Clinical Trials /

TAA Specific Cytotoxic T Lymphocytes in Patients With Pancreatic Cancer

NCT03192462

Description:

Status - CLOSED TO PATIENT ENROLLMENT (CNPE) Patients who have pancreatic cancer that has come back or has not gone away after treatment, including the standard treatment for this disease or patients who are not eligible for or have elected not to receive standard of care chemotherapy, and patients who will have surgery after treatment for pancreatic cancer are eligible for this study. This is a research study using special immune system cells called tumor-associated antigen (TAA)-specific cytotoxic T lymphocytes, a new experimental therapy. The proteins that are targeted in this study are called tumor-associated antigens (TAAs). These are cell proteins that are specific to the cancer cell. They do not show, or they show up in low quantities, on normal human cells. In this study, five common TAAs will be targeted. They are called NY-ESO-1, MAGEA4, PRAME, Survivin and SSX2. On a different study, patients have been treated and so far this treatment has shown to be safe. Investigators now want to try this treatment in patients with pancreatic cancer. These TAA-specific cytotoxic T lymphocytes (TAA-CTLs) are an investigational product not approved by the Food and Drug Administration. *Arm A and Arm B are closed to new patient enrollment.*

Related Conditions:
  • Pancreatic Adenocarcinoma
Recruiting Status:

Active, not recruiting

Phase:

Phase 1/Phase 2

URL:

https://clinicaltrials.gov/show/NCT03192462

Trial Eligibility

Document

Title

  • Brief Title: TAA Specific Cytotoxic T Lymphocytes in Patients With Pancreatic Cancer
  • Official Title: Tumor-Associated Antigen (TAA) Specific Cytotoxic T Lymphocytes Administered in Patients With Pancreatic Cancer

Clinical Trial IDs

  • ORG STUDY ID: H-40378 TACTOPS
  • NCT ID: NCT03192462

Conditions

  • Pancreatic Cancer

Interventions

DrugSynonymsArms
multiTAA specific T cellsGroup A (Closed to New Patient Enrollment)

Purpose

Status - CLOSED TO PATIENT ENROLLMENT (CNPE) Patients who have pancreatic cancer that has come back or has not gone away after treatment, including the standard treatment for this disease or patients who are not eligible for or have elected not to receive standard of care chemotherapy, and patients who will have surgery after treatment for pancreatic cancer are eligible for this study. This is a research study using special immune system cells called tumor-associated antigen (TAA)-specific cytotoxic T lymphocytes, a new experimental therapy. The proteins that are targeted in this study are called tumor-associated antigens (TAAs). These are cell proteins that are specific to the cancer cell. They do not show, or they show up in low quantities, on normal human cells. In this study, five common TAAs will be targeted. They are called NY-ESO-1, MAGEA4, PRAME, Survivin and SSX2. On a different study, patients have been treated and so far this treatment has shown to be safe. Investigators now want to try this treatment in patients with pancreatic cancer. These TAA-specific cytotoxic T lymphocytes (TAA-CTLs) are an investigational product not approved by the Food and Drug Administration. *Arm A and Arm B are closed to new patient enrollment.*

Detailed Description

      Status - CLOSED TO PATIENT ENROLLMENT (CNPE)

      The patient will give blood to make TAA-Specific cytotoxic T cells in a lab. These cells well
      be grown and frozen. If the TAA-Specific cytotoxic T cells can be made, the time from
      collection of the blood to manufacture of T cells for administration to the patient is about
      1 to 2 months.

      The cells will be infused by intravenous infusion (IV) into the patient over 1-10 minutes.
      The patient may be pre-treated with acetaminophen (Tylenol) and diphenhydramine (Benadryl).
      Acetaminophen (Tylenol) and diphenhydramine (Benadryl) are given to prevent a possible
      allergic reaction to the TAA-CTL administration.

      Patients will be given up to six doses of TAA-CTLs at monthly intervals. The treatments will
      be given by the Center for Cell and Gene Therapy at Houston Methodist Hospital (HMH).

      MEDICAL TESTS BEFORE TREATMENT:

        -  Physical exam.

        -  Blood tests to measure blood cells, kidney and liver function.

        -  Measurements of the patient's tumor by routine imaging studies and/or blood tests. The
           study will use the imaging study that was used before to follow the patient's tumor: CT,
           MRI, or PET.

        -  Blood test to check for pregnancy for female patients who can have children

      MEDICAL TESTS DURING TREATMENT:

      Standard medical tests will be conducted on the day of the second and subsequent infusions:

        -  Physical exams prior to each T cell infusion

        -  Blood tests to measure blood cells, kidney and liver function.

      MEDICAL TESTS AFTER TREATMENT:

      - Measurements the patient's tumor by routine imaging studies and/or blood tests done as per
      standard of care.

      To learn more about the way the TAA-CTLs are working in patient's body, an extra 20-40 mL
      (4-8 teaspoons) of blood will be taken before the infusion, at Weeks 1 and 2 after each
      infusion and at weeks 4, 6 and 8 and months 3, 6, 9 and 12 after the last infusion. The blood
      may be drawn from a central line at the time of the patient's regular blood tests.
      Investigators will use this blood to see how long the TAA-CTLs last, and to look at the
      immune system response to the patient's cancer.

      Study Duration: Patients will be active participants in this study for approximately one year
      after their last dose. Investigators will contact patients once a year for up to 4 additional
      years (total of 5 years follow-up) in order to evaluate disease response long-term.

      *Arm A and Arm B are closed to new patient enrollment.*

Trial Arms

NameTypeDescriptionInterventions
Group A (Closed to New Patient Enrollment)ExperimentalPatients with locally advanced or metastatic pancreatic adenocarcinoma who are responding following 3 cycles of first line chemotherapy will receive 6 infusions with a fixed dose of multiTAA specific T cells beginning on the 4th week of the 4th cycle of chemotherapy. MultiTAA T cell infusions will occur on day 21 (a chemotherapy "off" week) of each chemotherapy cycle starting on chemotherapy cycle 4.
  • multiTAA specific T cells
Group B (Closed to New Patient Enrollment)ExperimentalPatients with locally advanced or metastatic pancreatic adenocarcinoma who have failed first line chemotherapy or are intolerant or ineligible to receive standard of care chemotherapy will be evaluated in the clinic and receive 6 infusions (administered at monthly intervals) with a fixed dose of multiTAA specific T cells.
  • multiTAA specific T cells
Group C (Closed to New Patient Enrollment)ExperimentalPatients with resectable pancreatic adenocarcinoma following completion of neoadjuvant chemotherapy, radiotherapy or combination. These patients will receive 6 infusions with a fixed dose of multiTAA specific T cells. One infusion will occur 4 weeks prior to surgical resection (with an option to infuse up to one week earlier) and after the completion of all pre-operative chemotherapy and/or radiation. The subsequent 5 infusions will occur at monthly intervals beginning 8 weeks post-surgery. Following surgery all patients will additionally receive 3 months of standard of care (SOC) chemotherapy starting week 9 after surgery. Hence, SOC chemo will occur weeks 9-11, 13-15, and 17-19 post-surgery and multiTAA T cell infusions will occur at weeks 8, 12, 16, 20, and 24 post-surgery.
  • multiTAA specific T cells

Eligibility Criteria

        Status - CLOSED TO PATIENT ENROLLMENT (CNPE)

        Inclusion Criteria:

        PROCUREMENT:

          1. Any patient with biopsy proven pancreatic adenocarcinoma.

          2. Patients with life expectancy greater than or equal to 6 months.

          3. Age greater than or equal to 18 years

          4. Hgb greater than or equal to 7.0 g/dl (transfusions allowed)

        TREATMENT:

          1. Any patient with biopsy-proven pancreatic adenocarcinoma:

             Group A: Patients with locally advanced or metastatic adenocarcinoma who are
             responding (defined as stable disease or tumor volume reduction) following 3 cycles of
             first line chemotherapy

             Group B: Patients with locally advanced or metastatic adenocarcinoma who have failed
             first line chemotherapy or are intolerant, ineligible or unwilling to receive standard
             of care chemotherapy

             Group C: Patients with resectable pancreatic cancer who have completed planned
             neo-adjuvant chemotherapy, radiotherapy or combination

          2. Patients must have measurable or evaluable disease per RECIST 1.1 criteria.

          3. Patients with life expectancy greater than or equal to 12 weeks

          4. Age greater than or equal to 18

          5. Pulse oximetry of greater than 95 percent on room air in patients who previously
             received radiation therapy

          6. Patients with an ECOG score of ≤ 2 or Karnofsky score of 50 or greater

          7. Patients with bilirubin less than or equal to 2x upper limit of normal, AST less than
             or equal to 3x upper limit of normal, Hgb greater than or equal to 7.0 g/dl
             (transfusion allowed).

          8. Patients with a creatinine less than or equal to 2x upper limit of normal for age

          9. Patients should have been off other investigational therapy for one month prior to
             receiving treatment on this study.

         10. For Groups B or C patients must be off conventional therapy for at least 1 week prior
             to receiving treatment on this study.

         11. Informed Consent explained to, understood by and signed by patient. Patient given copy
             of informed consent.

         12. Due to unknown effects of this therapy on a fetus, pregnant women are excluded from
             this research. The male partner should use a condom. Females of child-bearing
             potential must be willing to utilize one of the more effective birth control methods
             during the study unless female has had a hysterectomy or tubal ligation.

        Exclusion Criteria:

        PROCUREMENT:

          1. Patients with severe intercurrent infection.

          2. Patients with active HIV infection (can be pending at this time)

        TREATMENT:

          1. Patients with severe intercurrent infection.

          2. Patients receiving systemic corticosteroids (Patients off steroids for at least 48
             hours are eligible)

          3. Pregnant

          4. HIV positive
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Number of patients with treatment related serious adverse events
Time Frame:7 months
Safety Issue:
Description:To determine the safety of up to 6 intravenous infusions of multiTAA-specific T cells in pancreatic cancer patients with metastatic, locally advanced unresectable, or resectable disease.

Secondary Outcome Measures

Measure:Progression Free Survival using the Kaplan-Meier method
Time Frame:5 years
Safety Issue:
Description:To evaluate the progression-free of patients after multiTAA-specific T cell infusions
Measure:Overall Survival using the Kaplan-Meier method
Time Frame:5 years
Safety Issue:
Description:To evaluate the overall survival of patients after multiTAA-specific T cell infusions

Details

Phase:Phase 1/Phase 2
Primary Purpose:Interventional
Overall Status:Active, not recruiting
Lead Sponsor:Baylor College of Medicine

Trial Keywords

  • Pancreatic Cancer
  • Immune-based therapies
  • CytotoxicT Lymphocytes

Last Updated

May 3, 2021