Escalated-Dose BEACOPP in the Treatment of Patients With Advanced-Stage Hodgkin's Lymphoma: 10 Years of Follow-Up of the GHSG HD9 Study

Andreas Engert(Centrum für Integrierte Onkologie), Volker Diehl(Centrum für Integrierte Onkologie), Jeremy Franklin(Centrum für Integrierte Onkologie), Andreas Lohri(Centrum für Integrierte Onkologie), Bernd Dörken(Centrum für Integrierte Onkologie), Wolf‐Dieter Ludwig(Centrum für Integrierte Onkologie), P. Koch(Centrum für Integrierte Onkologie), Mathias Hänel(Centrum für Integrierte Onkologie), Michael Pfreundschuh(Centrum für Integrierte Onkologie), Martin Wilhelm(Centrum für Integrierte Onkologie), Lorenz Trümper(Centrum für Integrierte Onkologie), Walter-Erich Aulitzky(Centrum für Integrierte Onkologie), Martin Bentz(Centrum für Integrierte Onkologie), Mathias Rummel(Centrum für Integrierte Onkologie), Orhan Sezer(Centrum für Integrierte Onkologie), Hans–Konrad Müller–Hermelink(Centrum für Integrierte Onkologie), Dirk Hasenclever(Centrum für Integrierte Onkologie), Markus Löffler(Centrum für Integrierte Onkologie)
Journal of Clinical Oncology
August 24, 2009
Cited by 498Open Access
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Abstract

PURPOSE: The HD9 trial of the German Hodgkin Study Group compared two different doses (baseline and escalated) of the bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPP) chemotherapy regimen in 1,196 patients with advanced-stage Hodgkin's lymphoma (HL). The previous analysis with 5 years median follow-up had indicated improved tumor control with BEACOPP escalated. Since the long-term safety and efficacy of this regimen has been debated, we report the 10-year follow-up. PATIENTS AND METHODS: Patients received one of three chemotherapy regimens: eight cycles of cyclophosphamide, vincristine, procarbazine, and prednisone (COPP) alternating with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD); eight cycles of BEACOPP baseline; or eight cycles of BEACOPP escalated. RESULTS: Median follow-up was 111 months. At 10 years, freedom from treatment failure (FFTF) was 64%, 70%, and 82% with OS rates of 75%, 80%, and 86% for patients treated with COPP/ABVD (arm A), BEACOPP baseline (arm B), and BEACOPP escalated (arm C), respectively (P < .001). BEACOPP escalated was significantly better than BEACOPP baseline in terms of FFTF (P < .0001) and OS (P = .0053). A total of 74 second malignancies (6.2%) were documented, including acute myeloid leukemia (0.4%, 1.5%, and 3.0%), non-Hodgkin's lymphoma (2.7%, 1.7%, and 1.0%), and solid tumors (2.7%, 3.4%, and 1.9%). The corresponding overall secondary malignancy rates were 5.7%, 6.6%, and 6.0%, respectively. CONCLUSION: The 10-year follow-up of the HD9 trial demonstrates a stabilized significant improvement in long-term FFTF and OS for BEACOPP escalated in advanced-stage HL. These results challenge ABVD as standard of care for this patient population.


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