PT - JOURNAL ARTICLE AU - MICHAEL H. WANG AU - WILSON ROA AU - KEITH WACHOWICZ AU - ATIYAH YAHYA AU - ALBERT MURTHA AU - JOHN AMANIE AU - JONATHAN CHAINEY AU - HARVEY QUON AU - SUNITA GHOSH AU - SAMIR PATEL TI - Early Metabolic Changes in 1H-MRSI Predictive for Survival in Patients With Newly Diagnosed High-grade Glioma AID - 10.21873/anticanres.15744 DP - 2022 May 01 TA - Anticancer Research PG - 2665--2673 VI - 42 IP - 5 4099 - http://ar.iiarjournals.org/content/42/5/2665.short 4100 - http://ar.iiarjournals.org/content/42/5/2665.full SO - Anticancer Res2022 May 01; 42 AB - Background: The purpose of this study was to evaluate the association of specific threshold values for changes in metabolic metrics measured from 1H magnetic resonance spectroscopic imaging (MRSI) to survival of patients with high-grade glioma treated with multimodality therapy. Patients and Methods: Forty-four patients with newly diagnosed high-grade glioma were prospectively enrolled. Serial MRI and MRSI scans provided measures of tumor choline, creatine, and N-acetylaspartate (NAA). Cox regression analyses adjusted for patient age, KPS, and delivery of concurrent chemotherapy were used to assess the association of changes in metabolic metrics with survival. Results: Median follow-up time for patients at risk was 13.4 years. Overall survival (OS) was longer in patients with ≤20% increase (vs. >20%) in normalized choline (p=0.024) or choline/NAA (p=0.024) from baseline to week 4 of RT. During this period, progression-free survival (PFS) was longer in patients with ≤40% increase (vs. >40%) in normalized choline (p=0.013). Changes in normalized creatine, choline/creatine, and NAA/creatine from baseline to mid-RT were not associated with OS. From baseline to post-RT, changes in metabolic metrics were not associated with OS or PFS. Conclusion: Threshold values for serial changes in choline metrics on mid-RT MRSI associated with OS and PFS were identified. Metabolic metrics at post-RT did not predict for these survival endpoints. These findings suggest a potential clinical role for MRSI to provide an early assessment of treatment response and could enable risk-adapted therapy in clinical trial development and clinical practice.