Lymphoblastic Leukemia, Acute, ChildhoodPhase 1NCT01861002
A Phase I Study of 5-Azacytidine in Combination With Chemotherapy for Children With Relapsed or Refractory ALL or AML
A Phase 1 study testing Azacytidine, Fludarabine and Cytarabine in people with Lymphoblastic Leukemia, Acute, Childhood and Myelogenous Leukemia, Acute, Childhood, run by Therapeutic Advances in Childhood Leukemia Consortium at 23 sites in 3 countries.
Trial summary
This is a Phase I study with a conditional cohort expansion phase to evaluate the feasibility of, and to obtain preliminary efficacy data about, pretreatment with Azacytidine (AZA) for 5 days followed by fludarabine/cytarabine chemotherapy regimen in pediatric acute myeloid leukemia (AML) and acute lymphoblastic… Read more about this study
- Who is it for?
- Ages 1 year to 21 years
- Conditions the study is for
- Lymphoblastic Leukemia, Acute, Childhood, Myelogenous Leukemia, Acute, Childhood
- What is being tested?
- Azacytidine, Fludarabine and Cytarabine
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 15 participants
- Where
- 23 sitesin 3 countries
- Study dates
- 22 May 2013to 28 Jul 2014
- Phase
- Phase 1
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 1 year to 21 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Patients must be ≥ 1 and ≤ 21 years of age.
- Diagnosis
- Patients with AML must have ≥5% blasts (by morphology) in the bone marrow.
- Patients with ALL must have an M2 or M3 marrow (≥5% blasts by morphology).
- Patients may have disease in the central nervous system (CNS) or other sites of extramedullary disease. No cranial irradiation is allowed during the protocol therapy.
- Patients with secondary AML are eligible.
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- Patients with Down syndrome and DNA fragility syndromes (such as Fanconi anemia, Bloom syndrome) are excluded.
- Karnofsky > 50% for patients > 16 years of age and Lansky > 50% for patients ≤ 16 years of age.
- Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study.
- Myelosuppressive chemotherapy - the eligibility criteria is different between phase I and expansion phase
- Phase I
- Any patient with AML in 1st or greater relapse, OR
- Any patient with ALL in 2nd or greater relapse, OR
- Patients with AML or ALL failed to go into remission after first or greater relapse, OR
- Patients with AML or ALL failed to go into remission from original diagnosis after two or more courses of induction attempts.
- Expansion phase - will be restricted to AML patients only
- Cytoreduction with hydroxyurea can be initiated and continued for up to 24 hours prior to the start of azacytidine. It is recommended to use hydroxyurea in patients with significant leukocytosis (WBC > 50,000/L) to control blast count before initiation of systemic protocol therapy.
- Patients who relapsed while they are receiving cytotoxic therapy (including AZA , decitabine, or vorinostat) At least 14 days must have elapsed since the completion of the cytotoxic therapy.
- Hematopoietic stem cell transplant: Patients who have experienced their relapse after a stem cell transplant are eligible, provided they have no evidence of acute or chronic Graft-versus-Host Disease (GVHD) and are at least 90 days post-transplant at the time of enrollment.
- Hematopoietic growth factors: It must have been at least 7 days since the completion of therapy with filgrastim or other growth factors at the time of enrollment. It must have been at least 14 days since the completion of therapy with pegfilgrastim (Neulasta®).
- Biologic (anti-neoplastic agent): At least 7 days after the last dose of a biologic agent. For agents that have known adverse events occurring beyond 7 days after administration, this period must be extended beyond the time during which adverse events are known to occur. The duration of this interval must be discussed with the study chair
- Monoclonal antibodies: At least 3 half-lives of the antibody must have elapsed after the last dose of monoclonal antibody. (i.e. Gemtuzumab = 36 days)
- Immunotherapy: At least 42 days after the completion of any type of immunotherapy, e.g. tumor vaccines.
- Radiation Therapy (XRT): Craniospinal XRT is prohibited during protocol therapy. No washout period is necessary for radiation given to non-CNS chloromas; ≥ 90 days must have elapsed if prior total body radiation or craniospinal radiation.
- Renal and hepatic function
- Patients must have adequate renal and hepatic functions as indicated by the following laboratory values:
- Patient must have a calculated creatinine clearance or radioisotope glomerular filtration rate (GFR) greater than or equal to 70ml/min/1.73m2 OR a normal serum creatinine based on age/gender.
- Direct bilirubin < 1.5 x upper limit of normal (ULN) for age or normal, AND alanine transaminase (ALT) < 5 x ULN for age.
- Adequate Cardiac Function Defined as: Shortening fraction greater than or equal to 27% by echocardiogram, OR ejection fraction greater than or equal 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.
- Patients and/or their parents or legal guardians must be capable of understanding the investigational nature, potential risks and benefits of the study. All patients and/or their parents or legal guardians must sign a written informed consent.
Who cannot join
- Patients will be excluded if they have a known allergy to any of the drugs used in the study.
- Patients will be excluded if they 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 will be excluded if there is a plan to administer non-protocol chemotherapy, radiation therapy, or immunotherapy during the study period.
- Patients will be excluded if they 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 with Down syndrome and DNA fragility syndromes (such as Fanconi anemia, Bloom syndrome) are excluded.
Trial locations and contacts
23 sites in 3 countries.
23 sites in 3 countries
United States19 sites
C.S. Mott Children's Hospital
Ann Arbor, Michigan, 48109-0914
Children's Healthcare of Atlanta, Emory University
Atlanta, Georgia, 30322
Johns Hopkins University
Baltimore, Maryland, 21287
Dana Farber
Boston, Massachusetts, 02215
Levine Children's Hospital at Carolinas Medical Center
Charlotte, North Carolina, 28203
Rainbow Babies & Children's Hospital
Cleveland, Ohio, 44106
Nationwide Childrens Hospital
Columbus, Ohio, 43205
University of Texas at Southwestern
Dallas, Texas, 75235
Cook Children's Medical Center
Fort Worth, Texas, 76104
Children's Mercy Hospitals and Clinics
Kansas City, Missouri, 64108
Childrens Hospital Los Angeles
Los Angeles, California, 90027
Children's Hospital of Wisconsin
Milwaukee, Wisconsin, 53226
Childrens Hospital & Clinics of Minnesota
Minneapolis, Minnesota, 55404-4597
Vanderbilt Children's Hospital
Nashville, Tennessee, 37232
Children's Hospital New York-Presbyterian
New York, New York, 10032
Primary Children's Medical Center
Salt Lake City, Utah, 84113
UCSF School of Medicine
San Francisco, California, 94143-0106
Seattle Children's Hospital
Seattle, Washington, 98105
Children's National Medical Center
Washington D.C., District of Columbia, 20010
Australia2 sites
Sydney Children's Hospital
Randwick, New South Wales, 2031
Children's Hospital at Westmead
Westmead, New South Wales, 2145
Canada2 sites
Sainte-Justine University Hospital Center
Montreal, Quebec, H3T-1C5
British Columbia Children's Hospital
Vancouver, British Columbia, V6H 3V4
About this study
This is a Phase I study with a conditional cohort expansion phase to evaluate the feasibility of, and to obtain preliminary efficacy data about, pretreatment with Azacytidine (AZA) for 5 days followed by fludarabine/cytarabine chemotherapy regimen in pediatric acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) patients who are refractory to primary treatment or who relapsed.
Read the detailed description
Growing evidence indicates that aberrant DNA hypermethylation is associated with leukemia development, drug resistance, and relapse. It has been shown that pretreating leukemia cells with AZA or decitabine could partially reverse the aberrant DNA methylation, restore the expression of tumor suppressor gene important for apoptosis, and sensitize cells to subsequent killing by cytotoxic agent. Since cytarabine and decitabine share the same mechanisms of resistance, we use AZA to test the novel epigenetic "priming" approach. This is a phase I clinical study with expansion phase, using hypomethylating agent, 5-azacytidine (AZA), in sequential with chemotherapy to evaluate whether epigenetic "priming" can reverse aberrant DNA methylation, overcome drug resistance, and increase response in relapsed/refractory AML.
The chemotherapy regimen to be used in this study is fludarabine and cytarabine. This regimen has substantial activity in leukemia and has been widely used in treating pediatric patients with relapsed/refractory AML and ALL in the past several decades. In BFM relapsed AML 2001/01 study, FLAG (fludarabine, cytarabine and G-CSF) chemotherapy regimen showed significant activity in AML with 4 year OS around 36%. Since the use of G-CSF in conjunction with fludarabine/cytarabine didn't improve the overall survival of patient in a randomized trial, only fludarabine and cytarabine will be used in this study to decrease the incidence of leukocytosis related complications. This regimen is very similar to the chemotherapy regimen proposed for the next relapsed AML trial within the Children's Oncology Group (COG). If this trial proves to be safe and active, it will provide the foundation and smooth transition to larger statistically powered nationwide phase II clinical trials by COG.
- Being tested
- Azacytidine, Fludarabine, Cytarabine, Intrathecal (IT) Cytarabine, Intrathecal Methotrexate (IT MTX)
- Keywords
- Relapse, Lymphoblastic, Leukemia, Azacytidine, Refractory, Myelogenous, Acute, Childhood, Pediatric, ALL, AML, Methylation, Epigenetic therapy
- Medical subject headings
- Precursor Cell Lymphoblastic Leukemia-Lymphoma, Leukemia, Myeloid, Recurrence, Leukemia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AzacytidineDrug
Also called 5 Azacytidine, Vidaza
Dose assigned at study entry (75 mg/m2/day). Given subcutaneously, once daily on days 1 to 5, for a total of 5 doses.
FludarabineDrug
Also called fludarabine phosphate, Fludara, 2-fluoro-ara-AMP, Oforta
30 mg/m2/dose, intravenous infusion over 30 minutes, once daily, on days 6 to 10, total 5 doses
CytarabineDrug
Also called Cytosar-U, Ara-C, Arabinosylcytosine, cytosine arabinoside
2000 mg/m2/dose intravenous infusion over 3 hours, starting 4 hours after the beginning of fludarabine, once daily, on days 6 to 10, total 5 doses.
Intrathecal (IT) CytarabineDrug
Also called (See Cytarabine)
Intrathecally to AML patients on day 1 of course 1 and 2.
- Omit on day 1 of course 1 if patient received IT therapy within 7 days prior to study enrollment
- IT therapy may be given during the end of course 1 disease evaluation and repeated every 7 days
- For patients with CNS disease, IT cytarabine can be given weekly until the CSF is clear. Two additional doses of IT cytarabine should be given weekly after the initial CSF clearing. It is permitted to change to intrathecal triple therapy (ITT) if persistent blasts are present in the CSF based on the treating physician's clinical judgment. Cytarabine dose defined by age:
- 30 mg for patients age 1-1.99
- 50 mg for patients age 2-2.99
- 70 mg for patients >3 years of age
ITT Dosing:
Age (yrs) - Dose Methotrexate (MTX), Hydrocortisone (HC), Cytarabine (ARAC):
- - 1.99 MTX: 8 mg, HC: 15 mg, ARAC: 30 mg
- - 2.99 MTX: 10 mg, HC: 25 mg, ARAC: 50 mg
- 3 - MTX: 12 mg, HC: 35 mg, ARAC: 70 mg
Intrathecal Methotrexate (IT MTX)Drug
Also called Otrexup, Rasuvo, Rheumatrex, Trexall
- Intrathecally to patients with ALL on day 1 of course 1 and 2.
- Omit IT MTX on Day 1 of course 1 if patient received IT therapy within 7 days prior to study enrollment
- IT therapy may be given during the end of course 1 disease evaluation and repeated every 7 days
- For patients with CNS 2 or 3 disease, IT MTX can be given weekly until the CSF is clear. Two additional doses of IT MTX should be given weekly after the initial clearing of the CSF. It is permitted to change to ITT if persistent blasts are present in the CSF. Methotrexate dose defined by age
- 8 mg for patients age 1-1.99
- 10 mg for patients age 2-2.99
- 12 mg for patients 3-8.99 years of age
- 15 mg for patients >9 years of age
Triple IT Therapy Dosing:
Age (yrs): Dose Methotrexate (MTX), Hydrocortisone (HC), Cytarabine (ARAC):
- - 1.99 MTX: 8 mg, HC: 8 mg, ARAC: 16 mg
- - 2.99 MTX: 10 mg, HC: 10 mg, ARAC: 20 mg
- - 8.99 MTX: 12 mg, HC: 12 mg, ARAC: 24 mg
- 9 MTX: 15 mg, HC: 15 mg, ARAC: 30 mg
| Study group | Role | What they receive |
|---|---|---|
| AML Arm | Experimental | Participants with Acute Myeloid Leukemia (AML)
Intervention:
* Azacytidine (Dose Level 1 @ 75 mg/m2/day)
* Fludarabine 30 mg/m2/dose
* Cytarabine 2000 mg/m2/dose
* Intrathecal (IT) Cytarabine Receives: Drug: Azacytidine; Drug: Fludarabine; Drug: Cytarabine; Drug: Intrathecal (IT) Cytarabine |
| ALL Arm | Experimental | Patients with Acute Lymphocytic Leukemia
Intervention:
* Azacytidine (Dose Level 1 @ 75 mg/m2/day)
* Fludarabine 30 mg/m2/dose
* Cytarabine 2000 mg/m2/dose
* Intrathecal Methotrexate (IT MTX) Receives: Drug: Azacytidine; Drug: Fludarabine; Drug: Cytarabine; Drug: Intrathecal Methotrexate (IT MTX) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Participants Who Experienced a Dose Limiting Toxicity (DLT)
To evaluate the side effects of giving Azacytidine before and during chemotherapy using the standard drugs Fludarabine, Cytarabine, IT Cytarabine (AML patients) and IT methotrexate (ALL patients)
Measured: From Day 1 to Day 42 (Cycle 1)
Secondary outcomes (1)
Disease Response Rate After Treatment
CR is defined as a bone marrow with < 5% blast by morphology, no evidence of extramedullary disease, and recovery of peripheral counts (ANC ≥ 1000/μl and platelet counts ≥ 100,000/μl). CR with incomplete count recovery (CRi) was defined as CR without recovery of ANC and/or platelets. Partial response (PR) was defined as complete disappearance of circulating blasts and a decrease of at least 50% of blasts in the bone marrow. Progressive disease (PD) was defined as an increase of at least 25% in the absolute number of bone marrow or circulating blasts, development of new sites of extramedullary disease, or other laboratory or clinical evidence of progression of disease. Stable disease (SD) referred to patient who did not satisfy the criteria for either CR, CRi, PR or PD.
Measured: Between Days 36-42 of Courses 1 and 2
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 May 2013 (estimated)
- Study start22 May 2013
- Primary completion28 Jul 2014
- Study completion28 Jul 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Lymphoblastic Leukemia, Acute, ChildhoodStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 15 participants (actual)
Sponsor and investigators
- Lead sponsor
- Therapeutic Advances in Childhood Leukemia Consortium
- Sponsor type
- University, hospital or other
- Collaborators
- Gateway for Cancer Research
- Responsible party
- Sponsor
- Investigators
- Weili Sun, MD, PhD, Study chair, Children's Hospital Los Angeles
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01861002
- Sponsor's protocol ID
- T2011-002
- Status last verified
- May 2021
- First submitted
- 21 May 2013
- Last updated
- 9 Jun 2021
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Sun W, Triche T Jr, Malvar J, Gaynon P, Sposto R, Yang X, Bittencourt H, Place AE, Messinger Y, Fraser C, Dalla-Pozza L, Salhia B, Jones P, Wayne AS, Gore L, Cooper TM, Liang G. A phase 1 study of azacitidine combined with chemotherapy in childhood leukemia: a report from the TACL consortium. Blood. 2018 Mar 8;131(10):1145-1148. doi: 10.1182/blood-2017-09-803809. Epub 2018 Jan 16. No abstract available.
PubMed 29339403