Background and purpose To refine the recursive partitioning analysis (RPA) classification for glioblastoma incorporating the MGMT methylation and IDH1 mutation status. Methods and Materials Three-hundred forty patients were treated with radiotherapy plus concurrent and adjuvant temozolomide in three tertiary-referral hospitals. MGMT methylation and IDH1 mutation status were available in all patients. Methylation of the MGMT (MGMTmeth) and mutation of IDH1 (IDH1mut) were observed in 42.4% and 6.2% of the patients, respectively. Results The median follow-up for survivors and all patients was 33.2 and 20.5 months, respectively. The median survival (MS) was 23.6 months. RPA was performed on behalf of the results of the Cox proportional hazards model. MGMT methylation generated the initial partition (MGMTmeth vs. MGMTunmeth) in the RPA. Three final RPA classes were identified; class I = MGMTmeth/IDH1mut or MGMTmeth/IDH1wt/GTR/KPS ≥ 90 (MS, 67.2 months); class II = MGMTmeth/IDH1wt/GTR/KPS < 90, MGMTmeth/IDH1wt/residual disease, MGMTunmeth/age < 50, or MGMTunmeth/age ≥ 50/GTR (MS, 24.0 months); class III = MGMTunmeth/age ≥ 50/residual disease (MS, 15.2 months). Conclusions A novel RPA classification for glioblastoma was formulated highlighting the impact of MGMTmeth and IDH1mut in the temozolomide era. This model integrating pertinent molecular information can be used effectively for the patient stratification in future clinical trials. An external validation is ongoing.
Bibliographical notePublisher Copyright:
© 2017 Elsevier B.V.
All Science Journal Classification (ASJC) codes
- Radiology Nuclear Medicine and imaging