Evidence map›Paper›PMID 35163421›Full record

ReviewInternational journal of molecular sciences2022

Molecular Aspects of Resistance to Immunotherapies-Advances in Understanding and Management of Diffuse Large B-Cell Lymphoma.

Aleksandra Kusowska, Matylda Kubacz, Marta Krawczyk, Aleksander Slusarczyk, Magdalena Winiarska, Malgorzata Bobrowicz

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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.

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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Role of RNA Splicing Mutations in Diffuse Large B Cell Lymphoma.International journal of general medicine · 2023
    Review
  12. Review
  13. Review
  14. Article
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 1 institution in 1 country.

Aleksandra KusowskaDepartment of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.ORCID 0000-0001-6808-9919
Matylda KubaczDepartment of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Marta KrawczykDepartment of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.ORCID 0000-0001-9487-1744
Aleksander SlusarczykDepartment of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.ORCID 0000-0002-4344-0191
Magdalena WiniarskaDepartment of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Malgorzata BobrowiczDepartment of Immunology, Medical University of Warsaw, 02-097 Warsaw, Poland.ORCID 0000-0002-9078-5168
Medical University of Warsaw · PL

Funding

European Research Council 805038/STIMUNO/ERC-2018-STGPolish National Science Centre 2019/35/D/NZ5/01191Polish National Science Centre 2020/39/O/NZ6/01434
6 · The paper itself

Abstract

Despite the unquestionable success achieved by rituximab-based regimens in the management of diffuse large B-cell lymphoma (DLBCL), the high incidence of relapsed/refractory disease still remains a challenge. The widespread clinical use of chemo-immunotherapy demonstrated that it invariably leads to the induction of resistance; however, the molecular mechanisms underlying this phenomenon remain unclear. Rituximab-mediated therapeutic effect primarily relies on complement-dependent cytotoxicity and antibody-dependent cell cytotoxicity, and their outcome is often compromised following the development of resistance. Factors involved include inherent genetic characteristics and rituximab-induced changes in effectors cells, the role of ligand/receptor interactions between target and effector cells, and the tumor microenvironment. This review focuses on summarizing the emerging advances in the understanding of the molecular basis responsible for the resistance induced by various forms of immunotherapy used in DLBCL. We outline available models of resistance and delineate solutions that may improve the efficacy of standard therapeutic protocols, which might be essential for the rational design of novel therapeutic regimens.

Indexed as

Drug Resistance, NeoplasmAnimalsAntineoplastic Agents, ImmunologicalHumansLymphoma, Large B-Cell, DiffuseRituximabTumor MicroenvironmentAntineoplastic Agents, ImmunologicalRituximabantibody-dependent cellular cytotoxicitycomplement-dependent cytotoxicitydiffuse large B-cell lymphomaimmunotherapy resistance

Identifiers

PMID35163421
PMCPMC8835809
OpenAlexW4212960121

What OpenQuestion holds

Textmetadata
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.