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一种剂量强化方案(NB96),用于诱导治疗,在 1 岁以上的高危神经母细胞瘤患儿中采用序贯高剂量化疗和干细胞解救。

A dose-intensive approach (NB96) for induction therapy utilizing sequential high-dose chemotherapy and stem cell rescue in high-risk neuroblastoma in children over 1 year of age.

机构信息

Department of Pediatric Hemato-Oncology, CHU Bordeaux, Children's Hospital, Place Amélie Rabat-Léon, Bordeaux, France.

出版信息

Pediatr Blood Cancer. 2011 Dec 1;57(6):965-71. doi: 10.1002/pbc.23232. Epub 2011 Jul 8.

Abstract

BACKGROUND

To improve outcome and overall survival (OS) in high-risk neuroblastoma, NB96 induction therapy was intensified using sequential high-dose chemotherapy and autologous stem cell rescue.

PROCEDURE

Twenty children were included in this pilot study undertaken at seven reference centers in France, between May 1995 and October 1996. Induction began with one cycle of conventional chemotherapy followed by six sequential cycles of high-dose chemotherapy comprising two cycles of etoposide 800 mg/m(2)/day over 3 days, two cycles of cyclophosphamide 2,000 mg/m(2)/day over 3 days, and two cycles of carboplatin 400 mg/m(2)/day over 5 days, followed by stem cell rescue.

RESULTS

Thirteen patients (13/20) received this induction with acceptable toxicity and adequate stem cell harvest. Of these, nine (9/13) underwent surgery according to the protocol, while one patient was given a consolidation regimen prior to surgery. No toxic death was recorded. At the end of induction, complete remission was achieved in 10 cases (50%), with six still alive in July 2009. The 5-year event-free survival and OS were 35 ± 11% and 40 ± 11%, respectively.

CONCLUSION

NB96 therapy is feasible and tolerated without lethal toxicity. Nevertheless, given the small sample size and absence of randomization in our study, the effectiveness of this strategy based on metastasis complete response rates and long-term outcome was not superior to other intensive chemotherapy regimens.

摘要

背景

为了提高高危神经母细胞瘤的治疗效果和总生存率(OS),NB96 诱导治疗采用序贯高剂量化疗和自体干细胞挽救。

方法

1995 年 5 月至 1996 年 10 月,法国 7 个参考中心开展了这项试点研究,共纳入 20 例儿童。诱导治疗开始时接受一个周期的常规化疗,随后进行 6 个周期的序贯高剂量化疗,包括两个周期的依托泊苷 800mg/m²/天,共 3 天,两个周期的环磷酰胺 2000mg/m²/天,共 3 天,以及两个周期的卡铂 400mg/m²/天,共 5 天,随后进行干细胞挽救。

结果

13 例患者(20 例中的 13 例)接受了这种诱导治疗,具有可接受的毒性和足够的干细胞采集。其中 9 例(13 例中的 9 例)根据方案进行了手术,而 1 例患者在手术前接受了巩固治疗方案。无治疗相关死亡。诱导结束时,10 例(50%)患者达到完全缓解,截至 2009 年 7 月,其中 6 例仍存活。5 年无事件生存率和 OS 分别为 35±11%和 40±11%。

结论

NB96 治疗方案可行且可耐受,无致死性毒性。然而,鉴于本研究样本量小且无随机分组,该基于转移完全缓解率和长期结果的策略的有效性并不优于其他强化化疗方案。

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