Evidence map›Paper›PMID 35279528›Full record

ArticleESMO open2022

Plasma Tie2 trajectories identify vascular response criteria for VEGF inhibitors across advanced biliary tract, colorectal and ovarian cancers.

C Zhou, J O'Connor, A Backen, J W Valle, J Bridgewater, C Dive, G C Jayson

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Aflibercept and Faricimab Equipotently Restore Endothelial Barrier Function.Investigative ophthalmology & visual science · 2026
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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

7 authors at 4 institutions in 1 country.

C ZhouCRUK Manchester Institute Cancer Biomarker Centre, University of Manchester, Manchester, UK.
J O'ConnorDivision of Cancer Sciences, University of Manchester, Manchester, UK; Division of Radiotherapy and Imaging, Institute of Cancer Research, London, UK.
A BackenDivision of Cancer Sciences, University of Manchester, Manchester, UK; The Christie NHS Foundation Trust, Manchester, UK.
J W ValleThe Christie NHS Foundation Trust, Manchester, UK.
J BridgewaterUniversity College Hospital Macmillan Cancer Centre, Huntley Street, London, UK.
C DiveCRUK Manchester Institute Cancer Biomarker Centre, University of Manchester, Manchester, UK.
G C JaysonDivision of Cancer Sciences, University of Manchester, Manchester, UK; The Christie NHS Foundation Trust, Manchester, UK. Electronic address: Gordon.Jayson@manchester.ac.uk.
University of Manchester · GBCancer Research UK Manchester Institute · GBThe Christie NHS Foundation Trust · GBUniversity College Hospital Macmillan Cancer Centre · GB

Funding

Cancer Research UK 29832Cancer Research UK C2930/A11428Cancer Research UK C480/A15578Cancer Research UK C5759/A27412Department of Health
6 · The paper itself

Abstract

backgroundVascular endothelial growth factor inhibitors (VEGFi) are compromised by a lack of validated biomarkers. Previously we showed that changes in the concentration of plasma Tie2 (pTie2) was a response biomarker for bevacizumab. Here, we investigated whether pTie2 can predict response and progression cross-tumour for generic VEGFi treatment. PATIENTS AND

methodsPatients (n = 124) with advanced biliary tract cancer (ABC) received cisplatin/gemcitabine with cediranib or placebo (ABC-03 trial). Concentrations of pTie2 were measured longitudinally from before treatment until disease progression. Data from patients with ovarian cancer (n = 92, ICON7 trial) and patients with colorectal cancer (CRC) (n = 70, Travastin trial) were also included.

resultsCediranib-treated ABC patients were deconvoluted into distinct groups where in one group pTie2 trajectories resembled those seen in placebo-treated patients and in another pTie2 significantly reduced (t-test P = 2.7 × 10

conclusionpTie2 is the first cross-tumour, generic VEGFi, vascular response biomarker to guide optimum use of VEGFi in clinical practice.

Indexed as

Biliary TractColorectal NeoplasmsOvarian NeoplasmsBiomarkers, TumorFemaleHumansVascular Endothelial Growth Factor ABiomarkers, TumorVascular Endothelial Growth Factor Aangiogenesisbile duct cancerresponse biomarkerTie2VEGF inhibitor

Identifiers

PMID35279528
PMCPMC9058891
OpenAlexW4220719464

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.