High-risk stage IIB Hodgkin lymphoma treated in the H10 and AHL2011 trials: total metabolic tumor volume is a useful risk factor to stratify patients at baseline
Cédric Rossi,
Marc André,
Jehan Dupuis,
Franck Morschhauser,
Bertrand Joly,
Julien Lazarovici,
Hervé Ghesquières,
Aspasia Stamatoullas,
Emmanuelle Nicolas-Virelizier,
Pierre Feugier,
Anne-Claire Gac,
Hannah Moatti,
Luc-Matthieu Fornecker,
Bénédicte Deau,
Clémentine Joubert,
Catherine Fortpied,
John Raemaekers,
Massimo Federico,
Salim Kanoun,
Michel Meignan,
Alexandra Traverse-Glehen,
Anne-Ségolène Cottereau,
René-Olivier Casasnova
Affiliations
Cédric Rossi
Department of Hematology, Dijon-Bourgogne University Hospital, Dijon; INSERM unit 1231, University of Burgundy Franche-Comté, France
Marc André
Department of Hematology, CHU UCL Namur, Université Catholique de Louvain, Yvoir, Belgium
Jehan Dupuis
Lymphoid Malignancies Unit, Henri Mondor University Hospital (AP-HP), Créteil, France
Franck Morschhauser
Groupe de Recherche sur les formes Injectables et les Technologies Associées (GRITA), Department of Haematology, CHU Lille, Université de Lille, Lille
Bertrand Joly
Department of Hematology, Hospital Sud Francilien, Corbeille-Essonnes, France
Julien Lazarovici
Department of Hematology, Université Paris-Saclay, Gustave Roussy, Villejuif, France
Hervé Ghesquières
Department of Hematology, Centre Hospitalier Lyon Sud and Université Claude Bernard Lyon-1, Pierre-Bénite, France
Aspasia Stamatoullas
Department of Hematology, Centre Henri Becquerel, Rouen, France
Emmanuelle Nicolas-Virelizier
Department of Hematology, Centre Léon Bérard, Lyon, France
Pierre Feugier
Hospital of Nancy, Vandoeuvre les Nancy, France
Anne-Claire Gac
Department of Haematology, Institut d'hématologie de Basse Normandie, Caen, France
Hannah Moatti
Department of Hematology, CHU Paris-GH St-Louis Lariboisière F-Widal - Hôpital Saint-Louis, Paris, France
Luc-Matthieu Fornecker
Department of Haematology, University Hospital of Strasbourg, Strasbourg, France
Bénédicte Deau
Department of Hematology, CHU Cochin, Paris, France
Clémentine Joubert
Lymphoma Academic Research Organisation, CHU Lyon-Sud, Lyon, France
Catherine Fortpied
European Organisation for Research and Treatment of Cancer, Brussels, Belgium
John Raemaekers
Department of Haematology, Radboud University Medical Center, Nijmegen, Netherlands
Massimo Federico
CHIMOMO department, University of Modena and Reggio Emilia, Policlinico, Modena, Italy
Salim Kanoun
Nuclear Medecine Unit, Institut universitaire du cancer Toulouse-Oncopole, Toulouse, France
Michel Meignan
LYSA Imaging, University Hospital H Mondor, Creteil, France
Alexandra Traverse-Glehen
Department of Pathology, Centre Hospitalier Lyon Sud and Université Claude Bernard Lyon-1, Pierre- Bénite, France
Anne-Ségolène Cottereau
Nuclear Medecine Department, Hôpital Cochin, AP-HP, Université de Paris, France
René-Olivier Casasnova
Department of Hematology, Dijon-Bourgogne University Hospital, Dijon; INSERM unit 1231, University of Burgundy Franche-Comté, France
Stage IIB Hodgkin lymphoma (HL) patients, with a mediastinum-to-thorax (M/T) ratio of ≥0.33 or extranodal localization have a poor prognosis and are treated either as limited or advanced stage. We compared these two approaches in patients included in two randomized phase III trials enrolling previously untreated early (H10) or advanced stage HL (AHL2011). We included HL patients with Ann-Arbor stage IIB with M/T ≥0.33 or extranodal involvement enrolled in the H10 or AHL2011 trials with available positron emission tomography at baseline (PET0) and after two cycles of chemotherapy (PET2). Baseline total metabolic tumor volume (TMTV) was calculated using the 41% SUVmax method. PET2 response assessment used the Deauville score. One hundred and fourty-eight patients were eligible, including 83 enrolled in the AHL2011 trial and 65 in the H10 trial. The median TMTV value was 155.5 mL (range, 8.3-782.9 mL), 165.6 mL in AHL2011 and 147 mL in H10. PET2 positivity rates were 16.9% (n=14) and 9.2% (n=6) in AHL2011 and H10 patients, respectively. With a median follow-up of 4.1 years (95% confidence interval [CI]: 3.9-4.4), overall 4-year PFS was 88.0%, 87.0% in AHL2011 and 89.2% in H10. In univariate and mutivariate analyses, baseline TMTV and PET2 response influenced significantly progression-free survival (hazard ratio [HR]=4.94, HR=3.49 respectively). Notably, among the 16 patients who relapsed, 13 (81%) had a baseline TMTV baseline ≥155 mL. Upfront ABVD plus radiation therapy or upfront escBEACOPP without radiotherapy provide similar patient’s outcome in high-risk stage IIB HL. TMTV is useful to stratify these patients at baseline.