Autologous T Cells Lentivirally Transduced to Express L1CAM-Specific Chimeric Antigen Receptors in Treating Patients With Locally Advanced and Unresectable or Metastatic Small Cell Neuroendocrine Prostate Cancer
Study Details
Study Description
Brief Summary
This phase I trial studies the side effects and best dose of autologous CD8+ and CD4+ lentivirally transduced to express L1CAM-specific chimeric antigen receptor (CAR) and EGFRt mutation specific T cells and to see how well they work in treating patients with small cell neuroendocrine prostate cancer (SCNPC) that has spread to nearby tissue or lymph nodes (locally advanced) and cannot be removed by surgery (unresectable) or has spread from where it first started (primary site) to other places in the body (metastatic). CAR T-cell therapy is a type of treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so they will attack tumor cells. T cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein on the patient's tumor cells is added to the T cells in the laboratory. Some solid tumor cells have an EGFR protein on their surface, and T cells can be modified with a receptor, called a chimeric antigen receptor (CAR), to help recognize this protein and kill these tumor cells. Large numbers of the CAR T cells are grown in the laboratory and given to the patient by infusion for treatment of certain cancers. These L1CAM-EGFRt mutation specific T cells may help the body's immune system identify and kill L1CAM-EGFRt locally advanced and unresectable or metastatic small cell neuroendocrine prostate cancers' tumor cells.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Detailed Description
OUTLINE: This is a dose-escalation study of autologous L1CAM-specific CAR+EGFRt+ T cells.
Patients undergo leukapheresis to obtain peripheral blood mononuclear cells (PBMCs) for T cell product manufacturing and may undergo bridging therapy at the discretion of the treating clinician on study. Patients then undergo lymphodepleting chemotherapy with cyclophosphamide intravenously (IV) and fludarabine IV on days -5, -4 and -33 or single agent bendamustine on days -4 and -3 at the discretion of the treating clinician and/or principal investigator (PI). Patients receive an autologous L1CAM-specific CAR+EGFRt+ T cell infusion on day 0. Based on disease response and persistence of CAR T cells, patients may receive additional lymphodepletion chemotherapy and an autologous L1CAM-specific CAR+EGFRt+ T cell infusion as soon as 6 weeks and no later than 24 weeks after the first infusion, or at the discretion of the PI. Patients undergo echocardiography (ECHO) or multigated acquisition scan (MUGA) during screening. Patients undergo x-ray imaging, computed tomography (CT), bone scan, and blood sample collection throughout the trial. Additionally, patients may undergo tissue biopsy on the trial.
After completion of study treatment, patients are followed up monthly for 3 months, then every 3 months up to 12 months then may undergo long-term follow-up annually for up to 15 years.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Treatment (autologous L1CAM-specific CAR+EGFRt+ T cells) Patients undergo leukapheresis to obtain PBMCs for T cell product manufacturing and may undergo bridging therapy at the discretion of the treating clinician on study. Patients then undergo lymphodepleting chemotherapy with cyclophosphamide IV and fludarabine IV on days -5, -4 and -33 or single agent bendamustine on days -4 and -3 at the discretion of the treating clinician and/or PI. Patients receive an autologous L1CAM-specific CAR+EGFRt+ T cells infusion on day 0. Based on disease response and persistence of CAR T cells, patients may receive additional lymphodepletion chemotherapy and an autologous L1CAM-specific CAR+EGFRt+ T cell infusion as soon as 6 weeks and no later than 24 weeks after the first infusion, or at the discretion of the PI. Patients also undergo ECHO or MUGA during screening. Patients undergo x-ray imaging, CT, bone scan, and blood sample collection throughout the trial. Additionally, patients may undergo tissue biopsy on the trial. |
Drug: Bendamustine
Given IV
Other Names:
Procedure: Biopsy
Undergo tissue biopsy
Other Names:
Procedure: Biospecimen Collection
Undergo blood sample collection
Other Names:
Procedure: Bone Scan
Undergo bone scan
Other Names:
Procedure: Bridge Therapy
Undergo bridging therapy
Procedure: Computed Tomography
Undergo CT
Other Names:
Drug: Cyclophosphamide
Given IV
Other Names:
Procedure: Echocardiography
Undergo ECHO
Other Names:
Drug: Fludarabine
Given IV
Other Names:
Procedure: Leukapheresis
Undergo leukapheresis
Other Names:
Procedure: Multigated Acquisition Scan
Undergo MUGA
Other Names:
Biological: T-cell Receptor-engineered T-cells
Given autologous L1CAM-specific CAR+EGFRt+ T cells IV
Other Names:
Procedure: X-Ray Imaging
Undergo chest x-ray
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Incidence of adverse events [Up to 12 months after last chimeric antigen receptor (CAR) T cell infusion]
The toxicities observed at each dose level will be summarized in terms of type (organ affected or laboratory determination such as absolute neutrophil count), severity (by National Cancer Institute [NCI] Common Terminology Criteria for Adverse Events [CTCAE] version 5.0 and nadir or maximum values for the laboratory measures), date of onset and attribution. Tables will be created to summarize these toxicities and side effects by dose level. All disease responses will be reported according to Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.
- Dose-limiting toxicity rates [Within 28 days of last CAR T cell infusion]
The toxicities observed at each dose level will be summarized in terms of type (organ affected or laboratory determination such as absolute neutrophil count), severity (by NCI CTCAE version 5.0 and nadir or maximum values for the laboratory measures), date of onset and attribution. Tables will be created to summarize these toxicities and side effects by dose level. All disease responses will be reported according to RECIST 1.1.
Secondary Outcome Measures
- Objective response [Up to 12 months after last CAR T cell infusion]
Will be determined using RECIST version 1.1 and will be summarized at each dose level, and the number and percent responding combined across dose levels.
- Radiographic progression free survival [Up to 12 months after last CAR T cell infusion]
Will be assessed using RECIST v 1.1 criteria for soft tissue metastases and Prostate Cancer Working Group 3 criteria. Survival and time to relapse/progression will be summarized both by pooling across dose levels and within each dose level. Will calculate survival curves and the median expected survival duration, using the Kaplan-Meier estimate.
- Overall survival [Up to 12 months after last CAR T cell infusion]
Will be assessed using RECIST v 1.1 criteria for soft tissue metastases and Prostate Cancer Working Group 3 criteria. Survival and time to relapse/progression will be summarized both by pooling across dose levels and within each dose level. Will calculate survival curves and the median expected survival duration, using the Kaplan-Meier estimate.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Participants must be ≥ 18 years of age
-
Able to understand and give written informed consent
-
Confirmation of small cell neuroendocrine prostate cancer (SCNPC) diagnosis by internal pathology review of initial or subsequent biopsy or other pathologic material at Fred Hutchinson Cancer Center/University of Washington
-
Previously treated with a platinum-based chemotherapy regimen for SCNPC
-
Participants may not have received prior therapy or plan to receive therapy (chemotherapy, immunotherapy and/or radiation therapy) or have undergone or plan to undergo major surgery within the last 3 weeks prior to leukapheresis AND initiation of lymphodepleting chemotherapy. Participants who have developed SCNPC in the context of prior androgen deprivation therapy (ADT) (i.e. medical/surgical castration) may continue on ADT at the discretion of their treating provider
-
Evidence of L1CAM positivity by immunohistochemistry review of the patient's archival/fresh tumor samples
-
Metastatic or locally advanced and unresectable disease
-
Adequate performance status (Eastern Cooperative Oncology Group [ECOG] 0 or 1)
-
Expected survival > 3 months
-
Fertile participants must be willing to use an effective contraceptive method before, during, and for at least 4 months after the CAR T cell infusion
-
Measurable disease per RECIST v1.1 criteria as determined by CT, MRI or positron emission tomography (PET) scan
-
Hemoglobin > 9 g/dL (prior to leukapheresis)
-
Absolute neutrophil count (ANC) > 1,500 per mm^3 (prior to leukapheresis)
-
Platelets > 100,000 per mm^3 (prior to leukapheresis)
-
Creatinine ≤ 1.5 x upper limit of normal (ULN) (prior to leukapheresis)
-
Bilirubin ≤ 1.5 x ULN (≤ 3 x ULN in patients with known Gilbert's syndrome) (prior to leukapheresis)
-
Aspartate transaminase (AST) ≤ 3.0 x ULN (prior to leukapheresis)
-
Alanine transaminase (ALT) ≤ 3.0 x ULN (prior to leukapheresis)
-
Alkaline phosphatase ≤ 3.0 x ULN (prior to leukapheresis)
-
All prior treatment related toxicity prior to leukapheresis ≤ grade 2 by National Cancer Institute (NCI) Common Toxicity Criteria (CTC) version (v) 5.0
Exclusion Criteria:
-
Participants with non-melanoma skin cancer are eligible, while participants with other prior malignancies must have had at least a 3-year disease-free interval
-
Participants with active human immunodeficiency virus (HIV) (testing not required per protocol but status noted). Participants with adequately treated HIV will be permitted to enroll. Adequately treated HIV will be defined as being on a stable regimen of highly active anti-retroviral therapy (HAART), CD4 count ≥ 350 cells/mcL, undetectable viral load on standard polymerase chain reaction (PCR)-based testing and not requiring antibiotics or antifungal agents for the prevention of opportunistic infections
-
Participants with active hepatitis B (defined as hepatitis B surface antigen [HBsAg] reactive) or known active hepatitis C virus (defined as HCV RNA is detected) infection. Participants with prior hepatitis B virus (HBV) infection are eligible. Participants with a history of hepatitis C virus (HCV) infection are eligible if they have been treated with curative intent and their hepatitis C PCR viral load is negative
-
Known history of unstable angina or myocardial infarction (MI) within 6 months or clinically significant cardiac arrhythmia (other than stable atrial fibrillation) requiring anti-arrhythmia therapy
-
New York Heart Association (NYHA) class III or IV congestive heart failure (CHF), clinically significant hypotension, uncontrolled symptomatic coronary artery disease, or a documented ejection fraction of < 35%
-
Known history of clinically significant active chronic obstructive pulmonary disease (COPD), or other moderate-to-severe chronic respiratory illness present within 6 months
-
Participants with clinically significant pulmonary dysfunction, as determined by medical history and physical exam should undergo pulmonary function testing. Those with an forced expiratory volume (FEV1) of < 50 % of predicted or diffusing capacity for carbon monoxide (DLCO) (corrected) < 40% will be excluded. Patients with > grade 1 dyspnea at rest or oxygen saturation < 94% on room air (resting)
-
Infection requiring intravenous antibiotic use within 2 weeks of leukapheresis or uncontrolled active infection
-
Baseline serum sodium level < 130 mEq/L
-
Research participant is not receiving systemically administered steroid therapy. Physiologic glucocorticoid replacement therapy for management of adrenal insufficiency is allowed (≤ 10 mg daily of prednisone or equivalent)
-
History of an autoimmune disease requiring immunosuppressant therapy within the past 5 years
-
Other concurrent medical or psychiatric conditions that, in the investigator's opinion, may be likely to confound study interpretation or prevent completion of study procedures and follow-up examinations
-
Known history of brain metastases.
-
Note: Brain imaging is not required to determine eligibility. However, this should be performed if there is clinical suspicion for brain metastases
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Fred Hutch/University of Washington Cancer Consortium | Seattle | Washington | United States | 98109 |
Sponsors and Collaborators
- Fred Hutchinson Cancer Center
- Bristol-Myers Squibb
Investigators
- Principal Investigator: Michael Schweizer, Fred Hutch/University of Washington Cancer Consortium
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- RG1123589
- NCI-2023-07464
- FH20229