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Role of 18F-FDG PET/CT in the diagnosis and management of multiple myeloma and other plasma cell disorders: a consensus statement by the International Myeloma Working Group.
Cavo, Michele; Terpos, Evangelos; Nanni, Cristina; Moreau, Philippe; Lentzsch, Suzanne; Zweegman, Sonja; Hillengass, Jens; Engelhardt, Monika; Usmani, Saad Z; Vesole, David H; San-Miguel, Jesus; Kumar, Shaji K; Richardson, Paul G; Mikhael, Joseph R; da Costa, Fernando Leal; Dimopoulos, Meletios-Athanassios; Zingaretti, Chiara; Abildgaard, Niels; Goldschmidt, Hartmut; Orlowski, Robert Z; Chng, Wee Joo; Einsele, Hermann; Lonial, Sagar; Barlogie, Bart; Anderson, Kenneth C; Rajkumar, S Vincent; Durie, Brian G M; Zamagni, Elena.
Affiliation
  • Cavo M; Seràgnoli Institute of Hematology, Bologna University School of Medicine, Bologna, Italy. Electronic address: michele.cavo@unibo.it.
  • Terpos E; Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
  • Nanni C; Nuclear Medicine, Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Moreau P; Haematology Department, University Hospital of Nantes, Nantes, France.
  • Lentzsch S; Columbia University Medical Center, New York, NY, USA.
  • Zweegman S; Department of Hematology, VU University Medical Center, Amsterdam, Netherlands.
  • Hillengass J; Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.
  • Engelhardt M; Department of Medicine, Hematology, Oncology & Stem Cell Transplantation, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Usmani SZ; Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC, USA.
  • Vesole DH; John Theurer Cancer Center at Hackensack UMC, Hackensack, NJ, USA.
  • San-Miguel J; Clínica Universidad de Navarra, CIMA, IDISNA, Pamplona, Spain.
  • Kumar SK; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
  • Richardson PG; Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Mikhael JR; Division of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA.
  • da Costa FL; Myeloma Clinic, Hematology Department, Instituto Português de Oncologia Francisco Gentil, Lisboa, Portugal.
  • Dimopoulos MA; Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.
  • Zingaretti C; Biostatistics and Clinical trial Unit, IRST-IRCCS, Meldola, Italy.
  • Abildgaard N; Department of Hematology, Odense University Hospital, Odense, Denmark.
  • Goldschmidt H; Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.
  • Orlowski RZ; The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Chng WJ; National University Cancer Institute, National University Health System, Singapore.
  • Einsele H; Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Lonial S; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA, USA.
  • Barlogie B; Tisch Cancer Institute/Multiple Myeloma Program, Mt. Sinai Cancer Institute, New York, NY, USA.
  • Anderson KC; Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Rajkumar SV; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
  • Durie BGM; Cedars-Sinai Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Zamagni E; Seràgnoli Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
Lancet Oncol ; 18(4): e206-e217, 2017 04.
Article in En | MEDLINE | ID: mdl-28368259
ABSTRACT
The International Myeloma Working Group consensus aimed to provide recommendations for the optimal use of 18fluorodeoxyglucose (18F-FDG) PET/CT in patients with multiple myeloma and other plasma cell disorders, including smouldering multiple myeloma and solitary plasmacytoma. 18F-FDG PET/CT can be considered a valuable tool for the work-up of patients with both newly diagnosed and relapsed or refractory multiple myeloma because it assesses bone damage with relatively high sensitivity and specificity, and detects extramedullary sites of proliferating clonal plasma cells while providing important prognostic information. The use of 18F-FDG PET/CT is mandatory to confirm a suspected diagnosis of solitary plasmacytoma, provided that whole-body MRI is unable to be performed, and to distinguish between smouldering and active multiple myeloma, if whole-body X-ray (WBXR) is negative and whole-body MRI is unavailable. Based on the ability of 18F-FDG PET/CT to distinguish between metabolically active and inactive disease, this technique is now the preferred functional imaging modality to evaluate and to monitor the effect of therapy on myeloma-cell metabolism. Changes in FDG avidity can provide an earlier evaluation of response to therapy compared to MRI scans, and can predict outcomes, particularly for patients who are eligible to receive autologous stem-cell transplantation. 18F-FDG PET/CT can be coupled with sensitive bone marrow-based techniques to detect minimal residual disease (MRD) inside and outside the bone marrow, helping to identify those patients who are defined as having imaging MRD negativity.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma Cells / Fluorodeoxyglucose F18 / Positron Emission Tomography Computed Tomography / Multiple Myeloma Type of study: Diagnostic_studies / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Lancet Oncol Journal subject: NEOPLASIAS Year: 2017 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma Cells / Fluorodeoxyglucose F18 / Positron Emission Tomography Computed Tomography / Multiple Myeloma Type of study: Diagnostic_studies / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Lancet Oncol Journal subject: NEOPLASIAS Year: 2017 Type: Article