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NCT Number: NCT05941169

Primary Metastatic Renal Cell Carcinoma Treated With Immunecheckpoint Inhibitors and Cytoreductive Nephrectomy

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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 0-1.
  • 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.

Exclusion criteria

NA

Treatment and study plan

Cytoreductive Nephrectomy

Procedure

The experimental intervention consists of cytoreductive nephrectomy (CN) or any ablative local therapy within 6 months and 1 year after start of systemic treatment. All types of ablative local therapy are allowed as a substitute for CN

Primary outcomes

  1. Overall Survival

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

    Overall Survival Using Kaplan Meier Survival analysis

Secondary outcomes

  1. Long term Quality of Life outcomes using validated EORTC Quality of Life Questionnaire (QLQ-C30)

    Time frame: Post operative follow-up period during 5 years

    using the Dutch validated EORTC Quality of Life Questionnaire (QLQ-C30)

  2. Surgical morbidity outcomes using Clavien Dindo classification of surgical morbidity

    Time frame: Post operative follow-up period during 5 years

    Clavien Dindo classification of surgical morbidity is used to classify morbidity outcomes

Other outcomes

  1. Clinical data and annotated tissue for translational research into mechanisms of treatment response and resistance.

    Time frame: post-operative follow-up period during 5 years

    In detail, we will examine the intratumor alteration of tumor infiltrating CD8, CD4, NK(T) cells (CD56+,CD3+-), and the distribution of these NK cells in the tumor, as these cells have been shown to be involved in anti-tumor responses in RCC.

Study contacts

Contact information is provided by the study sponsor or research team.

Adriaan Bins, MD PhD

CONTACT

[email protected]

020 5665955

Axel Bex, MD PhD

CONTACT

[email protected]

020 512 9111

Sponsors and collaborators

Lead sponsor

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

Other

Collaborators

  • Comprehensive Cancer Centre The Netherlands

Registry information

Official study title

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

Acronym: PrimerX

Important dates

Study start
2023
Primary completion
2030
Study completion
2031
First posted
Jul 12, 2023
Registry last updated
Jul 12, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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