Outcome of relapsed adult lymphoblastic leukemia depends on response to salvage chemotherapy, prognostic factors, and performance of stem cell transplantation

挽救疗法 医学 内科学 移植 化疗 肿瘤科 造血干细胞移植 化疗方案 外科
作者
Nicola Gökbuget,Daniel Stanze,Joachim Beck,Helmut Diedrich,Heinz‐August Horst,Andreas Hüttmann,Guido Kobbe,Karl‐Anton Kreuzer,Lothar Leimer,Albrecht Reichle,Markus Schaich,Stefan Schwartz,Hubert Serve,Michael Starck,Matthias Stelljes,Reingard Stuhlmann,Andreas Viardot,Knut Wendelin,Mathias Freund,Dieter Hoelzer
出处
期刊:Blood [American Society of Hematology]
卷期号:120 (10): 2032-2041 被引量:384
标识
DOI:10.1182/blood-2011-12-399287
摘要

Abstract Despite improvements in first-line therapies, published results on the treatment of relapsed adult acute lymphoblastic leukemia (ALL) show that prognosis is still poor. The aim of the present retrospective analysis of the German Multicenter Study Group for Adult ALL was to identify prognostic factors and options for improvement. A total of 547 patients with a median age of 33 years (range, 15-55) experiencing their first relapse (406 vs 141 shorter or longer than 18 months from diagnosis) were evaluated. The aim of salvage therapy was to achieve a complete remission (CR) with subsequent a stem cell transplantation (SCT). The CR rate (assessed in Philadelphia chromosome– and BCR-ABL–negative ALL without CNS involvement) after the first salvage in relapse after chemotherapy (n = 224) was 42%. After failure of first salvage (n = 82), the CR rate after second salvage was 33%. In relapse after SCT (n = 48) the CR rate after first salvage was 23%. The median overall survival after relapse was 8.4 months and survival was 24% at 3 years. Prognostic factors for survival were relapse localization, response to salvage, performance of SCT, and age. Overall survival appeared superior compared with previously published studies, likely because of the high rate of SCT in the present study (75%). Further improvement may be achieved with earlier relapse detection and experimental approaches in early relapse. The study is registered at www.clinicaltrials.gov as NCT00199056 and NCT00198991.
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