Evidence map›Paper›PMID 26646755›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2016

TP53 mutational status is predictive of pazopanib response in advanced sarcomas.

K Koehler, D Liebner, J L Chen

Open access · bronzeAbstract read
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 67 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

3 authors at 1 institution in 1 country.

K KoehlerDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus.
D LiebnerDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus Division of Bioinformatics, Department of Biomedical Informatics, The Ohio State University, Columbus, USA.
J L ChenDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University, Columbus Division of Bioinformatics, Department of Biomedical Informatics, The Ohio State University, Columbus, USA james.chen@osumc.edu.
The Ohio State University · US

Funding

Tissue and Pathology ResourcesU54CA168512 · NCI · SARC · PI BAKER, LAURENCE HOWARD, POLLOCK, RAPHAEL E. · 2012 to 2016
$11.0M
NCI NIH HHS U54 CA168512
6 · The paper itself

Abstract

backgroundTo investigate whether TP53 DNA mutational status impacts progression-free survival (PFS) in patients with advanced sarcomas (soft tissue sarcoma) treated with vascular endothelial growth factor receptors (VEGFR) inhibition. PATIENTS AND

methodsWe retrospectively reviewed 19 cases of patients treated at the Ohio State James Comprehensive Cancer Center with advanced sarcoma treated with VEGFR inhibition who also had next-generation sequencing of their tumors (via FoundationOne Heme panel). We evaluated TP53 as well as mutations that were observed in at least 20% of patients and evaluated its contribution to PFS using the Kaplan-Meier survival analysis of available radiology end points.

resultsMutations that were observed in at least 20% of patients included TP53 and Rb1. Only TP53 was predictive of PFS in the context of VEGFR inhibition. The PFS of patients with TP53 mutations was significantly greater than TP53 wild-type tumors with the median PFS of 208 versus 136 days, respectively [P = 0.036, hazards ratio 0.38 (95% confidence interval 0.09-0.83)].

conclusionsMutations in TP53 may serve as a predictive biomarker of response to VEGFR inhibition in patients with advanced sarcoma. Larger, prospective studies are necessary to confirm these findings.

Indexed as

Angiogenesis InhibitorsBase SequenceDisease-Free SurvivalFemaleGenetic MarkersHigh-Throughput Nucleotide SequencingHumansIndazolesKaplan-Meier EstimateMaleMiddle AgedMutationPyrimidinesReceptors, Vascular Endothelial Growth FactorRetinoblastoma ProteinRetrospective StudiesAngiogenesis InhibitorsGenetic MarkersIndazolespazopanibPyrimidinesReceptors, Vascular Endothelial Growth FactorRetinoblastoma ProteinSulfonamidesTP53 protein, humanTumor Suppressor Protein p53next-generation sequencingpazopanibsarcomaTP53VEGFR

Identifiers

PMID26646755
PMCPMC5006122
OpenAlexW2192184960

What OpenQuestion holds

Textmetadata
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.