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临床试验/NCT05817604
NCT05817604进行中(未招募)不适用

Stereotactic Body Radiotherapy (SBRT) for Medically Inoperable Localised Renal Tumors (SABINA Trial)

Consorci Sanitari de Terrassa1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
60
试验地点
1
主要终点
Local relapse-free survival

研究概览

简要总结

Study evaluating the activity and efficacy of Stereotactic Body Radiotherapy for the treatment of medically inoperable localized renal cancer

详细描述

Stereotactic Body Radiotherapy (SBRT) is a non-invasive alternative to surgery to control localized primary renal cell cancer (RCC) in medically inoperable patients. The kidney tumor has classically been considered radioresistant. Multiple retrospective series and few Phase II trial have studied the role of SBRT in localized renal tumors with favorable outcomes. Although large prospective studies are lacking, we evaluate the safety and effectiveness of SBRT for the treatment of renal cancer.

Participants will be allocated to recieve either single 26Gy fraction or Multifraction 3 - 5 fraction-squeme.

Assesment at regular intervals will estimate the activity and efficacy of the technique, evaluate tolerability, estimate survival, estimate distant failure rate, and renal function change after SABR.

Follow-up visits occur at 1month and every 3 months in the first year after SBRT, then every 6 months in the second year and then yearly until study closure.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histological diagnosis of Renal tumor and/or highly suspected malignant neoplasm by CT, MRI or PET.
  • Tumor Diameter >1cm - <7cm
  • Tumor visible on CT planning
  • Medically inoperable disease (or rejection of surgery)
  • Karnofsky Index >70%
  • >18 y.o.
  • Informed Consent signature
  • Exclusion criteria:
  • Non-oncological renal disease or autoinmunological disorder that does not recommend the treatment with radiotherapy.
  • Previous local/regional RT
  • Life expectancy <6 months
  • Concomitance with other antineoplastic drugs

排除标准

  • 未提供

结局指标

主要结局

Local relapse-free survival

时间窗: Participants should be followed continuously during 5 years

Local Control assessed by RECISTv1.1 criteria with TC, MRI or PET-scan

次要结局

  • Overall Survival(Participants should be followed continuously during 5 years)
  • Cancer Specific Survival(Participants should be followed continuously during 5 years)
  • Renal treatment-related adverse events(Participants should be followed continuously during 5 years)
  • Metastases-Free Survival(Participants should be followed continuously during 5 years)
  • Non-Renal treatment-related adverse events(Participants should be followed continuously during 5 years)

研究者

发起方
Consorci Sanitari de Terrassa
申办方类型
Other
责任方
Principal Investigator
主要研究者

Manuel Galdeano-Rubio

Radiation Oncologist, MD, MSc

Consorci Sanitari de Terrassa

研究点 (1)

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