Study to Evaluate Efficacy and Safety of Sunitinib in Renal Cell Carcinoma Progressed to 1L Immunotherapy Treatment. (INMUNOSUN)

Phase II Study to Evaluate Efficacy and Safety of Sunitinib Therapy in Patients With Metastatic Renal Clear Cell Carcinoma Who Have Progressed to First-line Immunotherapy Treatment (INMUNOSUN Study)

The therapeutic scenario of metastatic renal cancer is undergoing a new revolution with the appearance of a novel therapeutic strategy after the antiangiogenic treatments, that is the immunotherapy, in addition to the approval of new active drugs in the following lines of treatment.

There are currently two phase III trials in the first line of treatment in metastatic renal cancer that include different combinations of treatment based on immunotherapy. If results of these studies were positive, the therapeutic algorithm would be modified so that the remaining drugs would have to be repositioned within the therapeutic decision scheme.

Sunitinib has previously demonstrated its benefit in patients who had failed to prior treatment with cytokines, so it is likely to continue to be effective in patients who have become resistant to treatment with new drugs based on immune checkpoint blockade.

This phase II study is developed to evaluate the activity of sunitinib after treatment with immunotherapy-based regimens that are currently being developed within phase III clinical trials.

Study Overview

• Status: Completed
• Conditions: Clear Cell Renal Carcinoma
• Intervention / Treatment: Drug: Sunitinib

• Study Type: Interventional
• Enrollment (Actual): 23
• Phase: Phase 2

Contacts and Locations

Study Locations

• Spain
  • Barcelona, Spain, 08035
    • Hospital Universitari Vall d'Hebron
  • Barcelona, Spain, 08036
    • Hospital Clinic i Provincial de Barcelona
  • Córdoba, Spain, 14004
    • Complejo Hospitalario Regional Reina Sofía
  • Madrid, Spain, 28041
    • Hospital Universitario 12 de Octubre
  • Madrid, Spain, 28034
    • Hospital Ramon y Cajal
  • Madrid, Spain
    • Centro Integral Oncologico Clara Campal
  • Madrid, Spain
    • MD Anderson Cancer Center Madrid
  • Oviedo, Spain
    • Hospital Central de Asturias
  • Barcelona
    • L'Hospitalet de Llobregat, Barcelona, Spain, 08908
      • ICO Duran i Reynals

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• 1. Eighteen years or older on the day of consent
• 2. Documented histological or cytological diagnosis of renal cell cancer with a clear-cell component.
• 3. Patient must have progressed to at least one immune check point inhibitor-based therapy (antiPD1, anti-PDL1 o antiCTLA4) for the first line
• 4. Measurable disease per RECIST 1.1 as determined by the investigator
• 5. The subjects should not present disease that may be subsidiary of surgical treatment, radiotherapy or combined treatment with curative intent.
• 6. Recovery of toxicities related to any prior treatments to ≤ Grade 1 CTCAE v.4.03, unless adverse event(s) are clinically nonsignificant and/or stable on supportive therapy.
• 7. Eastern Cooperative Oncology Group Performance Status (PS) 0-2
• 8. Adequately controlled blood pressure (BP) with or without antihypertensive medication to maintain a BP <150/90 mmHg before the start of study treatment.

• 9. Adequate marrow function

  • Absolute neutrophil count (ANC) ≥ 1500/mm3 (≥ 1.5 GI/L).
  • Platelets ≥ 100,000/mm3 (≥ 100 GI/L).
  • Hemoglobin ≥ 9 g/dL (≥ 5,6 mmol/L).

• 10. Adequate liver function

  • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) < 2.5 × ULN.
  • Total bilirubin ≤ 1.5 × upper limit of normal (ULN).
• 11. Adequate kidney function: calculated creatinine clearance ≥ 30 mL/min (≥ 0.5 mL/sec) using the Cockroft-Gault equation
• 12. Proteinuria <2+ on urine test strip
• 13. Prothrombin Time (PT) or International Standard Ratio (INR) ≤ 1.2 x ULN.
• 14. Life expectancy >3 months.
• 15. Patient able to ingest study drug and meet study follow-up requirements.
• 16. Sexually active fertile subjects and their partners must agree to use medically accepted methods of contraception
• 17. Female subjects of childbearing potential must not be pregnant at screening.

Exclusion Criteria:

• 1. Previous treatments with sunitinib are not permitted for the advanced or localized disease.
• 2. Major surgery within 3 weeks of patient inclusion
• 3. Radiation therapy or embolization within 2 weeks of first dose of sunitinib
• 4. Previous treatment with immunosuppressive drugs such as cyclosporine, tacrolimus, azathioprine, or long-term oral glucocorticoids taken prior to (3 months) patient inclusion
• 5. Prior high-dose chemotherapy requiring hematopoietic stem cell rescue.
• 6. Current treatment on another clinical trial.
• 7. Treatment with known potent CYP3A4 inhibitors or inducers or that prolong the QT interval, within 7 days prior to the inclusion.
• 8. Prior radiation therapy to >25% of the bone marrow.
• 9. Uncontrolled brain metastases, spinal cord compression, carcinomatous meningitis, or leptomeningeal disease.
• 10. Any gastrointestinal malabsorption disorder or any other condition that, in the opinion of the investigator, may affect the absorption of sunitinib or increase the risk of bleeding or perforation.
• 11. Presence of an unhealed wound or active ulcer.
• 12. Diarrhea grade III/IV in the screening period.
• 13. Diagnosis of any second malignancy within the last 3 years, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix.
• 14. Clinically significant cardio-cerebrovascular disease within 6 months prior to initiation of treatment.
• 15. Ongoing cardiac dysrhythmias of NCI CTCAE grade ≥2, atrial fibrillation of any grade that require treatment.
• 16. Corrected QT interval (QTc) interval >500 msec.
• 17. Active hemoptysis within 6 weeks prior to initiation of study treatment.
• 18. Evidence of active bleeding or hemorrhagic diathesis.
• 19. Presence of endobronchial lesions and / or lesions that infiltrate large vessels.
• 20. Current treatment with therapeutic doses of Coumadin (low dose Coumadin up to 2 mg PO daily for deep vein thrombosis prophylaxis is allowed).

• 21. Other clinically significant alterations:

  • Known human immunodeficiency virus (HIV) infection.
  • Presence of an uncontrolled active infection.
  • Presence of uncontrolled or symptomatic hypothyroidism.
  • Moderate-severe liver disease (Child Pugh B-C).
  • Requirement for hemodialysis or peritoneal dialysis.
  • History of solid organ transplantation.
• 22. Pregnancy or breastfeeding.
• 23. Any disease that, in the opinion of the investigator, interferes with the patient's ability to participate in the clinical trial.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Sunitinib; Sunitinib 50 mg/day, 4 weeks on/2weeks off	Drug: Sunitinib; Sunitinib 50 mg/d; Other Names: Sutent

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Objective response rate	Percentage of patients with documented response according RECIST 1.1 criteria (complete response + partial response)	12 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Progression-free survival	Time from start of treatment to disease progression or death.	12 months
Time to progression	Time from start of treatment to disease progression or death due to the illness	12 months
Duration of the response	Time from first response to disease progression or death.	12 months
Overall survival	Time from start of treatment to death.	18 months
Clinical benefit	Percentage of patients with documented response or disease stabilization according RECIST 1.1 criteria	12 months
Number of individual events (hematologic events and not hematologic events)	Percentage of patients with each of the adverse event per grade	12 months

Collaborators and Investigators

• Sponsor: Spanish Oncology Genito-Urinary Group
• Collaborators: Pfizer; Apices Soluciones S.L.
• Investigators: Study Chair: Enrique Grande, MD, MD Anderson Cancer Center Madrid; Principal Investigator: Cristina Suárez, MD, Hospital Vall d'Hebron; Principal Investigator: Xavier García del Muro, MD, Hestia Duran I Reynals; Principal Investigator: Oscar Reig, MD, Hospital Clinic i Provincial de Barcelona; Principal Investigator: María J Méndez, MD, Complejo Hospitalario Regional Reina Sofía; Principal Investigator: Daniel Castellano, MD, Hospital Universitario 12 de Octubre; Principal Investigator: Teresa Alonso, MD, Hospital Universitario Ramon y Cajal

Study record dates

Study Major Dates

• Study Start (Actual): May 10, 2017
• Primary Completion (Actual): September 22, 2020
• Study Completion (Actual): September 22, 2020

Study Registration Dates

• First Submitted: February 23, 2017
• First Submitted That Met QC Criteria: February 23, 2017
• First Posted (Actual): February 28, 2017

Study Record Updates

• Last Update Posted (Actual): November 13, 2020
• Last Update Submitted That Met QC Criteria: November 12, 2020
• Last Verified: October 1, 2020

More Information

Terms related to this study

• Keywords: Clear Cell Renal Carcinoma; Sunitinib
• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Urologic Neoplasms; Urogenital Neoplasms; Neoplasms by Site; Kidney Diseases; Urologic Diseases; Adenocarcinoma; Neoplasms, Glandular and Epithelial; Kidney Neoplasms; Carcinoma, Renal Cell; Carcinoma; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Antineoplastic Agents; Angiogenesis Inhibitors; Angiogenesis Modulating Agents; Growth Substances; Growth Inhibitors; Protein Kinase Inhibitors; Sunitinib
• Other Study ID Numbers: SOGUG-2016-A- IEC(REN)-10; 2016-004011-12 (EudraCT Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No