Aprepitant as Antiemetic Prophylaxis in Patients With Acute Myeloid Leukemia Undergoing Induction Chemotherapy

Acute Myeloid Leukemia Clinical Trial

Official title:

A Phase II Open Label Study of Aprepitant as Antiemetic Prophylaxis in Patients With Acute Myeloid Leukemia Undergoing Induction Chemotherapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01334086
• Other study ID #: AML-11-001
• Status: Completed
• Phase: Phase 2
• Start date: September 2011
• Est. completion date: August 30, 2013

Study information

• Verified date: April 2021
• Source: University Health Network, Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chemotherapy induced nausea and vomiting (CINV) is a major adverse effect of chemotherapy. This study is determining the incidence of vomiting/retching of the standard induction chemotherapy regimen for patients with acute myeloid leukemia (AML) who are also receiving an antiemetic known as aprepitant. The standard frontline chemotherapy for patients with AML consists of cytarabine given as a 7 day continuous infusion plus 3 days of an anthracycline, most commonly daunorubicin, on days 1-3. This is known as the 3+7 regimen. Antiemetic treatments are usually given to patients for nausea and vomiting. Granisetron (a 5-HT3 receptor antagonist) is used on the 3 daunorubicin days and other antiemetics can be used for breakthrough nausea/vomiting. This study will test that the prophylactic use of aprepitant, in addition to the standard antiemetic regimen used at Princess Margaret Hospital (PMH), will reduce the incidence of delayed onset vomiting/retching by Day 5 in AML patients receiving the standard 3+7 regimen, compared to retrospective data using this regimen.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 41
• Est. completion date: August 30, 2013
• Est. primary completion date: August 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Acute myeloid leukemia (AML), any subtype including acute promyelocytic leukemia (APL). Patients with either de novo or secondary AML are eligible.
• No prior AML induction chemotherapy.
• Due to receive standard 3+7 induction chemotherapy using daunorubicin on Days 1-3, plus cytarabine continuous infusion daily on Days 1-7.
• Age 18 and over.
• Serum bilirubin < or = 1.5 times the upper limit of normal (ULN).
• Serum aspartate aminotransferase and alanine aminotransferase < or = 2.5 times the ULN.
• Serum creatinine < 200 umol/L

Exclusion Criteria:

• Uncontrolled nausea or vomiting within 48 hours prior to start of induction therapy. Grade 0-1 nausea is permitted at the start of induction.
• Known hypersensitivity to granisetron or aprepitant.
• Patients currently receiving treatment with strong CYP3A4 inhibitors or substrates and treatment cannot be either discontinued or switched to a different medication prior to starting study drug.
• Not able to swallow or absorb oral medications.
• Documented active central nervous system (CNS) leukemia or recent CNS hemorrhage.
• Concomitant use of:

1. Other investigational agents during induction therapy

2. Radiotherapy during, or one month prior to, induction therapy

3. Systemic corticosteroids

4. Other chemotherapy agents on Days 1-8

• Pregnant or breast feeding.

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute

Intervention

Drug:
• Aprepitant
Oral aprepitant will be given to the participant on Days 1-5 of standard induction treatment. A dose of 125 mg will be given on Day 1 and 80 mg will be given on Days 2-5.

Locations

Country	Name	City	State
Canada	Princess Margaret Hospital	Toronto	Ontario

Sponsors (2)

Lead Sponsor	Collaborator
University Health Network, Toronto	Merck Sharp & Dohme Corp.

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Participants With Incidence of Vomiting/Retching From Day 1 Through End of Day 5	Cumulative incidence will be determined by the patient self-assessment form, supplemented by the nursing inpatient records.	Day 1 through end of Day 5
Secondary	Presence of Nausea Per Day, on Days 1-8.		Days 1 to 8
Secondary	Daily Number of Vomiting or Retching Incidents From Days 1-8	This will be determined by both self-assessment form which will be filled out by the patient on a daily basis, and review of the nursing inpatient records.	Days 1 to 8
Secondary	Percentage of Participants Experiencing Vomiting or Retching From Days 1-8.	This will be determined by both self-assessment form which will be filled out by the patient on a daily basis, and review of the nursing inpatient records.	Days 1 to 8
Secondary	Percentage of Patients Experiencing Nausea From Days 1-8.		Days 1 to 8
Secondary	Percentage of Patients' Use of Supplemental Anti-emetics as Determined by the Total Number of Doses Per Day and in Total, From Days 1-8.		Days 1 to 8
Secondary	To Evaluate the Tolerance of Aprepitant by Documenting All Toxicities on Days 1-8 and All Unexpected Serious Adverse Events up to Day 30.		Days 1 to 8
Secondary	Severity of Nausea Per Day, on Days 1-8.		Days 1 to 8