Evidence map›Paper›PMID 41939906›Full record

ReviewFrontiers in immunology2026

CAR T-cell therapy induced pseudoprogression.

Erin A Dean

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

1 author.

Erin A DeanHematopoietic Stem Cell Transplantation and Cellular Therapy Program, Division of Hematology/Oncology, Department of Medicine, University of California Irvine, Orange, CA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudoprogression is defined as a seeming post-therapy increase in tumor burden on imaging that recedes on subsequent reimaging without additional therapy. The origins of pseudoprogression lie in the field of immunology with current understanding of the imaging finding coming mostly from experience with checkpoint inhibitors used for management of solid tumors. With the wider administration of chimeric antigen receptor (CAR) T-cell therapy for the treatment of hematologic malignancies, CAR T-cell induced pseudoprogression (CARTiPP) has also been noted although it has remained an underreported, although likely rare, adverse event lacking clear description and management guidelines. CARTiPP can obscure response assessment in patients and lead to serious clinical complications due to edema-driven compression of organs or tissue. This mini review summarizes the emergence of pseudoprogression with the rise of immunotherapy along with the modifications of radiologic guidelines for correct interpretation of scans as a key non-invasive technique for overcoming the associated diagnostic challenges. It discusses the limited available data on the nature of CARTiPP in the setting of the tumor microenvironment and its meaning for the care of patients receiving CAR T-cell therapy.

Indexed as

Immunotherapy, AdoptiveNeoplasmsReceptors, Chimeric AntigenT-LymphocytesAnimalsDisease ProgressionHumansTumor MicroenvironmentReceptors, Chimeric AntigenCAR T-cell therapyCARTiPPcheckpoint inhibitorshematologic malignanciesPET/CT scanpseudoprogressionsolid tumorstumor microenvironment

Identifiers

PMID41939906
PMCPMC13044004

What OpenQuestion holds

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LicenceCC BY
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.