首页> 美国卫生研究院文献>other >Phase II study of interleukin-12 for treatment of plateau phase multiple myeloma (E1A96): A trial of the Eastern Cooperative Oncology Group
【2h】

Phase II study of interleukin-12 for treatment of plateau phase multiple myeloma (E1A96): A trial of the Eastern Cooperative Oncology Group

机译:白细胞介素12治疗高原期多发性骨髓瘤(E1A96)的II期研究:东方合作肿瘤小组的一项试验

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The Eastern Cooperative Oncology Group (ECOG) conducted a phase II trial of interleukin-12 (IL-12) for plateau phase multiple myeloma. Patients were initially treated with IL-12 250 ng/kg I.V. daily for 5 days every 3 weeks. The trial was modified due to toxicity after the first 16 patients. IL-12 was given 300 ng/kg subcutaneously twice weekly for 24 weeks. Of 48 eligible patients, there were 4 objective responses (8.3%), all CR. The median survival and progression-free survival were 42.8 and 11.4 months. Unacceptable grade 3 or 4 non-hematologic toxicity (31% with IL-12 subcutaneously and 63% with IL-12 intravenously) was observed.
机译:东部肿瘤合作研究小组(ECOG)对高原期多发性骨髓瘤进行了白介素12(IL-12)的II期试验。患者最初接受IL-12 250 ng / kg I.V.治疗。每3周每天5天。最初的16例患者因毒性反应而修改了该试验。每周两次皮下给予IL-12 300 ng / kg,持续24周。在48例合格患者中,有4例客观缓解(8.3%),均为CR。中位生存期和无进展生存期分别为42.8和11.4个月。观察到不可接受的3或4级非血液学毒性(皮下注射IL-12时为31%,静脉注射IL-12时为63%)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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