A Phase I Clinical Study to Evaluate the Safety, the Tolerability, the Pharmacokinetic Characteristics and the Efficacy of ScTIL Injection (Genetically Modified Tumor Infiltrating Lymphocytes) in the Treatment of Advanced Malignant Solid Tumors

Chinese Academy of Medical Sciences & Peking Union Medical College

Status and phase: Not yet enrolling; Phase 1

Conditions: Advanced Tumor of Digestive Tract or Urinary System

Treatments: Biological: ScTIL injection

Study type: Interventional

Funder types: Other

Identifiers

NCT05499715

ScTIL-008-2022

Details and patient eligibility

About

This is an open-lable, single-arm, dose escalation and dose extension phase I clinical study of ScTIL designed to observe and evaluate the safety, the tolerance, the pharmacokinetic characteristics and the effectiveness of ScTIL in the treatment of advanced malignant solid tumors, in order to provide the basis for the future clinical research to explore the best recommended phase II dose (PR2D) and treatment scheme.

Full description

This study consists of two phases: the first phase will be the dose exploration phase (Phase I), followed by the dose extension phase.

In the dose escalation of the study, 3 subjects are enrolled for 1st treatment group, starting with single dose of ScTIL injection of 5x10^9 alone. If there is no dose limiting toxicity (DLT) observed, 3 subjects are enrolled into treatment groups successively in sequential order of: Group 2: ScTIL1.0x10^10; Group 3: ScTIL 2.0x10^10.

After the completion of ScTIL reinfusion for first subject of the 1st dose group, the subject will be observed for no less than 7 days. If no serious toxic and adverse events occurres, ScTIL reinfusion for the second and third subjects will be performed. If no DLT occurres by the 21th days after completion of reinfusion for the 3rd subject, The study will proceed to the next treatment group. If 1/3 of enrolled subjects have DLT, another 3 subjects will be enrolled. In any of the dose groups, if less than 1/6 subjects have DLT, subject enrollment for the next treatment group will start. If DLT occurs in more than 2/6 of subjects, the number of subjects in the previous dose group will be reviewed. If there were only 3 subjects, 3 more subjects will be enrolled. If DLT occurs in less than 1/6 subjects, the dose will be defined as the maximum tolerable dose (MTD), and the dose escalation phase of the study will be completed. If DLT occurs in more than 2/6 subjects in the first dose group, a dose reduction exploration will be performed or the study will be terminated upon decision made by the Safety Committee.

Appropriate doses will be selected by investigator for the dose extention phase study.

Enrollment: 48 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age ≥ 18 and ≤ 75, regardless of gender;

2. Eastern United States Cancer Collaborative Group (ECOG) physical condition score is 0 to1;

3. Anticipated survival > 3 months;

4. Advanced digestive tract tumor or urinary system tumor confirmed by histology or cytology;

5. Patients with unresectable locally advanced or metastatic malignant digestive or urinary system tumors who have failed at least the first-line standard treatment;

6. According to iRECIST standard, at least one tumor lesion can be measured by CT or MRI. Measurable tumor lesions are defined as the longest diameter ≥ 10mm and the scanning thickness does not exceed 5.0mm. For lymph node lesions, the short diameter ≥ 15mm;

7. PD-1 positive T cells in peripheral blood accounts for≥ 18% of total T lymphocytes (By detection standard of BD accuri C6 flow cytometer);

8. Voluntarily accept the use of peripheral blood cell apheresis to obtain cells for the preparation of ScTIL cells;

9. Sufficient bone marrow and organ functions:

   1. Hematology: neutrophils is equal to or higher than 1.5×10^9/L, platelets is equal to or higher than 75×10^9/L, hemoglobin is equal to or higher than 90g/L; total lymphocytes is equal to or higher than 60% of the lower limit of normal range;
   2. Liver function: Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) are both eqal to or lower than 2.5 times the upper limit of normal range (ULN) (if intrahepatic metastatic tumor exists, equal to lower than 5 times of ULN); total bilirubin (TBIL) is equal to or lower than 1.5 times of ULN;
   3. Kidney function: Creatinine (Cr) is equal to or lower than 1.5 times of ULN, or creatinine clearance is equal or higher than 60;
   4. Coagulation function: Activated partial prothrombin time (APTT) is equal to or shorter than1.5 times of ULN; international normalized ration (INR) is equal to or shorter than1.5 times of ULN;

10. Qualified patients with fertility (male and female) must agree to use reliable contraceptive methods (hormone or barrier method or abstinence, etc.) with their partners during the trial and at least 90 days after the last medication; The blood or urine pregnancy test within 7 days before the first use of the study drug in women of childbearing age (see Appendix 8 for the definition) must be negative;

11. Study subjects must obtain informed consent to this study and voluntarily sign a written informed consent before screening for enrollment..

Exclusion criteria

1. Central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence shows that the patient's central nervous system metastasis or meningeal metastasis has not been controlled, so it is not suitable to be included in the study according to the judgment of the researcher;

2. Patients who had in recent 5 years or currently have other malignant tunors, except for cured basal cell skin cancer, in situ cervical carcinoma, and in situ lung cancer, before signing the ICF;

3. Patients who received PD-L1 monoclonal antibody treatment within 12 weeks before apheresis (including but not limited to atilizumab and dovalizumab);

4. There was active infection within 1 week before apheresis, and systemic anti-infection treatment was currently required;

5. Currently suffering from interstitial lung disease;

6. Had received immunotherapy and had ≥ grade 3 IrAE;

7. Patients with active or had autoimmune diseases that may recur (such as systemic lupus erythematosus, rheumatoid arthritis, vasculitis, etc.); Except for patients with clinically stable autoimmune thyroid disease and well-controlled type I diabetes;

8. The adverse reaction of previous anti-tumor treatment has not recovered to CTCAE 5.0 grade evaluation ≤ 1 (except for the toxicity without safety risk judged by researchers such as hair loss);

9. Received anti-tumor treatment within 2 weeks before apheresis, including but not limited to chemotherapy, radiotherapy, immunotherapy, traditional Chinese medicine with anti-tumor indications, etc., except for the following:

   1. Nitrosourea or mitomycin C within 6 weeks before harvest;
   2. Oral fluorouracils and small molecule targeted drugs were taken 1 week before apheresis.

10. Received systemic glucocorticoid (prednisone >10mg/day or equivalent dose of similar drugs) or other immunosuppressant treatment within 2 weeks before apheresis; Except for the following cases: Intermittent use of local, eye, intra-articular, intranasal and inhaled glucocorticoids; Short term use of glucocorticoids for preventive treatment (e.g. prevention of contrast agent allergy);

11. Within 4 weeks before apheresis:

    1. Have received other unlisted clinical research drugs or treatments;
    2. Having undergone major organ surgery (excluding puncture biopsy) or significant trauma, or requires scheduled hospitalization during the trial period;
    3. Used live attenuated vaccine;

12. Hepatitis B: HBsAg (+) or HBeAg (+); Or anti HBe (+)/anti HBc (+) and the DNA quantity of hepatitis B is higher than the detection limit of the research center; Hepatitis C: anti HCV positive; Treponema pallidum antibody (+);

13. Have a history of immunodeficiency, including HIV antibody test positive;

14. Have a history of serious cardiovascular and cerebrovascular diseases, including but not limited to:

    1. There are serious cardiac rhythm or conduction abnormalities, such as ventricular arrhythmia requiring clinical intervention, II-III degree atrioventricular blockade, etc;
    2. Acute coronary syndrome, congestive heart failure, aortic dissection, stroke or other cardiovascular and cerebrovascular events ≥ grade 3 occurred within 6 months before the cell reinfusion;
    3. New York Heart Association (NYHA) cardiac function rating ≥ class II or left ventricular ejection fraction (LVEF) < 50%, or structural heart disease with high risk judged by other researchers;
    4. Clinically uncontrollable hypertension;

15. Serous cavity effusion beyond clinical control as judged unsuitable for being enrolled by the researcher;

16. Known alcohol or drug dependence;

17. Mental disorders or poor compliance;

18. Pregnant or lactating women;

19. The researcher believes that the subject has a history of other serious systemic diseases or is not suitable to participate in this clinical study due to other reasons.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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48 participants in 1 patient group

ScTIL injection

Experimental group

Description:

In the dose escalation of the study, starting with the dose of injection of 5x10\^9. If there is no DLT, followed by the second dose of 1.0x10\^10 until the third dose of 2.0x10\^10.

Treatment:

Biological: ScTIL injection