Positron Emission Tomography-Guided Treatment in Early-Stage Favorable Hodgkin Lymphoma: Final Results of the International, Randomized Phase III HD16 Trial by the German Hodgkin Study Group.


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 11 2019
Historique:
pubmed: 10 9 2019
medline: 17 6 2020
entrez: 10 9 2019
Statut: ppublish

Résumé

Combined-modality treatment (CMT) with 2× ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) and small-field radiotherapy is standard of care for patients with early-stage favorable Hodgkin lymphoma (HL). However, the role of radiotherapy has been challenged. Positron emission tomography (PET) after 2× ABVD (PET-2) might help to predict individual outcomes and guide treatment. Between November 2009 and December 2015, we recruited patients age 18 to 75 years with newly diagnosed, early-stage favorable HL for this international randomized phase III trial. Patients were assigned to standard CMT of 2× ABVD and 20-Gy involved-field radiotherapy or PET-guided treatment, omitting involved-field radiotherapy after negative PET-2 (Deauville score < 3). Primary objectives were to exclude inferiority of 10% or more in 5-year progression-free survival (PFS) of ABVD alone compared with CMT in a per-protocol analysis among PET-2-negative patients (noninferiority margin for hazard ratio, 3.01) and to confirm PET-2 positivity (Deauville score ≥ 3) as a risk factor for PFS among CMT-treated patients. We enrolled 1,150 patients. Median follow-up was 45 months. Among 628 PET-2-negative, per-protocol-treated patients, 5-year PFS was 93.4% (95% CI, 90.4% to 96.5%) with CMT and 86.1% (95% CI, 81.4% to 90.9%) with ABVD (difference 7.3% [95% CI, 1.6% to 13.0%]; hazard ratio, 1.78 [95% CI, 1.02 to 3.12]). Five-year overall survival was 98.1% (95% CI, 96.5% to 99.8%) with CMT and 98.4% (95% CI, 96.5% to 100.0%) with ABVD. Among 693 patients who were assigned to CMT, 5-year PFS was 93.2% (95% CI, 90.2% to 96.2%) among PET-2-negative patients and 88.4% (95% CI, 84.2% to 92.6%) in PET-2-positive patients ( In early-stage favorable HL, a positive PET after two cycles ABVD indicates a high risk for treatment failure, particularly when a Deauville score of 4 is used as a cutoff for positivity. In PET-2-negative patients, radiotherapy cannot be omitted from CMT without clinically relevant loss of tumor control.

Identifiants

pubmed: 31498753
doi: 10.1200/JCO.19.00964
doi:

Substances chimiques

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

Banques de données

ClinicalTrials.gov
['NCT00736320']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2835-2845

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

Michael Fuchs (M)

German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.

Helen Goergen (H)

German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.

Carsten Kobe (C)

Department of Nuclear Medicine, University of Cologne, Cologne, Germany.

Georg Kuhnert (G)

Department of Nuclear Medicine, University of Cologne, Cologne, Germany.

Andreas Lohri (A)

Cantonal Hospital Baselland, Liestal, Switzerland.
Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.

Richard Greil (R)

IIIrd Medical Department, Paracelcus Medical University and Salzburg Cancer Research Institute, Salzburg, Austria.
Salzburg Cancer Research Institute and AGMT (Arbeitsgemeinschaft Medikamentöse Tumortherapie), Salzburg, Austria.

Stephanie Sasse (S)

German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.

Max S Topp (MS)

Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.

Erhardt Schäfer (E)

Dres. med. Just/Düwel/Riesenberg/Steinke/Schäfer, Studiengesellschaft, Bielefeld, Germany.

Bernd Hertenstein (B)

Department of Internal Medicine I, Klinikum Bremen Mitte, Bremen, Germany.

Martin Soekler (M)

University of Tübingen, Tübingen, Germany.

Martin Vogelhuber (M)

Medizinische Klinik III, Universitätsklinik Regensburg, Regensburg, Germany.

Josée M Zijlstra (JM)

Amsterdam University Medical Center, Vrije Universiteit, Department of Hematology, Amsterdam, Netherlands.

Ulrich Bernd Keller (UB)

Department of Internal Medicine III, Klinikum "Rechts der Isar", Munich, Germany.

Stefan W Krause (SW)

Department of Internal Medicine 5, Haematology/Oncology, University of Erlangen, Erlangen, Germany.

Martin Wilhelm (M)

Department of Medical Oncology, Klinikum Nürnberg, Paracelsus Medical University, Nürnberg, Germany.

Georg Maschmeyer (G)

Department of Hematology, Oncology and Palliative Care, Klinikum Ernst von Bergmann, Potsdam, Germany.

Julia Thiemer (J)

Clinic for Hematology, Oncology and Immunology, Philipps University, Marburg, Germany.

Ulrich Dührsen (U)

Department of Haematology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Julia Meissner (J)

University of Heidelberg, Heidelberg, Germany.

Andreas Viardot (A)

Department of Internal Medicine III, University Hospital Ulm, Ulm, Germany.

Hans Eich (H)

Department of Radiotherapy, University Hospital of Muenster, Muenster, Germany.

Christian Baues (C)

Department of Radiotherapy, University of Cologne, Cologne, Germany.

Volker Diehl (V)

German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.

Andreas Rosenwald (A)

Institute of Pathology, Julius Maximilian University of Würzburg and Comprehensive Cancer Center Mainfranken, Würzburg, Germany.

Bastian von Tresckow (B)

German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.

Markus Dietlein (M)

Department of Nuclear Medicine, University of Cologne, Cologne, Germany.

Peter Borchmann (P)

German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.

Andreas Engert (A)

German Hodgkin Study Group (GHSG), Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, University of Cologne, Cologne, Germany.

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