Clinical trial · Interventional
Vaccine Therapy Plus Interleukin-2 in Treating Patients With Stage III, Stage IV, or Recurrent Follicular Lymphoma
Active Specific Immunotherapy for Follicular Lymphomas With Liposomes Containing Tumor-Derived Antigen and IL-2
NCT00020462CI-TRIAL-00017737completedPhase 1ClinicalTrials.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)
RATIONALE: Vaccines made from a person's cancer cells may make the body build an immune response to kill tumor cells. Combining vaccine therapy with interleukin-2 may be a more effective treatment for follicular lymphoma . PURPOSE: Phase I trial to study the effectiveness of vaccine therapy plus interleukin-2 in treating patients who have stage III, stage IV, or recurrent follicular lymphoma.
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 |
|---|---|---|---|
| Lymphoma | Lymphoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| aldesleukin | Biological | Aldesleukin | ALIAS |
| autologous tumor cell vaccine | Biological | — | UNRESOLVED |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically proven follicular center cell lymphoma with surface immunoglobulin (Ig) M, G, or A phenotype * Grade I (follicular small cleaved cell) * Grade II (follicular mixed small and large cell) * Grade III (follicular large cell) * Stage III, IV, or recurrent disease * Previously untreated with chemotherapy or monoclonal antibody therapy OR * Recurrent, residual disease or progressive disease after prior prednisone, doxorubicin, cyclophosphamide, and etoposide (PACE) chemotherapy * Peripheral lymph node of at least 2 cm and accessible for biopsy/harvest * No primary or secondary CNS lymphoma * Must not have any of the following: * Rapidly progressing lymphadenopathy * Bone marrow failure secondary to lymphoma * B symptoms * Neurovascular or organ compromise secondary to lymphoma PATIENT CHARACTERISTICS: Age: * 18 and over Performance status: * Karnofsky 70-100% Life expectancy: * More than 1 year Hematopoietic: * Not specified Hepatic: * ALT/AST no greater than 3.5 times upper limit of normal * Bilirubin no greater than 1.5 mg/dL unless secondary to Gilbert's disease * Hepatitis B surface antigen negative * Hepatitis C antibody negative Renal: * Creatinine no greater than 1.5 mg/dL Other: * HIV negative * No active infection * No other prior or concurrent malignancy except curatively treated squamous cell or basal cell skin cancer or effectively treated carcinoma in situ of the cervix * No medical or psychiatric condition that would preclude study * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: * See Disease Characteristics * No other concurrent biologic therapy for lymphoma Chemotherapy: * See Disease Characteristics * At least 3 months since prior PACE chemotherapy * No concurrent chemotherapy Endocrine therapy: * At least 2 weeks since prior steroid treatment * Less than 2 months of prior prednisone * No concurrent endocrine therapy for lymphoma Radiotherapy: * Prior radiotherapy to no more than 1 site allowed * At least 2 weeks since prior radiotherapy * No concurrent radiotherapy Surgery: * See Disease Characteristics * Lymph node biopsy performed within past month
References
Publications (1)
- RESULTNeelapu SS, Gause BL, Harvey L, Lee ST, Frye AR, Horton J, Robb RJ, Popescu MC, Kwak LW. A novel proteoliposomal vaccine induces antitumor immunity against follicular lymphoma. Blood. 2007 Jun 15;109(12):5160-3. doi: 10.1182/blood-2006-12-063594. Epub 2007 Mar 5. PMID 17339422