A Study of Cabozantinib and Nivolumab With Radiation Therapy for People With Renal Cell Carcinoma That Has Spread to the Brain

Brain Metastases Clinical Trial

Official title:

Phase 1b Study of the Safety of Concurrent Cabozantinib and Nivolumab With Radiation Therapy for Brain Metastases in Patients With Metastatic Renal Cell Carcinoma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06132945
• Other study ID #: 23-138
• Status: Recruiting
• Phase: Phase 1
• Start date: November 10, 2023
• Est. completion date: November 2027

Study information

• Verified date: May 2024
• Source: Memorial Sloan Kettering Cancer Center
• Contact: Ritesh Kotecha, MD
• Phone: 646-422-4839
• Email: kotechar[@]mskcc.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to find out whether the combination of cabozantinib, nivolumab, and radiation therapy is a safe and effective treatment that causes few or mild side effects in people with renal cell cancer that has spread to the brain. The researches will also look at how the study treatment affects the quality of life of participants. They will measure the quality of life by having participants complete questionnaires.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: November 2027
• Est. primary completion date: November 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Unresectable advanced or metastatic clear cell or non-clear cell RCC; all histologies acceptable except for chromophobe RCC

2. Brain metastases present, meeting the following criteria:

1. At least 1 brain metastasis measuring =0.5cm in any dimension (intracranial RANO-BM measurable disease required)

2. SRS is indicated per treating radiation oncologist

3. Surgical intervention for brain metastases is not planned

3. Able to undergo MRI Brain assessments for radiation planning.

4. Availability of archival tissue that enables the definitive diagnosis of RCC, accompanied by an associated pathology report. If archival tissue cannot be obtained, PI to provide documented confirmation patient can still enroll onto the study. Specimens can be collected by surgical resection or biopsy of the primary tumor or biopsy or resection of a metastatic lesion.

5. Age =18 years

6. KPS = 80

7. Adequate hematologic and end organ function, defined by the following laboratory results obtained within 14 days prior to the first study treatment:

1. ANC = 1500 cells/µL (without granulocyte colony stimulating factor support within 2 weeks prior to Cycle 1, Day 1)

2. WBC counts = 2500/µL

3. Lymphocyte count = 500/µL

4. Platelet count =100,000/µL (without transfusion within 2 weeks prior to Cycle 1, Day 1)

5. Hemoglobin =9.0 g/dL o Patients may be transfused or receive erythropoietic treatment to meet this criterion.

8. AST, ALT, and alkaline phosphatase = 2.5 x ULN, with the following exceptions:

1. Patients with documented liver metastases: AST and/or ALT = 5 x ULN

2. Patients with documented liver or bone metastases: alkaline phosphatase = 5 x ULN

9. Serum bilirubin = 1.5 x ULN

10. Patients with known Gilbert disease who have serum bilirubin level = 3 x ULN may be- enrolled.

11. INR and aPTT = 1.5 x ULN

a. This applies only to patients who are not receiving therapeutic anticoagulation; patients receiving therapeutic anticoagulation should be on a stable dose.

12. Creatinine = 1.5 x ULN or Calculated Creatinine clearance = 30mL/min by institutional standard measurement

13. 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

14. If any Grade =1 toxicities occurred in relation to prior treatment, patients must have recovered to baseline or = Grade 1 unless adverse events are clinically insignificant or stable on supportive medication if needed.

Exclusion Criteria:

1. Prior treatment with cabozantinib for RCC

2. Receipt of any small molecule kinase inhibitor (including investigational) or VEGFtargeted therapy within 2 weeks before the first dose of study treatment

o 2-week washout period was selected in order to facilitate rapid enrollment and treatment of patients given the target population with active brain metastases.

3. Patients requiring whole brain radiotherapy (WBRT).

4. Any prior brain radiotherapy within 28 days prior to enrollment

5. Incomplete healing from prior radiotherapy as determined by the treating radiation oncologist or treating investigator

6. Diagnosis of autoimmune condition that may worsen during immune checkpoint blockade, with the following exceptions:

o Diabetes type I, vitiligo, psoriasis, hypo- or hyperthyroid disease not requiring immunosuppressive treatment are eligible.

7. Any active or suspected autoimmune disease requiring systemic steroids > 10 mg daily prednisone (or equivalent) or other immunosuppression, except for:

• those not expected to reoccur

• Chronic physiologic replacement of =10mg prednisone (or equivalent) for treatment of adrenal insufficiency

• Steroids required for pre-medication reactions

• Local steroid use is permitted (e.g. intranasal, topical, inhaled, or local steroid injection, i.e. intra-articular)

8. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures

9. Uncontrolled hypercalcemia (= 1.5 mmol/L ionized calcium or Ca = 12 mg/dL or corrected serum calcium = ULN) or symptomatic hypercalcemia requiring continued use of bisphosphonate therapy or denosumab

10. Participation in an experimental drug study within 28 days of study enrollment

11. Pregnant and lactating women

12. History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins

13. Significant cardiovascular disease, such as New York Heart Association cardiac disease (Class II or greater), myocardial infarction within the previous 3 months, unstable arrhythmias, unstable angina, or EF < 50%

o 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.

14. Uncontrolled hypertension (>140 mm Hg systolic or >90 mm Hg diastolic) despite optimal antihypertensive treatment

15. QTcF > 500 msec within 28 days before the first dose of study treatment

16. Major surgical procedure within 14 days prior to Cycle 1, Day 1 or anticipation of need for a major surgical procedure during the course of the study

o Patients must have completed wound healing from major or minor surgery before first dose of study treatment

17. History of stroke or transient ischemic attack within 6 months prior to Cycle 1, Day 1

18. Significant vascular disease (e.g., aortic aneurysm requiring surgical repair or recent peripheral arterial thrombosis) within 6 months prior to Cycle 1, Day 1

19. Evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation)

o Clinically significant hematuria, hematemesis, or hemoptysis of >0.5 tsp (2.5ml) of red blood or other history of significant bleeding within 12 weeks before first dose of study treatment.

20. Clinical signs or symptoms of gastrointestinal obstruction or requirement for routine parenteral hydration, parenteral nutrition, or tube feeding

21. Evidence of abdominal free air not explained by paracentesis or recent surgical procedure

22. Serious, non-healing or dehiscing wound, active ulcer, or untreated bone fracture

23. Concomitant anticoagulation with coumarin agents, direct thrombin inhibitors, factor Xa inhibitor betrixaban, or platelet inhibitors. Other anticoagulants are allowed.

24. Abdominal fistula, GI perforation, bowel obstruction, or intra-abdominal abscess within 6 months before first dose of study treatment.

o Complete healing of intra-abdominal abscess must be confirmed before the first dose of study treatment

25. Cavitating pulmonary lesion(s) or known endotracheal or endobronchial disease manifestation

26. Lesions invading or encasing major blood vessels

27. Uncompensated or symptomatic hypothyroidism

28. History of solid organ or allogeneic stem cell transplant

29. Clinically significant active infection including HIV, Hepatitis B, Hepatitis C, acute COVID-19 infection, or other

• For patients with HIV infection, clinically significant/exclusionary features include: detectable viral load, CD4+ T cell count <300 cells/microL, or history of opportunistic infection

• For patients with HBV infection, clinically significant/exclusionary features include: HBV surface antigen positivity, detectable HBV DNA by polymerase chain reaction (PCR). Patients with prior HBV infection (HBV core Ab positive, HBV DNA undetectable by PCR, HBV surface antigen negative) are eligible for the study if they are already stable on entecavir or tenofovir

30. Inability to swallow tablets

31. Previously identified allergy or hypersensitivity to components of the treatment

32. Malignancy that requires anti-cancer directed therapy within the last 3 years. Exceptions include those cancers that are considered cured by local therapy (e.g. Basal cell carcinoma, squamous cell carcinoma, ductal carcinoma in situ of breast, bladder, or cervix) or other cancers that have low malignant potential and do not require systemic therapy (e.g. Gleason grade <6 prostate adenocarcinoma)

33. Patients in whom nivolumab treatment is not otherwise feasible (for example, for financial reasons)

Related Conditions & MeSH terms

• Brain Metastases
• Brain Neoplasms
• Carcinoma
• Carcinoma, Renal Cell
• Metastatic Renal Cell Carcinoma
• Neoplasm Metastasis

Intervention

Drug:
• Cabozantinib
Cabozantinib (40 mg PO daily)

Device:
• Nivolumab
Nivolumab (480 mg IV Day 1)

Radiation:
• Stereotactic Radiosurgery (SRS)
Radiation will be stereotactic radiosurgery, delivered over 1-5 fractions with a total dose of 18-30Gy depending on fractionation schedule per the discretion of the treating radiation oncologist.

Locations

Country	Name	City	State
United States	Memorial Sloan Kettering Basking Ridge (All Protocol Activities)	Basking Ridge	New Jersey
United States	Memorial Sloan Kettering Cancer Suffolk - Commack (All Protocol Activities)	Commack	New York
United States	Memorial Sloan Kettering Westchester (All Protocol Activities)	Harrison	New York
United States	Memorial Sloan Kettering Monmouth (All Protocol Activities)	Middletown	New Jersey
United States	Memorial Sloan Kettering Bergen (All Protocol Activities)	Montvale	New Jersey
United States	Memorial Sloan Kettering Cancer Center (All Protocol Activities)	New York	New York
United States	Memorial Sloan Kettering Nassau (All Protocol Activities)	Uniondale	New York

Sponsors (2)

Lead Sponsor	Collaborator
Memorial Sloan Kettering Cancer Center	Exelixis

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	percent of enrolled patients who are able to tolerate treatment	56-day safety monitoring period without unacceptable CNS toxicity. Unacceptable CNS toxicity is defined as any grade =3 treatment-emergent neurological disorder, per NCI CTCAE version 5.0 criteria	56-day
Secondary	rate of CNS adverse events	CNS adverse events will be reported as a proportion of patients who experience a CNS adverse event of any grade based on CTCAE 5.0	1 year
Secondary	objective response rate (ORR)	as measured by RANO-BM criteria	1 year

External Links

•   Memorial Sloan Kettering Cancer Center