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Active, Not Recruiting

NCT Number: NCT02306954

Study of High Dose Interleukin-2 (IL-2) and Stereotactic Body Radiation (SBRT) in Patients With Metastatic Renal Cancer

All patients will receive IL-2 (14 planned doses with an additional cycle 14 days after the first). Responding patients with regressing disease are eligible for up to 6 IL-2 cycles. Patients assigned to SBRT arm will receive two doses of SBRT on the Wednesday and Friday before the Monday on which IL-2 starts.

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This study is active but is not currently recruiting participants.

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Key information

About this study

All patients will receive IL-2 at 600,000 international units per kilogram (kg) by intraveneous bolus (IVB) every 8 hours for 14 planned doses with an additional cycle 14 days after the first. Responding patients with regressing disease are eligible for up to 6 IL-2 cycles. Patients assigned to SBRT arm will receive two doses of SBRT at 20 Gray (Gy) on the Wednesday and Friday before the Monday on which IL-2 starts.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histological confirmation of predominant conventional (clear cell) renal cancer
  • Patients must be ≥ 18 years of age
  • Tumors amenable to SBRT in lungs (central locations preferred), mediastinum, chest wall, bones with a soft tissue component (other than long bones), or liver, liver hilum and associated lymph nodes (inclusive of immediately adjacent masses), 1 - 3 foci; no minimum size, but none greater than 7 cm. Patients may have other metastases but only a maximum of 3 will be treated
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
  • Women of childbearing potential must have a negative serum or urine pregnancy test within 72 hours prior to the start of protocol treatment. In addition, women of childbearing potential as well as male patients must agree to take appropriate precautions to avoid pregnancy
  • Patients must agree to participate in the Prometheus IL-2 patient registry (PROCLAIM registry)
  • Patients must sign a study-specific consent form

Exclusion criteria

  • No metastatic site amenable to SBRT
  • Patients with brain metastases not candidates for radiosurgery alone
  • Previous radiation to sites proposed for SBRT
  • Patients with active systemic, pulmonary, or pericardial infection
  • Pregnant or lactating women, as treatment involves unforeseeable risks to the embryo or fetus
  • Evidence of ischemia on exercise tolerance test, stress thallium study, or baseline EKG
  • Clinically significant underlying pulmonary disease as measured by pulmonary function tests
  • Blood tests within protocol-specified range
  • Need for chronic steroids

Treatment and study plan

High dose IL-2

Biological

High Dose IL-2 is approved by the FDA for the treatment of renal cell cancer.

Other names: Proleukin

SBRT

Radiation

Patients assigned to SBRT arm will receive two doses of SBRT at 20 Gy on the Wednesday and Friday before the Monday on which IL-2 starts.

Primary outcomes

  1. Response Rate

    Time frame: 5 years

    The objective of this study is to compare the response rate among renal cell cancer (RCC) patients of high dose IL-2 to SBRT + IL-2 in patients with metastatic renal cancer

Secondary outcomes

  1. Response Rate in Patients Who Receive SBRT following Progression on IL-2

    Time frame: 5 years

    Measure the response of SBRT + IL-2 in patients with RCC who have disease progression after high-dose IL-2

Sponsors and collaborators

Lead sponsor

Providence Health & Services

Other

Collaborators

  • Cytokine Working Group
  • Prometheus Laboratories

Registry information

Official study title

Phase II Randomized Study of High Dose Interleukin-2 Versus Stereotactic Body Radiation (SBRT) and High Dose Interleukin-2 (IL-2) in Patients With Metastatic Renal Cancer

Important dates

Study start
2014
Primary completion
2020
Study completion
2026
First posted
Dec 3, 2014
Registry last updated
Jul 23, 2026

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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