A Phase I/II Study of Trametinib and Azacitidine for Patients With Newly Diagnosed Juvenile Myelomonocytic Leukemia
Risk Stratified Treatment for Patients With Newly Diagnosed Juvenile Myelomonocytic Leukemia: A Phase I/II Non-randomized Study of Trametinib and Azacitidine With or Without Chemotherapy (IND #164058)
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 1 Month to 21 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Time periods mentioned: 5 days, 28 days
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Dosing: Patients with newly diagnosed lower-risk JMML will be treated with daily azacitidine for 5 days in combination with daily trametinib for 28 days per course for up to 12 courses."
- "Patients with newly diagnosed high-risk JMML will be treated with daily azacitidine, fludarabine, and cytarabine for 5 days in combination with daily trametinib for 28 days per course for up to 2 courses."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests how safe and effective trametinib and azacitidine are for patients ages 1 month to 21 years with newly diagnosed juvenile myelomonocytic leukemia (JMML), a blood cancer. Patients with lower-risk JMML get these two drugs. Patients with high-risk JMML also get fludarabine and cytarabine.
This clinical trial will test the safety and efficacy of combining trametinib and azacitidine in patients with juvenile myelomonocytic leukemia (JMML). Newly diagnosed lower-risk JMML patients will receive trametinib and azacitidine. High-risk JMML patients will receive trametinib, azacitidine, fludarabine, and cytarabine.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Be 1 month to 21 years old when joining.
- Have JMML that meets the study’s blood, bone marrow, and gene test rules.
- Score above 50 on an age-based scale of daily activity and ability.
- Have no past leukemia treatment or stem cell transplant, except certain drugs allowed for a short time before study treatment.
- Have kidney and liver test results within study limits. The study leaders may waive liver limits if leukemia may affect the liver.
- Have a heart test showing that the heart pumps out at least 50% of its blood with each beat.
- If able to become pregnant, have a negative pregnancy test within 2 weeks before joining. Do not breastfeed during the study.
- If able to have children, agree to use approved birth control during the study and for at least 6 months after treatment.
Who can't join
- Have a known allergy to any study drug.
- Have an infection that is not improving with treatment. Patients must be off drugs that support blood pressure and have blood tests showing no infection for 48 hours.
- Plan to get chemotherapy, radiation, or immune-based cancer treatment outside this study during the study.
- Have another illness, mental health condition, or social issue that could make the study unsafe or prevent taking part or following study rules.
- Have Noonan syndrome or Down syndrome. Neurofibromatosis type 1 and CBL syndrome, also called Noonan-like syndrome, are allowed.
- Have previously used blood cell growth drugs, biologic cancer drugs, radiation, or any MEK inhibitor, a type of cancer drug.
- Take medicine to treat weakness in the heart’s main pumping chamber.
- Have or have had a blocked vein in the retina or fluid buildup under the retina, the light-sensing layer at the back of the eye.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: Age • Patients must be ≥ 1 month and ≤21 years of age at enrollment. Diagnosis • Patients must meet the 2022 International Consensus Classification criteria for JMML. The diagnosis is made based on the following criteria:. Clinical and hematologic features (the first 2 features are present in most cases; the last 2 are required): * Peripheral blood monocyte count ≥ 1 × 109/L\* * Splenomegaly† * Blast percentage in PB and BM \< 20% * Absence of BCR::ABL1 * This monocyte threshold is not reached in approximately 7% of cases. †Splenomegaly is absent in 3% of cases at presentation. II. Genetic studies (1 finding required): * Somatic mutation in PTPN11‡ or KRAS‡ or NRAS‡ or RRAS or RRAS2‡ * Clinical diagnosis of neurofibromatosis type 1 or germline NF1 mutation and loss of heterozygosity of NF1 or somatic biallelic loss of NF1 * Germline CBL mutation and loss of heterozygosity of CBL, or somatic mutation(s) in CBL§ * Germline mutations (indicating Noonan syndrome) need to be excluded. §Occasional cases with heterozygous splice site mutations. Performance Level * Karnofsky \> 50% for patients ≥ 16 years of age * Lansky \> 50% for patients \< 16 years of age. Prior Therapy * No prior leukemia directed therapy is permitted with the exception of: 1. Cytoreduction with hydroxyurea can be initiated and continued for up to 24 hours prior to the start of trametinib. 2. Cytoreduction with 6-mercaptopurine (6-MP) 6-MP can be initiated and continued for up to 72 hours prior to the start of trametinib. 3. Intrathecal (IT) cytarabine, IT methotrexate or triple IT therapy (cytarabine, methotrexate and hydrocortisone) within 7 days of enrollment as part of a diagnostic evaluation. No prior hematopoietic stem cell transplant is permitted. Adequate Renal Function Defined as: * Patient must have a calculated creatinine clearance or radioisotope GFR ≥ 70ml/min/1.73m2 OR a normal serum creatinine based on age/gender in the chart below: Maximum Serum Creatinine (mg/dL): * 1 month to \< 6 months old - Male: 0.4, Female 0.4 * 6 months to \<1 year old - Male 0.5, Female 0.5 * 1 to \< 2 years old - Male: 0.6, Female: 0.6 * 2 to \< 6 years old - Male:0.8, Female: 0.8 * 6 to \< 10 years old - Male: 1, Female: 1 * 10 to \< 13 years old - Male: 1.2, Female: 1.2 * 13 to \< 16 years old - Male: 1.5, Female: 1.4 * ≥ 16 years old - Male: 1.7, Female: 1.4 The threshold creatinine values in this Table were derived from the Schwartz formula for estimating GFR (Schwartz et al. J. Peds, 106:522, 1985) utilizing child length and stature data published by the CDC. Adequate Liver Function Defined as: * Direct bilirubin \< 1.5 x upper limit of normal (ULN) for age or normal, AND alanine transaminase (ALT) \< 5 x ULN for age. * The hepatic requirements are waived for patients with known or suspected liver involvement by leukemia and will not be evaluable for hepatotoxicity. This must be reviewed and approved by the study chair or vice chair. Adequate Cardiac Function Defined as: * Ejection fraction of \> or = to 50% by echocardiogram, OR * Ejection fraction of \> or = to 50% by radionuclide angiogram (MUGA). Reproductive Function * Female patients of childbearing potential must have a negative urine or serum pregnancy test confirmed within 2 weeks prior to enrollment. * Female patients with infants must agree not to breastfeed their infants while on this study. * Male and female patients of child-bearing potential must agree to use an effective method of contraception approved by the investigator during the study and for a minimum of 6 months after study treatment. Exclusion Criteria: * Patients cannot have a known allergy to any of the drugs used in the study. * Patients cannot have a systemic fungal, bacterial, viral, or other infection that is exhibiting ongoing signs/symptoms related to the infection without improvement despite appropriate antibiotics or other treatment. The patient needs to be off pressors and have negative blood cultures for 48 hours. * Patients cannot have a plan to administer non-protocol chemotherapy, radiation therapy, or immunotherapy during the study period. * Patients cannot have significant concurrent disease, illness, psychiatric disorder or social issue that would compromise patient safety or compliance with the protocol treatment or procedures, interfere with consent, study participation, follow up, or interpretation of study results. * Patients cannot have a clinical or molecular diagnosis of Noonan syndrome. Note: patients with either neurofibromatosis type 1 or Casitas B-lineage lymphoma (CBL) syndrome (also known as Noonan-like syndrome), are eligible to enroll. Patients with Down syndrome are excluded from the study. * Patient cannot have had prior use of hematopoietic growth factors, biologics (anti-neoplastic agent), or XRT. * Patients cannot be taking any medications for treatment of left ventricular systolic dysfunction. * Patients cannot have a history of or current evidence of retinal vein occlusion (RVO) or central serous retinopathy (CSR). * Patients cannot have had prior use of any MEK inhibitor.
Study sites (21)
AZ
- Phoenix Children's Hospital · Phoenix, AZ 85016Dana Salzberg, MD · Study contactMore trials in Phoenix
CA
- Children's Hospital Los Angeles · Los Angeles, CA 900027Jaime Stokke, MD · Study contactMore trials in Los Angeles
- University of California San Francisco · San Francisco, CA 94158Elliot Stieglitz, MD · Study contactMore trials in San Francisco
CO
- Children's Hospital of Colorado · Denver, CO 80045Kelly Faulk, MD · Study contactMore trials in Denver
DC
- Children's National Medical Center · Washington D.C., DC 20010Reuven Schore, MD · Study contactMore trials in Washington D.C.
FL
- University of Miami · Miami, FL 33136Julio Barredo, MD · Study contactMore trials in Miami
GA
- Children's Hospital of Atlanta · Atlanta, GA 30322Melinda Pauly, MD · Study contactMore trials in Atlanta
IL
- Lurie Children's Hospital of Chicago · Chicago, IL 60611Jenna Rossoff, MD · Study contactMore trials in Chicago
IN
- Indiana University/Riley Hospital for Children · Indianapolis, IN 46202Sandeep Batra, MD · Study contactMore trials in Indianapolis
MD
- Sidney Kimmel Cancer Center at Johns Hopkins · Baltimore, MD 21231Stacy Cooper, MD · Study contactMore trials in Baltimore
MI
- C.S. Mott Children's Hospital · Ann Arbor, MI 48109Jennifer Agrusa, MD · Study contactMore trials in Ann Arbor
MO
- Children's Mercy Hospital · Kansas City, MO 64108Keith August, MD · Study contactMore trials in Kansas City
NC
- Levine Children's Hospital at Carolinas · Charlotte, NC 28203Joel Kalpan, MD · Study contactMore trials in Charlotte
NY
- Memorial Sloan Kettering Cancer Center · New York, NY 10065Kavitha Ramaswamy, MD · Study contactMore trials in New York
OH
- Cincinnati Children's Hospital Medical Center · Cincinnati, OH 45229Lauren Pommert, MD · Study contactMore trials in Cincinnati
OR
- Oregon Health & Science University · Portland, OR 97239Bill Chang, MD · Study contactMore trials in Portland
PA
- Children's Hospital of Philadelphia · Philadelphia, PA 19104Sarah Tasian, MD · Study contactMore trials in Philadelphia
TN
- St. Jude Children's Research Hospital Memphis · Memphis, TN 38105Seth Karol, MD · Study contactMore trials in Memphis
TX
- Children's Medical Center · Dallas, TX 75235Tamra Slone, MD · Study contactMore trials in Dallas
UT
- Primary Children's Hospital · Salt Lake City, UT 84113Mallorie Heneghan, MD · Study contactMore trials in Salt Lake City
WA
- Seattle Children's Hospital · Seattle, WA 98105Mignon Loh, MD · Study contactMore trials in Seattle