Your browser doesn't support javascript.
loading
MR spectroscopic imaging predicts early response to anti-angiogenic therapy in recurrent glioblastoma.
Talati, Pratik; El-Abtah, Mohamed; Kim, Daniel; Dietrich, Jorg; Fu, Melanie; Wenke, Michael; He, Julian; Natheir, Sharif N; Vangel, Mark; Rapalino, Otto; Vaynrub, Anna; Arrillaga-Romany, Isabel; Forst, Deborah A; Yen, Yi-Fen; Andronesi, Ovidiu; Kalpathy-Cramer, Jayashree; Rosen, Bruce; Batchelor, Tracy T; Gonzalez, R Gilberto; Gerstner, Elizabeth R; Ratai, Eva-Maria.
Affiliation
  • Talati P; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • El-Abtah M; Department of Neurosurgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Kim D; Harvard Medical School, Boston, Massachusetts, USA.
  • Dietrich J; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Fu M; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Wenke M; Harvard Medical School, Boston, Massachusetts, USA.
  • He J; Massachusetts General Hospital, Cancer Center, Boston, Massachusetts, USA.
  • Natheir SN; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Vangel M; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Rapalino O; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Vaynrub A; Harvard Medical School, Boston, Massachusetts, USA.
  • Arrillaga-Romany I; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Forst DA; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Yen YF; Harvard Medical School, Boston, Massachusetts, USA.
  • Andronesi O; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Kalpathy-Cramer J; Harvard Medical School, Boston, Massachusetts, USA.
  • Rosen B; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Batchelor TT; Harvard Medical School, Boston, Massachusetts, USA.
  • Gonzalez RG; Massachusetts General Hospital, Cancer Center, Boston, Massachusetts, USA.
  • Gerstner ER; Massachusetts General Hospital, Cancer Center, Boston, Massachusetts, USA.
  • Ratai EM; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Neurooncol Adv ; 3(1): vdab060, 2021.
Article in En | MEDLINE | ID: mdl-34131648
ABSTRACT

BACKGROUND:

Determining failure to anti-angiogenic therapy in recurrent glioblastoma (GBM) (rGBM) remains a challenge. The purpose of the study was to assess treatment response to bevacizumab-based therapy in patients with rGBM using MR spectroscopy (MRS).

METHODS:

We performed longitudinal MRI/MRS in 33 patients with rGBM to investigate whether changes in N-acetylaspartate (NAA)/Choline (Cho) and Lactate (Lac)/NAA from baseline to subsequent time points after treatment can predict early failures to bevacizumab-based therapies.

RESULTS:

After stratifying based on 9-month survival, longer-term survivors had increased NAA/Cho and decreased Lac/NAA levels compared to shorter-term survivors. ROC analyses for intratumoral NAA/Cho correlated with survival at 1 day, 2 weeks, 8 weeks, and 16 weeks. Intratumoral Lac/NAA ROC analyses were predictive of survival at all time points tested. At the 8-week time point, 88% of patients with decreased NAA/Cho did not survive 9 months; furthermore, 90% of individuals with an increased Lac/NAA from baseline did not survive at 9 months. No other metabolic ratios tested significantly predicted survival.

CONCLUSIONS:

Changes in metabolic levels of tumoral NAA/Cho and Lac/NAA can serve as early biomarkers for predicting treatment failure to anti-angiogenic therapy as soon as 1 day after bevacizumab-based therapy. The addition of MRS to conventional MR methods can provide better insight into how anti-angiogenic therapy affects tumor microenvironment and predict patient outcomes.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Neurooncol Adv Year: 2021 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: Neurooncol Adv Year: 2021 Document type: Article Affiliation country: United States