Prospective Evaluation of Magnetic Resonance Imaging and [18F]Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography at Diagnosis and Before Maintenance Therapy in Symptomatic Patients With Multiple Myeloma Included in the IFM/DFCI 2009 Trial: Results of the IMAJEM Study

Philippe Moreau, Michel Attal, Denis Caillot, Margaret Macro, Lionel Karlin, Laurent Garderet, Thierry Facon, Lotfi Benboubker, Martine Escoffre-Barbe, Anne-Marie Stoppa, Kamel Laribi, Cyrille Hulin, Aurore Perrot, Gerald Marit, Jean-Richard Eveillard, Florence Caillon, Caroline Bodet-Milin, Brigitte Pegourie, Veronique Dorvaux, Carine Chaleteix, Kenneth Anderson, Paul Richardson, Nikhil C Munshi, Herve Avet-Loiseau, Aurelie Gaultier, Jean-Michel Nguyen, Benoit Dupas, Eric Frampas, Françoise Kraeber-Bodere, Philippe Moreau, Michel Attal, Denis Caillot, Margaret Macro, Lionel Karlin, Laurent Garderet, Thierry Facon, Lotfi Benboubker, Martine Escoffre-Barbe, Anne-Marie Stoppa, Kamel Laribi, Cyrille Hulin, Aurore Perrot, Gerald Marit, Jean-Richard Eveillard, Florence Caillon, Caroline Bodet-Milin, Brigitte Pegourie, Veronique Dorvaux, Carine Chaleteix, Kenneth Anderson, Paul Richardson, Nikhil C Munshi, Herve Avet-Loiseau, Aurelie Gaultier, Jean-Michel Nguyen, Benoit Dupas, Eric Frampas, Françoise Kraeber-Bodere

Abstract

Purpose Magnetic resonance imaging (MRI) and positron emission tomography-computed tomography (PET-CT) are important imaging techniques in multiple myeloma (MM). We conducted a prospective trial in patients with MM aimed at comparing MRI and PET-CT with respect to the detection of bone lesions at diagnosis and the prognostic value of the techniques. Patients and Methods One hundred thirty-four patients received a combination of lenalidomide, bortezomib, and dexamethasone (RVD) with or without autologous stem-cell transplantation, followed by lenalidomide maintenance. PET-CT and MRI were performed at diagnosis, after three cycles of RVD, and before maintenance therapy. The primary end point was the detection of bone lesions at diagnosis by MRI versus PET-CT. Secondary end points included the prognostic impact of MRI and PET-CT regarding progression-free (PFS) and overall survival (OS). Results At diagnosis, MRI results were positive in 127 of 134 patients (95%), and PET-CT results were positive in 122 of 134 patients (91%; P = .33). Normalization of MRI after three cycles of RVD and before maintenance was not predictive of PFS or OS. PET-CT became normal after three cycles of RVD in 32% of the patients with a positive evaluation at baseline, and PFS was improved in this group (30-month PFS, 78.7% v 56.8%, respectively). PET-CT normalization before maintenance was described in 62% of the patients who were positive at baseline. This was associated with better PFS and OS. Extramedullary disease at diagnosis was an independent prognostic factor for PFS and OS, whereas PET-CT normalization before maintenance was an independent prognostic factor for PFS. Conclusion There is no difference in the detection of bone lesions at diagnosis when comparing PET-CT and MRI. PET-CT is a powerful tool to evaluate the prognosis of de novo myeloma.

Figures

Fig. 1.
Fig. 1.
CONSORT diagram for IMAJEM trial. ASCT, autologous stem-cell transplantation; MRI, magnetic resonance imaging; PET-CT, positron emission tomography-computed tomography; RVD, lenalidomide, bortezomib, and dexamethasone.
Fig 2.
Fig 2.
Progression-free survival (PFS) and overall survival (OS) according to normalization of magnetic resonance imaging (MRI) and positron emission tomography-computed tomography (PET-CT) after three cycles of induction therapy. (A) PFS, MRI normalized versus positive (P = .42). (B) OS, MRI normalized versus positive (P = .67). (C) PFS, PET-CT normalized versus positive (P = .08). (D) OS, PET-CT normalized versus positive (P = .16).
Fig 3.
Fig 3.
Progression-free survival (PFS) and overall survival (OS) according to normalization of magnetic resonance imaging (MRI) and positron emission tomography-computed tomography (PET-CT) before maintenance therapy. (A) PFS, MRI normalized versus positive (P = .52). (B) OS, MRI normalized versus positive (P = .62). (C) PFS, PET-CT normalized versus positive (P = .011). (D) OS, PET-CT normalized versus positive (P = .033).
Fig 4.
Fig 4.
Progression-free survival (PFS) and overall survival (OS) according to normalization of PET-CT before maintenance therapy in arm A and arm B. (A) PFS, PET-CT normalized versus positive in arm A (eight cycles of lenalidomide, bortezomib, and dexamethasone; P = .22). (B) PFS, PET-CT normalized versus positive in arm B (lenalidomide, bortezomib, and dexamethasone plus frontline autologous stem-cell transplantation; P = .004). (C) OS, PET-CT normalized versus positive in arm B (P < .001).
Fig 5.
Fig 5.
Progression-free survival for patients with negative positron emission tomography-computed tomography and negative minimal residual disease by flow cytometry before maintenance (41 of 86; 48%) versus others (45 of 86; 52%; P = .05).

Source: PubMed

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