DC Vaccination in CML
Ključne riječi
Sažetak
Datumi
Posljednja provjera: | 12/31/2018 |
Prvo podneseno: | 08/24/2015 |
Predviđena prijava predata: | 09/03/2015 |
Prvo objavljeno: | 09/06/2015 |
Zadnje ažuriranje poslato: | 01/29/2019 |
Posljednje ažuriranje objavljeno: | 01/30/2019 |
Stvarni datum početka studija: | 06/30/2014 |
Procijenjeni datum primarnog završetka: | 06/30/2021 |
Predviđeni datum završetka studije: | 12/31/2021 |
Stanje ili bolest
Intervencija / liječenje
Biological: DC vaccine
Faza
Grupe ruku
Arm | Intervencija / liječenje |
---|---|
Experimental: DC vaccine Autologous DC pulsed with leukemia-associated peptides+adjuvant.
Ten vaccinations over 26 weeks with 10 x 106 freshly thawed DC Intradermal injections (1-2 ml volume) | Biological: DC vaccine Autologous DC pulsed with leukemia-associated peptides+adjuvant |
Kriteriji prihvatljivosti
Uzrast podoban za studiranje | 18 Years To 18 Years |
Polovi podobni za studiranje | All |
Prihvaća zdrave volontere | Da |
Kriterijumi | Inclusion Criteria: 1. Patients with bcr/abl-positive CML in stable cytogenetic / molecular remission after at least 18 months therapy with tyrosine kinase Inhibitors (TKI). The following groups of patients will be included: - complete cytogenetic remission (CCyR), but stable detection of bcr/abl-transcript on qPCR (at least on two different time points over a period of at least 6 months). A stable molecular remission is assumed, if the difference between the qPCR values does not exceed a factor 5 (< 0,5log). - No CCyR, but qPCR for bcr/abl transcript < 10% (= MCyR (Major cytogenetic Response)) after at least 24 months on 2nd generation TKI therapy. 2. Treatment with a TKI inhibitor and an additional anti leukemic drug is no exclusion criterion. 3. Age 18-80 years 4. Performance status of 0 or 1 according to WHO index or Karnofsky index >70 % 5. Life expectancy > 18 months 6. Hematological function should be at least partially conserved (platelets count >50.000/ μl, Hb > 8g/dl) 7. written informed consent 8. No breast feeding 9. if of childbearing potential, negative pregnancy test (serum/urine ß- HCG ( human chorionic gonadotropin )) and willingness to use highly effective contraceptive methods (Pearl Index <1, e.g.: birth control pill, loop, hormone implant, transdermal hormone patch, a combination of two barrier methods [condom and vaginal diaphragm] sterilisation or sexual abstinence) for the study duration and thereafter as long as under treatment with antileukemic drugs Exclusion Criteria: 1. Clinically relevant autoimmune disorders 2. Immunodeficiency syndromes 3. Known allergy to GM-CSF (granulocyte macrophage colony-stimulating factor), TNF-α (Tumor necrosis factor Alpha) , IL-4 (interleukine 4) or KLH (keyhole limpet hemocyanin) 4. Pregnancy (absence confirmed by serum/urine ß-HCG) or breastfeeding 5. Women of childbearing age without highly effective contraception 6. Active infectious disease requiring treatment 7. Continuous therapy with corticosteroids or other immunosuppressive drugs 8. Severe psychiatric disorders 9. Organ dysfunction: - Thrombin Time / Partial Thromboplastin Time > 1,5 x upper normal limit - creatinine > 2,0 mg/ml - Bilirubin > 3,0 mg/ml, ALAT/ASAT (Alanine aminotransferase/ aspartate aminotransferase) > 3x upper normal limit - pulmonary disfunction (dyspnea at rest or with minimal exertion) - clinically relevant coronary heart disease or ventricular arrhythmia, congestive heart failure > grade II NYHA (New York Heart Association) 10. Persons who are detained officially or legally to an official institute 11. Subjects for whom there is concern about compliance with the protocol procedures 12. Present History of substance abuse (drug or alcohol) or any other factor (e.g., serious psychiatric condition) that could limit the subject's ability to comply with study procedures |
Ishod
Primarne mjere ishoda
1. DC toxicity Parameters using CTC (Common toxicity criteria) [30 weeks]
Sekundarne mjere ishoda
1. Molecular/cytogenetic Response under vaccination as measured by qPCR for bcr/abl in % IS (International scale) [30 weeks]
2. T-cell Response: Antigen specific T-cell Response in % CD8+ T-cells for bcr/abl [30 weeks]
3. T-cell Response: Antigen specific T-cell Response in % CD4+ T-cells for bcr/abl [30 weeks]
4. T-cell Response: Antigen specific T-cell Response in % CD8+ T-cells for WT-1 (only in HLA-A2+ patients) [30 weeks]
5. T-cell Response: Antigen specific T-cell Response in % CD8+ T-cells for Proteinase 3 (only in HLA-A2+ patients) [30 weeks]