Clinical Trials /

E7 TCR T Cell Immunotherapy for High-Grade Cervical Intraepithelial Neoplasia

NCT04411134

Description:

Background: Human papillomavirus (HPV) can lead to High-Grade Cervical Intraepithelial Neoplasia (CIN 2,3). This type of lesion has a high risk of becoming cancer. T cells are part of the immune system. A new type of treatment involves modifying these cells and injecting them into the lesions to shrink them. Objective: To test if injecting a type of treatment directly into cervical lesions can be safely given as therapy for high-grade CIN. Eligibility: People ages 21 and older with CIN 2,3 caused by HPV-16 Design: Participants will be screened over at least 2 visits with: Tumor sample Blood and urine tests Medical and medication history Physical exam Pelvic exam and colposcopy to look at the cervix Participants will have a baseline visit. They may be admitted to the hospital. They may receive a large catheter inserted into a vein. They will have a vein assessment. Before they receive treatment, participants will have a biopsy of the cervix. They will have leukapheresis. Blood will be removed through a needle in the arm, circulated through a machine that takes out the while blood cells, then returned through a needle in the other arm. A central catheter may also be used. Participants will have the modified cells injected directly into their cervical lesions. They will recover in the hospital for 1-2 days. Participants will have follow-up visits 2 weeks, 31 days, 6 weeks, and 12 weeks after treatment. They may receive a second injection at the 31-day visit. Participants will be contacted once a year for 5 years after treatment. They will be followed for up to 15 years.

Related Conditions:
  • Cervical Intraepithelial Neoplasia
Recruiting Status:

Withdrawn

Phase:

Phase 1

Trial Eligibility

Document

Title

  • Brief Title: E7 TCR T Cell Immunotherapy for High-Grade Cervical Intraepithelial Neoplasia
  • Official Title: A Phase I Study of E7 TCR T Cell Immunotherapy for High-Grade Cervical Intraepithelial Neoplasia

Clinical Trial IDs

  • ORG STUDY ID: 200093
  • SECONDARY ID: 20-C-0093
  • NCT ID: NCT04411134

Conditions

  • Cervical Intraepithelial Neoplasia

Interventions

DrugSynonymsArms
E7 TCRArm 1

Purpose

Background: Human papillomavirus (HPV) can lead to High-Grade Cervical Intraepithelial Neoplasia (CIN 2,3). This type of lesion has a high risk of becoming cancer. T cells are part of the immune system. A new type of treatment involves modifying these cells and injecting them into the lesions to shrink them. Objective: To test if injecting a type of treatment directly into cervical lesions can be safely given as therapy for high-grade CIN. Eligibility: People ages 21 and older with CIN 2,3 caused by HPV-16 Design: Participants will be screened over at least 2 visits with: Tumor sample Blood and urine tests Medical and medication history Physical exam Pelvic exam and colposcopy to look at the cervix Participants will have a baseline visit. They may be admitted to the hospital. They may receive a large catheter inserted into a vein. They will have a vein assessment. Before they receive treatment, participants will have a biopsy of the cervix. They will have leukapheresis. Blood will be removed through a needle in the arm, circulated through a machine that takes out the while blood cells, then returned through a needle in the other arm. A central catheter may also be used. Participants will have the modified cells injected directly into their cervical lesions. They will recover in the hospital for 1-2 days. Participants will have follow-up visits 2 weeks, 31 days, 6 weeks, and 12 weeks after treatment. They may receive a second injection at the 31-day visit. Participants will be contacted once a year for 5 years after treatment. They will be followed for up to 15 years.

Detailed Description

      Background:

        -  Cervical Intraepithelial Neoplasia (CIN) is caused by persistent infection with the
           Human Papillomavirus (HPV).

        -  High-grade lesions are common, affecting 5% of the female population in the United
           States, and are more likely to progress to cervical cancer.

        -  Surgical and ablative therapies are effective but can lead to long-term morbidity. New
           treatment modalities are needed.

        -  E7 TCR T cells have demonstrated safety and clinical activity in treatment-refractory
           metastatic HPV+ cancers.

      Objectives:

      - To determine the safety of intralesional injection of E7 TCR T cells as therapy for high-
      grade CIN.

      Eligibility:

      - Patients greater than or equal to 21 years of age with HPV16-associated, high-grade CIN.

      Design:

        -  This is a phase I clinical trial with a 3+3 dose escalation design.

        -  Patients will receive intralesional injections of E7 TCR T cells.

        -  Patients will not receive a conditioning chemotherapy regimen or systemic aldesleukin.
    

Trial Arms

NameTypeDescriptionInterventions
Arm 1ExperimentalApproximately 3x10^8 or 1.5x10^9 E7 TCR T cells will be injected on day 0 and 1.5x10^9 E7 TCR T cells on day 31 (2 escalating dose levels)
  • E7 TCR
Arm 2ExperimentalThe MTD from among dose level 1 and dose level 2
  • E7 TCR

Eligibility Criteria

        -  INCLUSION CRITERIA:

          -  Patients must have histologically confirmed high-grade cervical intraepithelial
             neoplasia (CIN 2,3). Confirmation of high-grade cervical intraepithelial neoplasia
             (pathology report from outside institution is sufficient). Pathology confirming
             high-grade CIN must be within 3 months prior to initiation of study therapy. If
             needed, confirmatory biopsy of lesion(s) may be performed.

          -  HPV16+ CIN 2,3 and HLA-A*02:01 HLA type

          -  Patients may be treatment-naive or have received previous treatment for high-grade
             CIN. Patients who have received previous treatment are eligible if prior treatment was
             greater than or equal to 3 months before first dose of E7 TCR T cells and there is
             pathological confirmation of recurrent or persistent disease. If needed, confirmatory
             biopsy of lesion(s) may be performed.

          -  Patients can have either one lesion or multiple lesions with at least one lesion being
             visible on colposcopy to help facilitate intralesional administration of E7 TCR T
             cells.

          -  Age greater than or equal to 21 years. Because treatment for this disease is not
             recommended in patients <21 years of age, children and adolescents <21 years old are
             excluded from this study.

          -  ECOG performance status greater than or equal to 2.

          -  Patients must have adequate organ and marrow function as defined below:

               -  leukocytes greater than or equal to 3,000/mcL

               -  absolute neutrophil count greater than or equal to 1,500/mcL

               -  platelets greater than or equal to 100,000/mcL

               -  total bilirubin within 1.5X normal institutional limits

               -  AST(SGOT)/ALT(SGPT) less than or equal to 2.5 X institutional upper limit of
                  normal

               -  creatinine within normal institutional limits

               -  creatinine clearance Calculated creatinine clearance (CrCl) >50mL/min/1.73m^2 for
                  patient with creatinine levels above institutional normal (by the Chronic Kidney
                  Disease Epidemiology Collaboration (CKD-EPI) equation)

          -  Women of child-bearing potential must have a negative pregnancy test because E7 TCR T
             cells have unknown potential for teratogenic or abortifacient effects. Women of
             childbearing potential are defined as all women who are not post-menopausal or who
             have not had a hysterectomy. Postmenopausal will be defined as women over the age of
             55 who have not had a menstrual period in at least 1 year.

          -  The effects of E7 TCR T cells on the developing human fetus are unknown. For this
             reason, women of child-bearing potential must agree to use adequate contraception
             (intrauterine device, hormonal or barrier method of birth control, abstinence, tubal
             ligation or vasectomy) prior to study entry and for up to 4 months after treatment.
             Should a woman become pregnant or suspect she is pregnant while she is participating
             in this study, she should inform her treating physician immediately.

          -  Seronegative for HIV antibody. The experimental treatment being evaluated in this
             protocol depends on an intact immune system. Patients who are HIV seropositive can
             have decreased immune-competence and thus be less responsive to the experimental
             treatment.

          -  Seronegative for hepatitis B antigen and hepatitis C antibody. If hepatitis C antibody
             test is positive, then the patient must be tested for the presence of antigen by
             RT-PCR and be HCV RNA negative.

          -  Must be willing to participate in Gene Therapy Long Term Follow up Protocol, which
             will follow patients for up to 15 years per Food and Drug Administration (FDA)
             requirements.

          -  Ability of subject to understand and the willingness to sign a written informed
             consent document.

        EXCLUSION CRITERIA:

          -  Patients who are receiving any other investigational agents.

          -  Uncontrolled intercurrent illness including, but not limited to, active infection,
             symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or
             psychiatric illness/social situations that would limit compliance with study
             requirements.

          -  Because there is an unknown but potential risk for adverse events in nursing infants
             secondary to treatment of the mother with E7 TCR T cells, breastfeeding should be
             discontinued if the mother is treated with E7 TCR T cells. These potential risks may
             also apply to other agents used in this study.

          -  Patients with any form of systemic immunodeficiency, including acquired deficiency
             such as HIV or primary immunodeficiency such as Severe Combined Immunodeficiency
             Disease, are ineligible. The experimental treatment being evaluated in this protocol
             depends on an intact immune system. Patients who have decreased immune competence may
             be less responsive to the treatment.

          -  Patients on immunosuppressive drugs including systemic corticosteroids (inhaled or
             intranasal corticosteroids are allowed).

          -  Patients with a second active invasive cancer are not eligible.
      
Maximum Eligible Age:N/A
Minimum Eligible Age:21 Years
Eligible Gender:Female
Healthy Volunteers:No

Primary Outcome Measures

Measure:To determine the safety of intralesional injection of E7 TCR T cell therapy for highgrade CIN
Time Frame:3 months
Safety Issue:
Description:The fraction who experience a DLT based on the dose level and cell administration within the dose level will be determined and reported.The analysis will be entirely descriptive.

Details

Phase:Phase 1
Primary Purpose:Interventional
Overall Status:Not yet recruiting
Lead Sponsor:National Cancer Institute (NCI)

Trial Keywords

  • T Cell Receptor
  • Immunotherapy
  • Human Papillomavirus
  • Intralesional Injections
  • Cervical Cancer

Last Updated

July 8, 2020