Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2025 Jan 17;7(4):100967.
doi: 10.1016/j.xkme.2025.100967. eCollection 2025 Apr.

Pembrolizumab-Mediated Complete Remission of a PLA2R-Positive Paraneoplastic Membranous Nephropathy: A Case Report

Affiliations
Case Reports

Pembrolizumab-Mediated Complete Remission of a PLA2R-Positive Paraneoplastic Membranous Nephropathy: A Case Report

Rayane Benyahia et al. Kidney Med. .

Abstract

Management of paraneoplastic membranous nephropathy (MN) is directed toward the underlying malignancy, and prescriptions of immune checkpoint inhibitors (ICIs) are skyrocketing in the field of oncology. However, this drug category is usually discouraged for patients with autoimmune disorders (AIDs) because it might trigger immune-related adverse events (irAEs) in the form of flare-ups or even genesis of AID. Yet, nothing is known about the efficacy and safety of ICIs for cancers associated with paraneoplastic MN. Here, we report a rare case of PLA2R-positive MN related to a PDL1-positive locally advanced lung adenocarcinoma. Antineoplastic treatment with the anti-PD1 pembrolizumab as a first-line, single-drug therapy allowed for both cancer and nephropathy remissions. To date, to our knowledge, this is the first description of a (PLA2R-positive) paraneoplastic MN that was put into remission via an ICI monotherapy successfully targeting the associated neoplasia only, without additional immunosuppressive agents.

Keywords: Case report; immune checkpoint inhibitor; immune-related adverse event; lung adenocarcinoma; membranous nephropathy; pembrolizumab; phospholipase A2 receptor (PLA2R).

PubMed Disclaimer

Figures

Figure 1
Figure 1
Evolution of kidney function over time. (A) Serum creatinine concentration (μmol/L) over time. (B) Urinary protein-creatinine ratio (g/g) and serum albumin concentration (g/L) over time. Abbreviations: PET, positron emission tomography; TDM, tomodensitometry.

References

    1. Rovin B.H., Adler S.G., Barratt J., et al. Executive summary of the KDIGO 2021 Guideline for the Management of Glomerular Diseases. Kidney Int. 2021;100(4):753–779. - PubMed
    1. Bacchetta J., Juillard L., Cochat P., Droz J.P. Paraneoplastic glomerular diseases and malignancies. Crit Rev Oncol Hematol. 2009;70(1):39–58. - PubMed
    1. Murtas C., Bruschi M., Spinelli S., et al. Novel biomarkers and pathophysiology of membranous nephropathy: PLA2R and beyond. Clin Kidney J. 2024;17(1) - PMC - PubMed
    1. Anwar H., Sachpekidis C., Winkler J., et al. Absolute number of new lesions on 18F-FDG PET/CT is more predictive of clinical response than SUV changes in metastatic melanoma patients receiving ipilimumab. Eur J Nucl Med Mol Imaging. 2018;45(3):376–383. - PubMed
    1. Sethi S., Beck L.H., Glassock R.J., et al. Mayo Clinic consensus report on membranous nephropathy: proposal for a novel classification. Kidney Int. 2023;104(6):1092–1102. - PubMed

Publication types

LinkOut - more resources