Clinical Trials /

NY-ESO-1-specific T Cell Receptor (TCR) T Cell in Sarcoma

NCT03462316

Description:

The main purpose of this trial is to investigate the safety and tolerability of NY-ESO-1(TCR Affinity Enhancing Specific T cell Therapy)in the first-line treatment failed advanced bone and soft tissue sarcoma. The secondary purpose of this trial is to investigate the efficacy of NY-ESO-1(TCR Affinity Enhancing Specific T cell Therapy)in the first-line treatment failed advanced bone and soft tissue sarcoma.

Related Conditions:
  • Bone Sarcoma
  • Soft Tissue Sarcoma
Recruiting Status:

Recruiting

Phase:

Phase 1

Trial Eligibility

Document

Title

  • Brief Title: NY-ESO-1-specific T Cell Receptor (TCR) T Cell in Sarcoma
  • Official Title: To Evaluate the Efficacy of NY-ESO-1-specific T Cell Receptor (TCR) Affinity Enhancing Specific T Cell in Bone and Soft Tissue Sarcoma

Clinical Trial IDs

  • ORG STUDY ID: B2017-023-01
  • NCT ID: NCT03462316

Conditions

  • Bone Sarcoma
  • Soft Tissue Sarcoma

Interventions

DrugSynonymsArms
NY-ESO-1(TCR Affinity Enhancing Specific T cell Therapy)NY-ESO-1 TCR Specific T cell Therapy

Purpose

The main purpose of this trial is to investigate the safety and tolerability of NY-ESO-1(TCR Affinity Enhancing Specific T cell Therapy)in the first-line treatment failed advanced bone and soft tissue sarcoma. The secondary purpose of this trial is to investigate the efficacy of NY-ESO-1(TCR Affinity Enhancing Specific T cell Therapy)in the first-line treatment failed advanced bone and soft tissue sarcoma.

Detailed Description

      This is a one arm, open label, dose escalation, single dose phase I study. The investigators
      include first-line treatment failed advanced patients with bone or soft tissue sarcoma and
      without standard regimen;TCR-T cell therapy has made a breakthrough for tumors in recent
      years. Phase I/II trial of NY-ESO-1-specific TCR-T treatment for synovial sarcoma and
      melanoma, conducted by the Rosenberg team at the National Cancer Institute, showed that 61%
      Synovial cell sarcoma patients and 55% melanoma patients benefit from this treatment, without
      severe side effects found in T cell receptor (TCR) transduced T-Cell Immunotherapy.

      This clinical trial is mainly focused on cancer-testis antigen, because it is not expressed
      in normal cells. NY-ESO-1 antigen as one member of cancer-testis antigen, is commonly
      expressed in 10-50% of melanoma, lung, liver, esophageal, breast, prostate, bladder, thyroid
      and ovarian cancer cases, 60% of multiple myeloma cases, and 70-80% of synovial sarcoma.
      NY-ESO-1 expression was also found in 88.2% of myxoid liposarcomas, 61.1% of synovial
      sarcomas, 31.3% of osteosarcomas, 21.4% of pleomorphic liposarcomas, 16.7% of desmoplastic
      small round cell tumors, and 14.3% of chondrosarcomas. The NY-ESO-1 TCR cell therapy for
      synovial sarcoma and melanoma has benefited many patients, but its effect on bone and soft
      tissue sarcoma is still unknown. So the investigators plan to explore its efficacy.

      The patients must meet the two criteria: HLA-A*0201+ and NY-ESO-1 positive cells≥25% by
      immunohistochemistry. By this trial, the dose-limiting toxicity (DLT) and maximum tolerance
      (MTD) will be initially identified.
    

Trial Arms

NameTypeDescriptionInterventions
NY-ESO-1 TCR Specific T cell TherapyExperimentalNY-ESO-1 TCR specific T cells are prepared by lentiviral infection. Seven days before TCR-T cell reinfusion, the subjects received low-dose cyclophosphamide (15mg/kg/d x 3 days) and low-dose fludarabine (15mg/m2/d x 3 days) lymphocyte clearance. Four days later, TCR-T cells were transfused back (1 x 109-5 x 1010 was administered once or in stages). Then interleukin (IL)-2 subcutaneous injections (250,000 IU/twice/day) will be subcutaneously administered for 14 days concomitantly to each subject within 15-30 minutes after cell reinfusion. If the first three patients had no severe bone marrow suppression side effects (CTCAE was above grade 3) on low-dose lymphocyte clearance therapy, the dosage of cyclophosphamide (20 mg/kg/d x 3 days) and fludarabine (25 mg/m2/d x 3 days) could be increased for follow-up patients.
  • NY-ESO-1(TCR Affinity Enhancing Specific T cell Therapy)

Eligibility Criteria

        Inclusion Criteria:

          1. Sign an informed consent before undertaking any trial-related activities;

          2. Aged 14 to 70 years old;

          3. Patients withbone and soft tissue sarcoma in stage IV by licensed pathologist;

          4. First-line treatment failed advanced patients.

          5. With measurable lesions, the product of the two maximum vertical diameters should not
             be less than 5mm*5mm

          6. Meet the two screening indicators: HLA-A*0201+, NYESO-1+(≥25% by
             immunohistochemistry);

          7. Eastern Cooperative Oncology Group score 0-1; life expectancy is longer than 3 months;

          8. The patient did not receive anti-tumor therapy within 4 weeks before enrollment;

          9. A brain metastasis patient in a stable condition for one month after anti-tumor
             therapy can be included;

         10. Left ventricular ejection fraction≥50%;

         11. Lab test results meet the following requirements: white blood cell count≥3.0×10^9/L;
             absolute neutrophil count≥1.5 ×10^9/L (No human granulocyte colony stimulating factor
             support); absolute lymphocyte count≥0.7×10^9/L;blood platelet≥75 ×10^9/L;
             Hemoglobin≥10g/dL (No transfusion in the last 14 days); Prothrombin time or
             International normalized rate ≤1.5×normal upper limit, except taking anticoagulant
             therapy; thrombin time≤1.5×normal upper limit, except taking anticoagulant therapy;
             Serum creatinine: 1.5mg /dL (or 132.6 microns /L);a 24-hour creatinine clearance
             rate≥60mL/ min; Aspartate transaminase / serum glutamic oxaloacetic transaminase≤2.5
             ×upper limit of normal; Alanine aminotransferase/ serum glutamate pyruvate
             transaminase≤2.5 ×upper limit of normal; total bilirubin≤1.5×upper limit of normal.

             In the case of liver metastasis, glutamate transaminase and glutamate alanine
             transaminase should be less than 5 x ULN

         12. Women of child-bearing age who have not undergone sterilization before menopause must
             agree to use effective contraceptive measures at least 30 days from the start of the
             study treatment to the last drug use, and serum pregnancy test is negative 14 days
             before the first treatment.

         13. Men who have not received sterilization must agree to use effective contraception from
             the start of the study until at least 90 days after the last study medication is
             administered.

         14. During the whole test period, the subjects can regularly go to the enrolled research
             institutions for relevant detection, evaluation and management.

        Exclusion Criteria:

          1. other types of tumors; If the patient has a previous history of malignant tumor, the
             disease-free time of the patient needs > for 5 years.

          2. received major surgery, conventional chemotherapy, large-area radiotherapy, immune
             therapy or any biological anti-tumor therapy within 4 weeks before enrollment;

          3. allergic to ingredients in this trial;

          4. common terminology criteria for adverse events not return to under 2 level from
             previous surgery or treatment-related adverse reactions;

          5. poorly managed hypertension (systolic blood pressure >160 mmHg and / or diastolic
             blood pressure > 90 mmHg) or clinically serious (for example, active) cerebrovascular
             diseases such as cerebrovascular incident (within 6 months prior to signing the
             informed consent), myocardial infarction (within 6 months prior to signing the
             informed consent), unstable angina, grade II or above heart failure according to New
             York Heart Association Grading Congestive, or severe arrhythmia can not be controlled
             by medication or has a potential impact on the study; with consecutive three times of
             obvious abnormality on electrocardiogram or average QT corrected interval ≥450
             millisecond;

          6. combined with other serious organic and mental disorders;

          7. serious or active bacteria, viral or fungal infections that require systemic
             treatment;

          8. with autoimmune diseases: such as a history of inflammatory bowel disease or other
             autoimmune diseases determined by the investigator as unsuitable for the study (e.g.
             systemic lupus erythematosus,vasculitis, invasive pulmonary disease);

          9. within 4 weeks prior the infusion, received chronic systemic steroid cortisone,
             hydroxyurea, immunomodulatory treatment (for example: Interleukin 2, alpha or gamma
             interferon, granulocyte colony stimulating factor, mammalian target of rapamycin
             inhibitors, cyclosporine, Thymosin etc);

         10. with organ transplantation, autologous/allogeneic stem cell transplantation and renal
             replacement therapy;

         11. with uncontrolled diabetes, pulmonary fibrosis, interstitial lung disease, acute lung
             disease, or liver failure;

         12. alcohol and / or drug abuse;

         13. pregnant or lactating women;

         14. with any medical condition or disease determined by the investigators that may be
             detrimental to this trial;

         15. without legal capacity / limited behavior.

         16. receive any other gene therapy products before study
      
Maximum Eligible Age:70 Years
Minimum Eligible Age:14 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Number of Participants With Treatment-Related Adverse Events as Assessed by CTCAE v3.0
Time Frame:270 days
Safety Issue:
Description:safety evaluation(dose-limiting toxicity and the maximum tolerance)

Secondary Outcome Measures

Measure:clinical response rate
Time Frame:270 Days
Safety Issue:
Description:Overall Response Rate as assessed by RECIST criteria

Details

Phase:Phase 1
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Sun Yat-sen University

Last Updated

March 15, 2020