Current whole-body MRI applications in the neurofibromatoses

Shivani Ahlawat(Harvard University), Laura M. Fayad(Harvard University), Muhammad Shayan Khan(Harvard University), Miriam A. Bredella(Harvard University), Gordon J. Harris(Harvard University), D. Gareth Evans(Harvard University), Said Farschtschi(Harvard University), Michael A. Jacobs(Harvard University), Avneesh Chhabra(Harvard University), Johannes Salamon(Harvard University), Ralph Wenzel(Harvard University), Victor F. Mautner(Harvard University), Eva Dombi(Harvard University), Wenli Cai(Harvard University), Scott R. Plotkin(Harvard University), Jaishri O. Blakeley(Harvard University), Shivani Ahlawat(Harvard University), Srivandana Akshintala, Jeffrey C. Allen, Simone Ardern‐Holmes, Robert A. Avery, Amedeo A. Azizi, Dusica Babovic‐Vuksanovic, Annette Bakker, Andrea Baldwin, Fred G. Barker, Amanda L. Bergner, Chetan Bettegowda, Sucharita Bhaumik, Larissa T. Bilaniuk, Kim Bischoff, Jaishri Blakely(Harvard University), Diana Bradford, Miriam A. Bredella(Harvard University), Wenli Cai(Harvard University), John Carino, Avneesh Chabra(Harvard University), Patricia Ciavarelli, Wade Clapp, Stephen Connor, Albert Cornelius, Tambra Dahlheimer, Stephanie H. Davis, Peter de Blank, Vidya Dhote, Joni K. Doherty, Eva Dombi(Harvard University), William N. Dudley, Rachel Ershler, D. Gareth Evans(Harvard University), Laura M. Fayad(Harvard University), Cristina Fernández‐Valle, Rosalie E. Ferner, Michael J. Fisher(Harvard University), Barbara Franklin, Giulia Fulci, Tracy Galloway, Kathy Gardner, Richard Gedrich, Marco Giovannini, Amy Goldstein, Anne Goodwin(Harvard University), Stéphane Goutagny, David H. Gutmann, Theresa Hadlock, Chris Halpin, C. Oliver Hanemann, Kristina K. Hardy, Gordon J. Harris(Harvard University), Desirée Headley, Gena Heidary, Jonathan Heller, Cynthia M. Hingtgen, Trent R. Hummel, Susan Huson, Michael A. Jacobs(Harvard University), Jennifer Janusz, Diego Jaramillo, Justin T. Jordan, Allen Julian, Michel Kalamarides, Matthias A. Karajannis, Bonnie Klein-Tasman, Pamela Knight, Bruce R. Korf, Shannon Langmead, Theresa LaVallee, Fawn Leigh, Donita Lightner, Carol Lin, Robert Listernick, Grant Liu, Mevo Marco, Carole L. Marcus, Gabriella Mariani, Staci Martin, Victor Mautner(Harvard University), Vanessa L. Merker, Michael J. Ferguson(Harvard University), Chris Moertel, Jill A. Morris, Katrina Morris, Kathryn N. North, Fabio P. Nunes, Roger J. Packer, Laura Papi(Harvard University), Allyson Parry, Neha Patel, Jonathan M. Payne, Karen Peluso, Sebastian Perreault, Scott R. Plotkin(Harvard University), Tina Young Poussaint, Nancy Ratner, Karlyne M. Reilly, Vincent M. Riccardi, Kent A. Robertson, Claas Röhl, Deborah Rukin Gold, La Rosa Salvatore, Laura Schaffner Gray, Elizabeth K. Schorry, Claire Semerjian, Monica Sheridan, Chie‐Schin Shih, Carolyn Sidor, William H. Slattery, Miriam J. Smith(Harvard University), Kathy Sommer, Marigo Stathis, Matthew R. Steensma, Anat Stemmer‐Rachamimov, David A. Stevenson, Kari Struemph, Lara Sullivan, Mary Anne Tamula, Mary Thomas, Heather Thompson, James H. Tonsgard, Nicole J. Ullrich, Sharad K. Verma, David Viskochil, Ana-Maria Vranceanu, Ute Wahlländer, Karin S. Walsh, D. Bradley Welling, Ralph Wenzel(Harvard University), Trish Whitcomb, Brigitte C. Widemann, Victoria Williams, David S. Wolf, Pamela L. Wolters, Kaleb Yohay
Neurology
August 16, 2016
Cited by 88Open Access
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Abstract

OBJECTIVES: The Response Evaluation in Neurofibromatosis and Schwannomatosis (REiNS) International Collaboration Whole-Body MRI (WB-MRI) Working Group reviewed the existing literature on WB-MRI, an emerging technology for assessing disease in patients with neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and schwannomatosis (SWN), to recommend optimal image acquisition and analysis methods to enable WB-MRI as an endpoint in NF clinical trials. METHODS: A systematic process was used to review all published data about WB-MRI in NF syndromes to assess diagnostic accuracy, feasibility and reproducibility, and data about specific techniques for assessment of tumor burden, characterization of neoplasms, and response to therapy. RESULTS: WB-MRI at 1.5T or 3.0T is feasible for image acquisition. Short tau inversion recovery (STIR) sequence is used in all investigations to date, suggesting consensus about the utility of this sequence for detection of WB tumor burden in people with NF. There are insufficient data to support a consensus statement about the optimal imaging planes (axial vs coronal) or 2D vs 3D approaches. Functional imaging, although used in some NF studies, has not been systematically applied or evaluated. There are no comparative studies between regional vs WB-MRI or evaluations of WB-MRI reproducibility. CONCLUSIONS: WB-MRI is feasible for identifying tumors using both 1.5T and 3.0T systems. The STIR sequence is a core sequence. Additional investigation is needed to define the optimal approach for volumetric analysis, the reproducibility of WB-MRI in NF, and the diagnostic performance of WB-MRI vs regional MRI.


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