GT201 Injection in Combination With Teraplizumab Injection for Treatment of Patients With Non-small Cell Lung Cancer

Who can take part

• 1. Voluntarily join the study, signed informed consent form,, willing and able to comply with the study protocol
• 2. Age 18 to 70 years old
• 3. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1
• 4. Expected survival time of ≥ 12 weeks
• 5. Good function of vital organs
• 6. Subjects entering this study due to disease progression must have an imaging record of disease progression before tumor sampling
• 7. At least one measurable target lesion that meets the definition of RECIST v1.1 after tumor sampling

Who cannot take part

• 1.Patients with uncontrollable tumor-related pain as judged by the investigator; participants requiring analgesic medication must already have a stable analgesic regimen at the time of study entry; symptomatic lesions suitable for palliative radiotherapy should be completed prior to study entry
• 4.Those who have received other clinical trial drug treatment within 4 weeks before preconditioning by lymphodepletion,plan to participate in other clinical trial drug treatment during the study
• 2.Known mental illness, alcoholism, drug use or substance abuse
• 5.The investigators determine that other conditions that make the patient not suitable for enrollment
• 3.Pregnant or lactating women; or women who are pregnant, breastfeeding, or planning to become pregnant within 1 year after cell infusion