Baseline 18F-FDG Metabolic Tumor Volume Predicts Response to Rituximab Induction in Post-transplant Lymphoproliferative Disorders: A Multi-institutional Retrospective Study

Author:

Morland David1234,Kanagaratnam Lukshe5,Hubelé Fabrice6,Toussaint Elise7,Choquet Sylvain8,Kas Aurélie9,Caquot Pierre-Ambroise19,Haioun Corinne10,Itti Emmanuel11,Leprêtre Stéphane12,Decazes Pierre13,Bijou Fontanet14,Schwartz Paul15,Jacquet Caroline16,Chauchet Adrien17,Matuszak Julien18,Kamar Nassim19,Payoux Pierre20,Durot Eric21,

Affiliation:

1. Médecine Nucléaire, Institut Godinot, Reims, France

2. Laboratoire de Biophysique, UFR de Médecine, Université de Reims Champagne-Ardenne, Reims, France

3. CReSTIC, EA 3804, Université de Reims Champagne-Ardenne, Reims, France

4. Unità di Medicina Nucleare, TracerGLab, Dipartimento di Radiologia, Radioterapia ed Ematologia, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Roma, Italy

5. Unité d’Aide Méthodologique, Pôle Recherche et Santé Publique, CHU de Reims, Reims, France

6. Médecine Nucléaire, CHU de Strasbourg, ICANS, Strasbourg, France

7. Hématologie, CHU de Strasbourg, ICANS, Strasbourg, France

8. Hématologie, CHU Pitié-Salpêtrière Charles Foix, Sorbonne Université, AP-HP, Paris, France

9. Médecine Nucléaire, CHU Pitié-Salpêtrière Charles Foix, Sorbonne Université, AP-HP, Paris, France

10. Hématologie, CHU Henri Mondor, AP-HP, Créteil, France

11. Médecine Nucléaire, CHU Henri Mondor, AP-HP, Créteil, France

12. Inserm U1245 et Département d’Hématologie, Centre Henri Becquerel et Normandie Univ, UNIROUEN, Rouen, France

13. Médecine Nucléaire, Centre Henri Becquerel, Rouen, France

14. Hématologie, Institut Bergonié, Bordeaux, France

15. Médecine Nucléaire, Institut Bergonié, Bordeaux, France

16. Hématologie, CHU de Nancy, France

17. Hématologie, CHU de Besançon, France

18. Médecine Nucléaire, CHU de Besançon, France

19. Néphrologie et transplantation d’organes, CHU Rangueil, Toulouse, France

20. Médecine Nucléaire, CHU de Toulouse, France

21. Hématologie clinique, CHU de Reims, France

Abstract

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.

Publisher

Wiley

Subject

Hematology

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