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

Author:

Fuchs Michael1,Goergen Helen1,Kobe Carsten2,Kuhnert Georg2,Lohri Andreas34,Greil Richard56,Sasse Stephanie1,Topp Max S.7,Schäfer Erhardt8,Hertenstein Bernd9,Soekler Martin10,Vogelhuber Martin11,Zijlstra Josée M.12,Keller Ulrich Bernd13,Krause Stefan W.14,Wilhelm Martin15,Maschmeyer Georg16,Thiemer Julia17,Dührsen Ulrich18,Meissner Julia19,Viardot Andreas20,Eich Hans21,Baues Christian22,Diehl Volker1,Rosenwald Andreas23,von Tresckow Bastian1,Dietlein Markus2,Borchmann Peter1,Engert Andreas1

Affiliation:

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

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

3. Cantonal Hospital Baselland, Liestal, Switzerland

4. Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland

5. IIIrd Medical Department, Paracelcus Medical University and Salzburg Cancer Research Institute, Salzburg, Austria

6. Salzburg Cancer Research Institute and AGMT (Arbeitsgemeinschaft Medikamentöse Tumortherapie), Salzburg, Austria

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

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

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

10. University of Tübingen, Tübingen, Germany

11. Medizinische Klinik III, Universitätsklinik Regensburg, Regensburg, Germany

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

13. Department of Internal Medicine III, Klinikum “Rechts der Isar”, Munich, Germany

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

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

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

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

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

19. University of Heidelberg, Heidelberg, Germany

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

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

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

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

Abstract

PURPOSE 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. METHODS 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. RESULTS 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 ( P = .047). When using the more common liver cutoff (Deauville score, 4) for PET-2 positivity, the difference was more pronounced (5-year PFS, 93.1% [95% CI, 90.7% to 95.5%] v 80.9% [95% CI, 72.2% to 89.7%]; P = .0011). CONCLUSION 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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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