Evidence map›Paper›PMID 41068545›Full record

ArticleJournal of nephrology2025

Efficacy and safety of obinutuzumab on progressive IgA nephropathy: a case series.

Qingyun Ding, Cheng Xue, Xiang Gao, Xiaojing Tang, Sanli Zhang, Yawei Liu, Bing Dai

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Journal of nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Qingyun Ding *Division of Nephrology, Kidney Institute of PLA of China, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Cheng Xue *Division of Nephrology, Kidney Institute of PLA of China, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Xiang Gao *Division of Nephrology, Kidney Institute of PLA of China, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Xiaojing Tang *Division of Nephrology, Kidney Institute of PLA of China, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Sanli ZhangDivision of Nephrology, Kidney Institute of PLA of China, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Yawei LiuDivision of Nephrology, Kidney Institute of PLA of China, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China. lyw1025@163.com.
Bing DaiDivision of Nephrology, Kidney Institute of PLA of China, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China. daibin105@126.com.

Funding

National Natural Science Foundation of China 81970640National Natural Science Foundation of China 82370735
6 · The paper itself

Abstract

IgA nephropathy (IgAN) is the most prevalent glomerulonephritis globally, significantly contributing to kidney failure. B cells are central to its pathogenesis through IgA production. While rituximab is commonly used to deplete B cells, obinutuzumab, a type II anti-CD20 antibody, may provide more effective and sustained depletion. This report regards the efficacy and safety of obinutuzumab in patients with progressive IgAN refractory to other immunosuppressive therapies. We discuss three patients with progressive IgAN aged 21, 35, and 57 years. All patients exhibited significant proteinuria and hematuria, with kidney biopsies confirming IgAN. In addition to supportive care, they all showed favorable responses to initial immunosuppressive therapy but developed kidney function impairment and nephrotic-range proteinuria 2-4 years after discontinuing initial treatments. Following intolerance and/or poor response to a new round of immunosuppressive medications, one patient was switched from rituximab to obinutuzumab (1000 mg), while 2 patients received obinutuzumab (1000 mg, 2 doses). After 12 months of follow-up, all patients achieved sustained B-cell depletion, with a reduction in IgA/C3, proteinuria, and hematuria, and improvement in kidney function. Mild infusion reactions were noted, but no severe adverse events occurred. These findings provide preliminary, hypothesis-generating insights into the efficacy of obinutuzumab in progressive IgAN and highlight the need for further studies on these issues.

Indexed as

Antibodies, Monoclonal, HumanizedGlomerulonephritis, IGAAdultB-LymphocytesDisease ProgressionFemaleHumansImmunosuppressive AgentsKidneyMaleMiddle AgedTreatment OutcomeYoung AdultAntibodies, Monoclonal, HumanizedImmunosuppressive AgentsobinutuzumabAdverse eventIgA nephropathyObinutuzumabProteinuria

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.