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临床试验/NCT05941169
NCT05941169尚未招募不适用

A Prospective Study of Primary Metastatic Renal Cell Carcinoma Treated With Immunecheckpoint Inhibitors and Cytoreductive Nephrectomy vs Primary Tumour in Place

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)0 个研究点目标入组 750 人开始时间: 2023年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
750
主要终点
Overall Survival

研究概览

简要总结

The benefit of deferred Cytoreductive Nephrectomy (CN) has to be re-assessed in the context of IO +IO and IO + TKI systemic treatment. Given the benefit of CN in the setting of first generation immunotherapy, it is conceivable that both trials underestimated the benefit of CN, in absence of immunotherapy.

详细描述

In past years, much research has been done into the beneficial effects of cytoreductive nephrectomy in patients with metastatic renal cancer receiving systemic therapy with positive results. In the meantime systhemic therapy, and in particular immunotherapy, have changed. Patients with metastatic renal cancer are increasingly treated with immunocheckpoint inhibitors, but the effect of adding cytoreductive nephrectomy in this group of patients has not yet been investigated. The aim of this study is to investigate whether performing a cytoreductive nephrectomy has a beneficial effect on overall survival in patients with metastatic renal cancer receiving systemic therapy using immunocheckpoint inhibitors.

A randomized controlled trial. All eligible patients have already been enrolled in the PRO-RCC registry, a registry that collects prospective observational data, and have also given consent to be included in other studies as a control cohort. This design is called a TWiC (trial within cohort). After randomization, patients who are randomized into the therapy arm will receive a patient information via their treating physician. Upon participation, an informed consent will be signed and the patient will be scheduled for surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • Male or female patients age ≥ 18 years
  • Signed and written informed consent Note: Written and signed informed consent will be obtained before any study procedures, including study-specific-screening procedures, has been performed.
  • Informed consent obtained for being offered future experimental interventions within the PRO-RCC project.
  • Histologically confirmed diagnosis of metastatic clear cell, papillary or chromophobe renal cell carcinoma of intermediate to poor risk, including sarcomatoid features, with
  • World Health Organization (WHO) performance status of 0-
  • Surgical candidates based on surgeon and anesthetist assessment
  • Treatment with an IO combination (IO+IO or IO+TKI) as standard of care for metastatic RCC
  • Absence of progression at metastatic sites at time of identification (6month after start of systemic first line treatment). 9) Primary tumor in situ 10) Participation in the PRO-RCC prospective cohort.

排除标准

  • 未提供

研究组 & 干预措施

Cytoreductive Nephrectomy

Experimental

Cytoreductive Nephrectomy within 6 months to 1 year after start systemic therapy for metastatic Renal Cell Carcinoma

干预措施: Cytoreductive Nephrectomy (Procedure)

Standard of Care

No Intervention

Standard of Care for metastatic Renal Cell Carcinoma

结局指标

主要结局

Overall Survival

时间窗: defined as time from randomization to death of any cause during 5 years of follow-up

Overall Survival Using Kaplan Meier Survival analysis

次要结局

  • Surgical morbidity outcomes using Clavien Dindo classification of surgical morbidity(Post operative follow-up period during 5 years)
  • Long term Quality of Life outcomes using validated EORTC Quality of Life Questionnaire (QLQ-C30)(Post operative follow-up period during 5 years)

研究者

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

Adriaan D. Bins

Principal Investigator

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

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