TCR-T Cells in the Treatment of Advanced Pancreatic Cancer

Pancreatic Cancer Clinical Trial

— GB3010-02  

Official title:

To Investigate the Safety, Tolerability, Efficacy and Pharmacokinetics of T Cell Receptor T Cell Therapy in the Treatment of Advanced Pancreatic Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06054984
• Other study ID #: (2021) IEC No.288
• Status: Recruiting
• Phase: Early Phase 1
• Start date: September 7, 2021
• Est. completion date: September 7, 2024

Study information

• Verified date: March 2023
• Source: Ruijin Hospital
• Contact: ChenLeiWen
• Phone: 13761638756
• Email: wcl12161[@]rjh.com.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To investigate the safety, tolerability, efficacy and pharmacokinetics of TCR-T cells in the treatment of advanced pancreatic cancer

Description:

The aim of this clinical trial is to investigate the safety, tolerability, efficacy and pharmacokinetics of TCR-T cell therapy in patients with advanced pancreatic cancer by intravenous injection, in order to explore an effective cellular immunotherapy method for the treatment of advanced pancreatic cancer

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 18
• Est. completion date: September 7, 2024
• Est. primary completion date: June 7, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• To be eligible for the study, patients must meet all of the following criteria:

1. Male or female, aged 18-75 years;

2. Patients with advanced pancreatic cancer diagnosed by histology or cytology, patients who failed to respond to standard treatment, relapsed or voluntarily gave up;

3. Patients must have tumor tissue that expresses specific tumor antigens, such as mutations in RAS and/or TP53;

4. Patients must undergo HLA matching testing and meet the requirements of HLA matching.

5. At least one measurable or evaluable lesion =15 mm according to RECIST1.1 criteria;

6. Patients with ECOG < 2 and life expectancy =3 months;

7. a) Liver function: ALT/AST < 3 times the upper limit of normal value (ULN) and bilirubin =34.2µmol/L; b) renal function: creatinine < 220µmol/L; c) terminal oxygen saturation =95% in room air; d) Cardiac function: left ventricular ejection fraction (LVEF) =60%; e) Blood routine: absolute neutrophil count = 1×109/L; Platelet count =70×109/L; Absolute lymphocyte count =100 cells /µL;

8. The patients met the requirements of apheresis without any contraindications.

9. Women of childbearing age who have a negative urine pregnancy test at screening and before starting dosing and who have agreed to use highly effective contraception for at least 100 days after infusion; Female participants must agree not to donate eggs (oocytes, oocytes) for assisted reproductive purposes during the study and for 90 days after receiving the last study drug;

10. Male subjects with a fertile partner must consent to use an effective barrier method of contraception for at least 100 days after infusion; Must agree not to donate sperm for at least one year;

11. Sign an informed consent form.

Exclusion Criteria:

• Patients who met any of the following criteria were not eligible for inclusion in the

study:

1. Persons with severe mental disorders;

2. A positive virological test for any of the following: HIV; HCV; HBsAg; HBcAb was positive, and HBV DNA copy number and TPPA were positive.

3. Patients with severe allergic history or allergic constitution;

4. Severe underlying medical conditions such as evidence of other serious active viral, bacterial or uncontrolled systemic fungal infection; Active autoimmune disease or a history of autoimmune disease within 3 years;

5. A history of autoimmune diseases (e.g., Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus) leading to end-organ damage or requiring systemic immunosuppressive/systemic disease modulating drugs within the past 2 years;

6. Combined with organ dysfunction, such as renal insufficiency;

7. Had been enrolled in another clinical trial within 4 weeks before enrollment in the trial;

8. Those who were unable to comply with the study protocol and follow-up plan due to physiological, family, social, geographical and other factors;

9. Patients with contraindications to cyclophosphamide or fludarabine chemotherapy;

10. Subjects who required additional immunosuppressive drug therapy within 72 hours before TCR-T infusion, except for the treatment of adverse events during the trial;

11. Pregnant, lactating women, or men who plan to have children while participating in the study or within 100 days of receiving study treatment;

12. Any other condition considered by the investigator to be ineligible for enrollment.

Related Conditions & MeSH terms

• Pancreatic Cancer
• Pancreatic Neoplasms

Intervention

Drug:
• TCR-T Cells Injection(GB3010 Cells Injection)
The TCRT cells used in this clinical trial were derived from the patient's autologous peripheral-blood T cells and were genetically transduced to express a T-cell Receptor that recognizes the RAS/TP53.Patients were sequentially enrolled into 3 dose escalation groups(dose level 1-3) :5×10^8±20%,5×10^9±20%,5×10^10±20%.

Locations

Country	Name	City	State
China	Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine	ShangHai	Shanghai

Sponsors (2)

Lead Sponsor	Collaborator
Ruijin Hospital	Shanghai Essight Bio Co.,Ltd

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	To explore the correlation between the proliferation and persistence of TCRT cells in body and the efficacy	observe correlation of the PK parameters with response (CR, PR, relapse),PK parameters including peak (Cmax) of neoantigen-specific TCRT cells in blood and tumor tissue, time to peak (number of days to peakTCRT cells after infusion), Tmax) and AUC0-28 (area under the curve plotted against visit time by the number of neoantigen-specific TCRT cells in peripheral blood from day 0 to 28).	2years
Primary	Evaluate the Incidence of Treatment Related Adverse Events of TCRT cells in patients with advanced pancreatic cancer	collect adverse events (AE), serious adverse events (SAE), adverse events of special interest (AESI), and laboratory abnormalities (type, frequency, and severity)	2years
Primary	Characterize the Peak of Peripheral Blood Concentration and Area under the Peripheral Blood concentration versus time curve of TCRT cells and observe their proliferation and persistence in body	After infusion of neoantigen-specific TCRT cells, collect peak (Cmax) of neoantigen-specific TCRT cells in blood and tumor tissue, time to peak (number of days to peakTCRT cells after infusion), Tmax) and AUC0-28 (area under the curve plotted against visit time by the number of neoantigen-specific TCRT cells in peripheral blood from day 0 to 28). "If possible, AUC0-inf, terminal phase elimination rate constant (?z), elimination half-life (t1/2) will be evaluated."	2years
Secondary	Correlation of the pharmacokinetic profile of TCRT cells with the Incidence of CRS and ICANS events	collect changes in mutant cell concentration in peripheral blood and tumor tissue after TCRT cell reinfusion,observe correlation of these measures with CRS and ICANS events	2years
Secondary	Evaluate tumor size (mm) , tumor biomarker CA19-9 (U/ml), ORR/DCR/PFS and OS of patients with advanced pancreatic cancer	ORR at 2, 4, and 6 months after TCRT cell infusion (ORR=CR+PR). The primary efficacy outcome was the change in target tumor size (local control rate of target lesions). Secondary efficacy indicators: changes in tumor markers; Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS) and overall survival (OS) according to RECIST1.1 criteria	2years