Involved-Field Radiotherapy Is Equally Effective and Less Toxic Compared With Extended-Field Radiotherapy After Four Cycles of Chemotherapy in Patients With Early-Stage Unfavorable Hodgkin’s Lymphoma: Results of the HD8 Trial of the German Hodgkin’s Lymphoma Study Group

Author:

Engert Andreas1,Schiller Petra1,Josting Andreas1,Herrmann Richard1,Koch Peter1,Sieber Markus1,Boissevain Friederike1,de Wit Maike1,Mezger Jörg1,Dühmke Eckhart1,Willich Normann1,Müller Rolf-Peter1,Schmidt Bernhard F.1,Renner Helmut1,Müller-Hermelink Hans Konrad1,Pfistner Beate1,Wolf Jürgen1,Hasenclever Dirk1,Löffler Markus1,Diehl Volker1

Affiliation:

1. From the First Department of Internal Medicine, University Hospital of Cologne and Department of Radiotherapy, University Clinic of Cologne, Cologne; Medical Department and Department of Radiotherapy, University Clinic Münster, Münster; University Clinic Nürnberg, Nürnberg; University Clinic Hamburg, Hamburg; St Vincentius Hospital Karlsruhe, Karlsruhe; Department of Radiation Oncology, Ludwig Maximilian Universität München, München; Center of Radiotherapy, Katharinenhospital, Stuttgart; Center of...

Abstract

Purpose: To investigate whether radiotherapy can be reduced without loss of efficacy from extended field (EF) to involved field (IF) after four cycles of chemotherapy. Patients and Methods: Between 1993 and 1998, patients with newly diagnosed early-stage unfavorable HD were enrolled onto this multicenter study. Patients were randomly assigned to receive cyclophosphamide, vincristine, procarbazine, and prednisone (COPP) + doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) for two cycles followed by radiotherapy of 30 Gy EF + 10 Gy to bulky disease (arm A) or 30 Gy IF + 10 Gy to bulky disease (arm B). Results: Of 1,204 patients randomly assigned to treatment, 1,064 patients were informative and eligible for the arm comparison (532 patients in arm A; 532 patients in arm B). The median observation time was 54 months. Five years after random assignment, the overall survival (OSran) for all eligible patients was 91% and freedom from treatment failure (FFTFran) was 83%. Survival rates at 5 years after start of radiotherapy revealed no differences for arms A and B, respectively, in terms of FFTF (85.8% and 84.2%) and OS at 5 years (90.8% and 92.4%). There also were no differences between arms A and B, respectively, in terms of complete remission (98.5% and 97.2%), progressive disease (0.8% and 1.9%), relapse (6.4% and 7.7%), death (8.1% and 6.4%), and secondary neoplasia (4.5% and 2.8%). In contrast, acute side effects including leukopenia, thrombocytopenia, nausea, gastrointestinal toxicity, and pharyngeal toxicity were more frequent in the EF arm. Conclusion: Radiotherapy volume size reduction from EF to IF after COPP + ABVD chemotherapy for two cycles produces similar results and less toxicity in patients with early-stage unfavorable HD.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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