Dose-Intensified Combined Modality Treatment with 2 Cycles of BEACOPP Escalated Followed by 2 Cycles of ABVD and Involved Field Radiotherapy (IF-RT) Is Superior to 4 Cycles of ABVD and IFRT in Patients with Early Unfavourable Hodgkin Lymphoma (HL): An Analysis of the German Hodgkin Study Group (GHSG) HD14 Trial

Author:

Borchmann Peter1,Engert Andreas2,Pluetschow Annette2,Fuchs Michael2,Markova Jana3,Lohri Andreas4,Kral Zdenek5,Greil Richard6,Topp Max7,Villalobos Matthias8,Zijlstra Jose9,Soekler Martin10,Stein Harald11,Eich Hans Theodor12,Mueller Rolf Peter13,Diehl Volker14

Affiliation:

1. First Department of Internal Medicine, University of Cologne, Cologne, Germany

2. First department of Internal Medicine/German Hodgkin Study Group (GHSG), University of Cologne, Cologne, Germany

3. Hematologia, Fakultni Nemocnice Kralovske Vinohrady, Prague, Czech Republic

4. Dept. of Oncology/Hematology, Medical University Clinic, Liestal, Switzerland

5. Department of Internal Medicine and Hematology, University Hospitel of Brno, Brno, Czech Republic

6. Third Department of Internal Medicine, University of Salzburg, Salzburg, Austria

7. Department of Hematology and Oncology, University of Wuerzburg, Wuerzburg, Germany

8. Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany

9. Hematology, VU University Medical Centre Amsterdam, Amsterdam, Netherlands

10. Hematology and Oncology, University of Tuebingen, Tuebingen, Germany

11. Institute of Pathology, University Hospitel Benjamin Franklin Berlin, Berlin, Germany

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

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

14. First department of Internal Medicine/German Hodgkin Study Group (GHSG), University of Cologne, Cologne/Germany, Germany

Abstract

Abstract Purpose: Combined modality treatment consisting of 4 cycles of chemotherapy and IF-RT is the standard treatment for early unfavourable HL. Overall survival (OS) and freedom from treatment failure (FFTF) in this group of patients was 91% and 83%, respectively, at 5 years in our prior HD8 study. Thus, the rationale for HD14 was to improve on these results by increasing dose intensity using BEACOPP escalated. Methods: Between January 2003 and January 2007, 1.216 patients aged 16–60 with untreated early unfavourable stage HL (CS I, IIA with one of the following risk factors: large mediastinal mass (a), extranodal disease (b), elevated ESR (c), or ≥ 3 nodal areas (d); IIB with risk factors c and d) were randomized to either 4 cycles of ABVD (arm A) or 2x BEACOPP escalated followed by 2x ABVD (arm B). All patients received 30Gy IF-RT after chemotherapy. Primary objective was the improvement of the FFTF. Here we present the results of the predefined 3rd interim analysis within the prespecified group sequential test design. Results: Of the 1.216 patients included, 1.010 were evaluable for this analysis. Patient characteristics were well balanced between both arms. At 3 years, the FFTF for arm A is 90% (95% CI: 87%–93%), and for arm B 96% (95% CI: 94%–98%). Since the observed inverse normal test statistic exceeds the critical level, the null hypothesis of equal FFTF in each arm can already be rejected. The improved FFTF is mainly due to differences in progression and early relapses (arm A 5.9% versus arm B 1.8%). Protocol adherence for chemotherapy was high and not different in both arms (arm A 98.8%, am B 97.3%). Though the chemotherapy-intensity was higher in the experimental arm, safety was comparable to the standard treatment. Secondary neoplasias occurred in 8 patients in each arm so far. Conclusion: Based on the significantly superior FFTF of the intensified therapy (2x BEACOPP escalated + 2x ABVD + IF-RT) compared to the prior standard (4x ABVD + IF-RT), this more aggressive treatment strategy will become the new standard for early unfavourable HL patients within the GHSG. Whether the improved FFTF translates into an improved overall survival must be awaited. Future strategies should aim at identification of those patient subgroups that profit most from this approach.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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