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Impact of initial FDG-PET/CT and serum-free light chain on transformation of conventionally defined solitary plasmacytoma to multiple myeloma

Authors :
Salim Adib
Guillemette Fouquet
Olivier Decaux
Xavier Leleu
Zoé Van de Wyngaert
Céline Berthon
Valérie Coiteux
Stéphanie Guidez
Louis Terriou
Mathieu Wemeau
Thierry Facon
Hélène Demarquette
Damien Huglo
Margaret Macro
David Beauvais
Sarah Bonnet
Bénédicte Hivert
Charles Herbaux
Centre de Recherche Jean-Pierre AUBERT Neurosciences et Cancer - U1172 Inserm - U837 (JPArc)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Lille Nord de France (COMUE)-Université de Lille
Institut Mondor de Recherche Biomédicale (IMRB)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)-IFR10
Service de Médecine interne et immunologie clinique [Rennes] = internal medicine and clinical immunology [Rennes]
CHU Pontchaillou [Rennes]
Hôpital Claude Huriez [Lille]
CHU Lille
Therapies Interventionnelles Assistees Par l'Image et la Simulation
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Droit et Santé
university hospital
University Hospital
Université Lille Nord de France (COMUE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille
Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Therapies Interventionnelles Assistees Par l'Image et la Simulation - U 703 (Thiais)
Centre de Recherche Jean-Pierre AUBERT Neurosciences et Cancer - U837 (JPArc)
Source :
Clinical Cancer Research: An Official Journal of the American Association for Cancer Research, Clinical Cancer Research: An Official Journal of the American Association for Cancer Research, 2014, 20 (12), pp.3254--3260. ⟨10.1158/1078-0432.CCR-13-2910⟩, Clinical Cancer Research, Clinical Cancer Research, American Association for Cancer Research, 2014, 20 (12), pp.3254--3260. ⟨10.1158/1078-0432.CCR-13-2910⟩, Clinical Cancer Research, 2014, 20 (12), pp.3254--3260. ⟨10.1158/1078-0432.CCR-13-2910⟩
Publication Year :
2014
Publisher :
HAL CCSD, 2014.

Abstract

Purpose: Solitary plasmacytoma (SP) is a localized proliferation of monoclonal plasma cells in either bone or soft tissue, without evidence of multiple myeloma (MM), and whose prognosis is marked by a high risk of transformation to MM. Experimental Design: We studied the impact of FDG-PET/CT (2[18F]fluoro-2-deoxy-D-glucose positron emission tomography–computed tomography) on the risk of transformation of SP to overt MM among other markers in a series of 43 patients diagnosed with SP. Results: Median age was 57.5 years; 48% of patients had an abnormal involved serum-free light chain (sFLC) value, and 64% had an abnormal sFLC ratio at diagnosis. Thirty-three percent had two or more hypermetabolic lesions on initial PET/CT, and 20% had two or more focal lesions on initial MRI. With a median follow-up of 50 months, 14 patients transformed to MM with a median time (TTMM) of 71 months. The risk factors that significantly shortened TTMM at diagnosis were two or more hypermetabolic lesions on PET/CT, abnormal sFLC ratio and involved sFLC, and to a lesser extent at completion of treatment, absence of normalized involved sFLC and PET/CT or MRI. In a multivariate analysis, abnormal initial involved sFLC [OR = 10; 95% confidence interval (CI), 1–87; P = 0.008] and PET/CT (OR = 5; 95% CI, 0–9; P = 0.032) independently shortened TTMM. Conclusions: An abnormal involved sFLC value and the presence of at least two hypermetabolic lesions on PET/CT at diagnosis of SP were the two predictors of early evolution to myeloma in our series. This data analysis will need confirmation in a larger study, and the study of these two risk factors may lead to a different management of patients with SP in the future. Clin Cancer Res; 20(12); 3254–60. ©2014 AACR.

Details

Language :
English
ISSN :
10780432 and 15573265
Database :
OpenAIRE
Journal :
Clinical Cancer Research: An Official Journal of the American Association for Cancer Research, Clinical Cancer Research: An Official Journal of the American Association for Cancer Research, 2014, 20 (12), pp.3254--3260. ⟨10.1158/1078-0432.CCR-13-2910⟩, Clinical Cancer Research, Clinical Cancer Research, American Association for Cancer Research, 2014, 20 (12), pp.3254--3260. ⟨10.1158/1078-0432.CCR-13-2910⟩, Clinical Cancer Research, 2014, 20 (12), pp.3254--3260. ⟨10.1158/1078-0432.CCR-13-2910⟩
Accession number :
edsair.doi.dedup.....99315fcb9b18e972785a5ffff511ae8a
Full Text :
https://doi.org/10.1158/1078-0432.CCR-13-2910⟩