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Abstract

French

Background:

Adults with primary focal segmental glomerulosclerosis (FSGS) are frequently resistant to multiple immunosuppressive agents, which is associated with ongoing complications of nephrotic syndrome and a high risk of progression to end-stage renal disease (ESRD). Rituximab, a monoclonal antibody against the B cell CD20 antigen, has shown some preliminary evidence in treating nephrotic syndrome.

Objectives:

Describe the usage and the efficacy of rituximab for adults with FSGS in British Columbia (BC) (Canada) and perform a literature review of multi-immunosuppressive drug resistant FSGS in adult patients treated with rituximab to estimate the overall response rate.

Design:

Case series report and a literature review.

Patients:

For the case-series, all BC patients who received rituximab for a diagnosis of primary FSGS were included. The literature review included all cases of immunosuppressive-resistant FSGS patients treated with rituximab. We excluded transplant and pediatric patients in both groups.

Methods:

We describe all cases of adults with native-kidney FSGS resistant to conventional immunosuppressive medications from our provincial health database who were treated with rituximab from 2014 to 2018. A review of the existing literature was performed via PubMed, MEDLINE, and Embase using the following keywords: rituximab, focal segmental glomerulosclerosis, and FSGS up to August 2019.

Results:

We characterize four immunosuppressive-resistant FSGS patients who were treated with rituximab as part of our provincial program, all of whom showed a response to rituximab with a sustained remission. We found 29 specific cases in the literature of adults with native-kidney FSGS treated with rituximab after being resistant to other immunosuppressive medications, of whom 15 cases showed a response to rituximab. This has increased the total response rate from 15/29 (52%) to 19/33 (58%).

Limitations:

Literature on this topic is coming predominantly from case series. Prospective trials are needed to confirm efficacy, tolerability, and duration of remission.

Conclusions:

Due to the low number of currently reported cases and variable response rates, these four cases provide critical data to generate a more accurate understanding of the role of rituximab in adults with resistant FSGS. Adding these results to the confirmed literature cases of multiple-immunosuppressive-resistant FSGS patients treated with rituximab results in a total remission rate of 19/33 cases.

Keywords

focal segmental glomerular disease FSGS glomerulonephritis immunosuppressant resistant rituximab

Introduction

Focal segmental glomerulosclerosis (FSGS) occurs when the kidney develops segmental glomerular scarring.¹ Primary FSGS has a low rate of spontaneous remission and adults with primary FSGS are frequently resistant to multiple immunosuppressive agents.² Left untreated, FSGS is associated with ongoing complications of nephrotic syndrome and a 50% risk of disease progression to end-stage renal disease (ESRD) in 6 to 8 years.³ Conventional immunosuppressive treatment options such as corticosteroids, cyclophosphamide, mycophenolate mofetil (MMF), and calcineurin inhibitors have variable efficacy as well as significant long-term side-effects.⁴

Rituximab, a monoclonal antibody against the B cell CD20 antigen, has shown some preliminary evidence in treating nephrotic syndrome.⁵ However, much of the data on rituximab for FSGS treatment has been in the pediatric population.^6,7 Given the substantial cost of rituximab compared to other treatment options, it is likely to remain a treatment of last resort for FSGS.⁸ As such, we described the usage and the efficacy of rituximab for adults with FSGS in the province of British Columbia (Canada). We conducted a comprehensive literature review of multi-immunosuppressive drug-resistant FSGS in adult patients treated with rituximab to estimate an overall response rate.

Methods

In British Columbia, the provincial health database captures all patients with biopsy-proven glomerular disease and their associated immunosuppressive treatment. Rituximab is covered by the provincial government for FSGS resistant to other treatment options. We therefore sought to use this data infrastructure to describe all cases of adults (≥19 years) with native-kidney FSGS resistant to conventional immunosuppressive medications who were treated with rituximab from 2014 to 2018. Individual patients’ charts were accessed for demographic data, as well as patient’s complete medical and pharmacological history.

A detailed literature search for cases of immunosuppressive-resistant FSGS treated with rituximab up to August 2019 was performed via PubMed, MEDLINE, and Embase using the following keywords: rituximab, focal segmental glomerulosclerosis, and FSGS. Data on renal transplant patients and pediatric patients (age <19 years) were excluded, and only results for patients with primary FSGS resistant to at least 1 non-steroid immunosuppressive agent were included. For steroid-sensitive FSGS, only cases that were previously shown to be resistant to immunosuppressive agents other than rituximab where included.

As per KDIGO guidelines, complete remission (CR) for patients with primary FSGS is defined as a proteinuria <0.3 g/d (PCR < 30 mg/mmol or ACR < 30 mg/mmol).⁹ Partial remission (PR) is defined as a 50% reduction in proteinuria to a proteinuria level less than 3.5 g/d (PCR < 350 mg/mmol or ACR < 350 mg/mmol).⁹ For the purpose of this review, we defined a response to rituximab by (1) achieving CR or PR in patients with nephrotic range proteinuria at the time of rituximab treatment, or (2) maintaining CR/PR after tapering off corticosteroids in those patients with steroid-sensitive disease that were in remission on steroids at the time of rituximab treatment.

The dosage and regimen of rituximab, previous therapies, and markers of treatment response are summarized in Table 1.

Table 1.

A Description of Individual Adult Patients From the Existing Literature With Resistant FSGS Treated With Rituximab and Their Associated Outcome.

Reference	Sex	Ethnicity	FSGS Histological Subtype	Age^a (Years)	Previous Therapies	Duration of Disease(years)	Steroid-Sensitive	RTX Dosage	Proteinuria Prior to RTX	Proteinuria After RTX	SCr Prior to RTX (umol/L)	SCr After RTX (umol/L)	Albumin Prior to RTX (g/L)	Albumin After RTX (g/L)	Follow-up Time (Months)	Status at Last Follow-up
Fernandez-Fresnedo et al.⁵	M	N/A	NOS	19	CST, TAC, MMF	2	No	375 mg/m² weekly × 4	16g/d	14 g/d	106.1	168.0	—	—	12	No response
Fernandez-Fresnedo et al.⁵	M	N/A	Tip	29	CST, CYC, CsA, MMF	3	No	375 mg/m² weekly × 4	16.5g/d	21 g/d	79.6	70.7	—	—	12	No response
Fernandez-Fresnedo et al.⁵	M	N/A	NOS	34	CST, CsA, TAC, MMF	3	No	375 mg/m² weekly × 4	9.4g/d	11.3 g/d	123.8	123.8	—	—	14	No response
Fernandez-Fresnedo et al.⁵	M	N/A	NOS	19	CST, CsA, MMF	1.1	No	375 mg/m² weekly × 4	12g/d	14 g/d	79.6	97.2	—	—	18	No response
Fernandez-Fresnedo et al.⁵	M	N/A	NOS	55	CST, CsA	2	No	375 mg/m² weekly × 4	9.8g/d	10.5 g/d	79.6	70.7	-	-	24	No response
Fernandez-Fresnedo et al.⁵	M	N/A	Cellular variant	51	CST, CsA, MMF	8.9	No	375 mg/m² weekly × 4	12.7g/d	9.0 g/d	203.3	221	—	—	24	No response.
Fernandez-Fresnedo et al.⁵	M	N/A	NOS	20	CST, CsA, TAC, MMF	2.5	No	375 mg/m² weekly × 4	12.9g/d	3.2 g/d	150.2	141.4	—	—	12	Response PR with tapering of CST, TAC, and MMF.
Fernandez-Fresnedo et al.⁵	F	N/A	NOS	23	CST, CYC, CsA, MMF	7.9	No	375 mg/m² weekly × 8	23g/d	3.9 g/d	168.0	141.4	—	—	15	No response
Ochi et al.¹⁰	F	N/A	Collapsing	25	CST, CsA, Mizoribine	12	No	375 mg/m² single dose	6.5g/d	6-8 g/d	114.9	—	—	—	—	No response
Ochi et al.¹⁰	M	N/A	NOS	21	CST, CsA, CYC, MMF	9	No	375 mg/m² single dose	13g/d	15-20 g/d	185.6	—	—	—	—	No response
Ochi et al.¹⁰	F	N/A	Perihilar	27	CST, CsA	18	Yes	375 mg/m² × 4 doses	9.8g/d	0-1 g/d	44.2	—	—	—	—	Response CR not on other IS agents
Ochi et al.¹⁰	F	N/A	Tip	26	CST, CsA, CYC, MMF	19	Yes	375 mg/m² × 3 doses	3.6g/d	0-1 g/d	35.4	—	—	—	—	Response CR not on other IS agents
Marasà et al.¹¹	F	White	NOS	22	CST, CYC, Azathioprine	1	No	375 mg/m² and a second dose 32 months after	4g/d	0.27 g/d	71.6	48.6	26.8	38	48	Response CR and off other IS agents.
Kisner et al.¹²	M	N/A	N/A	51	CST, CsA	0.6	No	1000 mg single dose	1105.9 mg/mmol	441.3 mg/mmol	136.1	—	—	—	8	No response
Kisner et al.¹²	M	N/A	N/A	50	CST, CsA, TAC, MMF	2	Yes	1000 mg × 2 doses	485.6 mg/mmol	185.43 mg/mmol	110.5	—	—	—	22	Response PR maintained with CST, MMF, TAC.
Peters et al.¹³	M	N/A	N/A	20	CSA, CST, MMF, TAC	8	Yes	1000 mg × 2 doses with 2 week interval between doses	1g/d	“Nephrotic range proteinuria persisted”	170	“Renal function rapidly deteriorated”	—	—	7	No response
Cortazar et al.¹⁴	M	N/A	N/A	56	CST, CsA, TAC, MMF	N/A	Yes	Initially 1000 mg × 2 doses every 2-4 weeks and then every 4 months after	463 mg/mmol	<113 mg/mmol	97.2	88-132	32	40-50	83	Response PR
Cortazar et al.¹⁴	M	N/A	N/A	67	CST, MMF	N/A	Yes	Initially 1000mg × 2 doses every 2-4 weeks and then every 4 months after	441 mg/mmol	226-452 mg/mmol	114.9	111-133	—	30-40	70	No response Based on proteinuria, however prednisone was tapered off.
Cortazar et al.¹⁴	F	N/A	N/A	67	CST, CsA	N/A	Yes	Initially 1000 mg × 2 doses every 2-4 weeks and then every 4 months after	655 mg/mmol	0 mg/mmol	106	66-88	32	40-50	31	Response CR
Cortazar et al.¹⁴	F	N/A	N/A	54	CST, CsA, TAC, MMF, Abatacept	N/A	Yes	Initially 1000 mg × 2 doses every 2-4 weeks and then every 4 months after	554 mg/mmol	0-113 mg/mmol	70.7	44-88	22	37.5-40	13	Response PR
Cortazar et al.¹⁴	F	N/A	N/A	65	CST, CsA, MMF	N/A	No	Initially 1000 mg × 2 doses every 2-4 weeks and then every 4 months after	1559 mg/mmol	226-339 mg/mmol	144.4	155-177	23	30-40	29	Response PR
Cortazar et al.¹⁴	F	N/A	N/A	66	CST, CYC, MMF	N/A	No	Initially 1000 mg × 2 doses every 2-4 weeks and then every 4 months after	904 mg/mmol	226-339 mg/mmol	114.9	44-88	31	37.5-40	24	Response PR
Wee Leng et al.¹⁵	M	N/A	NOS	21	CST, CYC, CsA, MMF	3	Yes	500 mg × 4 doses 1 dose weekly, then 500mg × 6 doses 1 dose weekly	1200 mg/mmol	0-250 mg/mmol	100-150	0-100	19	—	—	Response PR
Jayaraman and Thomas¹⁶	M	White	N/A	62	CST, CsA, CYC	2	No	375 mg/m² × 4 doses total	200-400 mg/mmol	800-900 mg/mmol	100-200	100-200	25-30	15-20	21	No response
Ramachandran et al.¹⁷	M	N/A	Collapsing	19	CST, CYC, CsA, MMF, TAC	1.5	No	375 mg/m² × 4 doses 1 dose weekly	5g/d	1.2 g/d	62-80	80	<20	47	18	Response PR
Kronbichler et al.¹⁸	F	N/A	N/A	33	CST, CsA, CYC, MMF, TAC	29	Yes	375 mg/m² × 4 doses 1 dose weekly, and then 23 months later another 4 doses 1 weekly	689 mg/mmol	4.6 mg/mmol	67.2	68.9	—	48.5	55	Response CR and off other IS agents.
Kronbichler et al.¹⁸	M	N/A	N/A	32	CST, CsA, MMF	14	Yes	375 mg/m² × 4 doses 1 dose weekly	847.5 mg/mmol	9.6 mg/mmol	56.6	50.3	15.9	68	14	Response CR and off other IS agents.
Kronbichler et al.¹⁸	M	N/A	N/A	26	CST, CsA, CYC, MMF	2.6	Yes	375 mg/m² × 4 doses 1 dose weekly	Not detectable	6.4 mg/mmol	112.3	79.6	38	40	29	Response CR and off other IS agents.
Butterly et al.¹⁹	M	N/A	N/A	32	CST, MMF	N/A	N/A	1400 mg	1600 mg/mmol	465 mg/mmol	—	—	<15	30	4	No response
Barbour et al.⁸	F	Asian	NOS	41	CST, MMF, TAC, Galactose, CsA	32	No	375 mg/m² weekly × 4 doses and single 375mg/m² with CD20 reconstitution	4.95g/d	2.1 mg/mmol (ACR)	71	81	23	42	47	Response CR and off other IS agents.
Barbour et al.⁸	M	White	NOS	21	CST, MMF, TAC, CsA, CYC, Infliximab, Galactose	8	No	375 mg/m² weekly × 4 doses and single 375mg/m² with CD20 reconstitution	8.69g/d	55 mg/mmol (ACR)	168	270	30	36	55	Response PR and off other IS agents.
Barbour et al.⁸	F	White	NOS	26	CST, CYC, CsA, TAC	12	Yes	1 g every 2 weeks for 2 doses and single 1g dose with CD20 reconstitution	0.38g/d	0.79 g/d	63	70	35	38	30	Response PR off CST and with tapering TAC.
Barbour et al.⁸	M	Asian	NOS	19	CST, Chlorambucil, Levamisole, CYC, MMF, TAC	17	No	375 mg/m² weekly × 4 doses and single 375 mg/m² with CD20 reconstitution	8.30g/d	0.66 g/d	233	91	12	43	40	Response PR off CST and other IS agents.

Note. FSGS = focal segmental glomerulosclerosis; RTX = rituximab; SCr = serum creatinine; N/A = not available; NOS = not otherwise specified; CST = corticosteroids; TAC = tacrolimus; MMF = mycophenolate mofetil; CYC = cyclophosphamide; CsA = cyclosporine.

Age at RTX Administration.

Ethics approval, including a waiver of individual patient consent, was granted from the University of British Columbia Research and Ethics Board.

Results

Case Reports

Of the 121 patients in British Columbia who received rituximab for the treatment of glomerulonephritis (GN) from January 2014 to April 2018, 4 were adults with primary FSGS in the native kidney. Clinical and laboratory data are summarized in Table 1.

Patient 1 is a 41-year-old female who had previously failed combination therapy with prednisone, MMF, tacrolimus, and galactose. Her creatinine was 71 µmol/L, albumin 23 g/L, and proteinuria 4.95 g/d while on therapeutic tacrolimus level and MMF. She was treated with rituximab 375 mg/m² weekly for 4 doses followed by single 375 mg/m² doses with CD20 reconstitution (approximately every 7 months). She achieved CR 3 months after her first rituximab dose. One year after the initiation of rituximab she was tapered off all other immunosuppressive agents and remained in CR. Two years after her first rituximab dose, we started tapering her rituximab dosage yearly. Fifty-seven months after her first rituximab dose, her serum creatinine was 81 µmol/L, albumin 42 g/L, and an ACR of 2.1 mg/mmol consistent with a CR.

Patient 2 is a 21-year-old male, who had previously failed tacrolimus, cyclosporine, and was on prednisone and MMF. His serum creatinine was 168 µmol/L, albumin 30 g/L, and proteinuria 8.69 g/d. He was treated with rituximab 375 mg/m² weekly for 4 doses followed by single 375 mg/m² doses with CD20 reconstitution (approximately every 6 months). He achieved PR 3 months after his first rituximab dose. Seventeen months after the initiation of rituximab, he was tapered off all other immunosuppressive and remained in partial remission. Thirty-three months after his first rituximab dose, we began tapering his rituximab dosage yearly. Fifty-five months after is first rituximab dose, his serum creatinine was 270 µmol/L, albumin 36 g/L, and an ACR of 55 mg/mmol consistent with a PR. Unfortunately, his chronic kidney disease continued to progress likely on the basis of sclerosis.

Patient 3 is a 26-year-old female who was steroid-sensitive, but unable to taper off prednisone without a disease flare despite concurrent use of cyclophosphamide, cyclosporine, or tacrolimus. At the time of being treated with rituximab 1 g every 2 weeks for 2 doses, she was on tacrolimus 3 mg BID and prednisone 20 mg/d, with serum creatinine 63 µmol/L, albumin 35 g/L, and proteinuria 0.38 g/d. She achieved PR 2 months after her first rituximab dose. Following the two rituximab doses, she received rituximab 1 g with CD 20 reconstitution (approximately every 8 months). Thirty months after rituximab treatment, she was off all immunosuppression. At that time, her serum creatinine was 70 µmol/L, albumin 39 g/L, and proteinuria 0.79 g/d consistent with a PR.

Patients 4 is a 19-year-old male. He was diagnosed at 2 years of age with biopsy proven minimal change disease. He was steroid-sensitive, but unable to taper off prednisone despite being treated with chlorambucil, levamisole, cyclophosphamide, tacrolimus, and MMF. At 17 years of age, he received 1 course of rituximab 375 mg/m² weekly for 4 doses and remained relapse-free on no other immunosuppressive agent for 24 months. Two years later, he had a relapse with significant nephrotic syndrome and creatinine 233 µmol/L, albumin 12 g/L, and proteinuria 8.3 g/d. A repeat biopsy showed FSGS. He was on no immunosuppressive therapy at this point. He was treated with rituximab 375 mg/m² weekly for 4 doses followed by single 375 mg/m² doses with CD20 reconstitution (approximately every 11 months). He achieved PR 1 month after first rituximab dose. Twenty-three months after his first rituximab dose, we began tapering his rituximab dosage yearly. Forty months after his first rituximab dose, his serum creatinine was 91 µmol/L, albumin 43 g/L, and proteinuria of 0.66 g/day consistent with a PR.

Literature Search Results

Figure 1 shows our literature strategy. Patients from 11 studies met our inclusion criteria, including a total of 29 patients with FSGS (Table 1).^5,10-19 As per our definition, 15 of these cases showed a response to rituximab

Figure 1.

Flow diagram for the literature review.

The four new cases of immunosuppressive-resistant FSGS that were treated with rituximab and presented in this report increases the rate of response to this treatment from 15/29 (52%) to 19/33 (58%). From the total of the literature review and our 4 cases, of the 19 patients who showed response to treatment at the last follow-up time point, 8/19 (42%) were in complete remission and 11/19 (58%) were in partial remission.

Of the 31 patients with nephrotic range proteinuria at time of rituximab treatment, 17/31 (55%) responded to treatment; of which 7/17 (41%) achieved CR and 10/17 (59%) achieved PR. Of the 2 patients who were in remission (partial and complete) on steroids with or without other immunosuppressive agents, after rituximab both patients were able to maintain remission while tapering off steroids. Of the 2 patients, 1 patient was in complete remission and 1 was in partial remission.

Discussion

We performed a literature review of adult patients with FSGS resistant to multiple immunosuppressive agents to generate a more accurate assessment of the response rate to rituximab. Due to the low number of reported FSGS adult cases treated with rituximab to date, the 4 cases presented in this report provide meaningful data to support the role of rituximab in adults with multiple immunosuppressive-resistant FSGS. When our results were combined with the existing literature, the total response rate rises up to 58% (19/33) from originally 52% (15/29). We acknowledge that the literature to date for rituximab in adult FSGS patients is predominantly case series. This underscores the need for prospective clinical trials to better determine the efficacy, tolerability, and duration of remission of rituximab in FSGS.

There is evidence suggesting that rituximab induce remission in FSGS patients by two pathways. The first one is that CD20 positive B cells are involved in the immunopathogenesis of FSGS by the production of the circulating permeability factors, which disrupt podocyte integrity. This is thought to be the main cause of primary FSGS.²⁰ The second pathway is that rituximab reduces exposure to B-cell-induced local interleukine-4, which cause foot process effacement and proteinuria.²⁰ Our results demonstrate the potential efficacy of rituximab in both steroid resistant and steroid dependent FSGS. Patients 1, 2, and 4 were resistant to prednisone in combination with multiple other immunosuppressive agents, with persistent nephrotic range proteinuria and hypoalbuminemia. Rituximab resulted in proteinuria remission (complete remission in patient 1, partial remission in patient 2 and 4) that was sustained despite discontinuing all other immunosuppressive agents. Patient 3 had steroid-sensitive disease, but was not able to taper off prednisone despite concurrent use of other immunosuppressive agents. After rituximab, patient 3 was able to maintain proteinuric remission even after discontinuing prednisone and tapering of other immunosuppressive medications. By reporting all cases of adults with FSGS treated with rituximab in our province, we reduced the risk of bias from selective reporting of individual cases.

Currently, many adult FSGS patients either fail therapy with conventional immunosuppressive agents or only achieve proteinuria remission that is dependent upon the ongoing use of these medications.^{5,10,12,16-18} Long-term use of corticosteroids, cyclophosphamide, MMF, or calcineurin inhibitors is known to have multisystem side-effects. Some studies have looked at the long-term safety profile of rituximab in the rheumatoid arthritis population, the granulomatosis with polyangiitis (GPA), and microscopic polyangiitis (MPA) populations or systemic inflammatory and autoimmune disease population for up to 11 years.^21-24 Results of these studies are quite consistent with an incidence ratio of infection of 3.76 to 7.1 per 100 patient-years, and malignancy rate similar to the one seen in general population.^21,22,25 We propose that rituximab can be safely considered when other immunosuppressive options have been trialed and patients continue to have nephrotic range proteinuria or in patients who may have achieved proteinuric remission yet continue to rely on immunosuppressive agents with known long-term risks.

To compare rituximab long-term side-effects to side-effects of previous immunosuppressive agents, one consideration is its efficacy and need for ongoing treatment. The dosing regimen of rituximab used at our center was largely based on dosing reported in previous studies.^17,18,26 However, the dose which is commonly used in the adult literature was derived from doses used in refractory non-Hodgkin’s lymphoma.²⁶ To date, there has not been a study to determine the most efficacious dose and regimen in the adult FSGS population. A previous study of steroid-resistant FSGS cases has shown that there was an association between patients who received more doses of rituximab and a greater reduction of proteinuria.⁵

From the available literature and based on our center’s experience, most patients received four 375 mg/m² once-weekly doses of rituximab with stable remission status as far as several months from the time of rituximab administration. Additional single rituximab doses were given as infrequently as every 6 to 11 months thereafter as needed to maintain both CD20 depletion and proteinuria remission.^5,10-19

One factor that may contribute to which patients are able to maintain remission after rituximab therapy is the rate of CD20 reconstitution.²² Rituximab can reduce CD20-positive B cells in a single dose, selectively targeting the B cell population and potentially other immune cell populations affected by costimulatory pathways; however, the correlation between reconstitution of CD20-positive cells and FSGS relapse needs to be further studied.²⁷ At our institution, we used CD20 as the main marker to determine maintenance dosing because CD20 levels are early indicators of relapse in minimal change disease.²⁸ However, in the pediatric population despite there being an association between CD20 reconstitution with disease relapse, not all patients who had recovery of CD20 levels had worsening disease.²⁹ Since there are still individual differences in response to rituximab not associated with CD20 reconstitution,²⁹ the immunopathogenesis and response to rituximab in FSGS disease variants need to be further explored in future studies.

Although the optimal long-term rituximab maintenance therapy for particularly intractable cases is currently unknown, there is also potential for combined treatment using rituximab with other immunosuppressive medications.^30-33 Two pediatric studies have shown that MMF therapy when given post-rituximab may help maintain remission.^30,31 Other studies have previously shown that tacrolimus and rituximab efficacy in nephrotic syndrome increases when used in combination therapy with other agents such as MMF.^32,33 Therefore, although we present cases of FSGS resistant to multiple immunosuppressive agents that have responded to prolonged rituximab treatment, the optimal duration and type of maintenance therapy will require ongoing study and development.

Conclusion

In conclusion, the preliminary results gained from this study support a role for rituximab in adults with FSGS when conventional therapies have failed. Moving forward, further trials are needed to confirm our findings in a larger number of patients, to identify patient characteristics that can predict response to treatment, and to determine the optimal rituximab dosing regimen in this population.

Footnotes

Ethics Approval and Consent to Participate

Ethics approval, including a waiver of individual patient consent, was granted from the University of British Columbia Research and Ethics Board.

Consent for Publication

All authors provided consent for publication.

Availability of Data and Materials

Data generated and analyzed during this study are included in this published article.

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iD

Judith G. Marin

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Rituximab for Adults With Multi-Drug Resistant Focal Segmental Glomerulosclerosis: A Case Series and Review of the Literature

Abstract

Background:

Objectives:

Design:

Patients:

Methods:

Results:

Limitations:

Conclusions:

Keywords

Introduction

Methods

Results

Case Reports

Literature Search Results

Discussion

Conclusion

Footnotes

Ethics Approval and Consent to Participate

Consent for Publication

Availability of Data and Materials

Declaration of Conflicting Interests

Funding

ORCID iD

References