Midostaurin in MRD (Minimal Residual Disease) Positive Acute Myeloid Leukemia After Allogeneic Stem Cell Transplantation

University of Jena

Status and phase

Terminated

Phase 2

Conditions

Acute Myeloid Leukemia, Adult

Treatments

Drug: Midostaurin

Study type

Interventional

Funder types

Other

Identifiers

NCT03951961

2019-000136-26 (EudraCT Number)

MAURITIUS

Details and patient eligibility

About

The MAURITIUS trial is a single-arm, multicenter phase II study of single treatment with midostaurin being applied to AML (acute myeloid leukemia) patients with activating FLT3 (FMS-like tyrosine kinase3) mutations and either molecular relapse or persistent molecular positivity after allogeneic SCT. The leukemia-free survival (LFS), the achievement of "MRD low" as well as the incidence of GvHD after transplantation reflect the most relevant endpoints of this non-randomized clinical trial.

Full description

The clinical situation of AML (acute myeloid leukemia) relapse after intensive chemotherapy or even after allogeneic SCT represents a huge challenge in hematology. So far, no FLT3-TKI (Tyrosine kinase Inhibitor) has been approved for the treatment of relapsed or refractory AML with activating FLT3 mutations in the European Union.

For elderly and unfit patients at primary diagnosis and for patients with AML relapse after induction and consolidation chemotherapy (including those with allogeneic SCT) who are not eligible for any further intensive treatment approach, AML therapy with HMA (hypomethylating agents) represents the standard of care and is associated with an even worse prognosis in those patients who relapse with AML after transplantation.

The FLT3-TKI midostaurin has been approved for newly diagnosed AML patients with activating FLT3 mutations who receive intensive induction and subsequent consolidation chemotherapy including midostaurin maintenance restricted to patients who do not undergo allogeneic SCT. So far, there is no approval of FLT3-TKI treatment for patients with FLT3-mutated AML after allogeneic SCT. Recently, preliminary data of the RADIUS trial investigating midostaurin maintenance after allogeneic SCT could demonstrate the feasibility of midostaurin treatment in the setting of post-transplant AML patients. Importantly, only half of patients were able to complete 12 cycles of maintenance and in most cases midostaurin was prematurely ceased due to a higher rate of adverse events than expected. As a consequence of this clinical trial, there is a good rationale to investigate midostaurin maintenance after allogeneic SCT focusing on those AML patients with a high risk of hematologic relapse after transplantation.

In detail, MRD assessment provides a reliable method in the majority of patients with FLT3-mutated AML (e.g. by qPCR) to identify AML patients with the highest risk of relapse following allogeneic SCT. There are consistent data demonstrating that MRD positivity by means of NPM1 (Nuclophosphmin-1)mutation (i.e. 100 to 1000 copies of mutated NPM1 per 10,000 ABL (Abelson Murine Leukemia Viral Oncogene Homolog) transcripts or 1% to 10% NPM1/ABL, respectively, is associated with a 60-90% risk of hematologic relapse.

Thus, this clinically relevant subgroup of AML patients with activating FLT3 mutations who develop a molecular relapse or who are characterized by a persistent MRD positivity after intensive AML treatment represents the target population of this clinical trial. The rationale of this study is to treat AML patients with MRD positivity using single midostaurin treatment and to improve the clinical outcome of these patients by preventing hematologic relapse after allogeneic SCT by "targeted therapy" against activating FLT3 mutations.

Enrollment

1 patient

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with molecular relapse or persistent molecular positivity of AML after allogeneic SCT (stem cell Transplantation)
Detection of FLT3-ITD (Internal tandem duplication) or FLT3-TKD (tyrosine kinase domain) at primary diagnosis or at antecedent relapse of AML prior to allogeneic SCT
Sensitive MRD assessment based on qPCR (e.g. by means of NPM1 mutations)
absolute neutrophil count > 1,0 Gpt/L and Platelets > 50 Gpt/L
ECOG (Eastern Cooperative Oncology Group) performance status 0-2
glomerular filtration rate > 30 ml/min and serum bilirubin < 1.5 x upper limit of normal
Serum aspartate transaminase (AST) and/or alanine transaminase (ALT) ≤ 3.0 × ULN
Normal serum levels of potassium, magnesium, and corrected calcium
Written informed consent prior to any study procedures being performed
Age ≥ 18 years

Exclusion criteria

Acute promyelocytic leukemia (APL)
Hematological relapse of AML
Lack of a suitable MRD marker
Impaired ejection fraction (LVEF) < 45%
Patients with midostaurin treatment after allogeneic SCT or with ongoing TKI therapy < 4 weeks prior to inclusion
Treatment with an investigational drug within 5 half-lives preceding the first dose of study medication
History of acute or chronic pancreatitis
Active and uncontrolled infections
History of severe lung disease and/or relevant functional impairment
Medical indication for treatment with strong CYP3A4 inhibitors (e.g. voriconazole, posaconazole, clarithromycin)
Positive PCR for Human Immunodeficiency Virus (HIV) or Hepatitis B or C
Patients unable to swallow medication
Known hypersensitivity reaction to midostaurin or any excipient of midostaurin
Concomitant medications with known induction of CYP3A4 isoenzyme unless they can be discontinued or replaced prior to enrollment
Patients who have undergone major surgery ≤ 2 weeks prior to starting study drug or who have not recovered from side effects of such therapy
Patients who are pregnant or breast feeding, or females of reproductive potential not employing an effective method of birth control. Female patients must agree to an effective birth control throughout the study and for up to 4 months beyond.
Other medical conditions (e.g. corrected QT interval prolongation) that might interfere with midostaurin treatment
Substance abuse, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results