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临床试验/NCT05167994
NCT05167994招募中2 期

Preoperative Intensity-Modulated Radiotherapy (IMRT) Combined With Concurrent Anlotinib Hydrochloride and Penpulimab for Localized Extremity or Trunk Sarcoma

Cancer Institute and Hospital, Chinese Academy of Medical Sciences2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年5月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
30
试验地点
2
主要终点
Major wound complications

研究概览

简要总结

To investigate the safety and efficacy of preoperative IMRT and concurrent Anlotinib Hydrochloride for primary truncal or extremity soft tissue sarcoma; To investigate the Quality of life and extremity function post-combination treatment; To study the mechanism of radio-sensitizing effects of Anlotinib Hydrochloride and Penpulimab for primary truncal or extremity soft tissue sarcoma; To assess the relationship between the MRI imaging, pathological findings and local control.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age older than 18-yo
  • Histology proven soft tissue sarcoma of truncal or extremity, deemed appropriate for preoperative radiotherapy and conservative surgery by multidisciplinary discussion.
  • Histology reviewed by reference pathologist
  • Lesion can be assessed
  • Can tolerate radiotherapy and Anlotinib
  • Agree contraception.
  • Informed consent: All patients must sign a document of informed consent indicating their understanding of the investigational nature and risks of the study before any protocol related studies are performed

排除标准

  • No gross tumor post-resection in other center.
  • Contraindications to Anlotinib, including allergic to Anlotinb, active bleeding, ulcer, enteric perforation, enteric obstruction, uncontrolled hypertension, Grade 3 to 4 cardiac insufficiency (per NYHA criteria), and severe hepatic or renal insufficiency (Grade 4), etc.
  • Dermatofibrosarcoma protuberans(DFSP), Desmoids, etc.
  • Benign histology
  • Secondary cancer within 5 years (except cervical carcinoma in situ or early-stage skin basal cell carcinoma)
  • STS can be cured by extensive operation alone.
  • Previous irradiation to the same area
  • Radiological evidence of distant metastases
  • Other contraindications, can't tolerate operation or other treatment needed in this study.
  • Neoadjuvant chemotherapy given or planned.

结局指标

主要结局

Major wound complications

时间窗: 4-months post-surgery

次要结局

  • Pathological remission rate(2 weeks after operation)
  • Acute and late toxicities(acute toxicities were evaluated during and 3 months after IMRT, late toxicities were evaluted after 6 months)
  • Extremity function(pre-IMRT, end of IMRT, 1 months post-IMRT, and every 3 to 6 months during follow-up)
  • Overall Survival(2-year)
  • Local control(2-year)
  • Quality of Life(pre-IMRT, end of IMRT, 1 months post-IMRT, and every 3 to 6 months during follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

NINGNING LU

Principle Investigator

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

研究点 (2)

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