首页> 外文OA文献 >Phase I study of concurrent real-time tumor-tracking thoracic radiation therapy with paclitaxel and carboplatin in locally advanced non-small cell lung cancer
【2h】

Phase I study of concurrent real-time tumor-tracking thoracic radiation therapy with paclitaxel and carboplatin in locally advanced non-small cell lung cancer

机译:紫杉醇和卡铂同时进行实时肿瘤追踪胸腔放疗的第一阶段研究在局部晚期非小细胞肺癌中的应用

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

Introduction: Although paclitaxel with carboplatin and thoracic radiotherapy has improved survival for patients with locally advanced unresectable non-small cell lung cancer (NSCLC), the optimal dose of paclitaxel has not been well defined in Japan. This study was conducted to determine the maximum tolerated dose (MTD) and recommended dose (RD) of paclitaxel in combination with carboplatin and concurrent real-time tumor-tracking thoracic radiation therapy (thoracic RTRT). Patients and methods: Previously untreated patients with histologically confirmed, locally advanced unresectable NSCLC were eligible. Before treatment, gold markers were inserted into the lung and the mediastinum of all patients. RTRT comprised a total of 66 Gy at 2 Gy/fraction, 5 days/week, for 7 weeks. Patients received paclitaxel at a starting dose of 40 mg/m2 followed by carboplatin at a fixed area under the curve (AUC) of 2, as a weekly regimen with RTRT. The dose of paclitaxel was escalated by 5 mg/m2 per level. Results: Eight patients with locally advanced unresectable NSCLC were enrolled and treated with two dose levels of paclitaxel (40 mg/m2 and 45 mg/m2), carboplatin (AUC = 2) and RTRT. No dose limiting toxicities (DLTs) were observed at Level 1 (paclitaxel, 40 mg/m2 and carboplatin, AUC = 2). At Level 2 (paclitaxel, 45 mg/m2 and carboplatin, AUC = 2), two of five patients experienced DLTs, in the form of esophagitis and discontinuation of chemotherapy more than twice. The MTD and RD of paclitaxel were thus defined as 45 mg/m2 and 40 mg/m2, respectively. Conclusions: This phase I study was well tolerated and the RD of paclitaxel and carboplatin with RTRT is 40 mg/m2 at AUC = 2, respectively. Further studies are warranted to evaluate the efficacy of this regimen.
机译:简介:尽管紫杉醇联合卡铂和胸腔放疗可提高局部晚期不可切除的非小细胞肺癌(NSCLC)患者的生存率,但紫杉醇的最佳剂量在日本尚未明确。这项研究的目的是确定紫杉醇联合卡铂和同时进行实时肿瘤追踪胸腔放疗(胸腔RTRT)联合使用时紫杉醇的最大耐受剂量(MTD)和推荐剂量(RD)。患者和方法:先前未经治疗且经组织学确认,局部晚期不可切除的NSCLC的患者符合条件。治疗前,将金标记物插入所有患者的肺和纵隔。 RTRT包含总计66 Gy,每次2 Gy,每周5天,共7周。患者每周接受RTRT方案,以40 mg / m2的起始剂量接受紫杉醇,然后在曲线下的固定区域(AUC)为2的情况下接受卡铂。紫杉醇的剂量每级增加5 mg / m2。结果:招募了8例局部晚期不可切除的NSCLC患者,并用两种剂量水平的紫杉醇(40 mg / m2和45 mg / m2),卡铂(AUC = 2)和RTRT治疗。在第1级(紫杉醇,40 mg / m2和卡铂,AUC = 2)上未观察到剂量限制性毒性(DLT)。在第2级(紫杉醇,45 mg / m2和卡铂,AUC = 2)下,五分之二的患者经历了DLTs,以食管炎的形式出现,并且化疗终止了两次以上。因此,紫杉醇的MTD和RD分别定义为45 mg / m2和40 mg / m2。结论:I期研究耐受性良好,在AUC = 2时,RTRT的紫杉醇和卡铂的RD分别为40 mg / m2。有必要进行进一步的研究以评估该方案的疗效。

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