Interim PET-guided treatment for early-stage NLPHL: a subgroup analysis of the randomized GHSG HD16 and HD17 studies.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
10 08 2023
Historique:
accepted: 25 04 2023
received: 31 01 2023
medline: 11 8 2023
pubmed: 31 5 2023
entrez: 31 5 2023
Statut: ppublish

Résumé

The optimal first-line treatment for nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) diagnosed in early stages is largely undefined. We, therefore, analyzed 100 NLPHL patients treated in the randomized HD16 (early-stage favorable; n = 85) and HD17 (early-stage unfavorable; n = 15) studies. These studies investigated the omission of consolidation radiotherapy (RT) in patients with a negative interim positron emission tomography (iPET) (ie, Deauville score <3) after chemotherapy (HD16: 2× doxorubicin, bleomycin, vinblastine, and dacarbazine [ABVD]; HD17: 2× escalated bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone [BEACOPP] plus 2× ABVD). Patients with NLPHL treated in the HD16 and HD17 studies had 5-year progression-free survival (PFS) rates of 90.3% and 92.9%, respectively. Thus, the 5-year PFS did not differ significantly from that of patients with classical Hodgkin lymphoma treated within the same studies (HD16: P = .88; HD17: P = .50). Patients with early-stage favorable NLPHL who had a negative iPET after 2× ABVD and did not undergo consolidation RT tended to have a worse 5-year PFS than patients with a negative iPET who received consolidation RT (83% vs 100%; P = .05). There were 10 cases of NLPHL recurrence. However, no NLPHL patient died during follow-up. Hence, the 5-year overall survival rate was 100%. Taken together, contemporary Hodgkin lymphoma-directed treatment approaches result in excellent outcomes for patients with newly diagnosed early-stage NLPHL and, thus, represent valid treatment options. In early-stage favorable NLPHL, consolidation RT appears necessary after 2× ABVD to achieve the optimal disease control irrespective of the iPET result.

Identifiants

pubmed: 37257195
pii: 496128
doi: 10.1182/blood.2023019939
doi:

Substances chimiques

Bleomycin 11056-06-7
Doxorubicin 80168379AG
Dacarbazine 7GR28W0FJI
Vinblastine 5V9KLZ54CY
Cyclophosphamide 8N3DW7272P
Vincristine 5J49Q6B70F
Prednisone VB0R961HZT

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

553-560

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 by The American Society of Hematology.

Auteurs

Dennis A Eichenauer (DA)

First Department of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany.
German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.

Ina Bühnen (I)

First Department of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany.
German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.

Christian Baues (C)

German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.
Department of Radiation Oncology, University of Cologne, Cologne, Germany.

Carsten Kobe (C)

German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.
Department of Nuclear Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

Helen Kaul (H)

First Department of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany.
German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.

Richard Greil (R)

Salzburg Cancer Research Institute, Center for Clinical Cancer and Immunology Trials, Cancer Cluster Salzburg, Austrian Group for Medical Tumor Therapy, Paracelsus Medical University, Salzburg, Austria.

Alden Moccia (A)

Department of Medical Oncology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Swiss Group for Clinical Cancer Research, Bern, Switzerland.

Joseé M Zijlstra (JM)

Department of Hematology, Amsterdam UMC, Vrije universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Bernd Hertenstein (B)

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

Max S Topp (MS)

Second Department of Internal Medicine, University Hospital Würzburg, Würzburg, Germany.

Marianne Just (M)

Onkologische Schwerpunktpraxis Bielefeld, Bielefeld, Germany.

Bastian von Tresckow (B)

German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.
Department of Hematology and Stem Cell Transplantation, University Hospital Essen, University Duisburg-Essen, German Cancer Consortium (DKTK partner site Essen), Essen, Germany.

Hans-Theodor Eich (HT)

German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.
Department of Radiotherapy, University Hospital Münster, Münster, Germany.

Michael Fuchs (M)

First Department of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany.
German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.

Markus Dietlein (M)

German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.
Department of Nuclear Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

Sylvia Hartmann (S)

Dr. Senckenberg Institute of Pathology, Goethe University Frankfurt, Frankfurt am Main, Germany.

Andreas Engert (A)

First Department of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany.
German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.

Peter Borchmann (P)

First Department of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany.
German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany.

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