Nivolumab and Cabozantinib S-malate in Treating Patients with Advanced or Metastatic Kidney Cancer

Status: Active

Description

This phase II trial studies how well nivolumab and cabozantinib s-malate work in treating patients with kidney cancer that has spread to other places in the body. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Cabozantinib s-malate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving nivolumab and cabozantinib s-malate may work better in treating patients with advanced or metastatic kidney cancer.

Eligibility Criteria

Inclusion Criteria

  • Signed and dated Institutional Review Board (IRB)-approved informed consent form
  • Pathologic or histologically confirmed unresectable advanced or metastatic non-clear cell renal cell carcinoma (nccRCC)
  • 0 or 1 prior systemic therapies, including treatment in the adjuvant setting
  • Availability of a representative formalin fixed, paraffin embedded tumor specimen or fresh frozen tissue specimen that enables the definitive diagnosis of RCC, accompanied by an associated pathology report. Specimens can be collected by surgical resection or biopsy of the primary tumor or biopsy or resection of a metastatic lesion
  • Measurable disease, as defined by RECIST 1.1
  • Karnofsky performance status (KPS) >= 70
  • Recovery to baseline or =< grade 1 Common Terminology Criteria for Adverse Events (CTCAE) version (v) 4 from toxicities related to any prior treatments, unless adverse events (AE[s]) are clinically nonsignificant and/or stable on supportive therapy
  • Absolute neutrophil count (ANC) >= 1500 cells/uL (without granulocyte colony stimulating factor support within 2 weeks prior to cycle 1, day 1) (obtained within 14 days prior to the first study treatment)
  • White blood cell (WBC) counts >= 2500/uL and =< 15,000/uL without granulocyte colony-stimulating factor (G-CSF) (obtained within 14 days prior to the first study treatment)
  • Lymphocyte count >= 500/uL (obtained within 14 days prior to the first study treatment)
  • Platelet count >= 100,000/uL (without transfusion within 2 weeks prior to cycle 1, day 1) (obtained within 14 days prior to the first study treatment)
  • Hemoglobin >= 9.0 g/dL (without transfusion within 2 weeks prior to cycle 1, day 1) (obtained within 14 days prior to the first study treatment)
  • Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) =< 3 x upper limit of normal (ULN). ALP =< 5 x ULN if patient has documented bone metastases
  • Serum bilirubin =< 1.5 x ULN. Patients with known Gilbert disease who have serum bilirubin level =< 3 x ULN may be enrolled
  • Serum albumin >= 2.8 g/dl
  • International normalized ratio (INR) and activated partial thromboplastin time (aPTT) =< 1.3 x ULN within 14 days of first dose of study treatment. * This applies only to patients who are not receiving therapeutic anticoagulation; patients receiving therapeutic anticoagulation should be on a stable dose
  • Creatinine =< 2.0 x ULN or calculated creatinine clearance >= 30 mL/min
  • For women who are not postmenopausal (12 months of amenorrhea) or surgically sterile (absence of ovaries and/or uterus): agreement to use two adequate methods of contraception, including at least one method with a failure rate of =< 1% per year
  • Urine protein/creatinine ratio (UPCR) =< 1 mg/mg (=< 113.2 mg/mmol)
  • Sexually active fertile subjects and their partners must agree to use medically accepted methods of contraception (eg, barrier methods, including male condom, female condom, or diaphragm with spermicidal gel) during the course of the study and for 5 months after the last dose of study treatment for females and 7 months for males
  • Female subjects of childbearing potential must not be pregnant at screening. Females of childbearing potential are defined as premenopausal females capable of becoming pregnant (ie, females who have had any evidence of menses in the past 12 months, with the exception of those who are surgically sterile as described above). However, women who have been amenorrheic for 12 or more months are still considered to be of childbearing potential if the amenorrhea is possibly due to prior chemotherapy, antiestrogens, low body weight, ovarian suppression or other reasons
  • Capable of understanding and complying with the protocol requirements and must have signed the informed consent document

Exclusion Criteria

  • Prior treatment with an immunotherapy agent including high dose IL-2, anti-CTLA4, anti-PD1, and anti-PD-L1 agents
  • Prior treatment with cabozantinib for non-clear cell RCC
  • Receipt of any type of small molecule kinase inhibitor within 2 weeks of treatment
  • Receipt of any type of anti-cancer antibody, cytotoxic anticancer therapy, or any other investigational agents within 4 weeks of treatment start
  • Known malignancies of the brain or spinal cord or leptomeningeal disease
  • Patients requiring pain medication must be on a stable regimen at study entry
  • Any condition requiring systemic treatment with corticosteroids (> 10 mg daily prednisone equivalents) or other immunosuppressive medications within 14 days prior to first dose of study drug. Inhaled steroids and adrenal replacement steroids > 10 mg daily prednisone equivalents are allowed in the absence of autoimmune disease
  • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures (once monthly or more frequently)
  • Uncontrolled hypercalcemia (>= 1.5 mmol/L ionized calcium or calcium [Ca] >= 12 mg/dL or corrected serum calcium >= ULN) or symptomatic hypercalcemia requiring continued use of bisphosphonate therapy or denosumab
  • Diagnosis of another malignancy within 2 years before first dose of study treatment, except for superficial skin cancers, or localized, low grade tumors deemed cured and not treated with systemic therapy
  • Pregnant and lactating women
  • History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins
  • History of human immunodeficiency virus (HIV) infection
  • Patients with active or chronic hepatitis B or hepatitis C infection
  • Significant cardiovascular disease, such as New York Heart Association cardiac disease (class II or greater), myocardial infarction within the previous 6 months, unstable arrhythmias, unstable angina, or ejection fraction (EF) < 50%
  • Uncontrolled hypertension defined as sustained blood pressure (BP) > 150 mm Hg systolic or > 100 mm Hg diastolic despite optimal antihypertensive treatment
  • Patients with known coronary artery disease, congestive heart failure not meeting the above criteria must be on a stable medical regimen that is optimized in the opinion of the treating physician, in consultation with a cardiologist if appropriate
  • Major surgery (eg, gastrointestinal [GI] surgery, removal or biopsy of brain metastasis) within 8 weeks before first dose of study treatment. Complete wound healing from major surgery must have occurred 1 month before first dose and from minor surgery (eg, simple excision, biopsy, tooth extraction) at least 10 days before first dose. Subjects with clinically relevant ongoing complications from prior surgery are not eligible
  • History of stroke or transient ischemic attack within 6 months prior to cycle 1, day 1
  • Significant vascular disease (e.g., aortic aneurysm requiring surgical repair or recent peripheral arterial thrombosis) within 6 months prior to cycle 1, day 1
  • Evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation)
  • Clinical signs or symptoms of gastrointestinal obstruction or requirement for routine parenteral hydration, parenteral nutrition, or tube feeding
  • Evidence of abdominal free air not explained by paracentesis or recent surgical procedure
  • Patients with a history of abdominal fistula, gastrointestinal perforation, or intraabdominal abscess within 6 months prior to study enrollment
  • Other clinically significant disorders that would preclude safe study participation * Serious non-healing wound/ulcer/bone fracture * Uncompensated/symptomatic hypothyroidism * Moderate to severe hepatic impairment (Child-Pugh B or C)
  • Corrected QT interval calculated by the Fridericia formula (QTcF) > 500 ms per electrocardiogram (ECG) within 28 days before first dose of study treatment * Note: If a single ECG shows a QTcF with an absolute value > 500 ms, two additional ECGs at intervals of approximately 3 min must be performed within 30 min after the initial ECG, and the average of these three consecutive results for QTcF will be used to determine eligibility
  • Inability to swallow tablets or capsules
  • Previously identified allergy or hypersensitivity to components of the study treatment formulations
  • Patients with a history of non-compliance to medical regimens or who are considered potentially unreliable or will not be able to complete the entire study
  • Concomitant anticoagulation with oral anticoagulants (eg, warfarin, direct thrombin and Factor Xa inhibitors) or platelet inhibitors (eg, clopidogrel). Allowed anticoagulants are the following: * Low-dose aspirin for cardio protection (per local applicable guidelines) is permitted * Low-dose low molecular weight heparins (LMWH) are permitted * Anticoagulation with therapeutic doses of LMWH is allowed in subjects without known brain metastases who are on a stable dose of LMWH for at least 3 weeks before first dose of study treatment, and who have had no clinically significant hemorrhagic complications from the anticoagulation regimen or the tumor
  • Clinically significant hematuria, hematemesis, or hemoptysis of > 0.5 teaspoon (2.5 ml) of red blood, or other history of significant bleeding (eg, pulmonary hemorrhage) within 12 weeks before first dose
  • Cavitating pulmonary lesion(s) or known endotracheal or endobronchial disease manifestation
  • The subject has tumor invading or encasing any major blood vessels
  • The subject has evidence of tumor invading the GI tract (esophagus, stomach, small or large bowel, rectum or anus), or any evidence of endotracheal or endobronchial tumor within 28 days before the first dose of cabozantinib
  • Radiation therapy for bone metastasis within 2 weeks, any other radiation therapy within 4 weeks before first dose of study treatment. Systemic treatment with radionuclides within 6 weeks before the first dose of study treatment. Subjects with clinically relevant ongoing complications from prior radiation therapy are not eligible. Radiation for palliation is allowable on study

Locations & Contacts

New Jersey

Basking Ridge
Memorial Sloan Kettering Basking Ridge
Status: Active
Contact: Chung-Han (Joe) Lee
Phone: 646-422-4545
Email: leec4@mskcc.org
Middletown
Memorial Sloan Kettering Monmouth
Status: Active
Contact: Chung-Han (Joe) Lee
Phone: 646-422-4545
Email: leec4@mskcc.org
Montvale
Memorial Sloan Kettering Bergen
Status: Active
Contact: Chung-Han (Joe) Lee
Phone: 646-422-4545
Email: leec4@mskcc.org

New York

Commack
Memorial Sloan Kettering Commack
Status: Active
Contact: Chung-Han (Joe) Lee
Phone: 646-422-4545
Email: leec4@mskcc.org
New York
Memorial Sloan Kettering Cancer Center
Status: Active
Contact: Chung-Han (Joe) Lee
Phone: 646-422-4545
Email: leec4@mskcc.org
Uniondale
Memorial Sloan Kettering Nassau
Status: Active
Contact: Chung-Han (Joe) Lee
Phone: 646-422-4545
Email: leec4@mskcc.org
West Harrison
Memorial Sloan Kettering Westchester
Status: Active
Contact: Chung-Han (Joe) Lee
Phone: 646-422-4545
Email: leec4@mskcc.org

Trial Objectives and Outline

PRIMARY OBJECTIVE:

I. To evaluate the efficacy of combining cabozantinib s-malate (cabozantinib) and nivolumab in patients with advanced or metastatic renal cell carcinoma (RCC) of non-clear cell histology.

SECONDARY OBJECTIVES:

I. Progression free survival (PFS) and overall survival (OS).

II. Evaluate the objective response rate (ORR) by immune related Response Evaluation Criteria in Solid Tumors (irRECIST).

III. To investigate the safety of cabozantinib and nivolumab in patients with advanced RCC of non-clear cell histology.

IV. To prospectively bank blood and tumor samples to later develop biomarkers for treatment response.

V. Safety and efficacy of prophylactic clobetasol on prevention of cabozantinib associated palmar-plantar erythrodysesthesia syndrome.

VI. Changes in quality of life (QOL) according to the Hand-Foot Syndrome-14 (HFS14) questionnaire.

OUTLINE:

Patients receive cabozantinib s-malate orally (PO) once daily (QD) on days 1-28 and nivolumab intravenously (IV) over 30-60 minutes on days 1 and 15. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also apply clobetasol topically twice daily (BID) for the first 12 weeks in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 30-37 and 100 days and then periodically thereafter.

Trial Phase & Type

Trial Phase

Phase II

Trial Type

Treatment

Lead Organization

Lead Organization
Memorial Sloan Kettering Cancer Center

Principal Investigator
Chung-Han (Joe) Lee

Trial IDs

Primary ID 18-254
Secondary IDs NCI-2018-01907
Clinicaltrials.gov ID NCT03635892