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儿童晚期伯基特淋巴瘤的强化、超短期化疗。

Intensive, very short-term chemotherapy for advanced Burkitt's lymphoma in children.

作者信息

Spreafico Filippo, Massimino Maura, Luksch Roberto, Casanova Michela, Cefalo Graziella S, Collini Paola, Ferrari Andrea, Polastri Daniela, Terenziani Monica, Gasparini Marco, Fossati-Bellani Franca

机构信息

Department of Pediatric Oncology, Istituto Nazionale Tumori, Milan, Italy.

出版信息

J Clin Oncol. 2002 Jun 15;20(12):2783-8. doi: 10.1200/JCO.2002.08.088.

Abstract

PURPOSE

To improve the 63% event-free survival (EFS) achieved before 1986 in Murphy's stage III to IV Burkitt's lymphoma (BL), both chemotherapy and supportive care were intensified.

PATIENTS AND METHODS

From May 1987 to February 2001, 60 children, median age 9 years (range, 2.1 to 17 years), with advanced BL were enrolled onto two sequential institutional studies. From 1987 to 1992, 30 patients were stratified according to the absence (regimen IA, n = 19) or presence (regimen IB, n = 11) of bone marrow (BM) or CNS involvement. After 5-week cytoreductive chemotherapy consisting of vincristine, cyclophosphamide, doxorubicin, high-dose (HD) methotrexate (MTX), and intrathecal MTX or cytarabine, HD cytarabine and cisplatin were provided as a 4-day continuous infusion. Regimen IB was intensified by adding etoposide and HD ifosfamide and escalating MTX doses. Since 1992, regardless of BM or CNS status, 30 patients have been placed on regimen II, which is identical to IB but without ifosfamide. The scheduled duration of regimen II was 45 days.

RESULTS

EFS and disease-free survival at 5 years are 81% +/- 5% and 87% +/- 5%, respectively, for 59 assessable patients (73% +/- 8% and 85% +/- 7% for regimen IA + IB, 89% +/- 6%, EFS and disease-free survival, for regimen II; median follow-up, 6.7 years; range, 0.6 to 13.5 years). Six patients, two of whom were receiving regimen II, died as a result of initial treatment failure or relapse, and five patients, none receiving regimen II, died as a result of treatment-related complications.

CONCLUSION

This 45-day intensive chemotherapy program is the shortest schedule for disseminated BL and overcomes previously recognized risk factors such as BM and CNS infiltration.

摘要

目的

为提高1986年以前在Murphy III至IV期伯基特淋巴瘤(BL)中所取得的63%的无事件生存率(EFS),化疗和支持治疗均得到强化。

患者与方法

1987年5月至2001年2月,60名中位年龄9岁(范围2.1至17岁)的晚期BL患儿被纳入两项连续的机构研究。1987年至1992年,30例患者根据有无骨髓(BM)或中枢神经系统(CNS)受累进行分层(IA方案,n = 19;IB方案,n = 11)。在接受由长春新碱、环磷酰胺、阿霉素、大剂量(HD)甲氨蝶呤(MTX)和鞘内注射MTX或阿糖胞苷组成的为期5周的细胞减灭化疗后,给予HD阿糖胞苷和顺铂进行为期4天的持续输注。IB方案通过添加依托泊苷和HD异环磷酰胺并提高MTX剂量而得到强化。自1992年起,无论BM或CNS状态如何,30例患者接受II方案治疗,该方案与IB方案相同,但不含异环磷酰胺。II方案的预定疗程为45天。

结果

59例可评估患者的5年EFS和无病生存率分别为81%±5%和87%±5%(IA + IB方案为73%±8%和85%±7%,II方案的EFS和无病生存率为89%±6%;中位随访6.7年;范围0.6至13.5年)。6例患者死亡,其中2例接受II方案治疗,死于初始治疗失败或复发,5例患者死亡,均未接受II方案治疗,死于治疗相关并发症。

结论

这个为期45天的强化化疗方案是播散性BL最短的疗程,并且克服了先前公认的危险因素,如BM和CNS浸润。

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