ReviewInnere Medizin (Heidelberg, Germany)2025
[Management of side effects of CAR T cells].
Review in Innere Medizin (Heidelberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Chimeric antigen receptor (CAR) T cell therapy has significantly improved outcomes for patients with hematological neoplasms and the approval of six CAR T cell products has led to increasing routine use; however, CAR T cell therapy is associated with specific and sometimes severe side effects, which are summarized in this article. Cytokine release syndrome (CRS) is a frequent systemic inflammatory reaction triggered by the massive release of cytokines after CAR T cell activation. The symptoms range from mild fever to multiorgan failure. The management is stepwise using tocilizumab and corticosteroids depending on the severity, with recent data supporting the use of anakinra. Further targeted therapeutic agents appear to be promising. The immune effector cell-associated hemophagocytic lymphohistiocytosis-like syndrome (IEC-HS) is rare compared to CRS but life-threatening and is characterized by high ferritin levels, cytopenia and organ failure. Treatment includes anakinra, dexamethasone and other salvage medications, whereby recognition of the complication is essential. Immune effector cell-associated neurotoxicity syndrome (ICANS) is comparatively frequent, presenting with symptoms such as confusion, speech disturbances or seizures. The treatment depends on the severity and usually involves corticosteroids, anakinra and other immunosuppressants. Besides ICANS, a heterogeneous group of rarer neurological complications can also occur, which are often difficult to treat and not yet fully understood. Hematotoxicity with prolonged cytopenia (immune effector cell-associated hematotoxicity, ICAHT) is an increasingly recognized complication and its risk can be estimated before lymphocyte depletion using a simple score. Prolonged cytopenia substantially increases the risk of infections and explains why infections are the most frequent non-disease-related cause of death after CAR T cell treatment. In summary, since the first approval the management of CAR T cell-related side effects has markedly improved through a better understanding of the pathophysiology, identification of risk factors and especially early intervention strategies.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.