Favorable outcome for adolescents with acute lymphoblastic leukemia treated on Dana-Farber Cancer Institute Acute Lymphoblastic Leukemia Consortium Protocols

被引:137
作者
Barry, Elly
DeAngelo, Daniel J.
Neuberg, Donna
Stevenson, Kristen
Loh, Mignon L.
Asselin, Barbara L.
Barr, Ronald D.
Clavell, Luis A.
Hurwitz, Craig A.
Moghrabi, Albert
Samson, Yvan
Schorin, Marshall
Cohen, Harvey J.
Sallan, Stephen E.
Silverman, Lewis B.
机构
[1] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Biostat Sci, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Childrens Hosp, Dept Pediat, Boston, MA 02115 USA
[6] Univ Calif San Francisco, Dept Pediat Hematol Oncol, San Francisco, CA 94143 USA
[7] Lucile Packard Childrens Hosp, Dept Pediat, Palo Alto, CA USA
[8] Hosp St Justine, Dept Pediat Hematol Oncol, Montreal, PQ, Canada
[9] Ctr Hosp Quebec, Dept Pediat, Quebec City, PQ, Canada
[10] McMaster Univ, Dept Pediat, Hamilton, ON, Canada
[11] Univ Rochester, Med Ctr, Dept Pediat Hematol Oncol, Rochester, NY 14642 USA
[12] San Jorge Childrens Hosp, Dept Pediat Oncol, San Juan, PR USA
[13] Maine Med Ctr, Maine Childrens Canc Program, Dept Pediat Oncol, Portland, ME USA
[14] Tulane Hosp Children, Dept Pediat, New Orleans, LA USA
关键词
D O I
10.1200/JCO.2006.08.6397
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Historically, adolescents with acute lymphoblastic leukemia (ALL) have had inferior outcomes when compared with younger children. We report the outcome of adolescents treated on Dana-Farber Cancer Institute (DFCI; Boston, MA) ALL Consortium Protocols conducted between 1991 and 2000. Patients and Methods A total of 844 patients aged 1 to 18 years, with newly diagnosed ALL were enrolled onto two consecutive DFCI-ALL Consortium Protocols. We compared outcomes in three age groups: children aged 1 to 10 years (n = 685), young adolescents aged 10 to 15 years (n = 108), and older adolescents aged 15 to 18 years (n = 51). Results With a median follow-up of 6.5 years, the 5-year event-free survival (EFS) for those aged 1 to 10 years was 85% (SE, 1 %), compared with 77% (SE, 4%) for those aged 10 to 15 years, and 78% (SE, 6%) for those aged 15 to 18 years (P =.09). Adolescents were more likely to present with T-cell phenotype (P <.001) and less likely to have the TEL-AML1 fusion (P =.05). The incidence of pancreatitis and thromboembolic complications, but not asparaginase allergy, was higher in patients : 10 years of age compared with those younger than 10 years. However, there was no difference in the rate of treatment-related complications between the 10- to 15-year and 15- to 18-year age groups. Conclusion Adolescents were more likely to present at diagnosis with biologically higher risk disease (T-cell phenotype and absence of the TEL-AML1 fusion) and more likely to experience treatment-related complications than younger children. However, the 5-year EFS for older adolescents was 78% +/- 6%, which is superior to published outcomes for similarly aged patients treated with other pediatric and adult ALL regimens. Based on this experience, we currently are piloting our regimen in patients aged 18 to 50 years.
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页码:813 / 819
页数:7
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