Evidence map›Paper›PMID 30765854›Full record

ArticleScientific reports2019

Targeting Epidermal Growth Factor Receptor (EGFR) and Human Epidermal Growth Factor Receptor 2 (HER2) Expressing Bladder Cancer Using Combination Photoimmunotherapy (PIT).

Mohammad R Siddiqui, Reema Railkar, Thomas Sanford, Daniel R Crooks, Michael A Eckhaus, Diana Haines, Peter L Choyke, Hisataka Kobayashi, Piyush K Agarwal

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 70 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Mohammad R SiddiquiUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.
Reema RailkarUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.
Thomas SanfordUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.
Daniel R CrooksUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.
Michael A EckhausDiagnostic and Research Services Branch, Office of the Director, National Institutes of Health, Bethesda, MD - 20892, USA.
Diana HainesPathology Section, Pathology/Histotechnology Laboratory, Leidos Biomedical Research, Inc. Frederick National Laboratory for Cancer Research, Frederick, MD, 21702, USA.
Peter L ChoykeMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.
Hisataka KobayashiMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.ORCID 0000-0003-1019-4112
Piyush K AgarwalUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA. piyush.agarwal@nih.gov.
National Cancer Institute · USLeidos (United States) · USNational Institutes of Health · USNorthwestern University · US

Funding

Molecular Targeted Photoimmunotherapy for Bladder CancerZIABC011458 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AGARWAL, PIYUSH · 2012 to 2019
$3.5M
Targeting Metabolic Pathways in Bladder CancerZIABC011741 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AGARWAL, PIYUSH · 2016 to 2019
$796k
CCR NIH HHS HHSN261200800001CIntramural NIH HHS ZIA BC011458NCI NIH HHS HHSN261200800001EU.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) ZIABC011458-02
6 · The paper itself

Abstract

Bladder cancer (BC) is heterogeneous and expresses various cell surface targets. Photoimmunotherapy (PIT) involves monoclonal antibodies (MAbs) conjugated to a photoabsorber (PA), IR Dye 700Dx, and then activated by near infra-red light (NIR) to specifically target tumors. We have demonstrated that tumors expressing EGFR can be targeted with PIT. However, PIT may be less effective when a tumor lacks "overwhelming" expression of a single target such as EGFR. We present a combinatorial PIT approach for targeting BC expressing EGFR and HER2, using PA- labeled panitumumab (pan) and trastuzumab (tra), respectively. Human BC tissues and cell lines were analyzed for EGFR and HER2 expression. Efficacy of PA-labeled MAbs singly and in combination was analyzed. About 45% of BC tissues stain for both EGFR and HER2. In vitro, the combination of pan IR700 and tra IR700 with NIR was more efficacious than either agent alone. Tumor xenografts treated with combination PIT showed significant tumor growth retardation. Combination PIT is a promising approach for treating BC with low/moderate expression of surface receptors. In addition, given the molecular heterogeneity of bladder cancer, targeting more than one surface receptor may allow for more effective cell death across different bladder tumors.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalCell Line, TumorErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleHumansImmunotherapyInfrared RaysMice, NudePanitumumabPhotosensitizing AgentsPhototherapyTrastuzumabUrinary Bladder NeoplasmsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsPanitumumabPhotosensitizing AgentsTrastuzumab

Identifiers

PMID30765854
PMCPMC6375935
OpenAlexW2911800940

What OpenQuestion holds

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LicenceCC BY
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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.