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无 MYCN 扩增的非转移性和不可切除神经母细胞瘤婴儿减少治疗后取得良好效果:前瞻性 INES 99.1 研究结果。

Excellent outcome with reduced treatment in infants with nonmetastatic and unresectable neuroblastoma without MYCN amplification: results of the prospective INES 99.1.

机构信息

Unité d'Hémato-Oncologie, Hôpital des Enfants, Toulouse, France.

出版信息

J Clin Oncol. 2011 Feb 1;29(4):449-55. doi: 10.1200/JCO.2010.29.5196. Epub 2010 Dec 20.

Abstract

PURPOSE

To evaluate the efficacy of low-dose chemotherapy in infants with nonmetastatic and unresectable neuroblastoma (NB) without MYCN amplification.

PATIENTS AND METHODS

Infants with localized NB and no MYCN amplification were eligible in the SIOPEN Infant Neuroblastoma European Study 99.1 study. Primary tumor was deemed unresectable according to imaging defined risk factors. Diagnostic procedures and staging were carried out according to International Staging System recommendations. Children without threatening symptoms received low-dose cyclophosphamide (5 mg/kg/d × 5 days) and vincristine (0.05 mg/kg at day 1; CyV), repeated once to three times every 2 weeks until surgical excision could be safely performed. Children with either one threatening symptom or insufficient response to CyV were given carboplatin and etoposide (CaE), sometimes followed by vincristine, cyclophosphamide, and doxorubicin. No postoperative treatment was to be administered.

RESULTS

Between December 1999 and April 2004, 120 infants were included in the study. Eighty-eight had no threatening symptoms and 79 received CyV. CaE was given to 49 of them because of insufficient response. Thirty-two children had threatening symptoms, 30 of whom received CaE. Anthracyclines were given to 46 children. Surgery was attempted in 102 patients, leading to gross surgical excision in 93. Relapse occurred in 12 patients (nine local and three metastatic). Five-year overall and event-free survivals were 99% ± 1% and 90% ± 3%, respectively, with a median follow-up of 6.1 years (range, 1.6 to 9.1).

CONCLUSION

Low-dose chemotherapy without anthracyclines is effective in 62% of infants with an unresectable NB and no MYCN amplification, allowing excellent survival rates without jeopardizing their long-term outcome.

摘要

目的

评估低剂量化疗对无 MYCN 扩增的非转移性和不可切除神经母细胞瘤(NB)婴儿的疗效。

方法

SIOPEN 婴儿神经母细胞瘤欧洲研究 99.1 研究纳入局部 NB 且无 MYCN 扩增的婴儿。根据影像学定义的危险因素,将原发肿瘤视为不可切除。根据国际分期系统建议进行诊断程序和分期。无威胁症状的儿童接受低剂量环磷酰胺(5mg/kg/d×5 天)和长春新碱(第 1 天 0.05mg/kg;CyV),每 2 周重复一次至三次,直到可以安全进行手术切除。有一个威胁症状或对 CyV 反应不足的儿童给予卡铂和依托泊苷(CaE),有时随后给予长春新碱、环磷酰胺和多柔比星。不给予术后治疗。

结果

1999 年 12 月至 2004 年 4 月期间,该研究纳入了 120 名婴儿。88 名患儿无威胁症状,79 名患儿接受 CyV 治疗。由于反应不足,其中 49 名患儿给予 CaE。32 名患儿有威胁症状,其中 30 名患儿给予 CaE。46 名患儿给予蒽环类药物。102 名患儿尝试手术,93 名患儿实现大体手术切除。12 名患儿发生复发(9 例局部复发和 3 例远处转移)。5 年总生存率和无事件生存率分别为 99%±1%和 90%±3%,中位随访时间为 6.1 年(范围 1.6 至 9.1 年)。

结论

对于无 MYCN 扩增的不可切除 NB 婴儿,不使用蒽环类药物的低剂量化疗有效率为 62%,可实现良好的生存率,而不会危及长期预后。

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