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Combining FDG‐PET/CT with laboratory data yields superior results for prediction of relapse in multiple myeloma *
Author(s) -
Elliott Brian M.,
Peti Steven,
Osman Keren,
Scigliano Eileen,
Lee David,
Isola Luis,
Kostakoglu Lale
Publication year - 2011
Publication title -
european journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0902-4441
DOI - 10.1111/j.1600-0609.2010.01575.x
Subject(s) - medicine , multiple myeloma , positron emission tomography , progression free survival , nuclear medicine , bone marrow , pet ct , radiology , overall survival , oncology
Objectives:  The precise role of positron emission tomography (PET/CT) for predicting relapse/progression in multiple myeloma remains uncertain. We compared the predictive values of PET/CT, concurrent laboratory testing (labs), and their combination in prediction of 12‐month progression, as determined by current International Myeloma Working Group (IMWG) criteria. Methods:  PET/CT and labs (serum chemistry, β2‐microglobulin, immunofixation, bone marrow biopsy, serum free light chains) were reviewed, and date of relapse/progression was determined by IMWG criteria. Results:  The median time from therapy to PET/CT imaging was 12.0 months (1.0–110) and median time to progression (TTP) was 29.8 months (1.6–130+). Overall survival and survival‐without‐progression at last follow‐up were 84% and 49%, respectively. Sensitivity of PET/CT for predicting relapse/progression was lower than that of labs (0.67 vs. 0.89, ns), but PET/CT was more specific (0.89 vs. 0.79, ns). When labs and PET/CT data were combined, a positive result for either test was 89% sensitive and a positive result for both tests was 100% specific for predicting 12‐month progression of disease. Kaplan–Meier analysis showed significantly greater TTP for those with a negative vs. positive PET/CT ( P  = 0.0005), negative vs. positive labs ( P  < 0.0001), and both tests negative vs. both tests positive ( P  < 0.0001). Conclusions:  Combining PET/CT with laboratory data improves the accuracy of prediction of relapse/progression within 12 months compared with each test alone. Thus, integration of PET/CT into myeloma follow‐up is recommended, and the impact of this approach on management should be explored.

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