Measurement of metabolite levels and treatment‐induced changes in hepatic metastases of gastro‐esophageal cancer using 7‐T phosphorus magnetic resonance spectroscopic imaging

• Published in: NMR in biomedicine Vol. 37; no. 9; pp. e5155 - n/a
• Main Authors: Wildenberg, Lieke, Runderkamp, Bobby A., Seelen, Leonard W. F., Laarhoven, Hanneke W. M., Gosselink, Mark W. J. M., Kemp, Wybe J. M., Haj Mohammad, Nadia, Klomp, Dennis W. J., Prompers, Jeanine J.
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.09.2024
• Subjects: 7 T; Arrays; Body size; Cancer; Cancer therapies; Chemotherapy; Data acquisition; Esophageal cancer; Esophagus; Feasibility studies; Health services; Liver; Liver cancer; Liver diseases; liver metastasis; Magnetic resonance imaging; Magnetic resonance spectroscopy; Medical imaging; membrane turnover; Metabolites; Metastases; Metastasis; Patients; Phosphocholine; Phosphodiesters; Phosphomonoesters; Phosphorus; treatment response; Tumors; liver metastasis; 7 T; treatment response; magnetic resonance spectroscopy; cancer; membrane turnover; phosphorus
• ISSN: 0952-3480; 1099-1492; 1099-1492
• DOI: 10.1002/nbm.5155

Methods for early treatment response evaluation to systemic therapy of liver metastases are lacking. Tumor tissue often exhibits an increased ratio of phosphomonoesters to phosphodiesters (PME/PDE), which can be noninvasively measured by phosphorus magnetic resonance spectroscopy (31P MRS), and may be a marker for early therapy response assessment in liver metastases. However, with commonly used 31P surface coils for liver 31P MRS, the liver is not fully covered, and metastases may be missed. The objective of this study was to demonstrate the feasibility of 31P MRS imaging (31P MRSI) with full liver coverage to assess 31P metabolite levels and chemotherapy‐induced changes in liver metastases of gastro‐esophageal cancer, using a 31P whole‐body birdcage transmit coil in combination with a 31P body receive array at 7 T. 3D 31P MRSI data were acquired in two patients with hepatic metastases of esophageal cancer, before the start of chemotherapy and after 2 (and 9 in patient 2) weeks of chemotherapy. 3D 31P MRSI acquisitions were performed using an integrated 31P whole‐body transmit coil in combination with a 16‐channel body receive array at 7 T, with a field of view covering the full abdomen and a nominal voxel size of 20‐mm isotropic. From the 31P MRSI data, 12 31P metabolite signals were quantified. Prior to chemotherapy initiation, both PMEs, that is, phosphocholine (PC) and phosphoethanolamine (PE), were significantly higher in all metastases compared with the levels previously determined in the liver of healthy volunteers. After 2 weeks of chemotherapy, PC and PE levels remained high or even increased further, resulting in increased PME/PDE ratios compared with healthy liver tissue, in correspondence with the clinical assessment of progressive disease after 2 months of chemotherapy. The suggested approach may present a viable tool for early therapy (non)response assessment of tumor metabolism in patients with liver metastases. This study aimed to demonstrate the feasibility of 31P MRSI with full liver coverage to assess 31P metabolite levels and chemotherapy‐induced changes in liver metastases of gastro‐esophageal cancer at 7 T, using a 31P whole‐body transmit coil and 31P body receive array. Before chemotherapy, PME was higher in metastases compared with healthy liver. After 2 weeks of chemotherapy, PME remained elevated or increased further, resulting in increased PME/PDE ratios, in correspondence with clinical assessment of progressive disease after 2 months of chemotherapy.