Evidence map›Paper›PMID 42294511›Full record

ArticleGlomerular diseases

Clinical Remission as a Function of Exposure to Cyclophosphamide in Patients with Primary Membranous Nephropathy: A One-Year Cohort Study.

Swati Arora, Jorge E Rojas-Rivera, Madeline S Chung, Himanshu Patel, Rajshree Patil, Hitesh Bhatia, Luba R Muaddi, Omar Osman, Brad Rovin, Isabelle Ayoub

Abstract read
In one paragraph

Article in Glomerular diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Swati AroraAllegheny Health Network, Division of Nephrology, Drexel University, Pittsburgh, PA, USA.
Jorge E Rojas-RiveraSchool of Doctoral Studies, Autonoma University of Madrid, Madrid, Spain.
Madeline S ChungDepartment of Medicine, Division of Nephrology, The Ohio State University, Columbus, OH, USA.
Himanshu PatelDepartment of Nephrology and Renal Transplant, Zydus Hospital, Ahmedabad, India.
Rajshree PatilDepartment of Nephrology and Renal Transplant, Zydus Hospital, Ahmedabad, India.
Hitesh BhatiaDepartment of Medicine, Guthrie Robert Packer Hospital, Sayre, PA, USA.
Luba R MuaddiDivision of Nephrology, Cleveland Clinic Martin Health, Stuart, FL, USA.
Omar OsmanDivision of Nephrology, University of Kentucky, Lexington, KY, USA.
Brad RovinDepartment of Medicine, Division of Nephrology, The Ohio State University, Columbus, OH, USA.
Isabelle AyoubDepartment of Medicine, Division of Nephrology, The Ohio State University, Columbus, OH, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Primary membranous nephropathy (pMN) is a leading cause of nephrotic syndrome (NS) in adults. Cyclophosphamide (CYC) with glucocorticoids (GCs) is recommended for high and very high-risk patients, but the optimal treatment duration and cumulative dose remain unclear. This study aimed to compare the effectiveness and safety of short-duration (SD) versus long-duration (LD) oral CYC regimens in pMN patients with NS. Methods: We conducted a multicenter retrospective cohort study of 54 adult patients with biopsy-proven pMN treated with oral CYC in the USA and India between 2010 and 2022. Patients received either SD-CYC (≤3 months) or LD-CYC (>3 months). The primary outcome was overall remission (complete or partial) at 12 months. Secondary outcomes included complete remission (CR) rates and adverse events. Analyses were stratified by treatment duration and cumulative CYC dose. Results: Overall remission at 12 months was similar between SD and LD groups (73% vs. 83%, Conclusion: Short-term oral CYC combined with GC may be a safe alternative to LD-CYC regimens for achieving clinical remission in pMN. Although these findings align with recent evidence supporting the efficacy of low-dose CYC in pMN, well-designed clinical trials are still needed for more robust clinical validation.

Indexed as

Clinical remissionCyclophosphamideMembranous nephropathyNephrotic syndrome

Identifiers

PMID42294511
PMCPMC13263000

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.