Evidence map›Paper›PMID 36353222›Full record

ArticleFrontiers in medicine2022

Development of combinatorial antibody therapies for diffuse large B cell lymphoma.

Eric S Geanes, Stacey A Krepel, Rebecca McLennan, Stephen Pierce, Santosh Khanal, Todd Bradley

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. 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
0.4field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. A cytokine receptor-targeting chimera toolbox for expanding extracellular targeted protein degradation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. 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 2 institutions in 1 country.

Eric S GeanesGenomic Medicine Center, Children's Mercy Research Institute, Kansas City, MO, United States.
Stacey A KrepelGenomic Medicine Center, Children's Mercy Research Institute, Kansas City, MO, United States.
Rebecca McLennanGenomic Medicine Center, Children's Mercy Research Institute, Kansas City, MO, United States.
Stephen PierceGenomic Medicine Center, Children's Mercy Research Institute, Kansas City, MO, United States.
Santosh KhanalGenomic Medicine Center, Children's Mercy Research Institute, Kansas City, MO, United States.
Todd BradleyGenomic Medicine Center, Children's Mercy Research Institute, Kansas City, MO, United States.
Mercy Research · USUniversity of Missouri–Kansas City · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse large B-cell lymphoma (DLBCL), the most common form of lymphoma, is typically treated with chemotherapy combined with the immunotherapy rituximab, an antibody targeting the B cell receptor, CD20. Despite the success of this treatment regimen, approximately a third of DLBCL patients experience either relapse or have refractory disease that is resistant to rituximab, indicating the need for alternative therapeutic strategies. Here, we identified that CD74 and IL4R are expressed on the cell surface of both CD20 positive and CD20 negative B cell populations. Moreover, genes encoding

Indexed as

bispecific antibodycancer therapyCD20CD74diffuse large B cell lymphomaIL4Rlymphomarituximab

Identifiers

PMID36353222
PMCPMC9637670
OpenAlexW4307274164

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.