Evidence map›Paper›PMID 40270461›Full record

ReviewBritish journal of haematology2025

How we manage immune-mediated thrombotic thrombocytopenic purpura after rituximab failure or intolerance.

Julia Weisinger, Jehane Fadlallah, Bérangère Joly, Agnès Veyradier, Paul Coppo

Abstract readReview
In one paragraph

Review in British journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Tailored treatment of acute immune-mediated thrombotic thrombocytopenic purpura.Hematology. American Society of Hematology. Education Program · 2025
    Review
  5. Article
  6. Review
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

5 authors.

Julia WeisingerCentre de Référence des Microangiopathies Thrombotiques et Service d'hématologie, Hôpital Saint Antoine, Assistance Publique-Hôpitaux de Paris and Sorbonne Université, Paris, France.ORCID https://orcid.org/0009-0003-8337-2925
Jehane FadlallahCentre de Référence des Microangiopathies Thrombotiques et Service d'hématologie, Hôpital Saint Antoine, Assistance Publique-Hôpitaux de Paris and Sorbonne Université, Paris, France.
Bérangère JolyCentre de Référence des Microangiopathies Thrombotiques et Service d'hématologie, Hôpital Saint Antoine, Assistance Publique-Hôpitaux de Paris and Sorbonne Université, Paris, France.
Agnès VeyradierCentre de Référence des Microangiopathies Thrombotiques et Service d'hématologie, Hôpital Saint Antoine, Assistance Publique-Hôpitaux de Paris and Sorbonne Université, Paris, France.
Paul CoppoCentre de Référence des Microangiopathies Thrombotiques et Service d'hématologie, Hôpital Saint Antoine, Assistance Publique-Hôpitaux de Paris and Sorbonne Université, Paris, France.ORCID https://orcid.org/0000-0002-4618-2095

Funding

European Union MSCA TOLERATE 101072729Filière de Santé Maladies Rares Immuno-HématologiquesFrench Ministry of Health AOM12259French Ministry of Health P120118National Plan for Rare Diseases of the French Ministry of Health
6 · The paper itself

Abstract

The use of rituximab, a B-cell-depleting agent as a pre-emptive treatment in immune-mediated thrombotic thrombocytopenic purpura (iTTP), is the current standard of care. However, for patients refractory to rituximab or for those with contraindications, further treatment guidelines are scarce. Standard immunosuppressive or chemotherapeutic agents were used routinely in the past, but most of the data proving their efficacy are stemming from experience before the routine use of rituximab. Ciclosporin A and azathioprine seem to be effective in the pre-emptive setting, but their safety profile might limit their use. Extended or intensive rituximab administration may overcome refractoriness in some patients. New therapeutic options, such as new generation anti-CD20 antibodies like obinutuzumab or the plasma cell-directed therapy daratumumab, showed important efficacy in iTTP after rituximab failure, with a favourable safety profile. There are no available comparative studies for pre-emptive treatment options in iTTP; therefore, data from large databases and multicentre studies are essential. In this review, we summarize the possible treatment options in case of rituximab failure in iTTP and try to provide a recommendation based on available literature and our own experience.

Indexed as

Purpura, Thrombotic ThrombocytopenicRituximabAntibodies, Monoclonal, HumanizedHumansImmunosuppressive AgentsTreatment FailureAntibodies, Monoclonal, HumanizedImmunosuppressive AgentsRituximabpre‐emptive therapyrituximabTTP

Identifiers

PMID40270461
PMCPMC12166343

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.