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

Author:

Eichenauer Dennis A.12ORCID,Bühnen Ina12,Baues Christian23ORCID,Kobe Carsten24,Kaul Helen12,Greil Richard5,Moccia Alden67,Zijlstra Joseé M.8ORCID,Hertenstein Bernd9,Topp Max S.10,Just Marianne11,von Tresckow Bastian212ORCID,Eich Hans-Theodor213,Fuchs Michael12,Dietlein Markus24,Hartmann Sylvia14,Engert Andreas12,Borchmann Peter12

Affiliation:

1. 1First Department of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany

2. 2German Hodgkin Study Group, University Hospital Cologne, Cologne, Germany

3. 3Department of Radiation Oncology, University of Cologne, Cologne, Germany

4. 4Department of Nuclear Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany

5. 5Salzburg Cancer Research Institute, Center for Clinical Cancer and Immunology Trials, Cancer Cluster Salzburg, Austrian Group for Medical Tumor Therapy, Paracelsus Medical University, Salzburg, Austria

6. 6Department of Medical Oncology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland

7. 7Swiss Group for Clinical Cancer Research, Bern, Switzerland

8. 8Department of Hematology, Amsterdam UMC, Vrije universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands

9. 9Department of Internal Medicine I, Klinikum Bremen-Mitte, Bremen, Germany

10. 10Second Department of Internal Medicine, University Hospital Würzburg, Würzburg, Germany

11. 11Onkologische Schwerpunktpraxis Bielefeld, Bielefeld, Germany

12. 12Department of Hematology and Stem Cell Transplantation, University Hospital Essen, University Duisburg-Essen, German Cancer Consortium (DKTK partner site Essen), Essen, Germany

13. 13Department of Radiotherapy, University Hospital Münster, Münster, Germany

14. 14Dr. Senckenberg Institute of Pathology, Goethe University Frankfurt, Frankfurt am Main, Germany

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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