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T-CTL immune cell targeted therapy for the treatment of nasopharyngeal cancer

T-CTL immune cell targeted therapy for the treatment of nasopharyngeal cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016855
Enrollment
Unknown
Registered
2018-06-28
Start date
2018-07-01
Completion date
Unknown
Last updated
2018-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nasopharyngeal cancer

Interventions

initial patients:cell injection
Relapsed patients:cell injection

Sponsors

Qi Hui
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: The patients who diagnosed as nasopharyngeal cancer with at least one measurable objective tumor index (through imaging diagnosis, such as CT, MRI examination, the maximum diameter of the lesion is measured = 1cm). No history of other tumors (excluding squamous cell carcinomas that have been cured by surgery). Males or females age between 18 to 75 (including 18 and 75). ECOG score 0 or 1. Expected survival time = 3 months. Blood, liver, kidney function, and blood clot laboratory tests meet the following criteria within 7 days before the treatment starts: white blood cells (WBC) = 3.5×10^9/L, platelets (PLT) =80×10^9/L, neutrophils (ANC) = 1.5 × 10^9/L, hemoglobin (HGB) = 90g/L, aspartate aminotransferase (AST) <2.5×upper limit of normal (the ULN) (liver metastases <5 × ULN), Alanine transaminase (ALT) <2.5xULN (liver metastasis<5 x ULN), total bilirubin (TIBC) <1.5xULN, serum creatinine (CR) <1.0 x ULN, prothrombin time, partial coagulation Live enzyme time, plasma fibrinogen, thrombin time were within the normal range. Subjects must take contraception during the entire study period. The subject has signed the informed consent form to understand the purpose of the study, the study steps and the study content and voluntarily participate in the study.

Exclusion criteria

Exclusion criteria: Subjects who meet any of the following conditions cannot participate in this study: 1. Patients with clinical symptoms of brain metastases (except radiotherapy control); 2. has active viral or bacterial infections and cannot be controlled with appropriate anti-infective treatments; 3. with HIV and syphilis, hepatitis B virus or hepatitis C virus infection; 4. suffering from mental illness or other conditions cannot cooperate with research treatmen; 5. Allergic to any of the components of the intervention; 6. rheumatic diseases; 7. has accepted the organ transplant; 8. Poor compliance; 9. Pregnant or nursing.

Design outcomes

Primary

MeasureTime frame
survival rate;complications;tumor control rate;life quality;Health economic index;

Secondary

MeasureTime frame
Local recurrence rate ;distant metastases rate;

Countries

China

Contacts

Public ContactQi Hui

Shenzhen People's Hospital

qihui214@126.com+86 13602662926

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026