. Zanubrutinib led to clinical improvement, and rituximab was later added to further reduce proteinuria. These cases underscore the critical role of kidney biopsy in clarifying diagnosis and underlying mechanisms. In this case series, the treatment regimen centered on next-generation BTKis enabled patients to achieve concurrent favorable renal and hematologic remission with good tolerability.

## Linked entities

- **Proteins:** C3 (complement C3)
- **Chemicals:** orelabrutinib (PubChem CID 91667513), chlorambucil (PubChem CID 2708), zanubrutinib (PubChem CID 135565884)
- **Diseases:** chronic lymphocytic leukemia (MONDO:0004948), membranoproliferative glomerulonephritis (MONDO:0002461), nephrotic syndrome (MONDO:0005377)

## Full-text entities

- **Genes:** PLA2G1B (phospholipase A2 group IB) [NCBI Gene 5319] {aka PLA2, PLA2A, PPLA2}, CD79B (CD79b molecule) [NCBI Gene 974] {aka AGM6, B29, IGB, Igbeta}, BTK (Bruton tyrosine kinase) [NCBI Gene 695] {aka AGMX1, AT, ATK, BPK, IGHD3, IMD1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, IGHV3OR16-7 (immunoglobulin heavy variable 3/OR16-7 (pseudogene)) [NCBI Gene 28309] {aka IGHV3/OR16-7, IGHV3OR167}, ATM (ATM serine/threonine kinase) [NCBI Gene 472] {aka AT1, ATA, ATC, ATD, ATDC, ATE}, HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, CD200 (CD200 molecule) [NCBI Gene 4345] {aka MOX1, MOX2, MRC, OX-2}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, CD22 (CD22 molecule) [NCBI Gene 933] {aka SIGLEC-2, SIGLEC2}, C1QA (complement C1q A chain) [NCBI Gene 712] {aka C1QD1}, FCER2 (Fc epsilon receptor II) [NCBI Gene 2208] {aka BLAST-2, CD23, CD23A, CLEC4J, FCE2, FCErII}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, SPN (sialophorin) [NCBI Gene 6693] {aka CD43, GALGP, GPL115, LEU-22, LSN}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, CD5 (CD5 molecule) [NCBI Gene 921] {aka LEU1, T1}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, RB1 (RB transcriptional corepressor 1) [NCBI Gene 5925] {aka OSRC, PPP1R130, RB, p105-Rb, p110-RB1, pRb}, PLA2R1 (phospholipase A2 receptor 1) [NCBI Gene 22925] {aka CLEC13C, PLA2-R, PLA2G1R, PLA2IR, PLA2R}
- **Diseases:** pneumonia (MESH:D011014), diarrhea (MESH:D003967), glomerulonephritis (MESH:D005921), glomerular damage (MESH:D007674), lymphadenopathy (MESH:D008206), hypoalbuminemia (MESH:D034141), Waldenstrom macroglobulinemia (MESH:D008258), CLL (MESH:D015451), skin petechiae (MESH:D011693), nephrotic (MESH:D009404), end-stage renal disease (MESH:D007676), AL amyloidosis (MESH:D000075363), B-cell malignancy (MESH:D016393), edema (MESH:D004487), oliguria (MESH:D009846), immune abnormalities (MESH:D007154), hypogammaglobulinemia (MESH:D000361), ankle edema (MESH:D016512), interstitial nephritis (MESH:D009395), Monoclonal gammopathy (MESH:D010265), MCD (MESH:D009402), TMA (MESH:D057049), cryoglobulinemia (MESH:D003449), toxicity (MESH:D064420), tumor (MESH:D009369), sepsis (MESH:D018805), membranous nephropathy (MESH:D015433), cytogenetic (MESH:D002869), DDD (MESH:D015432), thrombocytopenia (MESH:D013921), proteinuria (MESH:D011507), Binet B (MESH:D006509), leukemic (MESH:D007938), splenomegaly (MESH:D013163), Renal involvement (MESH:C565423), cytopenias (MESH:D006402), lymphomatous (MESH:D013967), anemia (MESH:D000740), lymphocytosis (MESH:D008218), Rai III (MESH:C564523), leukocytosis (MESH:D007964), complement-mediated injury (MESH:D020274), infection (MESH:D007239), lymphoproliferative disorder (MESH:D008232), C3 glomerulonephritis (MESH:C567033), acute kidney injury (MESH:D058186), autoimmune diseases (MESH:D001327)
- **Chemicals:** chlorambucil (MESH:D002699), telmisartan (MESH:D000077333), rituximab (MESH:D000069283), uric acid (MESH:D014527), BTKi (-), ibrutinib (MESH:C551803), creatinine (MESH:D003404), Zanubrutinib (MESH:C000629551), valsartan (MESH:D000068756), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606], Treponema pallidum (species) [taxon 160], Human immunodeficiency virus (species) [taxon 12721], Hepatitis C [taxon 11103]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12855336/full.md

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Source: https://tomesphere.com/paper/PMC12855336