Absence of secondary malignant neoplasms in children with high-risk acute lymphoblastic leukemia treated with dexrazoxane

被引:88
作者
Barry, Elly V.
Vrooman, Lynda M.
Dahlberg, Suzanne E.
Neuberg, Donna S.
Asselin, Barbara L.
Athale, Uma H.
Clavell, Luis A.
Larsen, Eric C.
Moghrabi, Albert
Samson, Yvan
Schorin, Marshall A.
Cohen, Harvey J.
Lipshultz, Steven E.
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 Biostat & Computat Biol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Univ Rochester, Med Ctr, Div Pediat Oncol, Rochester, NY 14642 USA
[5] McMaster Univ, Div Pediat Hematol Oncol, Hamilton, ON, Canada
[6] Univ Montreal, Div Hematol & Oncol, Hosp St Justine, Montreal, PQ H3C 3J7, Canada
[7] Univ Quebec, Ctr Hosp, Ste Foy, PQ G1V 2M3, Canada
[8] San Jorge Childrens Hosp, Div Pediat Oncol, San Juan, PR USA
[9] Maine Childrens Canc Program, Dept Pediat Hematol Oncol, Scarborough, ME USA
[10] Inova Fairfax Hosp Children, Sect Pediat Hematol Oncol, Falls Church, VA USA
[11] Stanford Univ, Sch Med, Dept Pediat, Palo Alto, CA 94304 USA
[12] Univ Miami Miller Sch Med, Dept Pediat, Miami, FL USA
关键词
D O I
10.1200/JCO.2007.12.2481
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Dexrazoxane is a drug used to prevent anthracycline-induced cardiotoxicity. A recent report found an association between the use of dexrazoxane and the risk of developing secondary malignant neoplasms (SMNs) in children with Hodgkin's disease. We report the absence of an association of SMNs in children with acute lymphoblastic leukemia (ALL) treated on Dana-Farber Cancer Institute ALL Consortium Protocol 95-01. Patients and Methods Two hundred five children with high-risk (HR) ALL were randomly assigned to receive doxorubicin alone (n = 100) or doxorubicin with dexrazoxane (n = 105) during the induction and intensification phases of multiagent chemotherapy. We compared incidence of SMNs in these two groups. Results With a median follow-up of 6.2 years, no differences in the incidence of SMNs were noted between the group that received dexrazoxane and the group that did not (P = .66). One SMN (a melanoma located outside of the cranial radiation field) occurred in a patient who was randomly assigned to doxorubicin alone. No SMNs were observed in patients randomly assigned to receive dexrazoxane. Conclusion Dexrazoxane was not associated with an increased risk of SMNs in children treated for HR ALL. Given the potential importance of dexrazoxane as a cardioprotectant, we recommend that dexrazoxane continue to be used and studied in doxorubicin-containing pediatric regimens.
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收藏
页码:1106 / 1111
页数:6
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