Clinical trial · Interventional
CIK Cell Transfusion Plus Chemotherapy as Adjuvant Therapy for Stage IB-IIIA Non-Small Cell Lung Cancer (NSCLC)
A Phase 2,Open-label Study of Autologous Cytokine-Induced Killer Cell Transfusion Plus Chemotherapy as Adjuvant Therapy for Stage IB-IIIA Non-Small Cell Lung Cancer
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Few patients would like to participate ,since CIK cell transfusion was a new treatment and its efficacy was doubted.
Summary
Brief summary (as posted)
Non - small cell lung cancer ( NSCLC ) accounts for more than 80% of lung cancer. The main treatment for early stage patients is surgical resection, but about 30% -70% patients will relapse. Postoperative chemotherapy is the major systemic treatment for surgical resection NSCLC patients. However, data show only 5-10% improvement in overall survival with systemic adjuvant chemotherapy. It is necessary to further improve the survival time of patients with lung cancer. Biological treatment is becoming a new treatment modality for Cancer following with surgery, radiotherapy and chemotherapy, and has been confirmed as an effective adjuvant treatment in comprehensive cancer treatment. Cytokine induced killer cells ( CIK) characterized as fast amplification, strong anti-cancer activity and broad anti-tumor spectrum is most widely used and thought to be the first choice for the new generation of anti-tumor adoptive immunotherapy. This Phase II study is investigating the efficacy of Autologous Cytokine-Induced Killer Cell Transfusion plus Chemotherapy as adjuvant therapy for stage IB-IIIA NSCLC.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Autologous CIK Transfusion plus Chemotherapy | Drug | — | UNRESOLVED |
| chemotherapy alone | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Group A
- description
- Autologous CIK Transfusion plus Chemotherapy
- interventionNames
- Drug: Autologous CIK Transfusion plus Chemotherapy
- type
- ACTIVE_COMPARATOR
- label
- Group B
- description
- chemotherapy alone
- interventionNames
- Drug: chemotherapy alone
Primary outcomes (1)
- measure
- the relapse rate
- timeFrame
- 30 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Stage IB-IIIA post-surgery NSCLC patients with histologically confirmed. 2. with an Eastern CooperativeOncology Group performance status of 0 or 1, 3. at least 18 years of age 4. adequate bone marrow reserve and organ function including calculated creatinine clearance 45 mL/min based on the standard Cockcroft and Gault formula 5. patients had fully recovered from its acute effects. Exclusion Criteria: 1. HIV positive 2. autoimmune disease 3. immune deficiency disorder 4. organ transplantation 5. received high dose glucocorticoid or other immune depressant within 4 weeks 6. active clinically serious infections (\> grade 2 NCI-CTC version 3.0) 7. life threatening medical condition
References
Publications (0)
Data not yet available