Clinical Research Directory

Inclusion Criteria: * 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. Exclusion Criteria: * 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; * 2.Known mental illness, alcoholism, drug use or substance abuse; * 3.Pregnant or lactating women; or women who are pregnant, breastfeeding, or planning to become pregnant within 1 year after cell infusion; * 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; * 5.The investigators determine that other conditions that make the patient not suitable for enrollment.