Oral Arsenic Trioxide for NPM1-mutated AML

The University of Hong Kong (HKU)

Status and phase: Enrolling; Phase 2

Conditions: NPMc+ AML

Treatments: Drug: Oral Arsenic Trioxide Formulation

Study type: Interventional

Funder types: Other

Identifiers

NCT04689815

NPM1001

Details and patient eligibility

About

A prospective open-label phase 2 study will be designed to assess the efficacy of oral arsenic trioxide plus azacitidine in preventing relapses in patients with NPM1-mutant AML. After screening and eligibility assessment, patients will receive treatment with oral arsenic trioxide plus azacitidine for 12 months. The recruitment period will last for 24 months and it will take approximately 36 months for study completion.

Full description

Eligible subjects with NPM1 MRD positivity will receive oral arsenic trioxide (oral-As2O3) (Arsenol ®) (5-10mg per day, from days 1-7 per cycle), ascorbic acid (1g per day, from days 1 - 7 per cycle) plus azacitidine (75mg/m2 per day subcutaneously, from days 1 to 3 per cycle). Each cycle of oral-As2O3 plus azacitidine will be given once every 28 days. The total duration of treatment is 12 months (12 cycles). Treatment will be day-care and outpatient based. Reduction in the dosage and duration of oral-As2O3 is required if the subject is experiencing adverse events (AEs). In case of grade 3 or above toxicity, the dosage of oral-As2O3 will be reduced to 5mg per day. Changes or interruption in dosages, their dates and time points will be recorded on the dosage administration record and the electronic case report form (eCRF).

Enrollment: 50 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Adults ≥ 18 years
2. Diagnosis of AML with NPM1 mutation
3. Positive MRD for NPM1 mutation after completion of consolidation in transplant-ineligible patients
4. Positive MRD for NPM1 mutation after allogeneic HSCT
5. bilirubin ≤ 1.5 x upper limit normal (ULN); alanine aminotransferase (ALT) ≤ 2 x ULN or aspartate aminotransferase (AST) ≤ 2 x ULN; and prothrombin time versus control <3 seconds at screening
6. Glomerular filtration rate ≥ 50 mL/min (by MDRD equation or Cockcroft-Gault formula)
7. Corrected QT interval (QTc) (by Framingham formula) <500ms.
8. Able to give a written informed consent and fully comply to the requirements of the study.

Exclusion criteria

1. Patients on other investigational therapies
2. Prior exposure to azacitidine, decitabine or arsenic trioxide
3. Uncontrolled graft-versus-host disease (GVHD)
4. Eastern Cooperative Oncology Group (ECOG) performance status > 2

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

Oral arsenic trioxide-Azacitidine

Experimental group

Description:

12 monthly cycles of oral arsenic trioxide (oral-As2O3) (Arsenol ®) (5-10mg per day, from days 1-7 per cycle), ascorbic acid (1g per day, from days 1 - 7 per cycle) plus azacitidine (75mg/m2 per day subcutaneously, from days 1 to 3 per cycle).

Treatment:

Drug: Oral Arsenic Trioxide Formulation