Botensilimab and Balstilimab versus Nivolumab and Ipilimumab for the Treatment Advanced Clear Cell Renal Cell Carcinoma, ARCITECT Trial
This phase II trial tests how well botensilimab and balstilimab versus nivolumab and ipilimumab works to treat patients with clear cell renal cell carcinoma that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Immunotherapy with monoclonal antibodies, such as botensilimab, balstilimab, nivolumab and ipilimumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. They work by binding to a substance in the body, including tumor cells, to help the body's immune system kill the tumor cells. Combination nivolumab and ipilimumab is the standard frontline treatment for patients with advanced clear cell carcinoma; however, even with good initial response, most patients still progress on this therapy. Giving botensilimab and balstilimab may be more safe and effective than standard treatment for patients with advanced clear cell renal cell carcinoma.
Inclusion Criteria
- Patient must have Eastern Cooperative Oncology Group (ECOG) performance status (PS) of ≤ 2 within 28 days of cycle 1 day 1 (C1D1)
- Age ≥ 18 years old at the time of informed consent
- Patient must have histological confirmation of renal carcinoma (RCC) with clear cell component including advanced RCC (not amenable to curative surgery or radiation therapy) or metastatic RCC
- Patient must have measurable disease by CT or MRI per Response Evaluation Criteria in Solid Tumors (RECIST 1.1) criteria. Radiated lesions cannot be used as measurable lesions unless there is clear evidence of progression
- Patient must have defined International Metastatic RCC Database Consortium (IMDC) risk categorization of either favorable, intermediate or poor based on clinical variables of increased risk (below). * No risk factors (0) = favorable risk * 1-2 risk factors = intermediate risk * ≥ 3 risk factors = poor risk NOTE: Patients with all IMDC risk factors are eligible, but will be stratified according to IMDC risk, and initial analysis will be based on the IMDC intermediate and poor risk patients. IMDC Risks: * Karnofsky PS (KPS) less than 80% * Less than 1 year from diagnosis including original localized disease to randomization (if applicable) * Hemoglobin less than the lower limit of normal * Corrected calcium concentration greater than 10 mg/dL * Absolute neutrophil count (ANC) greater than the upper limit of normal (ULN) * Platelet count greater than the ULN
- Patient must have either a formalin-fixed, paraffin-embedded (FFPE) tissue block or unstained tumor tissue sections, obtained from a metastatic lesion, preferably within 3 months or no more than 12 months with an associated pathology report. This tissue must be identified prior to registration. Confirmation of sufficient archival tissue must be obtained after informed consent and the tissue must be shipped to the appropriate lab by end of cycle 2. Biopsies should be excisional, incisional, or core needle. Fine needle aspiration is unacceptable for submission. Biopsies of bone lesions that do not have a soft tissue component are also unacceptable for submission. This sample is required to be eligible for the trial. If a patient is having a standard of care biopsy, part of that sample may be utilized for eligibility
- White blood cell (WBC) ≥ 2,000/uL within 28 days prior to registration
- ANC ≥ 1,000/uL; without growth factor support (within 28 days prior to registration)
- Hemoglobin (Hgb) ≥ 8.0 g/dL; ≥ 7 days without packed red blood cell (PRBC) transfusion (within 28 days prior to registration)
- Platelets ≥ 75,000/uL; without platelet transfusion (within 28 days prior to registration)
- Calculated creatinine clearance (CrCl)* ≥ 40 mL/min (within 28 days prior to registration) * Cockcroft-Gault formula will be used to calculate creatinine clearance
- Total bilirubin ≤ 1.5 × upper limit of normal (ULN) (within 28 days prior to registration) *EXCEPT participants with Gilbert syndrome who must have a total bilirubin level of < 3.0 x ULN
- Aspartate aminotransferase (AST) ≤ 3.0 × ULN (within 28 days prior to registration)
- Alanine aminotransferase (ALT) ≤ 3.0 × ULN (within 28 days prior to registration)
- Human immunodeficiency virus (HIV) positive patients may be eligible if either: * Patients with CD4 > 200 cells/mm3 OR * Patients with HIV viral load undetectable
- Active hepatitis B virus (HBV) or active hepatitis C virus (HCV) patients may be eligible if: * Patients with HBV infection are eligible if hepatitis B surface antigen and HBV deoxyribonucleic acid (DNA) are negative * Patients with HCV infection are eligible if HCV ribonucleic acid (RNA) is negative
- Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]) within 1 week prior to cycle 1 day 1
- WOCBP must agree to follow instructions for method(s) of contraception
- Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception
Exclusion Criteria
- Prior adjuvant or systemic therapy for RCC
- Prior treatment with an anti-PD1 or anti-PDL1 agent, anti-CTLA4 antibody or a vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitor (TKI) or anti-VEGF antibody including in the adjuvant setting
- Radiotherapy within 2 weeks prior to cycle 1 day 1
- Expected to require any other form of systemic or localized antineoplastic therapy while on trial (including maintenance therapy with another agent, radiation therapy, and/or surgical resection)
- Currently known active and definitive central nervous system (CNS) metastases. Patients who have treated brain metastases (with either surgical resection or stereotactic radiosurgery (SRS)) may be eligible. Patients must not have taken any steroids ≤ 2 weeks prior to randomization for the purpose of managing their brain metastases. Repeat imaging after SRS or surgical resection is not required so long as baseline MRI is within 4 weeks of registration. Patients with multiple brain metastases treated with SRS (with or without whole brain radiotherapy [WBRT]), are not excluded. Patients with definitive CNS metastases treated with only WBRT are ineligible. Patients with potential CNS metastases that are too small for treatment with either SRS or surgery (e.g. 1-2 mm) and/or are of uncertain etiology are potentially eligible, but need to be discussed with and approved by the sponsor-investigator
- Persistent toxicity of National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 grade > 1 severity that is related to prior therapy. NOTE: Sensory neuropathy or alopecia of grade ≤ 2 are acceptable
- Known severe (grade ≥ 3) hypersensitivity reactions to fully human monoclonal antibodies, antibody, or severe reaction to immuno-oncology agents, such as colitis or pneumonitis requiring treatment with steroids; or has a history of interstitial lung disease, any history of anaphylaxis, or uncontrolled asthma
- Known condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days of randomization. Inhaled or topical steroids, and adrenal replacement steroid doses <10 mg daily prednisone equivalent are permitted in the absence of active autoimmune disease. NOTE: Corticosteroid use as a premedication for IV contrast allergies/reactions is allowed
- Active known or suspected autoimmune disease that required systemic treatment within 2 years of the start of study drug (i.e., with use of disease-modifying agents, corticosteroids, or immunosuppressive drugs). Subjects with type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger (e.g., celiac disease) are permitted to enroll
- Uncontrolled adrenal insufficiency based on investigator discretion
- Active infection requiring systemic therapy within 14 days of cycle 1 day 1
- Clinically significant (i.e., active) cardiovascular disease: cerebral vascular accident/stroke or myocardial infarction within 6 months of enrollment, unstable angina, congestive heart failure (New York Heart Association class ≥ II), or serious uncontrolled cardiac arrhythmia requiring medication
- Legally incapacitated or has limited legal capacity
- Pregnant or breastfeeding
- Prior allogeneic tissue/solid organ transplant, except for corneal transplants
- Major surgery (e.g., nephrectomy) less than 28 days prior to cycle 1 day 1
- Prior malignancy active within the previous 2 years from screening except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast
- Any condition including medical, emotional, psychiatric, or logistical that, in the opinion of the Investigator, would preclude the participant from adhering to the protocol or would increase the risk associated with study participation or study treatment administration or interfere with the interpretation of safety results
- Receipt of a live/attenuated vaccine within 30 days of first study treatment. The use of inactivated seasonal influenza vaccines (eg, Fluzone®) will be permitted on study without restriction
Additional locations may be listed on ClinicalTrials.gov for NCT05928806.
See trial information on ClinicalTrials.gov for a list of participating sites.
PRIMARY OBJECTIVE:
I. Determine the objective response rate (ORR) of botensilimab + balstilimab in patients with treatment naïve metastatic clear cell renal cell carcinoma (ccRCC) relative to the ORR of patients treated with nivolumab + ipilimumab.
SECONDARY OBJECTIVES:
I. Determine duration of response (DOR) for patients who have a complete response (CR) or partial response (PR).
II. Determine the 12- & 24-month landmark progression free survival (PFS).
III. Determine treatment free survival (TFS).
IV. Determine the safety of botensilimab + balstilimab relative to nivolumab + ipilimumab.
EXPLORATORY OBJECTIVES:
I. Evaluate the relationship between percentage of regulatory T cell (Treg) and efficacy outcomes (ORR, landmark PFS, TFS).
II. Evaluate existing predictive/associated biomarker models for efficacy of the two regimens.
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM A INDUCTION: Patients receive botensilimab intravenously (IV) over 30 minutes on days 1 and 22 of cycle 1 and balstilimab IV over 30 minutes on days 1 and 22 of cycles 1 and 2. Treatment repeats every 6 weeks for up to 2 cycles in the absence of disease progression or unacceptable toxicity.
ARM A MAINTENANCE: Patients receive botensilimab IV over 30 minutes on day 1 of cycles 3-4 and balstilimab IV over 30 minutes on days 1, 22, 43 and 64 of cycles 3-9. Treatment repeats every 12 weeks for up to 7 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo computed tomography (CT) scan and/or magnetic resonance imaging (MRI), as well as blood sample collection throughout the study.
ARM B INDUCTION: Patients receive nivolumab IV over 30 minutes and ipilimumab IV over 30 minutes on days 1 and 22 of each cycle. Treatment repeats every 6 weeks for up to 2 cycles in the absence of disease progression or unacceptable toxicity.
ARM B MAINTENANCE: Patients receive nivolumab IV over 30 minutes on days 1, 29 and 57 of each cycle. Treatment repeats every 12 weeks for up to 7 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan and/or MRI as well as blood sample collection throughout the study.
After completion of study treatment, patients are followed up at 30 and 90 days, and then every 3 months for 3 years from start of study treatment and then every 6 months until 5 years from start of study treatment.
Trial PhasePhase II
Trial Typetreatment
Lead OrganizationMedStar Georgetown University Hospital
Principal InvestigatorMichael B. Atkins
- Primary IDSTUDY00006333
- Secondary IDsNCI-2023-08597
- ClinicalTrials.gov IDNCT05928806