Prognostic relevance of 18-F FDG PET/CT in newly diagnosed multiple myeloma patients treated with up-front autologous transplantation

Author:

Zamagni Elena1,Patriarca Francesca2,Nanni Cristina3,Zannetti Beatrice1,Englaro Emanuela4,Pezzi Annalisa1,Tacchetti Paola1,Buttignol Silvia2,Perrone Giulia1,Brioli Annamaria1,Pantani Lucia1,Terragna Carolina1,Carobolante Francesca2,Baccarani Michele1,Fanin Renato2,Fanti Stefano3,Cavo Michele1

Affiliation:

1. “Seràgnoli” Institute of Hematology, Bologna University School of Medicine, Bologna, Italy;

2. Hematologic Clinic, Department of Experimental and Clinical Medical Sciences, Udine University, Udine, Italy;

3. Institute of Nuclear Medicine, Bologna University School of Medicine, Bologna, Italy; and

4. Institute of Nuclear Medicine, S. Maria della Misericordia Hospital, Udine, Italy

Abstract

Abstract We prospectively analyzed the prognostic relevance of positron emission tomography–computed tomography (PET/CT) at diagnosis, after thalidomide-dexamethasone (TD) induction therapy and double autotransplantation (ASCT) in 192 newly diagnosed multiple myeloma (MM) patients. Presence at baseline of at least 3 focal lesions (FLs; 44% of cases), a standardized uptake value (SUV) > 4.2 (46%), and extramedullary disease (EMD; 6%) adversely affected 4-year estimates of progression-free survival (PFS; ≥ 3 FLs: 50%; SUV > 4.2: 43%; presence of EMD: 28%). SUV > 4.2 and EMD were also correlated with shorter overall survival (OS; 4-year rates: 77% and 66%, respectively). Persistence of SUV > 4.2 after TD induction was an early predictor for shorter PFS. Three months after ASCT, PET/CT was negative in 65% of patients whose 4-year rates of PFS and OS were superior to those of PET-positive patients (PFS: 66% and OS: 89%). In a multivariate analysis, both EMD and SUV > 4.2 at baseline and persistence of fluorodeoxyglucose (FDG) uptake after ASCT were independent variables adversely affecting PFS. PET/CT involvement at diagnosis, after novel agent-based induction and subsequent ASCT is a reliable predictor of prognosis in MM patients. This study is registered at www.clinicaltrials.gov as NTC01341262.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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