Positron Emission Tomography-Driven Strategy in Advanced Hodgkin Lymphoma: Prolonged Follow-Up of the AHL2011 Phase III Lymphoma Study Association Study.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 04 2022
Historique:
pubmed: 7 1 2022
medline: 6 5 2022
entrez: 6 1 2022
Statut: ppublish

Résumé

The AHL2011 study (ClinicalTrials.gov identifier: NCT01358747) demonstrated that a positron emission tomography (PET)-driven de-escalation strategy after two cycles of bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPP) provides similar progression-free survival (PFS) and overall survival (OS) and reduces early toxicity compared with a nonmonitored standard treatment. Here, we report, with a prolonged follow-up, the final study results. Patients with advanced Hodgkin lymphoma (stage III, IV, or IIB with mediastinum/thorax ratio > 0.33 or extranodal involvement) age 16-60 years were prospectively randomly assigned between 6 × BEACOPP and a PET-driven arm after 2 × BEACOPP delivering 4 × ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) in PET2- and 4 × BEACOPP in PET2+ patients. PET performed after four cycles of chemotherapy had to be negative to complete the planned treatment. In total, 823 patients were enrolled including 413 in the standard arm and 410 in the PET-driven arm. With a 67.2-month median follow-up, 5-year PFS (87.5% The extended follow-up confirms the continued efficacy and favorable safety of AHL2011 PET-driven strategy, which is noninferior to standard six cycles of BEACOPP. PET4 provides additional prognostic information to PET2 and allows identifying patients with particularly poor prognosis.

Identifiants

pubmed: 34990281
doi: 10.1200/JCO.21.01777
doi:

Substances chimiques

Bleomycin 11056-06-7
Procarbazine 35S93Y190K
Vincristine 5J49Q6B70F
Vinblastine 5V9KLZ54CY
Etoposide 6PLQ3CP4P3
Dacarbazine 7GR28W0FJI
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT01358747']

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1091-1101

Auteurs

René-Olivier Casasnovas (RO)

Department of Hematology, University Hospital F. Mitterrand and Inserm UMR 1231, Dijon, France.

Reda Bouabdallah (R)

Department of Hematology, Institut P. Calmette, Marseille, France.
Department of Hematology, Hopital privé de Provence, Aix en Provence, France.

Pauline Brice (P)

Department of Hematology, APHP, Hopital Saint Louis, Paris, France.

Julien Lazarovici (J)

Department of Hematology, Institut G. Roussy, Villejuif, France.

Hervé Ghesquieres (H)

Department of Hematology, Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, et Université Claude Bernard Lyon-1, Pierre Bénite, France.

Aspasia Stamatoullas (A)

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

Jehan Dupuis (J)

Lymphoid Malignancies Unit, Henri Mondor University Hospital, Créteil, France.

Anne-Claire Gac (AC)

Department of Hematology, Institut d'hématologie de basse normandie, Caen, France.

Thomas Gastinne (T)

Department of Hematology, University Hospital of Nantes, Nantes, France.

Bertrand Joly (B)

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

Krimo Bouabdallah (K)

Department of Hematology, University Hospital of Bordeaux, Bordeaux, France.

Emmanuelle Nicolas-Virelizier (E)

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

Pierre Feugier (P)

Department of Hematology, University Hospital of Nancy, Vandoeuvre les Nancy, France.

Franck Morschhauser (F)

Department of Hematology, CHU Lille, Unité GRITA, Université de Lille 2, Lille, France.

David Sibon (D)

Department of Hematology, Hopital Necker, Paris, France.

Christophe Bonnet (C)

Department of Hematology, University Hospital Liege, Liege, Belgium.

Alina Berriolo-Riedinger (A)

Department of Nuclear Medicine, Centre G.F. Leclerc, Dijon, France.

Véronique Edeline (V)

Department of Nuclear Medicine, Hopital R. Huguenin, Institut Curie, St-Cloud, France.

Marie Parrens (M)

Department of Pathology, University Hospital of Bordeaux and Inserm UMR 1053, Bordeaux, France.

Diane Damotte (D)

Department of Pathology, Université de Paris et GH Paris Centre APHP, Paris, France.

Diane Coso (D)

Department of Hematology, Institut P. Calmette, Marseille, France.

Marc André (M)

Department of Hematology, CHU UCL Namur, Université catholique de Louvain, Yvoir, Belgium.
Pole Mont, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Brussels, Belgium.

Michel Meignan (M)

Department of Nuclear Medicine, University Hospital H. Mondor, Creteil, France.

Cédric Rossi (C)

Department of Hematology, University Hospital F. Mitterrand and Inserm UMR 1231, Dijon, France.

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