Phase Ib Feasibility Trial of Neoadjuvant Nivolumab/Lirilumab in Cisplatin-Ineligible Muscle-Invasive Bladder Cancer

Uncategorized

Phase Ib Feasibility Trial of Neoadjuvant Nivolumab/Lirilumab in Cisplatin-Ineligible Muscle-Invasive Bladder Cancer

Condition: Bladder Cancer

Intervention:

  • Drug: Nivolumab
  • Drug: Nivolumab/Lirilumab

Purpose: Patients with muscle-invasive bladder cancer (MIBC) who can not receive cisplatin therapy will receive nivolumab or nivolumab/lirilumab before a planned surgical procedure called a radical cystectomy (RC) to remove the bladder. Nivolumab works by attaching to and blocking a molecule called Programmed Death-1 (PD-1). Lirilumab attaches to and blocks a group of molecules called Killer Cell Immunoglobulin-Like Receptor (KIR). PD-1 and KIR are proteins present mainly on immune system cells, and each controls part of the immune system by shutting it down. It is hoped that by binding to and inactivating these proteins, these drugs can enhance the body’s ability to detect, attack and destroy cancer cells. The purpose of this research study is to see whether nivolumab alone or combination of nivolumab and lirilumab given before surgery is effective in treating people who have bladder cancer, and to examine the side effects, good and bad, associated with nivolumab and lirilumab.

Study Type: Interventional

Clinical Trials Identifier NCT 8-digits: NCT03532451

Sponsor: PrECOG, LLC.

Primary Outcome Measures:

  • Measure: Number of Participants with Treatment-Related Adverse Events as Assessed by CTCAE V5.0
  • Time Frame: 30 months
  • Safety Issue:

Secondary Outcome Measures:

  • Measure: Change in CD8+ Tumor-Infiltrating Lymphocytes (TIL) Density
  • Time Frame: 54 months
  • Safety Issue:
  • Measure: Percent Change in CD8+ TIL Density
  • Time Frame: 54 months
  • Safety Issue:
  • Measure: Number of Patients unable to undergo RC
  • Time Frame: 30 months
  • Safety Issue:
  • Measure: Complete Response Rate
  • Time Frame: 30 months
  • Safety Issue:
  • Measure: Recurrence-Free Survival (RFS)
  • Time Frame: 54 months
  • Safety Issue:
  • Measure: Immunohistochemistry (IHC) Change
  • Time Frame: 54 months
  • Safety Issue:
  • Measure: Peripheral Blood Mononuclear Cell (PBMC) T-Cell Subset Change
  • Time Frame: 54 months
  • Safety Issue:

Estimated Enrollment: 43

Study Start Date: March 22, 2019

Phase: Phase 1

Eligibility:

  • Age: minimum 18 Years maximum N/A
  • Gender: All

Criteria: – Patients must have histologically confirmed MIBC (T2-T4a, N0-N1, M0 per American Joint Commission on Cancer [AJCC]) pure or mixed histology urothelial carcinoma. Clinical node-positive (N1) patients are eligible provided the lymph nodes (LNs) are confined to the true pelvis and are within the planned surgical LN dissection template. – The initial TURBT that showed muscularis propria invasion should be within 8 weeks prior to beginning study therapy. Patients must have sufficient baseline tumor tissue from either initial or repeat TURBTs. The local site pathologist will be asked to estimate and record the rough approximate percentage of viable tumor in the TURBT sample (initial or repeat TURBT with highest tumor content) to document at least 20% viable tumor content prior to registration. – Patients must be ineligible for cisplatin-based chemotherapy due to any of the following: – Creatinine clearance(CrCl) <60 mL/min with Easter Cooperative Oncology Group (ECOG) Performance Status (PS) 0-1 – Hearing impaired ≥ Grade 2 by CTCAE criteria – Neuropathy ≥ Grade 2 by CTCAE criteria – Heart failure New York Heart Association (NYHA) ≥ III – Patients must be medically fit for TURBT and RC. – Age ≥ 18 years. – Ability to understand and willingness to sign Institutional Review Board (IRB)-approved informed consent. – Willing to provide tumor tissue, blood, and urine samples for research. – Adequate organ function as measured by the following criteria, obtained ≤ 4 weeks prior to registration: – Absolute Neutrophil Count (ANC) ≥ 1000/mm³ (stable off growth factor within 4 weeks of first study drug administration) – Platelets ≥ 100,000/mm³ – Hemoglobin ≥ 8 g/dL – Serum Creatinine Clearance ≥ 30 mL/min using the Cockcroft-Gault formula – Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) ≤ 3x Upper Limit of Normal (ULN) – Total Bilirubin ≤ 1.5x ULN (in the absence of previously diagnosed Gilbert’s disease) – Women must not be pregnant or breastfeeding since we do not know the effects of nivolumab and lirilumab on the fetus or breastfeeding child. – Sexually active women of child-bearing potential with a non-sterilized male partner and sexually active men must agree to use 2 methods of adequate contraception (hormonal plus barrier or 2 barrier forms) OR abstinence prior to study entry, for the duration of study participation, and for 5 months for women and 7 months for men following last dose of study drugs. – Active or prior documented autoimmune disease within the past 2 years prior to Screening or other immunosuppressive agent within 14 days of study treatment. – Patients may not have locally advanced unresectable or metastatic urothelial carcinoma as assessed on baseline radiographic imaging obtained within 28 days prior to study registration. – Patients may not have concurrent upper urinary tract (i.e. ureter, renal pelvis) invasive urothelial carcinoma. Patients with history of non-invasive (Ta, Tis) upper tract urothelial carcinoma that has been definitively treated with at least one post-treatment disease assessment (i.e. cytology, biopsy, imaging) that demonstrates no evidence of residual disease are eligible. – Patients may not have another malignancy that could interfere with the evaluation of safety or efficacy of the study drugs. Patients with a prior malignancy will be allowed without study chair approval in the following circumstances: – Not currently active and diagnosed at least 3 years prior to the date of registration. – Non-invasive diseases such as low risk cervical cancer or any cancer in situ. – Localized (early stage) cancer treated with curative intent (without evidence of recurrence and intent for further therapy), and in which no chemotherapy was indicated.(e.g. low/intermediate risk prostate cancer, etc.). – Patients may not have received any prior immune checkpoint inhibitor (i.e. anti-KIR, anti-PD-1, anti-PD-L1, or other). – Patients may not have undergone major surgery (e.g. intra-thoracic, intra-abdominal or intra-pelvic), open biopsy or significant traumatic injury or specific anti-cancer treatment ≤ 4 weeks prior to starting study drug, or patients who have had percutaneous biopsies or placement of vascular access device ≤ 1 week prior to starting study drug, or who have not recovered from side effects of such procedure or injury. – Patients must not have clinically significant cardiac disease. – Patients may not have chronic active liver disease or evidence of acute or chronic Hepatitis B Virus (HBV) or Hepatitis C (HCV). – Patients may not have known diagnosis of human immunodeficiency virus (HIV) infection. Testing is not required in absence of clinical suspicion. – Patients may not have known diagnosis of any condition (e.g. post-hematopoietic or solid organ transplant, pneumonitis, inflammatory bowel disease, etc.) that requires chronic immunosuppressive therapy. Usage of non-steroidal anti-inflammatory medications (NSAIDS) for the treatment of osteoarthritis and uric acid synthesis inhibitors for the treatment of gout are permitted. – Patients with any serious and/or uncontrolled concurrent medical conditions (e.g. active or uncontrolled infection, uncontrolled diabetes) or psychiatric illness that could, in the investigator’s opinion, cause unacceptable safety risks or potentially interfere with the completion of the treatment according to the protocol are not eligible. – Patients may not have any live viral vaccine used for prevention of infectious diseases within 4 weeks prior to study drug(s). – Patients unwilling or unable to comply with the protocol.

Contact:

  • Carolyn Andrews, RN
  • 267-207-4070

Locations:

  • Moffitt Cancer Center
  • Tampa Florida 33612 United States
  • Montefiore Medical Center
  • Bronx New York 10461 United States
  • Oregon Health & Science University
  • Portland Oregon 97239 United States
  • University of TX Southwestern
  • Dallas Texas 75390 United States
  • University of Virginia
  • Charlottesville Virginia 22903 United States
  • University of Washington
  • Seattle Washington 98109 United States

View trial on ClinicalTrials.gov

X