Evidence map›Paper›PMID 34710981›Full record

SynthesisAsian Pacific journal of cancer prevention : APJCP2021

Overexpression of c-Met is Associated with Poor Prognosis in Glioblastoma Multiforme: A Systematic Review and Meta-Analyses.

Jellyca Anton, Sudibio Sudibio, Handoko Handoko, Tiara Bunga Mayang Permata, Henry Kodrat, Endang Nuryadi, Henry Sofyan, Eka Susanto, Rahmad Mulyadi, Renindra Ananda Aman and 1 more

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Asian Pacific journal of cancer prevention : APJCP, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 7 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

11 authors at 2 institutions in 1 country.

Jellyca AntonDepartment of Radiation Oncology, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.
Sudibio SudibioDepartment of Radiation Oncology, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.
Handoko HandokoDepartment of Radiation Oncology, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.ORCID 0000000228349090
Tiara Bunga Mayang PermataDepartment of Radiation Oncology, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.ORCID 0000-0002-5890-5545
Henry KodratDepartment of Radiation Oncology, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.ORCID 0000-0003-3782-7901
Endang NuryadiDepartment of Radiation Oncology, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.ORCID 0000-0003-1029-1748
Henry SofyanFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Eka SusantoFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Rahmad MulyadiFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Renindra Ananda AmanFaculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Soehartati GondhowiardjoDepartment of Radiation Oncology, Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.ORCID 0000-0002-9446-4361
University of Indonesia · IDRumah Sakit Umum Pusat Nasional Dr. Cipto Mangunkusumo · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study is to evaluate the association of c-Met overexpression with survival of glioblastoma multiforme (GBM) patients.

methodsA systematic review with meta-analyses was conducted on related articles from PubMed, EBSCOhost, Scopus, and Cochrane databases with last updated search on October 31, 2020. A total of 7 studies regarding c-Met overexpression and overall survival (OS) and/or progression free survival (PFS) are included in this study.

resultsAll studies used immunohistochemistry to examine the expression of c-Met protein. The results showed that the positive rate of c-Met overexpression was detected in approximately 33,9% - 60,5% of GBM patients. c-Met overexpression was related to worse OS (HR: 1,74; 95% CI: 1,482-2,043; Z=6,756; p<0,001) and PFS (HR: 1,66; 95% CI: 1,327-2,066; Z=4,464; p<0,001) in GBM patients. Low heterogeneity of subjects was found in both OS and PFS analyses, I2 values were 7,8% and 0,0%, respectively.

conclusionIn conclusion, c-Met overexpression is significantly related to shorter OS and PFS in GBM patients, so c-Met can be considered as a potential prognostic indicator in GBM.

Indexed as

Brain NeoplasmsGlioblastomaHumansKaplan-Meier EstimatePrognosisProgression-Free SurvivalProto-Oncogene Proteins c-metMET protein, humanProto-Oncogene Proteins c-metc-MetGlioblastoma MultiformePrognosissurvival

Identifiers

PMID34710981
PMCPMC8858257
OpenAlexW3211124867

What OpenQuestion holds

Textmetadata
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.