首页> 外文期刊>Clinical oncology >British National Lymphoma Investigation: pilot studies of neoadjuvant chemotherapy in clinical stage Ia and IIa Hodgkin's disease.
【24h】

British National Lymphoma Investigation: pilot studies of neoadjuvant chemotherapy in clinical stage Ia and IIa Hodgkin's disease.

机译:英国国家淋巴瘤调查:临床Ia期和IIa期霍奇金病新辅助化疗的初步研究。

获取原文
获取原文并翻译 | 示例
       

摘要

In order to improve treatment in early Stage IA and IIA Hodgkin's disease, the British National Lymphoma Investigation (BNLI) has evaluated two neoadjuvant chemotherapy regimens with involved field radiotherapy. This article reports the results of the methotrexate, vinblastine and prednisolone (MVP) study in 39 patients and updates the previous report on vinblastine, bleomycin and methotrexate (VBM) in 30 patients. Both studies recruited clinical Stage IA or IIA Hodgkin's disease patients with intermediate risk of relapse into a prospective multicentre Phase II study. They received two cycles of chemotherapy followed by involved field radiotherapy and then four further cycles of chemotherapy. For MVP the 5-year survival is 97% and for VBM it is 93%. The 5-year event-free survival rates are 71% and 87% respectively. The acute pulmonary and haematological toxicity occurring with VBM was not acceptable and therefore the MVP study was performed. There was less toxicity with this regimen although modest acute pulmonary toxicity was still observed. However, in view of the length of treatment with MVP (9 months) and the excellent results reported by the Manchester group, future efforts of the BNLI are to be directed towards a new short course chemotherapy regimen, VAPEC-B (vincristine, doxorubicin, prednisolone, etoposide, cyclophosphamide and bleomycin).
机译:为了改善IA和IIA早期霍奇金氏病的治疗,英国国家淋巴瘤调查(BNLI)对涉及野外放疗的两种新辅助化疗方案进行了评估。本文报告了39例患者的甲氨蝶呤,长春碱和泼尼松龙(MVP)研究的结果,并更新了30例患者中有关长春碱,博来霉素和甲氨蝶呤(VBM)的报道。两项研究均将具有中度复发风险的临床IA或IIA霍奇金病患者纳入一项前瞻性多中心II期研究。他们接受了两个周期的化学疗法,然后进行了现场放疗,然后又进行了四个周期的化学疗法。对于MVP,五年生存率为97%,对于VBM为93%。 5年无事件生存率分别为71%和87%。 VBM引起的急性肺和血液毒性不可接受,因此进行了MVP研究。尽管仍观察到中等程度的急性肺毒性,但该方案的毒性较小。但是,考虑到MVP的治疗时间(9个月)以及曼彻斯特小组报告的出色结果,BNLI的未来工作将针对一种新的短程化疗方案VAPEC-B(长春新碱,阿霉素,泼尼松龙,依托泊苷,环磷酰胺和博来霉素)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号