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18F-FDG PET/CT focal, but not osteolytic, lesions predict the progression of smoldering myeloma to active disease.
Zamagni, E; Nanni, C; Gay, F; Pezzi, A; Patriarca, F; Bellò, M; Rambaldi, I; Tacchetti, P; Hillengass, J; Gamberi, B; Pantani, L; Magarotto, V; Versari, A; Offidani, M; Zannetti, B; Carobolante, F; Balma, M; Musto, P; Rensi, M; Mancuso, K; Dimitrakopoulou-Strauss, A; Chauviè, S; Rocchi, S; Fard, N; Marzocchi, G; Storto, G; Ghedini, P; Palumbo, A; Fanti, S; Cavo, M.
Afiliação
  • Zamagni E; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Nanni C; Institute of Nuclear Medicine, Bologna University School of Medicine, Bologna, Italy.
  • Gay F; Myeloma Unit, Division of Hematology, University of Turin, Torino, Italy.
  • Pezzi A; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Patriarca F; Hematologic Clinic, Department of Clinical and Morphological Research, Udine University, Udine, Italy.
  • Bellò M; Institute of Nuclear Medicine, Department of Imaging, University of Turin, Torino, Italy.
  • Rambaldi I; Institute of Nuclear Medicine, Bologna University School of Medicine, Bologna, Italy.
  • Tacchetti P; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Hillengass J; Department of Hematology and Oncology, University of Heidelberg, Heidelberg, Germany.
  • Gamberi B; Hematology Unit, Department of Oncology, Azienda Ospedaliera ASMN, IRCCS, Reggio Emilia, Italy.
  • Pantani L; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Magarotto V; Myeloma Unit, Division of Hematology, University of Turin, Torino, Italy.
  • Versari A; Institute of Nuclear Medicine, Azienda Ospedaliera ASMN, IRCCS, Reggio Emilia, Italy.
  • Offidani M; Hematology Clinic, AOU Ospedali Riuniti di Ancona, Ancona, Italy.
  • Zannetti B; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Carobolante F; Hematologic Clinic, Department of Clinical and Morphological Research, Udine University, Udine, Italy.
  • Balma M; Institute of Nuclear Medicine, Department of Imaging, University of Turin, Torino, Italy.
  • Musto P; Hematology Unit, IRCCS Referral Cancer Centre of Basilicata, Rionero in Vulture, Italy.
  • Rensi M; Institute of Nuclear Medicine, S. Maria della Misericordia Hospital, Udine, Italy.
  • Mancuso K; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Dimitrakopoulou-Strauss A; Department of Nuclear Medicine, German Cancer Research Center, Heidelberg, Germany.
  • Chauviè S; Medical Physics Department, Santa Croce and Carlo Hospital, Cuneo, Italy.
  • Rocchi S; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Fard N; Department of Radiology, German Cancer Research Center, Heidelberg, Germany.
  • Marzocchi G; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Storto G; Unit of Nuclear Medicine, IRCCS Referral Cancer Centre of Basilicata, Rionero in Vulture, Italy.
  • Ghedini P; Institute of Nuclear Medicine, Bologna University School of Medicine, Bologna, Italy.
  • Palumbo A; Myeloma Unit, Division of Hematology, University of Turin, Torino, Italy.
  • Fanti S; Institute of Nuclear Medicine, Bologna University School of Medicine, Bologna, Italy.
  • Cavo M; 'Seràgnoli' Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
Leukemia ; 30(2): 417-22, 2016 Feb.
Article em En | MEDLINE | ID: mdl-26490489
ABSTRACT
Identification of patient sub-groups with smoldering multiple myeloma (SMM) at high risk of progression to active disease (MM) is an important goal. 18F-FDG PET/CT (positron emission tomography (PET) integrated with computed tomography (PET/CT) using glucose labelled with the positron-emitting radionuclide (18)F) allows for assessing early skeletal involvement. Identification of osteolytic lesions by this technique has recently been incorporated into the updated International Myeloma Working Group criteria for MM diagnosis. However, no data are available regarding the impact of focal lesions (FLs) without underlying osteolysis on time to progression (TTP) to MM. We hence prospectively studied a cohort of 120 SMM patients with PET/CT. PET/CT was positive in 16% of patients (1 FL 8, 2 FLs 3, >3 FLs 6, diffuse bone marrow involvement 2). With a median follow-up of 2.2 years, 38% of patients progressed to MM, in a median time of 4 years, including 21% with skeletal involvement. The risk of progression of those with positive PET/CT was 3.00 (95% confidence interval 1.58-5.69, P=0.001), with a median TTP of 1.1 versus 4.5 years for PET/CT-negative patients. The probability of progression within 2 years was 58% for positive versus 33% for negative patients. In conclusion, PET/CT positivity significantly increased the risk of progression of SMM to MM. PET/CT could become a new tool to define high-risk SMM.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteólise / Tomografia por Emissão de Pósitrons / Mieloma Múltiplo Tipo de estudo: Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteólise / Tomografia por Emissão de Pósitrons / Mieloma Múltiplo Tipo de estudo: Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article