Baseline 18F-FDG Metabolic Tumor Volume Predicts Response to Rituximab Induction in Post-transplant Lymphoproliferative Disorders: A Multi-institutional Retrospective Study
David Morland,
Lukshe Kanagaratnam,
Fabrice Hubelé,
Elise Toussaint,
Sylvain Choquet,
Aurélie Kas,
Pierre-Ambroise Caquot,
Corinne Haioun,
Emmanuel Itti,
Stéphane Leprêtre,
Pierre Decazes,
Fontanet Bijou,
Paul Schwartz,
Caroline Jacquet,
Adrien Chauchet,
Julien Matuszak,
Nassim Kamar,
Pierre Payoux,
K-VIROGREF Study Group*,
Eric Durot
Affiliations
David Morland
1 Médecine Nucléaire, Institut Godinot, Reims, France
Lukshe Kanagaratnam
5 Unité d’Aide Méthodologique, Pôle Recherche et Santé Publique, CHU de Reims, Reims, France
Fabrice Hubelé
6 Médecine Nucléaire, CHU de Strasbourg, ICANS, Strasbourg, France
Elise Toussaint
7 Hématologie, CHU de Strasbourg, ICANS, Strasbourg, France
Sylvain Choquet
8 Hématologie, CHU Pitié-Salpêtrière Charles Foix, Sorbonne Université, AP-HP, Paris, France
Aurélie Kas
9 Médecine Nucléaire, CHU Pitié-Salpêtrière Charles Foix, Sorbonne Université, AP-HP, Paris, France
Pierre-Ambroise Caquot
1 Médecine Nucléaire, Institut Godinot, Reims, France
Corinne Haioun
10 Hématologie, CHU Henri Mondor, AP-HP, Créteil, France
Emmanuel Itti
11 Médecine Nucléaire, CHU Henri Mondor, AP-HP, Créteil, France
Stéphane Leprêtre
12 Inserm U1245 et Département d’Hématologie, Centre Henri Becquerel et Normandie Univ, UNIROUEN, Rouen, France
Pierre Decazes
13 Médecine Nucléaire, Centre Henri Becquerel, Rouen, France
Fontanet Bijou
14 Hématologie, Institut Bergonié, Bordeaux, France
Paul Schwartz
15 Médecine Nucléaire, Institut Bergonié, Bordeaux, France
Caroline Jacquet
16 Hématologie, CHU de Nancy, France
Adrien Chauchet
17 Hématologie, CHU de Besançon, France
Julien Matuszak
18 Médecine Nucléaire, CHU de Besançon, France
Nassim Kamar
19 Néphrologie et transplantation d’organes, CHU Rangueil, Toulouse, France
Post-transplant lymphoproliferative disorder (PTLD) is a rare complication of immunosuppression. Sequential treatment is commonly proposed, combining induction with rituximab (R-induction) followed by either continuation of treatment or addition of chemotherapy depending on response. Response to R-induction, often assessed by CT scan, is a major predictor of overall survival (OS). The aim of the study was to analyze predictive factors of R-induction response, including total metabolic tumor volume (TMTV), and investigate the role of 18F-FDG PET/CT in response assessment. This retrospective multicenter study is based on patients with PTLD included in the K-VIROGREF cohort. Only patients treated by R-induction with a baseline 18F-FDG PET/CT were included. Response to R-induction was assessed by 18F-FDG PET/CT. The optimal threshold of TMTV for rituximab response was determined using receiver operating characteristic curves. Univariate and multivariate analyses were conducted to identify predictive factors of response. A total of 67 patients were included. Survival characteristics were similar to those previously reported: the complete response rate to R-induction was 30%, the 3-year OS estimate was 66%, and the treatment-related mortality was 4%. The optimal threshold for TMTV to predict R-induction response was 135 cm3. The response rate to R-induction was 38% in the 21 patients with TMTV ≥ 135 cm3 and 72% in the 46 patients with TMTV < 135 cm3. TMTV was a significant predictor of response, both at univariate and multivariate analyses (odd ratios = 3.71, P = 0.022). Baseline TMTV is predictive of response to R-induction. Early assessment of patient response is feasible with 18F-FDG PET/CT.