Study of Ponatinib (Iclusig) for Prevention of Relapse After Allogeneic Stem Cell Transplantation (Allo-SCT) in FLT3-ITD AML Patients (PONALLO)

• ClinicalTrials.gov Identifier: NCT03690115
• Recruitment Status: Recruiting
• First Posted: October 1, 2018
• Last Update Posted: August 5, 2021
• Sponsor: Versailles Hospital
• Information provided by (Responsible Party): Patrice Chevallier, Nantes University Hospital

Tracking Information

• First Submitted Date: April 4, 2018
• First Posted Date: October 1, 2018
• Last Update Posted Date: August 5, 2021
• Actual Study Start Date: December 2, 2019
• Estimated Primary Completion Date: December 2, 2021 (Final data collection date for primary outcome measure)
• Current Primary Outcome Measures (submitted: September 27, 2018): Relapse incidence at 2 years from transplant [ Time Frame: 2 years ]
• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: September 27, 2018)

• Overall survival [ Time Frame: 2 years ]
  time interval from the graft (day 0) until the date of last follow-up or death
• Leukemia free survival [ Time Frame: 2 years ]
  time interval from the date of the graft (day 0) until the date of last follow-up, death or relapse
• Non-relapse mortality (NRM) [ Time Frame: day 100 ]
  incidence of mortality due to all causes except relapse after transplant, considering that cause of death for patients having relapsed but dying from another cause is relapse
• Acute and chronic GVHD [ Time Frame: 2 years ]
  NIH score
• Influence of Ponatinib on Immune reconstitution PB lymphocyte cells [ Time Frame: 1 years ]
  an immunophenotype of PB lymphocytes will be performed by flow cytometry at +3, +6, +9 and +12 months post-transplant to study the reconstitutions of CD3, CD4 and CD8 T cells, B and NK cells. The results will be expressed as absolute counts (Giga/L). We want to establish the potential influence of ponatinib on the reconstitution of these cells
• Inflence of Ponatinib on Chimerism of Donor peripheral blood and CD3 T cells [ Time Frame: 1 years ]
  Donor peripheral blood and CD3 T cells chimerism will be studied using molecular markers and RT-PCR at day +30, +60, +90, and +6, +12 months post-transplant. We want to establish the potential influence of ponatinib on the chimerism post-transplant.
• Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 [ Time Frame: 2 years ]

• Original Secondary Outcome Measures: Same as current
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Study of Ponatinib (Iclusig) for Prevention of Relapse After Allogeneic Stem Cell Transplantation (Allo-SCT) in FLT3-ITD AML Patients
• Official Title: Phase 2 Study of Ponatinib (Iclusig) for Prevention of Relapse After Allogeneic Stem Cell Transplantation (Allo-SCT) in FLT3-ITD AML Patients: the PONALLO Trial."

Brief Summary

Recent advances in acute myeloid leukemia (AML) have been characterized by a better understanding of disease biology. As such, FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) have been recognized as conferring a poor prognosis. The FLT3-ITD molecular mutation is observed in about one-quarter of patients diagnosed with AML. Patients presenting with this abnormality are referred for early allogeneic stem-cell transplantation (allo-SCT). However, some data suggest that FLT3-ITD remains associated with a poor prognosis even after allo-SCT because of higher risk of relapse and strategies for preventing relapse in the post-transplant setting are required (Hu et al, Expert Rev Hematol, 2014). For example, in a large cohort of patients (Brunet et al, JCO, 2012), the incidence of relapse for FLT3-ITD AML patients after allo-SCT was 30% at 2-years, significantly higher compared to FLT3-ITD negative patients (p=0.006).

Ponatinib (Iclusig®) is an orally available, tyrosine kinase inhibitor with a unique binding mechanism allowing inhibition of BCR-ABL kinases, including those with the T315I point mutation. Ponatinib also has in vitro inhibitory activity against a discrete set of kinases implicated in the pathogenesis of other hematologic malignancies, including FLT3, KIT, fibroblast growth factor receptor 1 (FGFR1), and platelet derived growth factor receptor α (PDGFRα). In vitro activity of ponatinib in AML has been already demonstrated (Gozgit et al, Mol Cancer Ther, 2011; Smith et al, Blood 2013). If some trials are on-going to test ponatinib alone or in combination with chemotherapy in FLT3-ITD AML (Clinical.trials.gov), no study is dedicated to the use of ponatinib in the post-transplant setting in order to prevent relapse in these patients.

The main goal of this study will be to determine the maximal tolerated dose (MDT) of ponatinib after allo-SCT in FLT3-ITD AML patients, then to investigate the efficacy of ponatinib in a larger cohort of patients

• Detailed Description: Not Provided
• Study Type: Interventional
• Study Phase: Phase 2
• Study Design: Allocation: N/A; Intervention Model: Single Group Assignment; Masking: None (Open Label); Primary Purpose: Treatment
• Condition: Leukemia, Myeloid, Acute

Intervention

Drug: Ponatinib 30 MG

Administration of ponatinib after allo-SCT transplant in FLT3-ITD AML patient

Study Arms

Experimental: Experimental

Administration of ponatinib after allo-SCT transplant in FLT3-ITD AML patient

Intervention: Drug: Ponatinib 30 MG

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Recruiting
• Estimated Enrollment (submitted: September 27, 2018): 77
• Original Estimated Enrollment: Same as current
• Estimated Study Completion Date: June 2024
• Estimated Primary Completion Date: December 2, 2021 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Engraftment
• Controlled GVHD
• Positive FLT-3 ITD AML in cytologic complete remission
• Have an Eastern Cooperative Oncology Group (ECOG) performance status < 2
• Have adequate renal function: Serum creatinine ≤ 1.5 × upper limit of normal (ULN) for institution
• Have adequate hepatic function: Total serum bilirubin ≤ 1.5 × ULN, unless due to Gilbert's syndrome; Alanine aminotransferase (ALT) ≤ 2.5 × ULN, or ≤ 5 × ULN if leukemic infiltration of the liver is present ; Aspartate aminotransferase (AST) ≤ 2.5 × ULN, or ≤ 5 × ULN if leukemic infiltration of the liver is present
• Have normal pancreatic status: Serum lipase and amylase ≤ 1.5 × ULN
• Have normal QTcF interval on screening electrocardiogram (ECG) evaluation,defined as QTcF of ≤ 450 ms in males or ≤ 470 ms in females.
• Platelets ≥ 100 Giga/l; Neutrophils ≥ 1 Giga/l
• Have a negative pregnancy test documented prior to enrollment (for females of childbearing potential).
• Agree to use an effective form of contraception with sexual partners throughout study participation (for female and male patients who are fertile).
• Provide written informed consent.
• Be willing and able to comply with scheduled visits and study procedures.

Exclusion Criteria:

• HIV positive, active Hepatitis B or C
• Childbearing or childbreast feeding women
• Women or men without effective contraceptive barrier if needed
• Previous myocardial infarction, or cerebral vascular accident, pancreatitis
• Respiratory insufficiency defined as DLCO <40% of the corrected value
• Creatinine clearance ≤ 50ml/min
• Contra-indication to ponatinib
• Previous or concurrent second malignancy except for adequately treated basal cell carcinoma of the skin, curatively treated in situ carcinoma of the cervix, curatively treated solid cancer, with no evidence of disease for at least 2 years
• Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule

• Patients at high or very high risk of cardiovascular disease with any of the following

  1. Established cardiovascular disease Cardiac disease:

     • Congestive heart failure greater than class II NYHA or
     • Left ventricular ejection fraction (LVEF) < 50% or
     • Unstable angina (anginal symptoms at rest) or
     • New onset angina (began within the last 3 months) or
     • Myocardial infarction, coronary/peripheral artery disease, congestive heart failure, cerebrovascular accident including transient ischemic attack within the past 12 months or
     • History of thrombolic or embolic events Arrhythmias
     • Any history of clinically significant cardiac arrhythmias requiring anti-arrhythmic therapy.
  2. Diabetes Mellitus,

  3. Arterial Hypertension,

     • Uncontrolled hypertension defined as systolic blood pressure greater than 140 mmHg or diastolic pressure greater than 90 mmHg, despite optimal medical management and optimal measurement (http://www.has-sante.fr/portail/display.jsp?id=c_272459)
     • Any history of hypertension with
     • Hypertensive encephalopathy
     • Posterior leucoencephalopathy
     • Aortic or artery dissection
  4. Familial dysplipidemia.
  5. Taking medications that are known to be associated with Torsades de Pointes (see

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years to 70 Years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Contacts

Contact: Laure MORISSET; +33139239785; lmorisset@ch-versailles.fr

• Listed Location Countries: France

Administrative Information

• NCT Number: NCT03690115
• Other Study ID Numbers: P1701_ PONALLO
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

• IPD Sharing Statement: Not Provided
• Current Responsible Party: Patrice Chevallier, Nantes University Hospital
• Original Responsible Party: Same as current
• Current Study Sponsor: Versailles Hospital
• Original Study Sponsor: Same as current
• Collaborators: Not Provided
• Investigators: Not Provided
• PRS Account: Versailles Hospital
• Verification Date: August 2021