Evidence map›Paper›PMID 27310651›Full record

SynthesisJAMA oncology2016

Association of the Extent of Resection With Survival in Glioblastoma: A Systematic Review and Meta-analysis.

Timothy J Brown, Matthew C Brennan, Michael Li, Ephraim W Church, Nicholas J Brandmeir, Kevin L Rakszawski, Akshal S Patel, Elias B Rizk, Dima Suki, Raymond Sawaya and 1 more

2 registry-linked trialsAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in JAMA oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 625 papers, 14 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
625citing papers in PubMed, 14 pooled it
–field-weighted citation impact
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.

NCT05318612 phase3active not recruitingnot on this mapstarted 2022, after this paper: background citation

(Cost)Effectiveness of MR-guided LITT Therapy in Patients With Primary Irresectable Glioblastoma: a Prospective Multicenter Randomized Controlled Trial (EMITT)

TypeinterventionalSponsorRadboud University Medical CenterRan2022 to 2027Enrolled238ConditionsPrimary GlioblastomaArmsLaser Interstitial Thermal Therapy (LITT), Biopsy
NCT06551909 narecruitingnot on this mapstarted 2024, after this paper: background citation

Radioimmunotherapy in Solid Tumors (Aim 2- Stereotactic Neoadjuvant Radiotherapy for Glioblastoma)

TypeinterventionalSponsorIRCCS San RaffaeleRan2024 to 2027Enrolled30ConditionsGlioblastomaArmsNeoaddjuvant Stereotactic Radiotherapy with Simultaneous Integrated Boost
3 · Its place in the literature

Who cites it

625 citing papers in PubMed, 14 syntheses or guidelines pooled it.

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  18. Enhanced Glioblastoma Detection ThroughMagnetic resonance in medicine · 2026
    Article
  19. Article
  20. Laser Interstitial Thermal Therapy for Brain Tumors: A Prospective Multicenter Analysis of Patients From the LAANTERN Study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article

565 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Timothy J BrownDepartment of Medicine, University of Texas Southwestern Medical Center, Dallas.
Matthew C BrennanAnn Barshinger Cancer Center, Lancaster General Health, Lancaster, Pennsylvania.
Michael LiDepartment of Neurosurgery, University of Rochester Medical Center, Pittsford, New York.
Ephraim W ChurchDepartment of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.
Nicholas J BrandmeirDepartment of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.
Kevin L RakszawskiDepartment of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.
Akshal S PatelDepartment of Neurosurgery, Swedish Cerebrovascular Institute, Seattle, Washington.
Elias B RizkDepartment of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.
Dima SukiDivision of Surgery, Department of Neurosurgery, University of Texas MD Anderson Cancer Center, Houston.
Raymond SawayaDivision of Surgery, Department of Neurosurgery, University of Texas MD Anderson Cancer Center, Houston.
Michael GlantzDepartment of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

importanceGlioblastoma multiforme (GBM) remains almost invariably fatal despite optimal surgical and medical therapy. The association between the extent of tumor resection (EOR) and outcome remains undefined, notwithstanding many relevant studies.

objectiveTo determine whether greater EOR is associated with improved 1- and 2-year overall survival and 6-month and 1-year progression-free survival in patients with GBM. DATA SOURCES: Pubmed, CINAHL, and Web of Science (January 1, 1966, to December 1, 2015) were systematically reviewed with librarian guidance. Additional articles were included after consultation with experts and evaluation of bibliographies. Articles were collected from January 15 to December 1, 2015. STUDY SELECTION: Studies of adult patients with newly diagnosed supratentorial GBM comparing various EOR and presenting objective overall or progression-free survival data were included. Pediatric studies were excluded. DATA EXTRACTION AND SYNTHESIS: Data were extracted from the text of articles or the Kaplan-Meier curves independently by investigators who were blinded to each other's results. Data were analyzed to assess mortality after gross total resection (GTR), subtotal resection (STR), and biopsy. The body of evidence was evaluated according to Grading of Recommendations Assessment, Development, and Evaluation (GRADE) criteria and PRISMA guidelines. MAIN OUTCOME AND MEASURES: Relative risk (RR) for mortality at 1 and 2 years and progression at 6 months and 1 year.

resultsThe search produced 37 studies suitable for inclusion (41 117 unique patients). The meta-analysis revealed decreased mortality for GTR compared with STR at 1 year (RR, 0.62; 95% CI, 0.56-0.69; P < .001; number needed to treat [NNT], 9) and 2 years (RR, 0.84; 95% CI, 0.79-0.89; P < .001; NNT, 17). The 1-year risk for mortality for STR compared with biopsy was reduced significantly (RR, 0.85; 95% CI, 0.80-0.91; P < .001). The risk for mortality was similarly decreased for any resection compared with biopsy at 1 year (RR, 0.77; 95% CI, 0.71-0.84; P < .001; NNT, 21) and 2 years (RR, 0.94; 95% CI, 0.89-1.00; P = .04; NNT, 593). The likelihood of disease progression was decreased with GTR compared with STR at 6 months (RR, 0.72; 95% CI, 0.48-1.09; P = .12; NNT, 14) and 1 year (RR, 0.66; 95% CI, 0.43-0.99; P < .001; NNT, 26). The quality of the body of evidence by the GRADE criteria was moderate to low. CONCLUSION AND RELEVANCE: This analysis represents the largest systematic review and only quantitative systematic review to date performed on this subject. Compared with STR, GTR substantially improves overall and progression-free survival, but the quality of the supporting evidence is moderate to low.

Indexed as

BrainBrain NeoplasmsDisease-Free SurvivalGlioblastomaHumansRiskTreatment Outcome

Identifiers

PMID27310651
PMCPMC6438173

What OpenQuestion holds

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Registered trials

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.