Omega -3 Fatty Acid in Combination With Tyrosine Kinase Inhibitors in Chronic Myeloid Leukemia

NCT ID: NCT04006847

Last Updated: 2022-07-01

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-09-14
• Study Completion Date: 2021-05-21

Brief Summary

This is a Phase I/II single site, open label clinical trial. The purpose of the Phase I portion is to determine the safety, tolerability, and recommended Phase II dose of Eicosapentaenoic Acid (EPA) when given daily in combination with a Tyrosine Kinase Inhibitor (TKI) in subjects with Chronic Myeloid Leukemia (CML) in chronic stable phase. The recommended Phase II dose will be the maximum tolerated dose (MTD) of EPA as determined by the evaluation of dose-limiting toxicities (DLTs). The Phase II portion will subsequently examine the Anti-CML effects of EPA when administered with a TKI at the recommended Phase II dose. This efficacy objective will be done by evaluating BCR-ABL p210 quantitative PCR blood levels every 3 months to 1 year.

Detailed Description

Targeting CML leukemia stem cells is of paramount importance in successfully preventing cancer relapse. EPA metabolite, Δ12-PGJ3 may represent a new chemotherapeutic agent for leukemia that targets leukemia stem cells. Selective targeting of cancer stem cells may be potentially a highly effective treatment for cancer. As most CML patients treated with a TKI will reach a complete cytogenetic response, quantification of residual BCR-ABL transcripts by quantitative reverse transcription PCR (RT-qPCR) is a critical tool to further monitor response kinetics. Addition of EPA to TKI may help decrease residual BCR-ABL positive (Ph+) leukemia stem cells.

Conditions

Chronic Myeloid Leukemia, Chronic Phase

Study Design

• Allocation Method: NA
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Eicosapentaenoic Acid (EPA)

Phase I: TKI with escalating/de-escalating doses of EPA to determine MTD.

Phase I dose levels: Dose Level 1 = EPA 1500 mg orally once per day; Dose Level 2 = EPA 2000 mg orally once per day; Dose Level 3 = EPA 3000 mg orally once per day; Dose Level -1 = EPA 1000 mg orally once per day; Dose Level -2 = EPA 500 mg orally once per day.

Phase II: TKI administered in combination with the recommended Phase II dose of EPA

Group Type: EXPERIMENTAL

Eicosapentaenoic Acid

Intervention Type: DRUG

Eicosapentaenoic Acid once per day orally

Tyrosine kinase inhibitor

Intervention Type: DRUG

Tyrosine kinase inhibitor to be administered at subjects' pre-study dose

Interventions

Eicosapentaenoic Acid

Eicosapentaenoic Acid once per day orally

Intervention Type: DRUG

Tyrosine kinase inhibitor

Tyrosine kinase inhibitor to be administered at subjects' pre-study dose

Intervention Type: DRUG

Other Intervention Names

Omega-3 fatty acid; TKI; Imatinib; Dasatinib; Nilotinib; Bosutinib

Eligibility Criteria

Inclusion Criteria

1. Male or female ≥18 years of age.

2. Confirmed diagnosis of CML ≥ 18 months from diagnosis.

3. Current concomitant treatment with TKI therapy (Imatinib, Dasatinib, Nilotinib or Bosutinib; excluding Ponatinib). TKI therapy should be stable (same drug and dose) for at least 3 months prior to study enrollment.

4. One of the following confirmed:

1. BCR-ABL p210 at stable molecular disease (e.g., MMR stable but not CMR)

2. HR but no MMR.

5. Stable molecular response defined as 2 sequential BCR-ABL p210 levels done in the same lab with less than ½ log reduction of BCR-ABL (BA) 3-6 months apart.

6. ECOG PS of ≤ 3

7. Adequate organ function, as defined by the following:

ANC ≥ 500 cells/mm3 Platelet count ≥ 50,000 cells/mm3 Serum bilirubin ≤ 1.5 x ULN AST and ALT ≤ 2.5 x ULN Alkaline phosphatase ≤ 2.5 x ULN

8. WOCP as defined as defined as not surgically sterile or not one year post-menopausal, must have a negative result for a serum or urine pregnancy test within 7 days of initial receipt of study drug. Surgically sterile is defined as having had a hysterectomy, tubal ligation, or oophorectomy.

9. WOCP must use a medically accepted method of contraception and must agree to continued use of this method for the duration of the study and for 30 days after last dose of study drug. Acceptable methods of contraception include abstinence, barrier method with spermicide, intrauterine device (IUD) known to have a failure rate of less than 1% per year, or steroidal contraceptive (oral, transdermal, implanted, or injected) in conjunction with a barrier method.

10. Male subjects capable of producing offspring, must use a medically accepted method of birth control and agree to continued use of this method for the duration of the study and for 30 days after last dose of study drug because of the possible effects on spermatogenesis. Acceptable methods of contraception include abstinence, barrier method with spermicide, WOCP partner's use of an IUD known to have a failure rate of less than 1% per year, WOCP partner's use of steroidal contraceptive (oral, implanted or injected) in conjunction with a barrier method, WOCP partner is surgically sterile or 1 year postmenopausal. In addition, male subjects may not donate sperm for the duration of the study and for 30 days after last dose of study drug.

Exclusion Criteria

1. Has a malignancy or infection requiring active treatment

2. Has a known HIV infection, Hepatitis B , or Hepatitis C infection

3. Has a known symptomatic congestive heart failure (CHF), unstable angina or cardiac arrhythmia

4. Is using Aspirin or NSAID or COX-I

5. Is known to be non-compliant to medications.

6. Has, in the opinion of the physician investigator, an uncontrolled medical or psychiatric disorder.

7. Has active central nervous system (CNS) leukemia.

8. Is preceding allogeneic stem HSCT.

9. Has a known T 315 I mutation.

10. Is taking FISH oil at EPA dose > 500 mg

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Milton S. Hershey Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Seema Naik, MD

Assistant Professor, Cancer Institutue

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Seema Naik, MD

Role: PRINCIPAL_INVESTIGATOR

Penn State Cancer Institute

Locations

Penn State Cancer Institute

Hershey, Pennsylvania, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

17-085

Identifier Type: -

Identifier Source: org_study_id