Revumenib with Cytarabine, Daunorubicin and Midostaurin for the Treatment of Patients with NPM1 and FLT3 Mutated Acute Myeloid Leukemia
This phase I trial tests safety, side effects and best new dose of revumenib in combination with cytarabine, daunorubicin and midosataurin for the treatment of patients with NPMI and FLT3 mutated acute myeloid leukemia (AML). Revumenib is in a class of medications called menin inhibitors. It works by blocking the action of an abnormal menin-MLL complex that signals cancer cells to multiply. This may help keep cancer cells from growing and may kill them. Chemotherapy drugs, such as cytarabine, daunorubicin and midosataurin, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving revumenib with cytarabine, daunorubicin and midosataurin may be safe and tolerable in treating patients with NPMI and FLT3 mutated AML.
Inclusion Criteria
- Patients with AML who are newly diagnosed according to the World Health Organization (WHO) 2022 Classification and previously untreated except for hydroxyurea. All-trans retinoic acid (ATRA) pretreatment for suspected acute promyelocytic leukemia (APL) for less than 5 days is allowed. Eligible patients with AML arising from an antecedent hematologic disease (AHD) including myelodysplastic syndrome (MDS), may have been treated for their prior hematologic disease (except for allogenic transplant)
- Patients must be ≥ 18 and < 75 years old
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
- Presence of FLT3-ITD and/or TKD mutation(s) AND NPM1 mutation in bone marrow or peripheral blood
- DOSE ESCALATION PHASE ONLY: Presence of any of the following adverse risk genetic characteristics: * 2022 European Leukemia Net (ELN) adverse risk genetic features: ** t(6;9)(p23.3;q34.1)/DEK::NUP214 ** t(v;11q23.3)/KMT2A-rearranged ** t(9;22)(q34.1;q11.2)/BCR::ABL1 ** t(8;16)(p11.2;p13.3)/KAT6A::CREBBP ** inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2)/ GATA2, MECOM(EVI1) ** t(3q26.2;v)/MECOM(EVI1)-rearranged ** −5 or del(5q); −7; −17/abn(17p) ** Complex karyotype, monosomal karyotype ** Mutations in either one of these genes: ASXL1, BCOR, EZH2, RUNX1, SF3B1, SRSF2, STAG2, U2AF1, and/or ZRSR2 ** Mutated TP53 * NPM1 + FLT3-ITD + DNMT3A mutation
- Left ventricular ejection fraction (LVEF) ≥ 50% by MUGA or ECHO at screening
- Adequate renal function as demonstrated by a calculated creatinine clearance ≥ 60 mL/min; determined by the Cockcroft Gault formula
- Aspartate aminotransferase (AST) ≤ 2.5 × upper limit of nornal (ULN) and alanine aminotransferase (ALT) ≤ 2.5 × ULN * Unless considered due to leukemic organ involvement
- Total bilirubin ≤ 1.5 × ULN * Unless considered due to leukemic organ involvement. * Note: Subjects with Gilbert's Syndrome may have a total bilirubin > 1.5 × ULN per discussion with the sponsor-investigator
- Resolution of adverse reactions to prior drug therapy (such as hydroxyurea) to ≤ grade 1
- Eligible for intensive cytarabine/daunorubicin (7+3) chemotherapy based on the opinion of the treating physician
- Male subjects must agree to refrain from unprotected sex and sperm donation from initial study drug administration until 90 days after the last dose of study drug
- Females of childbearing potential (i.e., not postmenopausal for at least 1 year or not surgically sterile) must have negative results by a serum or urine pregnancy test performed within 7 days of day 1
- Ability to understand and the willingness to sign a written informed consent document. (Providing consents in as many languages as possible is encouraged)
- Consolidation should occur between 1-4 weeks following count recovery after induction and remission (must be confirmed by labs to document maximal response) is established. Subjects will receive medium intensity cytarabine -based consolidation in combination with midostaurin and revumenib if the following criteria are fulfilled: * An induction response < 5% blasts in the bone marrow and absolute neutrophil count (ANC) >1000 and platelet (PLT) >75000 for whom documented path report is submitted. * Sufficiently fit (performance status < 3) * Resolution of any adverse reactions to no greater than grade 1 severity
- QTc using Fridericia’s correction [QTcF]) > 450 msec. Drugs that prolong QTc should be avoided if possible. A list of common QTc prolonging drugs and alternatives that are not QTc prolonging can be found in the protocol document
- Subject is known to be positive for hepatitis B or C infection with the exception of those with an undetectable viral load within 3 months. (Hepatitis B or C testing is not required). Subjects with serologic evidence of prior vaccination to hepatitis B virus (HBV) (i.e., hepatitis B surface antigen negative [HBs Ag-], and anti hepatitis B surface positive [HBs+]) are allowed
Exclusion Criteria
- Subject has acute promyelocytic leukemia, inversion (16), t(8;21) AML as described below. Contact Sponsor-Investigator with questions. Inversion 16 and t(8;21): core binding factor (CBF) chromosomal abnormalities may be assessed by molecular (PCR), metaphase cytogenetics, or fluorescence in situ hybridization (FISH)
- Subject has known active central nervous system (CNS) involvement with AML
- Subject has received a strong CYP3A4 inducer within 7 days prior to the initiation of study treatment
- Strong CYP3A4 inhibitors are contraindicated except strong CYP3A4 inhibitor antifungal azole medications (systemic itraconazole, ketoconazole, posaconazole, voriconazole). For strong CYP3A4 inhibitor antifungal azole medications, the starting dose of revumenib has to be adjusted
- Subject has tested positive for HIV (due to potential drug-drug interaction between antiretroviral medications and midostaurin/revumenib). Note: HIV testing is not required
- Subject has consumed grapefruit, grapefruit products, Seville oranges (including marmalade containing Seville oranges) or star fruit within 3 days prior to the initiation of study treatment
- Subject has a cardiovascular disability status of New York Heart Association class ≥ 2. Class 2 is defined as cardiac disease in which patients are comfortable at rest but ordinary physical activity results in fatigue, palpitations, dyspnea, or anginal pain
- Subject has a significant history of renal, neurologic, psychiatric, endocrinologic, metabolic, immunologic, hepatic, cardiovascular disease, or any other medical condition that in the opinion of the investigator would adversely affect his/her participating in this study
- Subject has chronic respiratory disease that requires continuous oxygen use
- Subject has a malabsorption syndrome or other condition that precludes enteral route of administration
- Subject exhibits evidence of other clinically significant uncontrolled condition(s) including, but not limited to uncontrolled systemic infection
- Subject has a history of other malignancies prior to study entry, with the exception of: * Adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of breast; * Basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin; * Previous malignancy confined and surgically resected (or treated with other modalities) with curative intent. * Prior malignancies treated with (surgery+/- chemotherapy+/- radiation) that have remained disease free for at least two years after completion of therapy
- Subject treated with any form of chemotherapy, immunotherapy, or investigative agent within 1 month of enrollment
- Patients who have had prior exposure to a menin inhibitor
Additional locations may be listed on ClinicalTrials.gov for NCT06313437.
Locations matching your search criteria
United States
Massachusetts
Boston
PRIMARY OBJECTIVE:
I. To determine the safety and recommended phase 2 dose (RP2D) of revumenib in combination with 7+3 + midostaurin induction chemotherapy and intermediate intensity dose cytarabine with midostaurin (miDAC) + midostaurin consolidation chemotherapy.
SECONDARY OBJECTIVES:
I. To determine the complete response (CR) rate at end of induction chemotherapy and the end of cycle 1 of consolidation chemotherapy.
II. To determine the flow minimal residual disease negativity (MRD-) rate (MRD sensitive flow cytometry) at the end of induction chemotherapy and the end of cycle 1 of consolidation chemotherapy.
III. To determine molecular MRD- rate (by NPM1 MRD testing, FLT3 ITD MRD testing and duplex sequencing) at the end of induction chemotherapy and the end of cycle 1 of consolidation chemotherapy.
IV. To determine recurrence free survival (RFS) and overall survival (OS) at 6 months and 1 year after initiation of therapy.
OUTLINE: This is a dose-escalation study of revumenib followed by a dose-expansion study.
INDUCTION: Patients receive daunorubicin intravenously (IV) on days 1-3, cytarabine IV continuously on days 1-7, midostaurin orally (PO) twice per day (BID) on days 8-21 and revumenib PO BID on days 8-28 of each cycle. Treatment repeats every 28 days for up to 1 cycle in the absence of disease progression or unacceptable toxicity. Patients who achieve CR receive consolidation 1-4 weeks after count recovery, patients who do not achieve complete remission receive re-induction.
RE-INDUCTION: Patients receive daunorubicin IV on days 1-2, cytarabine IV continuously on days 1-5, midostaurin PO BID on days 8-21 and revumenib PO BID on days 8-28 of each cycle. Treatment repeats every 28 days for up to 1 cycle in the absence of disease progression or unacceptable toxicity. Patients who achieve CR receive consolidation 1-4 weeks after count recovery.
CONSOLIDATION: Patients receive cytarabine IV every 12 hours (Q12H) on days 1, 3 and 5, midostaurin PO BID on days 8-21 and revumenib PO BID on days 8-28. Treatment repeats every 28 days for up to 1 cycle in the absence of disease progression or unacceptable toxicity.
Patients undergo multigated acquisition (MUGA) scan or echocardiography (ECHO) during screening, and bone marrow aspiration and biopsy and blood sample collection throughout the study.
After completion of study treatment, patients are followed up at 30 days and every 3 months for up to 2 years.
Trial PhasePhase I
Trial Typetreatment
Lead OrganizationDana-Farber Harvard Cancer Center
Principal InvestigatorRichard M. Stone
- Primary ID24-021
- Secondary IDsNCI-2024-04789
- ClinicalTrials.gov IDNCT06313437