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

被引:115
作者
Josting, Andreas
Mueller, Horst
Borchmann, Peter
Baars, Joke W.
Metzner, Bernd
Doehner, Hartmut
Aurer, Igor
Smardova, Lenka
Fischer, Thomas
Niederwieser, Dietger
Schaefer-Eckart, Kerstin
Schmitz, Norbert
Sureda, Anna
Glossmann, Jan
Diehl, Volker
DeJong, Daphne
Hansmann, Martin-Leo
Raemaekers, John
Engert, Andreas
机构
[1] Univ Cologne, German Hodgkin Study Grp, D-5000 Cologne 41, Germany
[2] Hosp Oldenburg, Oldenburg, Germany
[3] Univ Ulm, Ulm, Germany
[4] Univ Hosp Magdeburg, Magdeburg, Germany
[5] Univ Hosp Leipzig, Leipzig, Germany
[6] Klinikum Nurnberg Nord, Nurnberg, Germany
[7] Asklepios Klin St Georg, Hamburg, Germany
[8] Univ Hosp Frankfurt, Frankfurt, Germany
[9] Antoni Van Leeuwenhoekziekenhuis, Amsterdam, Netherlands
[10] Radboud Univ Nijmegen Med Ctr, Nijmegen, Netherlands
[11] Univ Hosp Ctr Rebro, Zagreb, Croatia
[12] Gen Teaching Hosp, Prague, Czech Republic
[13] Hosp Santa Creu & Sant Pau, Barcelona, Spain
关键词
BONE-MARROW-TRANSPLANTATION; STEM-CELL TRANSPLANTATION; COLONY-STIMULATING FACTOR; SEQUENTIAL CHEMORADIOTHERAPY; COMBINATION CHEMOTHERAPY; PROGNOSTIC-FACTORS; SALVAGE TREATMENT; RANDOMIZED-TRIAL; DISEASE STATUS; THERAPY;
D O I
10.1200/JCO.2010.30.5771
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. J Clin Oncol 28:5074-5080.(C) 2010 by American Society of Clinical Oncology
引用
收藏
页码:5074 / 5080
页数:7
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