...
首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >A phase I/II study of gemcitabine-concurrent proton radiotherapy for locally advanced pancreatic cancer without distant metastasis
【24h】

A phase I/II study of gemcitabine-concurrent proton radiotherapy for locally advanced pancreatic cancer without distant metastasis

机译:吉西他滨同时质子放疗用于局部晚期胰腺癌且无远处转移的I / II期研究

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: We conducted the study to assess the feasibility and efficacy of gemcitabine-concurrent proton radiotherapy (GPT) for locally advanced pancreatic cancer (LAPC). Materials and methods: Of all 50 patients who participated in the study, 5 patients with gastrointestinal (GI)-adjacent LAPC were enrolled in P-1 (50 Gy equivalent [GyE] in 25 fractions) and 5 patients with non-GI-adjacent LAPC in P-2 (70.2 GyE in 26 fractions), and 40 patients with LAPC regardless of GI-adjacency in P-3 (67.5 GyE in 25 fractions using the field-within-a-field technique). In every protocol, gemcitabine (800 mg/m 2/week for 3 weeks) was administered concurrently. Every patient received adjuvant chemotherapy including gemcitabine after GPT within the tolerable limit. Results: The median follow-up period was 12.5 months. The scheduled GPT was feasible for all except 6 patients (12%) due to acute hematologic or GI toxicities. Grade 3 or greater late gastric ulcer and hemorrhage were seen in 5 patients (10%) in P-2 and P-3. The one-year freedom from local-progression, progression-free, and overall survival rates were 81.7%, 64.3%, and 76.8%, respectively. Conclusion: GPT was feasible and showed high efficacy. Although the number of patients and the follow-up periods are insufficient, the clinical results seem very encouraging.
机译:目的:我们进行了这项研究,以评估吉西他滨并发质子放射治疗(GPT)对局部晚期胰腺癌(LAPC)的可行性和有效性。材料和方法:在所有参与研究的50位患者中,有5位胃肠道(GI)邻近的LAPC患者被纳入P-1(25分数为50 Gy当量[GyE])和5位非GI邻近的患者LA-2在P-2中(70.2 GyE,分为26个分数),以及40例LAPC患者,而与P-3中的GI无关(在25分数中,采用场内技术的67.5 GyE)。在每个方案中,吉西他滨(800 mg / m 2 /周,共3周)同时给药。每位患者接受GPT后在容许范围内接受辅助化疗,包括吉西他滨。结果:中位随访期为12.5个月。由于急性血液学或胃肠道毒性,预定的GPT对除6例患者(12%)以外的所有患者均可行。 P-2和P-3的5例患者(10%)出现3级或更高级别的晚期胃溃疡和出血。一年无局部进展,无进展和总生存率分别为81.7%,64.3%和76.8%。结论:GPT是可行的,并具有较高的疗效。尽管患者人数和随访时间不足,但临床结果似乎令人鼓舞。

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