Association of the Extent of Resection With Survival in Glioblastoma

医学 胶质母细胞瘤 分级(工程) 相对风险 梅德林 内科学 外科 置信区间 政治学 工程类 土木工程 法学 癌症研究
作者
Timothy J. Brown,Matthew Brennan,Michael J. Li,Ephraim W. Church,Nicholas Brandmeir,Kevin Rakszawski,Akshal Patel,Elias Rizk,Dima Suki,Raymond Sawaya,Michael Glantz
出处
期刊:JAMA Oncology [American Medical Association]
卷期号:2 (11): 1460-1460 被引量:903
标识
DOI:10.1001/jamaoncol.2016.1373
摘要

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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