Extent of Tumor Resection and Survival in Pediatric Patients With High-Grade Gliomas: A Systematic Review and Meta-analysis.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 08 2022
Historique:
entrez: 16 8 2022
pubmed: 17 8 2022
medline: 19 8 2022
Statut: epublish

Résumé

Pediatric patients with high-grade gliomas have a poor prognosis. The association among the extent of resection, tumor location, and survival in these patients remains unclear. To ascertain whether gross total resection (GTR) in hemispheric, midline, or infratentorial pediatric high-grade gliomas (pHGGs) is independently associated with survival differences compared with subtotal resection (STR) and biopsy at 1 year and 2 years after tumor resection. PubMed, EBMR, Embase, and MEDLINE were systematically reviewed from inception to June 3, 2022, using the keywords high-grade glioma, pediatric, and surgery. No period or language restrictions were applied. Randomized clinical trials and cohort studies of pHGGs that stratified patients by extent of resection and reported postoperative survival were included for study-level and individual patient data meta-analyses. Study characteristics and mortality rates were extracted from each article. Relative risk ratios (RRs) were pooled using random-effects models. Individual patient data were evaluated using multivariate mixed-effects Cox proportional hazards regression modeling. The PRISMA reporting guideline was followed, and the study was registered a priori. Hazard ratios (HRs) and RRs were extracted to indicate associations among extent of resection, 1-year and 2-year postoperative mortality, and overall survival. A total of 37 studies with 1387 unique patients with pHGGs were included. In study-level meta-analysis, GTR had a lower mortality risk than STR at 1 year (RR, 0.69; 95% CI, 0.56-0.83; P < .001) and 2 years (RR, 0.74; 95% CI, 0.67-0.83; P < .001) after tumor resection. Subtotal resection was not associated with differential survival compared with biopsy at 1 year (RR, 0.82; 95% CI, 0.66-1.01; P = .07) but had decreased mortality risk at 2 years (RR, 0.89; 95% CI, 0.82-0.97; P = .01). The individual patient data meta-analysis of 27 articles included 427 patients (mean [SD] age at diagnosis, 9.3 [5.9] years), most of whom were boys (169 of 317 [53.3%]), had grade IV tumors (246 of 427 [57.7%]), and/or had tumors that were localized to either the cerebral hemispheres (133 of 349 [38.1%]) or midline structures (132 of 349 [37.8%]). In the multivariate Cox proportional hazards regression model, STR (HR, 1.91; 95% CI, 1.34-2.74; P < .001) and biopsy (HR, 2.10; 95% CI, 1.43-3.07; P < .001) had shortened overall survival compared with GTR but no survival differences between them (HR, 0.91; 95% CI, 0.67-1.24; P = .56). Gross total resection was associated with prolonged survival compared with STR for hemispheric (HR, 0.29; 95% CI, 0.15-0.54; P < .001) and infratentorial (HR, 0.44; 95% CI, 0.24-0.83; P = .01) tumors but not midline tumors (HR, 0.63; 95% CI, 0.34-1.19; P = .16). Results of this study show that, among patients with pHGG, GTR is independently associated with better overall survival compared with STR and biopsy, especially among patients with hemispheric and infratentorial tumors, and support the pursuit of maximal safe resection in the treatment of pHGGs.

Identifiants

pubmed: 35972743
pii: 2795183
doi: 10.1001/jamanetworkopen.2022.26551
pmc: PMC9382445
doi:

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2226551

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Auteurs

Rami Hatoum (R)

University of Montréal School of Medicine, Montréal, Quebec, Canada.

Jia-Shu Chen (JS)

The Warren Alpert Medical School of Brown University, Providence, Rhode Island.

Pascal Lavergne (P)

Department of Neurological Surgery, University of Washington, Seattle.

Nathan A Shlobin (NA)

Department of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Andrew Wang (A)

Department of Neurosurgery, David Geffen School of Medicine at UCLA (University of California, Los Angeles).
College of Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, California.

Lior M Elkaim (LM)

Division of Neurology and Neurosurgery, McGill University, McGill University Health Center, Montreal, Quebec, Canada.

Philippe Dodin (P)

Medical Library, Centre Hospitalier Universitaire (CHU) Sainte-Justine Children's, Montréal, Quebec, Canada.

Charles P Couturier (CP)

Department of Neurology and Neurosurgery, Montréal Neurological Institute-Hospital, Montréal, Quebec, Canada.

George M Ibrahim (GM)

Division of Neurosurgery, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Aria Fallah (A)

Department of Neurosurgery, David Geffen School of Medicine at UCLA (University of California, Los Angeles).
Department of Pediatrics, David Geffen School of Medicine at UCLA.

Dominic Venne (D)

Division of Neurosurgery, Ste Justine Hospital, University of Montréal, Montréal, Quebec, Canada.

Sebastien Perreault (S)

Department of Neurology, CHU Sainte-Justine, Montréal, Quebec, Canada.

Anthony C Wang (AC)

Department of Neurosurgery, David Geffen School of Medicine at UCLA (University of California, Los Angeles).
Department of Pediatrics, David Geffen School of Medicine at UCLA.

Nada Jabado (N)

Department of Human Genetics, McGill University, Montréal, Quebec, Canada.
Department of Pediatrics, McGill University and McGill University Health Centre Research Institute, Montréal, Quebec, Canada.

Roy W R Dudley (RWR)

Neurosurgery Service, Department of Surgery, McGill University and McGill University Health Centre Research Institute, Montréal, Quebec, Canada.

Alexander G Weil (AG)

Division of Neurosurgery, Ste Justine Hospital, University of Montréal, Montréal, Quebec, Canada.
Neurosurgery Service, Department of Surgery, University of Montreal Hospital Center, Montréal, Quebec, Canada.
Sainte-Justine University Hospital Research Center, Montréal, Quebec, Canada.

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