Evidence map›Paper›PMID 38026793›Full record

ReviewHemaSphere2023

CAR-T Cell Therapy for Classical Hodgkin Lymphoma.

Mikalai Katsin, Dmitri Dormeshkin, Alexander Meleshko, Alexandr Migas, Simon Dubovik, Natalya Konoplya

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in HemaSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07524816 (Treatment Method of Patients With Refractory and Relapsed CD-19 Positive Leukemia and Lymphoma Using Academic Anti-CD19 CAR-T Human Cells), which is not on this map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 7% of its field
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.

NCT07524816 recruitingnot on this map

Treatment Method of Patients With Refractory and Relapsed CD-19 Positive Leukemia and Lymphoma Using Academic Anti-CD19 CAR-T Human Cells

Typeobservational_patient_registrySponsorN.N. Alexandrov National Cancer CentreRan2021 to 2029Enrolled76ConditionsLarge B-Cell Lymphoma (LBCL)ArmsCAR-T cell therapy
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Is escalated BEACOPP dead? Rethinking standards in hodgkin lymphoma treatment.Medical oncology (Northwood, London, England) · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

6 authors at 4 institutions in 1 country.

Mikalai KatsinVitebsk Regional Clinical Cancer Centre, Vitebsk, Belarus.
Dmitri DormeshkinInstitute of Bioorganic Chemistry of the National academy of Sciences of Belarus, Minsk, Belarus.ORCID https://orcid.org/0000-0003-2505-3005
Alexander MeleshkoBelarusian Research Center for Pediatric Oncology and Hematology, Minsk, Belarus.ORCID https://orcid.org/0000-0001-6964-3635
Alexandr MigasImunovakcina, UAB, Vilnius, Lithuania.ORCID https://orcid.org/0000-0002-7013-9847
Simon DubovikInstitute of Bioorganic Chemistry of the National academy of Sciences of Belarus, Minsk, Belarus.
Natalya KonoplyaN.N. Alexandrov National Cancer Center of Belarus, Minsk, Belarus.
National Academy of Sciences of Belarus · BYBelarusian Research Center For Pediatric Oncology and Hematology · BYN.N. Alexandrov National Cancer Centre · BYVitebsk State Medical University · BY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical Hodgkin lymphoma (cHL) is a malignancy characterized by the presence of Hodgkin and Reed-Sternberg (HRS) cells within a complex tumor microenvironment (TME). Despite advances in conventional therapies, a subset of cHL patients experience relapse or refractory disease, necessitating the exploration of novel treatment strategies. Chimeric antigen receptor T cell (CAR-T cell) therapy has emerged as a promising approach for the management of cHL, harnessing the power of genetically modified T cells to recognize and eliminate tumor cells. In this article, we provide an overview of the pathogenesis of cHL, highlighting the key molecular and cellular mechanisms involved. Additionally, we discuss the rationale for the development of CAR-T cell therapy in cHL, focusing on the identification of suitable targets on HRS cells (such as CD30, CD123, LMP1, and LMP2A), clonotypic lymphoma initiating B cells (CD19, CD20), and cells within the TME (CD123, CD19, CD20) for CAR-T cell design. Furthermore, we explore various strategies employed to enhance the efficacy and safety of CAR-T cell therapies in the treatment of cHL. Finally, we present an overview of the results obtained from clinical trials evaluating the efficacy of CAR-T cell therapies in cHL, highlighting their potential as a promising therapeutic option. Collectively, this article provides a comprehensive review of the current understanding of cHL pathogenesis and the rationale for CAR-T cell therapy development, offering insights into the future directions of this rapidly evolving field.

Identifiers

PMID38026793
PMCPMC10656097
OpenAlexW4388775208

What OpenQuestion holds

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LicenceCC BY-NC
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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.