Clinical trial · Interventional
Ruxolitinib in the Treatment of Chronic Lymphocytic Leukemia
A Phase I/II Trial of Ruxolitinib (Jakafi) in Patients With Chronic Lymphocytic Leukemia Who Are Unfit for Conventional First-line Therapy Due to Age or 17p Deletions
NCT02015208CI-TRIAL-00024027completedPhase 1 / Phase 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)
The purpose of this study is to determine if Ruxolitinib, an inhibitor of cytokine-signaling, is effective in the treatment of patients with Chronic Lymphocytic Leukemia for whom conventional chemotherapy is either too toxic or ineffective.
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 |
|---|---|---|---|
| Chronic Lymphocytic Leukemia | Chronic Lymphocytic Leukemia | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Ruxolitinib | Drug | Ruxolitinib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Ruxolitinib
- description
- Ruxolitinib will be administered over a 28-day cycle, which will be repeated 6 more times in the absence of intolerable toxicity, disease progression, patient withdrawal of consent, or investigator decision to end therapy. The dose and schedule have been adapted from the product monograph for myelofibrosis. The starting dose will be 20 mg orally twice a day with normal .platelet and absolute neutrophil counts and no hepatic and renal impairment.
- interventionNames
- Drug: Ruxolitinib
Primary outcomes (1)
- measure
- Clinical response rate
- timeFrame
- at 7 months
Secondary outcomes (1)
- measure
- number of patients with adverse events
- timeFrame
- participants will be followed for an average of 8 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age greater than 65 years unless a 17p deletion is present in more than 20% of circulating tumor cells, in which case age can be younger than 65 years. 2. Diagnosis of CLL meeting published diagnostic criteria. 3. CLL requiring treatment on the basis of National Cancer Institute (NCI) working group criteria. 4. Not previously treated with cytotoxic drugs or antibodies but may have received glucocorticoid monotherapy, local radiation, or splenectomy. 5. Unfit for full dose FCR chemotherapy. 6. Platelets \>50x10\*\*9/L. Neutrophils\>.75x10\*\*9/L. 7. At least 1 lymph node \>1.5 cm or splenomegaly as detected by CT scan. Exclusion Criteria: 1. Fit for full-dose FCR as initial treatment. 2. Progressive multifocal leukoencephalopathy (PML). 3. Clinically significant bacterial, fungal, parasitic or viral infection, which require therapy. 4. Richter's transformation or prolymphocytic leukemia. 5. Uncontrolled autoimmune hemolytic anemia or idiopathic thrombocytopenia purpura. 6. Prior exposure to chemotherapy for CLL with the exception of glucocorticoids, local radiation, or splenectomy. 7. History of prior malignancy, with the exception of the following: i. Malignancy treated with curative intent and with no evidence of active disease for more than 2 years. ii. Adequately treated skin cancer. iii. Adequately treated cervical carcinoma in situ. 8. Currently active clinically significant cardiovascular disease. 9. History of stroke or intracranial hemorrhage within 6 months prior to enrollment. 10. Renal failure requiring dialysis and patients with moderate and severe renal impairment with platelet counts less than 100,000/ml. 11. Hepatic impairment.
References
Publications (2)
- BACKGROUNDTomic J, Lichty B, Spaner DE. Aberrant interferon-signaling is associated with aggressive chronic lymphocytic leukemia. Blood. 2011 Mar 3;117(9):2668-80. doi: 10.1182/blood-2010-05-285999. Epub 2011 Jan 4. PMID 21205928
- DERIVEDXia M, Luo TY, Shi Y, Wang G, Tsui H, Harari D, Spaner DE. Effect of Ibrutinib on the IFN Response of Chronic Lymphocytic Leukemia Cells. J Immunol. 2020 Nov 15;205(10):2629-2639. doi: 10.4049/jimmunol.2000478. Epub 2020 Oct 16. PMID 33067379