NCT04370301RecruitingPhase 2
Reduced Intensity Haploidentical Transplantation for the Treatment of Primary or Secondary Myelofibrosis
Pilot Study of JAK Inhibitor Therapy Followed by Reduced Intensity Haploidentical Transplantation for Patients With Myelofibrosis
Source: ClinicalTrials.gov · Last updated 20 Jul 2026
Brief summary (registry, in English)
This initial cohort of this phase II trial studied the outcomes of using a JAK inhibitor prior to reduced intensity haploidentical (Haplo) transplantation for the treatment of primary or secondary myelofibrosis (MF). The primary risk of using Haplo HCT in patients with MF is graft failure. In the first cohort, all patients engrafted. There were no instances of graft failure. However, a large number of patients did have graft versus host disease as a complication of their transplant. JAK inhibitors have since been approved for the indication of graft versus host disease treatment. And we are also using them for graft versus host disease prevention in a study of MF patients with sibling and unrelated donors. Therefore, we are opening a new cohort of the current study using the JAK inhibitor prior to, during and after Haplo transplant. Our goal is to decrease graft versus host disease in patients receiving a Haplo MF transplant without increasing the risk of graft failure.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- First submitted
- 28 Apr 2020
- Start date
- 9 Feb 2021
- Primary completion date
- 30 Apr 2027
- Lead sponsor
- Fred Hutchinson Cancer Center
- Diseases
- Myeloproliferative neoplasms
- NCT number
- NCT04370301
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 20
- From 9 Feb 2021 to the primary completion date, 30 Apr 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- PART 1: JAK INHIBITOR ADMINISTRATION EXCLUSION CRITERIA
- History of prior allogeneic transplant
- PART 2: ALLOGENEIC STEM CELL TRANSPLANT EXCLUSION CRITERIA
- Active or recent (prior 6 month) invasive fungal infection without infectious disease (ID) consult and approval
Other illness
- Uncontrolled viral or bacterial infection at the time of study enrollment
- Known HIV positivity
Lab values
- Contraindication to receiving a JAK inhibitor including:
- Patients who have known hypersensitivity to JAK inhibitors
- Clinical or laboratory evidence of significant renal or hepatic impairment including cirrhosis
- Active uncontrolled infection
- Known human immunodeficiency virus (HIV) positivity
- Women who are pregnant or trying to conceive
- Caution should be used in patients with platelets \< 100 though adjustments in dose can be made to accommodate anyone with platelets \> 50
- Availability of an human leukocyte antigen (HLA)-identical or 1-allele-mismatched related donor or an HLA 10 of 10 matched unrelated donor
Other
- Leukemic transformation (\> 20% blasts)
- Pregnant or breastfeeding
Who the study is looking for
- PART 1: JAK INHIBITOR ADMINISTRATION INCLUSION CRITERIA
- Age between 18 and 70 years
- Diagnosis of primary myelofibrosis (PMF) as defined by the 2016 World Health Organization classification system or diagnosis of secondary MF as defined by the International Working Group (IWG) for Myeloproliferative Neoplasms Research and Treatment criteria
- Patients meeting the criteria for intermediate-1, intermediate-2 or high-risk disease by the Dynamic International Prognostic Scoring System (DIPSS)-plus scoring system (DIPSS may be used if all data from DIPSS are not available)
- Ability to understand and the willingness to sign a written informed consent document (or legally authorized representative)
- Patient must be a potential hematopoietic stem cell transplant candidate
- PART 2: ALLOGENEIC STEM CELL TRANSPLANT INCLUSION CRITERIA
- Meeting criteria for 1st phase as above, at time of initiation of JAK inhibitor, including ability to understand and willingness to sign a written informed consent (or legally authorized representative). Patients arriving to our institution for transplant and not enrolled in Part 1 may still be enrolled in Part 2 if Part 1 criteria met. These patients will have Part 1 endpoints transcribed from medical records
- Received JAK inhibitor for at least 8 weeks immediately prior to conditioning and be willing to continue until 9-12 months post-transplant as tolerated
- Karnofsky performance status score \>= 70
- Calculated creatinine clearance using the Cockcroft-Gault formula or 24 hour (hr) urine creatinine clearance must be \> 60 ml/min
- Total serum bilirubin must be \< 3 mg/dL unless the elevation is thought to be due to Gilbert's disease or hemolysis
- Transaminases must be \< 3 x the upper limit of normal
- Patients with clinical or laboratory evidence of liver disease will be evaluated for the cause of liver disease, its clinical severity in terms of liver function, and the degree of portal hypertension. Patients with fulminant liver failure, cirrhosis with evidence of portal hypertension or bridging fibrosis, alcoholic hepatitis, hepatic encephalopathy, or correctable hepatic synthetic dysfunction evidenced by prolongation of the prothrombin time, ascites related to portal hypertension, bacterial or fungal abscess, biliary obstruction, chronic viral hepatitis with total serum bilirubin \> 3 mg/dL, and symptomatic biliary disease will be excluded
- Diffusion capacity of the lung for carbon monoxide (DLCO) corrected \> 60% normal; may not be on supplemental oxygen
- Left ventricular ejection fraction \> 40% OR shortening fraction \> 26%
- Comorbidity Index \< 5 at the time of pre-transplant evaluation
- DONOR: Patients must be screened prior to transplant for donor-specific anti-HLA antibodies (DSA). Patients with DSA will be reviewed by the principal investigator and considered for desensitization treatment
- DONOR: Children are preferred over siblings and parents
- DONOR: Younger donors are preferred over older donors
- DONOR: ABO matched donors are preferred over minor ABO mismatched and over major ABO mismatch donors
Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Fred Hutch/University of Washington Cancer Consortium Coordinator of this site? Confirm its status | Seattle | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.