Ferumoxytol-Enhanced MR Lymphography for Detection of Metastatic Lymph Nodes in Genitourinary Malignancies: A Prospective Study.

Adam R Metwalli, Peter L Choyke, William Dahut, Liza Lindenberg, Paula M Jacobs, Bradford J Wood, Lindsay S Rowe, Soroush Rais-Bahrami, Peter A Pinto, Edmond Paquette, Baris Turkbey, Ravi A Madan, Mukesh Harisinghani, James L Gulley, Deborah E Citrin, Andrea B Apolo, Piyush K Agarwal, Stephanie A Harmon, Joanna H Shih, Marcin Czarniecki

Journal: AJR. American journal of roentgenology 2020;214(1):105-113

PMID: 31613660

Abstract

The objective of our study was to evaluate the utility of ferumoxytol-enhanced MR lymphography (MRL) in detection of metastatic lymph nodes (LNs) in patients with prostate, bladder, and kidney cancer. This phase 2 single-institution study enrolled patients with confirmed prostate (arm 1), bladder (arm 2), and kidney (arm 3) cancer and evidence of suspected LN involvement. Participants underwent ferumoxytol-enhanced MRL 24 and 48 hours after IV injection of 7.5 mg Fe/kg of ferumoxytol. A retrospective quantitative analysis was performed to determine the optimal timing for ferumoxytol-enhanced MRL using percentage change in normalized signal intensity (SI) from baseline to 24 and 48 hours after injection, which were estimated using the linear mixed-effects model in which time (24 vs 48 hours), diseases status, and time and disease status interaction were the fixed-effects independent variables. Differences in normalized SI values between subgroups of lesions were estimated by forming fixed-effects contrasts and tested by the Wald test. Thirty-nine patients ( = 30, arm 1; = 6, arm 2; = 3, arm 3) (median age, 65 years) with 145 LNs (metastatic, = 100; benign, = 45) were included. LN-based sensitivity, specificity, positive predictive value, and negative predictive value of ferumoxytol-enhanced MRL was 98.0%, 64.4%, 86.0%, and 93.5%, respectively. Sensitivity and specificity of ferumoxytol-enhanced MRL did not vary by LN size. Metastatic LNs showed a significantly higher percentage decrease of normalized SI on MRL at 24 hours after ferumoxytol injection than at 48 hours after ferumoxytol injection ( = 0.023), whereas the normalized SI values for nonmetastatic LNs were similar at both imaging time points ( = 0.260). Ferumoxytol-enhanced MRL shows high sensitivity in the detection of metastatic LNs in genitourinary cancers independent of LN size. The SI difference between benign and malignant LNs on ferumoxytol-enhanced MRL appears similar 24 and 48 hours after ferumoxytol injection, suggesting that imaging can be performed safely within 1 or 2 days of injection. Although ferumoxytol-enhanced MRL can be useful in settings without an available targeted PET agent, issues of iron overload and repeatability of ferumoxytol-enhanced MRL remain concerns for this method.

Address: Molecular Imaging Program, Center for Cancer Research (CCR), National Cancer Institute (NCI), National Institutes of Health (NIH), 10 Center Dr, Rm B3B85, Bethesda, MD 20892.; Biometric Research Branch, Division of Cancer Treatment and Diagnosis, NCI, NIH, Rockville, MD.; Clinical Research Directorate, Frederick National Laboratory for Cancer Research, (Sponsored by the National Cancer Institute), Frederick, MD.; Urologic Oncology Branch, CCR, NCI, NIH, Bethesda, MD.; Genitourinary Malignancies Branch, CCR, NCI, NIH, Bethesda, MD.; Radiation Oncology Branch, CCR, NCI, NIH, Bethesda, MD.; Department of Radiology, Harvard Medical School, Massachusetts General Hospital, Boston, MA.; Department of Surgery, Division of Urology, Howard University Hospital, Washington, DC.; Inova Medical Group Urology, Inova Fairfax Hospital, Fairfax, VA.; Department of Urology, University of Alabama at Birmingham, Birmingham, AL.; Department of Radiology, University of Alabama at Birmingham, Birmingham, AL.; Center for Interventional Oncology, CCR, NCI, NIH, Bethesda, MD.; Cancer Imaging Program, CCR, NCI, NIH, Bethesda, MD.
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