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

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          Abstract

          IMPORTANCE

          Glioblastoma 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.

          OBJECTIVE

          To 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.

          RESULTS

          The 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.

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          Author and article information

          Contributors
          Journal
          101652861
          43608
          JAMA Oncol
          JAMA Oncol
          JAMA oncology
          2374-2437
          2374-2445
          5 August 2018
          01 November 2016
          28 March 2019
          : 2
          : 11
          : 1460-1469
          Affiliations
          Department of Medicine, University of Texas Southwestern Medical Center, Dallas
          Ann Barshinger Cancer Center, Lancaster General Health, Lancaster, Pennsylvania
          Department of Neurosurgery, University of Rochester Medical Center, Pittsford, New York
          Department of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania
          Department of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania
          Department of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania
          Department of Neurosurgery, Swedish Cerebrovascular Institute, Seattle, Washington
          Department of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania
          Division of Surgery, Department of Neurosurgery, University of Texas MD Anderson Cancer Center, Houston
          Division of Surgery, Department of Neurosurgery, University of Texas MD Anderson Cancer Center, Houston
          Department of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania
          Author notes

          Author Contributions: Drs Brown and Glantz had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.

          Study concept and design: Brown, Brennan, Li, Church, Brandmeir, Rakszawski, Patel, Glantz.

          Acquisition, analysis, or interpretation of data: Brown, Brennan, Church, Brandmeir, Rakszawski, Rizk, Suki, Sawaya, Glantz.

          Drafting of the manuscript: Brown, Rakszawski, Glantz.

          Critical revision of the manuscript for important intellectual content: All authors.

          Statistical analysis: Brown, Church, Brandmeir, Rakszawski, Rizk, Glantz.

          Administrative, technical, or material support: Li, Glantz.

          Study supervision: Patel, Rizk, Glantz.

          Additional Contributions: The Penn State Hershey George T. Harrell Health Science Library provided systematic review training to the study authors.

          Corresponding Author: Michael Glantz, MD, Department of Neurosurgery, Penn State Milton S. Hershey Medical Center, 30 Hope Dr, Mail Code EC110, Hershey, PA 17033 ( mglantz@ 123456hmc.psu.edu ).
          Article
          PMC6438173 PMC6438173 6438173 nihpa978186
          10.1001/jamaoncol.2016.1373
          6438173
          27310651
          18d86c14-68ee-4b7a-ba4f-104391981218
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