The Role of Extent of Resection in IDH1 Wild-Type or Mutant Low-Grade Gliomas

Author:

Patel Toral1,Bander Evan D23,Venn Rachael A2,Powell Tiffany2,Cederquist Gustav Young-Min2,Schaefer Peter M2,Puchi Luis A2,Akhmerov Akbarshakh2,Ogilvie Shahiba2,Reiner Anne S4,Moussazadeh Nelson23,Tabar Viviane2

Affiliation:

1. Department of Neurological Surgery, The University of Texas Southwestern Medical Center, Dallas, Texas

2. Depart-ment of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, New York

3. Department of Neurological Surgery, Weill Cornell Medical Center, New York, New York

4. Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York

Abstract

Abstract BACKGROUND Maximizing extent of resection (EOR) improves outcomes in adults with World Health Organization (WHO) grade II low-grade gliomas (LGG). However, recent studies demonstrate that LGGs bearing a mutation in the isocitrate dehydrogenase 1 (IDH1) gene are a distinct molecular and clinical entity. It remains unclear whether maximizing EOR confers an equivalent clinical benefit in IDH mutated (mtIDH) and IDH wild-type (wtIDH) LGGs. OBJECTIVE To assess the impact of EOR on malignant progression-free survival (MPFS) and overall survival (OS) in mtIDH and wtIDH LGGs. METHODS We performed a retrospective review of 74 patients with WHO grade II gliomas and known IDH mutational status undergoing resection at a single institution. EOR was assessed with quantitative 3-dimensional volumetric analysis. The effect of predictor variables on MPFS and OS was analyzed with Cox regression models and the Kaplan–Meier method. RESULTS Fifty-two (70%) mtIDH patients and 22 (30%) wtIDH patients were included. Median preoperative tumor volume was 37.4 cm3; median EOR of 57.6% was achieved. Univariate Cox regression analysis confirmed EOR as a prognostic factor for the entire cohort. However, stratifying by IDH status demonstrates that greater EOR independently prolonged MPFS and OS for wtIDH patients (hazard ratio [HR] = 0.002 [95% confidence interval {CI} 0.000-0.074] and HR = 0.001 [95% CI 0.00-0.108], respectively), but not for mtIDH patients (HR = 0.84 [95% CI 0.17-4.13] and HR = 2.99 [95% CI 0.15-61.66], respectively). CONCLUSION Increasing EOR confers oncologic and survival benefits in IDH1 wtLGGs, but the impact on IDH1 mtLGGs requires further study.

Funder

NIH

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Surgery

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