Dose Intensity of Chemotherapy in Patients With Relapsed Hodgkin's Lymphoma

Author:

Josting Andreas1,Müller Horst1,Borchmann Peter1,Baars Joke W.1,Metzner Bernd1,Döhner Hartmut1,Aurer Igor1,Smardova Lenka1,Fischer Thomas1,Niederwieser Dietger1,Schäfer-Eckart Kerstin1,Schmitz Norbert1,Sureda Anna1,Glossmann Jan1,Diehl Volker1,DeJong Daphne1,Hansmann Martin-Leo1,Raemaekers John1,Engert Andreas1

Affiliation:

1. From the University of Cologne, German Hodgkin Study Group; University of Cologne, Köln; Hospital of Oldenburg, Oldenburg; University of Ulm, Ulm; University Hospital Magdeburg, Magdeburg; University Hospital Leipzig, Leipzig; Klinikum Nürnberg Nord, Nürnberg; Asklepios Klinik St Georg, Hamburg; University Hospital Frankfurt, Frankfurt, Germany; The Netherlands Cancer Institute, Antoni Van Leeuwenhoekziekenhuis, Amsterdam; Radboud University Medical Center Nijmegen, Nijmegen, the Netherlands; University...

Abstract

Purpose High-dose chemotherapy (HDCT) followed by autologous stem-cell transplantation (PBSCT) has become the standard treatment for patients with relapsed Hodgkin's lymphoma (HL). The intensity of treatment needed is unclear. This European intergroup study evaluated the impact of sequential high-dose chemotherapy (SHDCT) before myeloablative therapy. Patients and Methods Patients with histologically confirmed, relapsed HL were treated with two cycles of dexamethasone, cytarabine, and cisplatin, and those without disease progression were randomly assigned. In the standard arm (A), patients received myeloablative therapy with carmustine, BEAM (carmustine, etoposide, cytarabine, and melphalan) followed by PBSCT. Patients in the experimental arm (B) also received sequential cyclophosphamide, methotrexate, and etoposide in high-doses before BEAM. Freedom from treatment failure (FFTF) was the primary end point. Remission rates, overall survival (OS), and toxicity of treatment were secondary end points. Results From a total of 284 patients included, 241 responding patients were randomly assigned after two cycles of dexamethasone, cytarabine, and cisplatinum. Patients treated in arm B had longer treatment duration and experienced more toxicity and protocol violations (P < .05). Mortality was similar in both arms (20% and 18%). With a median observation time of 42 months, there was no significant difference in terms of FFTF (P = .56) and OS (P = .82) between arms. FFTF at 3 years was 62% (95% CI, 56% to 68%) and OS was 80% (95% CI, 75% to 85%). Patients with stage IV, early relapse, multiple relapse, anemia, or B symptoms had a higher risk of recurrence (P < .001). Conclusion Compared with conventional high-dose chemotherapy, additional SHDCT is associated with more adverse effects and does not improve the prognosis of patients with relapsed HL.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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