Deferred Cytoreductive Nephrectomy in Synchronous Metastatic Renal Cell Carcinoma: The NORDIC-SUN-Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNiels Fristrup

About this trial

BACKGROUND: For synchronous metastatic renal cell carcinoma (RCC), surgical resection of the primary tumor in the presence of distant metastases has been the standard of therapy for select patients followed by systemic therapy. In the era of TKIs two randomized trials, CARMENA and SURTIME, have questioned the role and timing of surgery in these patients, results point towards no surgery or a deferred approach.

RATIONALE: The antitumor activity of immune checkpoint blockage (ICB) is more potent than other therapy in mRCC. The deferred cytoreductive nephrectomy approach ensures systemic therapy for all patients, avoid systemic treatment delay, and spare surgery in patients with progressive tumors. Current data only point towards a survival benefit for cytoreductive nephrectomy in intermediate risk patients, but not in poor risk patients

HYPOTHESIS: Deferred cytoreductive nephrectomy after initial nivolumab combined with ipilimumab or a TKI/IO-combination will improve OS in patients with synchronous metastatic RCC and ≤3 IMDC risk features

This is an open, randomized, multicenter comparison trial, designed to evaluate the effect of deferred cytoreductive nephrectomy compared with no surgery following initial nivolumab combined with ipilimumab or a TKI-combination, in mRCC patients with IMDC intermediate and poor risk.

Eligibility criteria

Qualifiers

Signed written informed consent obtained prior to any study specific procedures.

Patient must be willing and able to comply with the protocol.

Age ≥18.

Core needle biopsy proven metastatic renal cell carcinoma - all histologic subtypes acceptable.

Disqualifiers

Prior systemic treatment for mRCC

Other cancer within 3 years (except in situ basal cell carcinoma and localised prostate cancer with undetectable PSA).

Major surgical procedure, open surgical biopsy, or significant traumatic injury within 28 days prior to enrollment

Clinically significant (i.e active) cardiovascular disease for example cerebrovascular accidents (< 6 months before inclusion), myocardial infarction (< 6 months before inclusion), unstable angina, New York Heart Association (NYHA) grade II or greater congestive heart failure.

Trial design

Treatments tested in this trial

  • Cytoreductive nephrectomy
  • Tissue sampling

Treatment groups

400 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Niels Fristrup

Lead sponsor

Aarhus University Hospital

Sponsor institution

Aarhus University Hospital

Collaborator