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FSGS treatment

3 cited papers · March 31, 2026 · Powered by Researchly AI

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Focal segmental glomerulosclerosis (FSGS) is a leading cause of kidney disease worldwide and one of the most common glomerular causes leading to end-stage kidne…

Focal segmental glomerulosclerosis (FSGS) is a leading cause of kidney disease worldwide and one of the most common glomerular causes leading to end-stage kidney disease (ESKD).1Amir et al. (2020)2

The management of FSGS remains a therapeutic challenge due to intolerance or resistance to current immunomodulatory treatments. Rupesh et al. (2020)

1
Focal Segmental Glomerulosclerosis.Rosenberg Avi Z, Kopp Jeffrey B2017Clinical journal of the American Society of Nephrology : CJASN
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2
Focal Segmental Glomerulosclerosis: State-of-the-Art and Clinical Perspective.Shabaka Amir, Tato Ribera Ana et al.2020Nephron
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  • Primary FSGS — Thought to be caused by circulating permeability factors leading to podocyte foot process effacement, usually presenting with nephrotic syndrome and responsive to immunosuppression.
1Amir et al. (2020)2
  • Extracorporeal Therapies — Includes plasma exchange, immunoadsorption, and low-density lipoprotein apheresis; shown to have potential beneficial outcomes in drug-resistant and recurrent FSGS patients.
3Rupesh et al. (2020)3
  • Anti-TGF-β Therapy (Fresolimumab) — A human monoclonal antibody inactivating all forms of TGF-β, evaluated in treatment-resistant primary FSGS. Trachtman et al. (2011)
1
Focal Segmental Glomerulosclerosis.Rosenberg Avi Z, Kopp Jeffrey B2017Clinical journal of the American Society of Nephrology : CJASN
View
2
Focal Segmental Glomerulosclerosis: State-of-the-Art and Clinical Perspective.Shabaka Amir, Tato Ribera Ana et al.2020Nephron
View
3
Extracorporeal Therapies in the Treatment of Focal Segmental Glomerulosclerosis.Raina Rupesh, Wang Joseph et al.2020Blood purification
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Diagram
FSGS Diagnosis
 │
 ▼
Classification of FSGS Type
 ┌───────────────────────────────────┐
 │ Primary │ Secondary │ Genetic │
 └───────────────────────────────────┘
 │
 ▼
First-Line Treatment
 (Immunosuppression: Corticosteroids/High-dose Prednisone)
 │
 ▼
Partial/No Remission?
 │
 ├──► Extracorporeal Therapies
 │ (Plasma Exchange, Immunoadsorption, LDL Apheresis)
 │
 └──► Investigational Agents
 (Fresolimumab / Anti-TGF-β)
Table
TreatmentMechanismKey Finding
Extracorporeal TherapiesRemoval of circulating permeability factorsBeneficial in drug-resistant and recurrent FSGS
Obinutuzumab + DaratumumabB cell/plasma cell targetingEnabled plasmapheresis discontinuation and significant proteinuria reduction in rituximab-refractory post-transplant FSGS
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  • Fresolimumab was evaluated only as a single-dose phase I study in 16 patients, limiting conclusions about long-term efficacy; one patient developed a primitive neuroectodermal tumor 2 years post-treatment, raising safety concerns. Trachtman et al. (2011)
  • FSGS is a histological pattern with diverse etiologies — primary, secondary, genetic, and virus-associated — each requiring tailored management.
1
  • Extracorporeal therapies such as plasma exchange and immunoadsorption offer benefit in drug-resistant and recurrent FSGS.
2
  • Obinutuzumab combined with daratumumab shows promise as a rescue strategy in post-transplant FSGS refractory to rituximab and plasmapheresis.
  • Anti-TGF-β therapy with fresolimumab was well tolerated in a phase I study of treatment-resistant FSGS, warranting further investigation.
1
Focal Segmental Glomerulosclerosis.Rosenberg Avi Z, Kopp Jeffrey B2017Clinical journal of the American Society of Nephrology : CJASN
View
2
Extracorporeal Therapies in the Treatment of Focal Segmental Glomerulosclerosis.Raina Rupesh, Wang Joseph et al.2020Blood purification
View
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  1. "Rituximab vs obinutuzumab in nephrotic syndrome randomized trials"
  2. "Circulating permeability factors in primary FSGS pathogenesis"
  3. "Genetic FSGS mutations podocin nephrin treatment outcomes"

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