Anti-GPC3 CAR T for Recurrent or Refractory Lung Squamous Cell Carcinoma

Lung Squamous Cell Carcinoma Clinical Trial

Official title:

Preliminary Clinical Study of Autologous T Cells Modified Chimeric Antigen Receptor (CAR) Targeting GPC3 for the Treatment of Recurrent or Refractory Lung Squamous Cell Carcinoma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02876978
• Other study ID #: CG1003
• Status: Recruiting
• Phase: Phase 1
• First received: August 9, 2016
• Last updated: August 23, 2016
• Start date: March 2016
• Est. completion date: April 2019

Study information

• Verified date: August 2016
• Source: Carsgen Therapeutics, Ltd.
• Contact: Li Zonghai, MD
• Phone: 86-21-54489926
• Email: zonghaili[@]carsgen.com
• Is FDA regulated: No
• Health authority: China: National Health and Family Planning CommissionChina: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to observe and confirm the safety, tolerance and cell pharmacokinetics of lentivirus-transduced CAR-GPC3 T cells (CAR-GPC3 T cells targeting GPC3)

Description:

A single-center, open-label pilot study to determine the safety, tolerance and engraftment potential of CAR-GPC3 T cells in subjects with GPC3+ positive lung squamous cell carcinoma.

Primary objectives:

Observe and determine the safety and tolerance in escalating dose infusion of CAR-GPC3 T cells (CAR T cells targeting GPC3) transduced with the lentiviral vector, and the survival of the CAT-GPC3 T cells in vivo, referred to as engraftment potential.

Secondary objectives:

The following indexes are monitored for curative effect of CAR-GPC3 T cells on lung squamous cell carcinoma:

1. Objective response rate (ORR), is defined as the ratio of patients diagnosed as partial remission (PR) to complete remission (CR) according to RECIST 1.1 criteria.

2. Progression free survival (PFS), is defined as the duration from baseline to PD (audited and confirmed by independent imaging), or to the day of any death event. The earlier one shall prevail.

3. Time to tumor progression (TTP), is defined as the duration from baseline to disease starts to get worse or spreads to other parts of the body.

4. Overall survival (OS), is defined as the time period from the 1st day of treatment to the day of death for any reason. For patients who are still alive at the data analysis day, OS data is subject to the last confirmed time of survival patients.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: April 2019
• Est. primary completion date: October 2017
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Men or women aged 18~70 years old

2. Subjects are diagnosed as refractory, recurrent ,metastatic, advanced lung squamous cell carcinoma by histological and cytological methods including specific lesion-targeted brush biopsy, lavage and fine needle aspiration;

3. Have at least one new measurable tumor lesion compared with previous irradiated region

4. Tumor tissues samples confirmed as GPC3-positive

5. Expected survival=12 weeks

6. ECOG scored as 0-1 or KPS grading > 80

7. ANC=1500/nm3

8. PLT=100000/mm3

9. Hb=9.0g/dL

10. Serum creatinine=2.5mg/dL,CCR=50ml/min (renal malfunction defined as CCR<50ml/min according to Cockroft-Gault formula)

11. ALT and AST=2.5ULN; for liver metastasis,ALT and AST =5ULN

12. Serum TBiL=3.0mg/dL, TBiL=2.5ULN

13. PT: INR < 1.7 or extended PT to normal value < 4s

14. Adequate venous access for apheresis or venous blood collection, and no other contraindication of blood cell separation

15. Patients with willingness to be in this study and able to provide informed consent

16. Capable of receiving treatment and follow up, included subjects are required to receive treatment in the enrolled centre

17. Women of childbearing age are required to take acceptable measures to minimize the possibility of pregnancy during whole session. Women of childbearing age must have negative results of serum or urine tests within 24 hours prior to infusion. Women subjects must not be in lactation;

Exclusion Criteria:

1. CAR-T positive rate < 10%

2. pregnant women or women in lactation

3. active HBV or HCV infection

4. HIV/AIDS infection

5. active infection

6. previously suffered from diseases or concurrent diseases as followed:

• patients confirmed as severe autoimmune diseases in long-term (over 2 months) need of systemic immune inhibitors (steroid) or as immune-mediated symptomatic diseases including ulcerative colitis, Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus (SLE), autoimmune vasculitis (for example, Wegener's granulomatosis)

• subjects with previous diagnosis as motor neurone disease caused by autoimmunity

• subjects previously suffered from toxic epidermal necrolysis (TEN)

• subjects with any mental diseases including dementia, mental status change that may impinge the understanding and performance of informed consent and related questionnaire

• subjects with severe, uncontrollable diseases judged by investigators that may hinder them receiving this treatment

• subjects with previously active malignant tumors including basal or squamous skin cancer, superficial bladder cancer, and in situ breast carcinoma within 5 years who had been completely cured without the need of follow-up treatment are not excluded.

7. during ongoing treatment using systemic steroid or steroid inhalants

8. previous treatment used gene therapy products

9. previous experience of immunotherapies including CIK, DC, DC-CIK, LAK for the treatment of cancer

10. allergic to immunotherapies or related drugs

11. patients in need of treatment for heart disease with =2 NYHA or for poor controlled hypertension

12. subjects with unstable or active peptic ulcer or alimentary tract hemorrhage

13. subjects with previous organ transplantation or ready for organ transplantation

14. subjects in need of anticoagulant therapy treatment (warfarin or heparin)

15. subjects judged by investigators as not appropriate for this study

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Squamous Cell
• Lung Squamous Cell Carcinoma

Intervention

Genetic:
• CAR-GPC3 T Cells
Intravenous infusion of CAR-GPC3 T cells is conducted 1 - 2 days following lymphodepletion.

Drug:
• Fludarabine
30 mg/m^2/day x 4 days
• Cyclophosphamide
500 mg/m^2/day x 2 days

Locations

Country	Name	City	State
China	Shanghai Chest Hospital,Shanghai Jiaotong University	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Carsgen Therapeutics, Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and tolerance: Occurrence of study related adverse events	Occurrence of study related adverse events, defined as laboratory toxicities and clinical events that are possibly, likely or definitely related to study treatment at any time from the infusion until week 24. This will include infusive toxicity, and any toxicity possibly related to the CAR-GPC3 T cells.	24 weeks	Yes
Secondary	Engraftment: the DNA vector copies per mL blood of CAR-GPC3 T cells	The DNA vector copies per mL blood of CAR-GPC3 T cells on week 4 after the first infusion by Q-PCR. Q-PCR for CAR-GPC3 vector sequences will also be performed after infusion thereafter until any 2 sequential tests are negative documenting loss of CAR-GPC3 T cells within 2 years.	2 years	Yes