Evidence map›Paper›PMID 31362435›Full record

ArticleCancers2019

Extent of Resection, MGMT Promoter Methylation Status and Tumor Location Independently Predict Progression-Free Survival in Adult Sporadic Pilocytic Astrocytoma.

Christine Jungk, Annekathrin Reinhardt, Rolf Warta, David Capper, Andreas von Deimling, Christel Herold-Mende, Andreas Unterberg

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 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

7 authors at 2 institutions in 1 country.

Christine JungkDivision of Experimental Neurosurgery, Department of Neurosurgery, University Hospital Heidelberg, D-69120 Heidelberg, Germany. christine.jungk@med.uni-heidelberg.de.
Annekathrin ReinhardtDepartment of Neuropathology, German Cancer Consortium (DKTK), CCU Neuropathology, German Cancer Research Center, Institute of Pathology, University of Heidelberg, D-69120 Heidelberg, Germany.
Rolf WartaDivision of Experimental Neurosurgery, Department of Neurosurgery, University Hospital Heidelberg, D-69120 Heidelberg, Germany.
David CapperDepartment of Neuropathology, German Cancer Consortium (DKTK), CCU Neuropathology, German Cancer Research Center, Institute of Pathology, University of Heidelberg, D-69120 Heidelberg, Germany.
Andreas von DeimlingDepartment of Neuropathology, German Cancer Consortium (DKTK), CCU Neuropathology, German Cancer Research Center, Institute of Pathology, University of Heidelberg, D-69120 Heidelberg, Germany.
Christel Herold-MendeDivision of Experimental Neurosurgery, Department of Neurosurgery, University Hospital Heidelberg, D-69120 Heidelberg, Germany.
Andreas UnterbergDivision of Experimental Neurosurgery, Department of Neurosurgery, University Hospital Heidelberg, D-69120 Heidelberg, Germany.
Heidelberg University · DEGerman Cancer Research Center · DE

Funding

Anni-Hofmann-Foundation N/A
6 · The paper itself

Abstract

In adults, pilocytic astrocytomas (PA) account for less than 2% of gliomas, resulting in uncertainty regarding the clinical course and optimal treatment, particularly in cases where gross total resection (GTR) could not be achieved. Moreover, information on molecular markers and their prognostic impact is sparse. In order to improve risk stratification, we analyzed our institutional series of 58 patients aged 17 years and older with histology-proven intracranial PA World Health Organization grade I for clinical and molecular prognosticators. Anaplastic and NF1-associated tumors were excluded. O-6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status was determined by pyrosequencing or 450k/850k DNA methylation array. A univariate log-rank test and multivariate StepAIC were applied to identify prognostic factors. The median age was 30 years (range 17-66). Tumors were located in the cerebral/cerebellar hemispheres, midline structures and cerebello-pontine angle in 53%, 38% and 9%. MGMT promoter methylation was present in eight patients (14%). GTR (39/58 patients) significantly reduced the likelihood of tumor recurrence (

Indexed as

adultgross total resectionMGMT promoter methylation statuspilocytic astrocytomaprogression-free survivaltumor location

Identifiers

PMID31362435
PMCPMC6721291
OpenAlexW2965441596

What OpenQuestion holds

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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.