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Prospective Study of the Dendritic Cells Load the Livin Peptide to Non-Small-Cell Lung Cancer (NSCLC) Radiotherapy Sensitization

Prospective Study of the Dendritic Cells Load the Livin Peptide to Non-Small-Cell Lung Cancer (NSCLC) Radiotherapy Sensitization

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002369
Enrollment
Unknown
Registered
2012-07-24
Start date
2012-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Non-Small-Cell Lung Cancer (NSCLC)

Interventions

DC loaded Livin + radiotherapy group:immunotherapy and radiotherapy
DC loaded MUC-1 + radiotherapy group:immunotherapy and radiotherapy

Sponsors

Cancer Institute of People's Liberation Army, Third Military Medical University Xinqiao hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Confirmed non-small-cell lung cancer (NSCLC) by pathological and histological/cytologic examination; 2. Performance status is good, PS3 months; 4. 18 years old or over 18 years old; 5. Always have responded to radiotherapy; 6. Always have responded to autoimmune cellular therapy; 7. The liver function, renal, bone marrow was essentially normal; 8. Chemotherapy and molecular targeted therapy clearance phase should be 2 weeks or more; 9. The patient volunteered to conduct the study, and good compliance, could cooperate to observation of experiments, and freely given informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe dysfunction of life viscera; 2. Associated with other malignant tumor; 3. Have autoimmune diseases; 4. During pregnancy and nursing (women of reproductive age Should do a pregnancy test); 5. During active stage of acute or chronic infectious diseases; 6. Have clear allergic history in medicine or belong to allergies; 7. Actively participate in other clinical trials; 8. Those determined by the researchers to be unsuitable to participate in the (clinical) trial or under certain conditions.

Design outcomes

Primary

MeasureTime frame
immtmity indicator;clinical indicators;the toxic and side effect;

Countries

China

Contacts

Public ContactJianguo Sun
sunjg09@yahoo.com.cn+86 13983155736

Outcome results

None listed

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