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

NCT ID: NCT03066427

Last Updated: 2020-11-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-05-10
• Study Completion Date: 2020-09-22

Brief Summary

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.

Conditions

Clear Cell Renal Carcinoma

Keywords

Clear Cell Renal Carcinoma; Sunitinib

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Sunitinib

Sunitinib 50 mg/day, 4 weeks on/2weeks off

Group Type: EXPERIMENTAL

Sunitinib

Intervention Type: DRUG

Sunitinib 50 mg/d

Interventions

Sunitinib

Sunitinib 50 mg/d

Intervention Type: DRUG

Other Intervention Names

Sutent

Eligibility Criteria

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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Pfizer

INDUSTRY

Sponsor Role: collaborator

Apices Soluciones S.L.

INDUSTRY

Sponsor Role: collaborator

Spanish Oncology Genito-Urinary Group

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Enrique Grande, MD

Role: STUDY_CHAIR

MD Anderson Cancer Center Madrid

Cristina Suárez, MD

Role: PRINCIPAL_INVESTIGATOR

Hospital Vall d'Hebron

Xavier García del Muro, MD

Role: PRINCIPAL_INVESTIGATOR

Hestia Duran i Reynals

Oscar Reig, MD

Role: PRINCIPAL_INVESTIGATOR

Hospital Clínic i Provincial de Barcelona

María J Méndez, MD

Role: PRINCIPAL_INVESTIGATOR

Complejo Hospitalario Regional Reina Sofia

Daniel Castellano, MD

Role: PRINCIPAL_INVESTIGATOR

Hospital Universitario 12 de Octubre

Teresa Alonso, MD

Role: PRINCIPAL_INVESTIGATOR

Hospital Universitario Ramon y Cajal

Locations

ICO Duran i Reynals

L'Hospitalet de Llobregat, Barcelona, Spain

Hospital Universitari Vall d'Hebron

Barcelona, , Spain

Hospital Clínic i Provincial de Barcelona

Barcelona, , Spain

Complejo Hospitalario Regional Reina Sofía

Córdoba, , Spain

Hospital Ramón Y Cajal

Madrid, , Spain

Hospital Universitario 12 de Octubre

Madrid, , Spain

Centro Integral Oncologico Clara Campal

Madrid, , Spain

MD Anderson Cancer Center Madrid

Madrid, , Spain

Hospital Central de Asturias

Oviedo, , Spain

Countries

Spain

Other Identifiers

2016-004011-12

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

SOGUG-2016-A- IEC(REN)-10

Identifier Type: -

Identifier Source: org_study_id