Clinical trial · Interventional
Tumor Lysate Pulsed Dendritic Cell Immunotherapy for Patients With Brain Tumors
Phase ll Trial of Tumor Lysate-Pulsed Dendritic Cell Immunotherapy for Patients With Atypical or Malignant, Primary or Metastatic Brain Tumors of the Central Nervous System
NCT00576537CI-TRIAL-00038443completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This research is being determine whether vaccinations with your own immune cells called " dendritic cells " can activate your immune system to fight your brain tumor.
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 |
|---|---|---|---|
| Glioblastoma | Glioblastoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Dendritic Cell Immunotherapy | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Dendritic Cell Immunotherapy
- description
- Patients who consent to participate in the study and receive the Dendritic Cell vaccine manufactured from their own tumor cells.
- interventionNames
- Biological: Dendritic Cell Immunotherapy
Primary outcomes (1)
- measure
- Evaluate the safety/toxicity of subcutaneous injections of autologous dendritic cells
- timeFrame
- One year
- description
- Cytotoxic T lymphocyte (CTL) precursor frequency
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: * No age or gender limit, though minimal weight limitations for apheresis is about 15 - 20 Kg. * Both male and female of childbearing age entering the protocol must use a medically accepted form of birth control during the study, will be required to have a negative pregnancy test for female. * patients with atypical malignant brain tumor will be eligible. * Patients must have a Karnofsky performance score of at least 60% * patients may be maintained on glucocorticoid therapy at the lowest possible dose. * Baseline hematologic studies and chemistry profiles must meet the criteria. * Tumor specimen of adequate size to yield protein concentration in sufficient quantity. * Tumor-lysate peptide must be generated in sufficient quantity to pulse the APC's for vaccination. * Patient must have no prior sensitivity to the components of the dendritic cell vaccine. * Patient must agree to consider an autopsy in the event of death in an attempt to learn more concerning the nature of this treatment and tumor biology. * Patient must be capable of signing IRB approved Research Consent and Release of medical Records form. Exclusion Criteria: * Severe pulmonary, cardiac or other systemic disease associated with an unacceptable anesthetic or operative risk. * The presence of an acute infection requiring active treatment will be criteria for delay or exclusion. * Patients with a known history of an autoimmune disorder. * Inability to give informed consent. * Pregnancy.
References
Publications (1)
- DERIVEDJouanneau E, Black KL, Veiga L, Cordner R, Goverdhana S, Zhai Y, Zhang XX, Panwar A, Mardiros A, Wang H, Gragg A, Zandian M, Irvin DK, Wheeler CJ. Intrinsically de-sialylated CD103(+) CD8 T cells mediate beneficial anti-glioma immune responses. Cancer Immunol Immunother. 2014 Sep;63(9):911-24. doi: 10.1007/s00262-014-1559-2. Epub 2014 Jun 4. PMID 24893855