医学
内科学
淋巴细胞白血病
置信区间
年轻人
儿科
外科
白血病
作者
Adele K. Fielding,Susan Richards,Rajesh Chopra,Hillard M. Lazarus,Mark R. Litzow,Georgina Buck,Ian Durrant,Selina M. Luger,David I. Marks,Ian M. Franklin,Andrew McMillan,Martin S. Tallman,Jacob M. Rowe,Anthony H. Goldstone
出处
期刊:Blood
[American Society of Hematology]
日期:2006-10-10
卷期号:109 (3): 944-950
被引量:764
标识
DOI:10.1182/blood-2006-05-018192
摘要
Abstract Most adults with acute lymphoblastic leukemia (ALL) who achieve complete remission (CR) will relapse. We examined the outcome of 609 adults with recurring ALL, all of whom were previously treated on the Medical Research Council (MRC) UKALL12/ECOG2993 study, where the overall survival (OS) of newly diagnosed patients is 38% (95% confidence interval [CI] = 36%-41%) at 5 years. By contrast, OS at 5 years after relapse was 7% (95% CI = 4%-9%). Factors predicting a good outcome after salvage therapy were young age (OS of 12% in patients younger than 20 years vs OS of 3% in patients older than 50 years; 2P < .001) and short duration of first remission (CR1) (OS of 11% in those with a CR1 of more than 2 years versus OS of 5% in those with a CR1 of less than 2 years; 2P < .001). Treatment received in CR1 did not influence outcome after relapse. In a very highly selected subgroup of patients who were able to receive HSCT after relapse, some were long-term survivors. We conclude from a large, unselected series with mature follow-up that most adults with recurring ALL, whatever their prior treatment, cannot be rescued using currently available therapies. Prevention of recurrence is the best strategy for long-term survival in this disease.
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