Evidence map›Paper›PMID 30323890›Full record

ArticleOncotarget2018

RN765C, a low affinity EGFR antibody drug conjugate with potent anti-tumor activity in preclinical solid tumor models.

Oi Kwan Wong, Thomas-Toan Tran, Wei-Hsien Ho, Meritxell Galindo Casas, Melinda Au, Marjorie Bateman, Kevin C Lindquist, Arvind Rajpal, David L Shelton, Pavel Strop and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  6. Article
  7. Antibody drug conjugates: hitting the mark in pancreatic cancer?Journal of experimental & clinical cancer research : CR · 2023
    Review
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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

11 authors at 4 institutions in 2 countries.

Oi Kwan WongOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Thomas-Toan TranOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Wei-Hsien HoOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Meritxell Galindo CasasOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Melinda AuOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Marjorie BatemanOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Kevin C LindquistOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Arvind RajpalOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
David L SheltonOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Pavel StropOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Shu-Hui LiuOncology R&D, Cancer Immunology Discovery Unit, Pfizer Inc., South San Francisco, CA, USA.
Pfizer (United States) · USAllogene Therapeutics (United States) · USBristol-Myers Squibb (United States) · USWalmart (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) is a clinically validated target and often overexpressed in some solid tumors. Both EGFR tyrosine kinase inhibitors and ligand-blocking antibodies have been approved for treatment of NSCLC, head and neck cancers and colorectal cancers. However, clinical response is limited and often accompanied by significant toxicities due to normal tissue expression. To improve the effectiveness of targeting EGFR while minimizing the toxicities on normal tissues, we developed a low-affinity anti-EGFR antibody drug conjugate (ADC), RN765C. Potent

Indexed as

antibody-drug conjugateEGFRnon-small cell lung cancersite-specific conjugationtarget therapy

Identifiers

PMID30323890
PMCPMC6173368
OpenAlexW2892197301

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.