Utility and prognostic value of 18 F-FDG positron emission tomography-computed tomography scans in patients with newly diagnosed multiple myeloma.
Mohammed A AljamaM Hasib SidiqiFrancis K BuadiMartha Q LacyMorie A GertzAngela DispenzieriDavid DingliEli MuchtarAmie L FonderSuzanne R HaymanMiriam A HobbsWilson I GonsalvesRahma M WarsameTaxiarchis V KourelisYi Lisa HwaPrashant KapoorRobert A KyleNelson R LeungRonald S GoSundararajan Vincent RajkumarShaji K KumarPublished in: American journal of hematology (2018)
Positron emission tomography-computed tomography (PET-CT) can identify bony lesions, assess disease burden, and detect extramedullary disease (EMD) in patients with multiple myeloma. We retrospectively reviewed records of patients who underwent PET-CT within 60 days of a new diagnosis (before therapy commenced) to identify the nature and prognostic impact of PET-CT abnormalities. Patients (N = 313) were seen from April 2005 through June 2017. Of the 234 patients (75%) with focal lesions (FLs), 182 (58%) had at least 3 FLs, 38 (12%) had EMD, and 204 (65%) had documented myelomatous lytic lesions. The median maximum standardized uptake value (SUVmax ) for the entire cohort was 5.9 (range 1.5-48.3). Presence of at least 3 FLs and EMD predicted inferior overall survival (OS); median OS was 57.8 months for patients with 3 or more FLs and 103.6 months for patients with fewer than 3 FLs (P = .003). The median OS was 45.5 and 71.8 months for patients with and without EMD, respectively (P = .004). No clear SUVmax cutoff was predictive of progression-free survival or OS. PET-CT is a valuable tool for assessing disease burden and could provide prognostic information about a contemporary cohort of patients with newly diagnosed myeloma who received treatment with novel agents.
Keyphrases
- pet ct
- positron emission tomography
- newly diagnosed
- computed tomography
- multiple myeloma
- pet imaging
- end stage renal disease
- free survival
- ejection fraction
- magnetic resonance imaging
- stem cells
- healthcare
- prognostic factors
- peritoneal dialysis
- bone marrow
- risk factors
- magnetic resonance
- mesenchymal stem cells
- patient reported outcomes