首页> 美国卫生研究院文献>Neuro-oncology Advances >TRLS-09. RTOG1119: PHASE II RANDOMIZED STUDY OF WHOLE BRAIN RADIOTHERAPY / STEREOTACTIC RADIOSURGERY IN COMBINATION WITH CONCURRENT LAPATINIB IN PATIENTS WITH BRAIN METASTASIS FROM HER2-POSITIVE BREAST CANCER
【2h】

TRLS-09. RTOG1119: PHASE II RANDOMIZED STUDY OF WHOLE BRAIN RADIOTHERAPY / STEREOTACTIC RADIOSURGERY IN COMBINATION WITH CONCURRENT LAPATINIB IN PATIENTS WITH BRAIN METASTASIS FROM HER2-POSITIVE BREAST CANCER

机译:TRLS-09。 RTOG1119:合并HER2阳性乳腺癌的脑转移患者全脑放疗/定性放射外科手术治疗与并发拉帕替尼联合治疗的第二阶段随机研究

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 addition of trastuzumab to cytotoxic chemotherapy has improved outcomes for patients with HER2 positive breast cancer. Increased survival coupled with limited blood-brain barrier (BBB) penetration of trastuzumab may contribute to the increased incidence of brain metastasis in these patients. Half of these patients die of intracranial disease progression rather than extracranial disease. Therefore, strategies to improve survival must include increased CNS disease control in these patients. Lapatinib crosses the BBB and demonstrates modest activity against intracranial metastases. Based upon preclinical data and results of a phase I study, we hypothesized that lapatinib plus WBRT /SRS can improve the intracranial disease control compared to WBRT / SRS alone. A randomized phase II trial of WBRT (37.5 Gy/3 weeks) or SRS plus or minus concurrent lapatinib (daily 1000 mg for 6 weeks) was initiated. CNS penetrating HER2 targeted therapy is permitted throughout the study, but patients not on trastuzumab, pertuzumab or any other breast cancer therapy at study entry are not permitted to begin this therapy while on protocol treatment, but may begin it 24 hours after completion of protocol treatment. Eligibility includes HER2+ breast cancer with at least one measurable, unirradiated parenchymal brain metastasis. The two populations targeted for accrual include patients with 1) newly diagnosed, multiple brain metastases or 2) progressive brain metastases after stereotactic radiosurgery (SRS) or surgical resection of 1–3 metastases. Prior lapatinib is allowed. Patients are stratified by breast-specific graded prognostic assessment; use of non-CNS penetrating HER2 targeted therapy; and prior SRS or surgical resection. The primary endpoint is complete response rate in the brain 12 weeks after WBRT. Secondary endpoints include objective response rate, lesion-specific response rate, CNS progression-free survival, and overall survival. 140 of 143 target accrual have enrolled (4/22/2019).
机译:将曲妥珠单抗添加到细胞毒性化学疗法中可改善HER2阳性乳腺癌患者的结局。曲妥珠单抗增加的生存率和有限的血脑屏障(BBB)渗透可能导致这些患者脑转移的发生率增加。这些患者中有一半死于颅内疾病而不是颅外疾病。因此,提高生存率的策略必须包括加强这些患者的中枢神经系统疾病控制。拉帕替尼跨过血脑屏障,并表现出适度的抗颅内转移活性。基于临床前数据和I期研究的结果,我们假设拉帕替尼联合WBRT / SRS与单独使用WBRT / SRS相比可以改善颅内疾病的控制。开始了一项WBRT(37.5 Gy / 3周)或SRS加或减并发拉帕替尼(每天1000 mg,共6周)的II期随机试验。在整个研究过程中均允许CNS穿透HER2靶向治疗,但在研究开始时不允许未接受曲妥珠单抗,帕妥珠单抗或任何其他乳腺癌治疗的患者在接受方案治疗时开始这种治疗,但可以在方案治疗完成后24小时开始。资格包括具有至少一种可测量的,未辐射的实质性脑转移的HER2 +乳腺癌。应计入的两个人群包括:1)新诊断,多发脑转移或2)立体定向放射外科(SRS)或手术切除1-3个转移的进行性脑转移的患者。允许事先使用拉帕替尼。通过乳房特异性分级的预后评估对患者进行分层。使用非CNS穿透性HER2靶向治疗;和先前的SRS或手术切除。主要终点是WBRT后12周大脑的完全缓解率。次要终点包括客观缓解率,病变特异性缓解率,​​CNS无进展生存期和总体生存期。 143个目标应计项目中的140个已注册(4/22/2019)。

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