Molecular-Based Recursive Partitioning Analysis Model for Glioblastoma in the Temozolomide Era: A Correlative Analysis Based on NRG Oncology RTOG 0525.

Autor:	Bell EH; Department of Radiation Oncology, The Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital, Columbus, Ohio., Pugh SL; NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania., McElroy JP; The Ohio State University Center for Biostatistics, Columbus, Ohio., Gilbert MR; National Institutes of Health, Bethesda, Maryland., Mehta M; University of Maryland Medical Systems, Baltimore, Maryland (during trial)6now with Miami Cancer Institute, Coral Gables, Florida., Klimowicz AC; University of Calgary, Calgary, Alberta, Canada., Magliocco A; Moffitt Cancer Center, Tampa, Florida., Bredel M; University of Alabama, Birmingham, Alabama., Robe P; Utrecht Cancer Center, Utrecht, Netherlands., Grosu AL; University of Freiburg, Freiburg, Germany., Stupp R; University Hospital Zurich, Zürich, Switzerland., Curran W Jr; Emory University, Atlanta, Georgia., Becker AP; Department of Radiation Oncology, The Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital, Columbus, Ohio., Salavaggione AL; Department of Radiation Oncology, The Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital, Columbus, Ohio., Barnholtz-Sloan JS; Case Comprehensive Cancer Center, Case Western Reserve University School of Medicine, Cleveland, Ohio., Aldape K; MD Anderson Cancer Center, Houston, Texas., Blumenthal DT; Tel-Aviv Sourasky Medical Center, Tel Aviv, Israel., Brown PD; MD Anderson Cancer Center, Houston, Texas., Glass J; Thomas Jefferson University Hospital, Philadelphia, Pennsylvania., Souhami L; McGill University Health Centre, Montreal, Québec, Canada., Lee RJ; Intermountain Medical Center, Murray, Utah., Brachman D; Arizona Oncology Services Foundation, Tucson, Arizona., Flickinger J; UPMC-Shadyside Hospital, Pittsburgh, Pennsylvania., Won M; NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania., Chakravarti A; Department of Radiation Oncology, The Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital, Columbus, Ohio.
Jazyk:	angličtina
Zdroj:	JAMA oncology [JAMA Oncol] 2017 Jun 01; Vol. 3 (6), pp. 784-792.
DOI:	10.1001/jamaoncol.2016.6020
Abstrakt:	Importance: There is a need for a more refined, molecularly based classification model for glioblastoma (GBM) in the temozolomide era. Objective: To refine the existing clinically based recursive partitioning analysis (RPA) model by incorporating molecular variables. Design, Setting, and Participants: NRG Oncology RTOG 0525 specimens (n = 452) were analyzed for protein biomarkers representing key pathways in GBM by a quantitative molecular microscopy-based approach with semiquantitative immunohistochemical validation. Prognostic significance of each protein was examined by single-marker and multimarker Cox regression analyses. To reclassify the prognostic risk groups, significant protein biomarkers on single-marker analysis were incorporated into an RPA model consisting of the same clinical variables (age, Karnofsky Performance Status, extent of resection, and neurologic function) as the existing RTOG RPA. The new RPA model (NRG-GBM-RPA) was confirmed using traditional immunohistochemistry in an independent data set (n = 176). Main Outcomes and Measures: Overall survival (OS). Results: In 452 specimens, MGMT (hazard ratio [HR], 1.81; 95% CI, 1.37-2.39; P < .001), survivin (HR, 1.36; 95% CI, 1.04-1.76; P = .02), c-Met (HR, 1.53; 95% CI, 1.06-2.23; P = .02), pmTOR (HR, 0.76; 95% CI, 0.60-0.97; P = .03), and Ki-67 (HR, 1.40; 95% CI, 1.10-1.78; P = .007) protein levels were found to be significant on single-marker multivariate analysis of OS. To refine the existing RPA, significant protein biomarkers together with clinical variables (age, Karnofsky Performance Status, extent of resection, and neurological function) were incorporated into a new model. Of 166 patients used for the new NRG-GBM-RPA model, 97 (58.4%) were male (mean [SD] age, 55.7 [12.0] years). Higher MGMT protein level was significantly associated with decreased MGMT promoter methylation and vice versa (1425.1 for methylated vs 1828.0 for unmethylated; P < .001). Furthermore, MGMT protein expression (HR, 1.84; 95% CI, 1.38-2.43; P < .001) had greater prognostic value for OS compared with MGMT promoter methylation (HR, 1.77; 95% CI, 1.28-2.44; P < .001). The refined NRG-GBM-RPA consisting of MGMT protein, c-Met protein, and age revealed greater separation of OS prognostic classes compared with the existing clinically based RPA model and MGMT promoter methylation in NRG Oncology RTOG 0525. The prognostic significance of the NRG-GBM-RPA was subsequently confirmed in an independent data set (n = 176). Conclusions and Relevance: This new NRG-GBM-RPA model improves outcome stratification over both the current RTOG RPA model and MGMT promoter methylation, respectively, for patients with GBM treated with radiation and temozolomide and was biologically validated in an independent data set. The revised RPA has the potential to contribute to improving the accurate assessment of prognostic groups in patients with GBM treated with radiation and temozolomide and to influence clinical decision making. Trial Registration: clinicaltrials.gov Identifier: NCT00304031.
Databáze:	MEDLINE
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