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.


Journal

Haematologica
ISSN: 1592-8721
Titre abrégé: Haematologica
Pays: Italy
ID NLM: 0417435

Informations de publication

Date de publication:
01 12 2022
Historique:
received: 30 05 2022
pubmed: 1 6 2022
medline: 3 12 2022
entrez: 31 5 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35638548
doi: 10.3324/haematol.2021.280004
pmc: PMC9713544
doi:

Substances chimiques

Bleomycin 11056-06-7
Dacarbazine 7GR28W0FJI
Doxorubicin 80168379AG
Vinblastine 5V9KLZ54CY

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2897-2904

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Auteurs

Cédric Rossi (C)

Department of Hematology, Dijon-Bourgogne University Hospital, Dijon; INSERM unit 1231, University of Burgundy Franche-Comté, France. cedric.rossi66@gmail.com.

Marc André (M)

Department of Hematology, CHU UCL Namur, Université Catholique de Louvain, Yvoir, Belgium.

Jehan Dupuis (J)

Lymphoid Malignancies Unit, Henri Mondor University Hospital (AP-HP), Créteil, France.

Franck Morschhauser (F)

Groupe de Recherche sur les formes Injectables et les Technologies Associées (GRITA), Department of Haematology, CHU Lille, Université de Lille, Lille.

Bertrand Joly (B)

Department of Hematology, Hospital Sud Francilien, Corbeille-Essonnes, France.

Julien Lazarovici (J)

Department of Hematology, Université Paris-Saclay, Gustave Roussy, Villejuif, France.

Hervé Ghesquières (H)

Department of Hematology, Centre Hospitalier Lyon Sud and Université Claude Bernard Lyon-1, Pierre-Bénite, France.

Aspasia Stamatoullas (A)

Department of Hematology, Centre Henri Becquerel, Rouen, France.

Emmanuelle Nicolas-Virelizier (E)

Department of Hematology, Centre Léon Bérard, Lyon, France.

Pierre Feugier (P)

Hospital of Nancy, Vandoeuvre les Nancy, France.

Anne-Claire Gac (AC)

Department of Haematology, Institut d'hématologie de Basse Normandie, Caen, France.

Hannah Moatti (H)

Department of Hematology, CHU Paris-GH St-Louis Lariboisière F-Widal - Hôpital Saint-Louis, Paris, France.

Luc-Matthieu Fornecker (LM)

Department of Haematology, University Hospital of Strasbourg, Strasbourg, France.

Bénédicte Deau (B)

Department of Hematology, CHU Cochin, Paris, France.

Clémentine Joubert (C)

Lymphoma Academic Research Organisation, CHU Lyon-Sud, Lyon, France.

Catherine Fortpied (C)

European Organisation for Research and Treatment of Cancer, Brussels, Belgium.

John Raemaekers (J)

Department of Haematology, Radboud University Medical Center, Nijmegen, Netherlands.

Massimo Federico (M)

CHIMOMO department, University of Modena and Reggio Emilia, Policlinico, Modena, Italy.

Salim Kanoun (S)

Nuclear Medecine Unit, Institut universitaire du cancer Toulouse-Oncopole, Toulouse, France.

Michel Meignan (M)

LYSA Imaging, University Hospital H Mondor, Creteil, France.

Alexandra Traverse-Glehen (A)

Department of Pathology, Centre Hospitalier Lyon Sud and Université Claude Bernard Lyon-1, Pierre- Bénite, France.

Anne-Ségolène Cottereau (AS)

Nuclear Medecine Department, Hôpital Cochin, AP-HP, Université de Paris, France.

René-Olivier Casasnova (RO)

Department of Hematology, Dijon-Bourgogne University Hospital, Dijon; INSERM unit 1231, University of Burgundy Franche-Comté, France.

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