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Detection of early response to temozolomide treatment in brain tumors using hyperpolarized 13 C MR metabolic imaging
Author(s) -
Park Ilwoo,
Bok Robert,
Ozawa Tomoko,
Phillips Joanna J.,
James C. David,
Vigneron Daniel B.,
Ronen Sabrina M.,
Nelson Sarah J.
Publication year - 2011
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.22563
Subject(s) - temozolomide , medicine , nuclear medicine , glioblastoma , magnetic resonance imaging , brain tumor , u87 , glioma , pathology , cancer research , radiology
Purpose: To demonstrate the feasibility of using DNP hyperpolarized [1‐ 13 C]‐pyruvate to measure early response to temozolomide (TMZ) therapy using an orthotopic human glioblastoma xenograft model. Materials and Methods: Twenty athymic rats with intracranial implantation of human glioblastoma cells were divided into two groups: one group received an oral administration of 100 mg/kg TMZ ( n = 10) and the control group received vehicle only ( n = 10). 13 C 3D magnetic resonance spectroscopic imaging (MRSI) data were acquired following injection of 2.5 mL (100 mM) hyperpolarized [1‐ 13 C]‐pyruvate using a 3T scanner prior to treatment (day D0), at D1 (days from treatment) or D2. Results: Tumor metabolism as assessed by the ratio of lactate to pyruvate (Lac/Pyr) was significantly altered at D1 for the TMZ‐treated group but tumor volume did not show a reduction until D5 to D7. The percent change in Lac/Pyr from baseline was statistically different between the two groups at D1 and D2 ( P < 0.008), while percent tumor volume was not ( P > 0.2). Conclusion: The results from this study suggest that metabolic imaging with hyperpolarized [1‐ 13 C]‐pyruvate may provide a unique tool that clinical neuro‐oncologists can use in the future to monitor tumor response to therapy for patients with brain tumors. J. Magn. Reson. Imaging 2011;33:1284–1290. © 2011 Wiley‐Liss, Inc.