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接受右丙亚胺治疗的高危急性淋巴细胞白血病儿童未发生继发性恶性肿瘤。

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

作者信息

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

机构信息

Departments of Pediatric Oncology, Dana-Farber Cancer Institute, 44 Binney St, Boston, MA 02115, USA.

出版信息

J Clin Oncol. 2008 Mar 1;26(7):1106-11. doi: 10.1200/JCO.2007.12.2481.

Abstract

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.

摘要

目的

右丙亚胺是一种用于预防蒽环类药物所致心脏毒性的药物。最近的一份报告发现,右丙亚胺的使用与霍奇金病患儿发生继发性恶性肿瘤(SMN)的风险之间存在关联。我们报告了在达纳-法伯癌症研究所急性淋巴细胞白血病(ALL)协作组方案95-01治疗的急性淋巴细胞白血病患儿中,未发现SMN与之存在关联。

患者与方法

205例高危(HR)ALL患儿在多药化疗的诱导和强化阶段被随机分配,分别单独接受阿霉素治疗(n = 100)或阿霉素联合右丙亚胺治疗(n = 105)。我们比较了这两组中SMN的发生率。

结果

中位随访6.2年,接受右丙亚胺治疗的组与未接受右丙亚胺治疗的组之间,SMN的发生率没有差异(P = 0.66)。1例随机分配至单独接受阿霉素治疗的患者发生了1例SMN(位于颅脑放疗野之外的黑色素瘤)。随机分配接受右丙亚胺治疗的患者中未观察到SMN。

结论

在接受HR ALL治疗的儿童中,右丙亚胺与SMN风险增加无关。鉴于右丙亚胺作为心脏保护剂的潜在重要性,我们建议在含阿霉素的儿科治疗方案中继续使用和研究右丙亚胺。

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