Phase I Study of Mitoxantrone and Etoposide Combined With Hydroxychloroquine, for Relapsed Acute Myelogenous Leukemia

NCT ID: NCT02631252

Last Updated: 2018-02-23

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-08-18
• Study Completion Date: 2017-10-02

Brief Summary

This is an open label phase I clinical trial of hydroxychloroquine (HCQ) ,when it is combined with the usual medications for acute myeloid leukemia, mitoxantrone and etoposide. The purpose of this study is to find the safest and most effective dose of hydroxychloroquine with these medications. The investigators will be testing to see if it can increase the effectiveness of mitoxantrone and etoposide.

Detailed Description

Hydroxychloroquine is not FDA (United States Food and Drug Administration) approved for AML and is considered an investigational drug in this study. It has helped make chemotherapy more effective in animals. The investigators will be testing to see if it can increase the effectiveness of mitoxantrone and etoposide. It has been combined with other types of chemotherapy for humans with other types of cancer. Most of the patients were able to take hydroxychloroquine safely at the doses studied in this clinical trial.

Hydroxychloroquine is approved by the FDA for malaria, rheumatoid arthritis, and other autoimmune diseases. Mitoxantrone is approved by the FDA for use in AML, and it is one of the most common drugs used in the treatment of AML. Etoposide is not approved by the FDA for AML. It is approved for small cell lung cancer and testicular cancer. It is commonly used in AML.

The primary objective of this trial is to determine the recommend phase 2 dose (RP2D) for HCQ combined with mitoxantrone and etoposide, while secondary objectives include efficacy estimates of this combination at the RP2D, a safety and tolerability profile of this combination, as well as the correlation of pharmacodynamic assessments of autophagy inhibition with dose and clinical response.

Conditions

Leukemia, Acute Myelogenous

Study Design

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

Study Groups

Open-label, Single-arm

Hydroxychloroquine + Mitoxantrone + Etoposide

Hydroxychloroquine is given up to 21 days, started concurrently with both Mitoxantrone, administered by IVPB over 15 minutes each day for 5 days and Etoposide, administered intravenously over 2 hours each day for 5 days

Group Type: EXPERIMENTAL

Hydroxychloroquine

Intervention Type: DRUG

Doses ranging from 600-1400mg daily in divided twice daily doses and administered orally.

Mitoxantrone

Intervention Type: DRUG

Dose: 10mg/m2 IVPB in 50ml NS

Etoposide

Intervention Type: DRUG

Dose: 100 mg/m2 administered intravenously in 500 ml of 0.9% sodium chloride

Interventions

Hydroxychloroquine

Doses ranging from 600-1400mg daily in divided twice daily doses and administered orally.

Intervention Type: DRUG

Mitoxantrone

Dose: 10mg/m2 IVPB in 50ml NS

Intervention Type: DRUG

Etoposide

Dose: 100 mg/m2 administered intravenously in 500 ml of 0.9% sodium chloride

Intervention Type: DRUG

Other Intervention Names

Plaquenil; Dihydroxyanthracenedione, DHAD; Toposar®; EPEG

Eligibility Criteria

Inclusion Criteria

1. Able to understand and have the ability to provide written consent

2. Age > 18 years old to <80 years old

3. Patients with AML in the first morphologic relapse as defined by >5% reappearance of leukemia blasts in the bone marrow not attributable to any other cause (Appendix I) who have not yet received chemotherapy for the current relapse

4. Eastern Cooperative Oncology Group Performance Status of 0 -2 (see Appendix II)

5. Adequate organ function

1. Serum creatinine ≤ 1.5 mg/dl and calculated creatinine clearance ≥ 50 mL/min (using the Cockcroft-Gault equation CL creatinine = (140-age) x body mass X 0.85 if female)/72 x creatinine where age is given in years, body mass is given in kg and creatinine is given in mg/dL)

2. Aspartate aminotransferase (AST) ≤ 5x the upper limit of normal Alanine aminotransferase (ALT) < 5x the upper limit of normal

3. Direct bilirubin ≤ 1.5 mg/dl Note: As many eligible patients will be pancytopenic secondary to their disease or prior treatments, hematologic abnormalities will not be used as a criteria for entry or exclusion

6. Left ventricular ejection fraction (LVEF) ≥50 %

7. Females of child-bearing potential must have a negative pregnancy test during screening and all subjects must agree to use an effective method of contraception. A woman is eligible to enter and participate in the study if she is of:

1. Non-childbearing potential (i.e., physiologically incapable of becoming pregnant) including any female who has had a hysterectomy or has had a bilateral oophorectomy (ovariectomy).

2. Childbearing potential, has a negative serum pregnancy test during the screening period and agrees to avoid sexual activity or use accepted methods of contraception from screening through follow-up.

Men with a female partner of childbearing potential are eligible to enroll and participate in the study if they have had either a prior vasectomy or agree to avoid sexual activity or use appropriate barrier contraception from screening through post-treatment follow-up.

Exclusion Criteria

1. Acute promyelocytic leukemia

2. Prior chemotherapy regimen given for 1st relapse, not including the use of hydroxyurea or plasmapheresis that is used prior to the initiation of chemotherapy.

3. Previous use of mitoxantrone and etoposide combination therapy within the preceding 180 days of screening.

4. Symptomatic central nervous system (CNS) involvement

5. Uncontrolled, life-threatening infection that is not responding to antimicrobial therapy

6. History of psychiatric disorder which may compromise compliance with the protocol or which does not allow for appropriate informed consent

7. Current receiving any other anti neoplastic investigational agents

8. Prior autologous or allogeneic stem cell transplantation

9. Concurrent malignancy. Exceptions: Patients who have been disease-free for 5 years, or subjects with a history of completely resected non-melanoma skin cancer or successfully treated in situ carcinoma are eligible. Subjects with concurrent malignancies that are indolent or definitely treated may be enrolled.

10. Women who are pregnant or breastfeeding

11. Evidence of severe or uncontrolled systemic disease (e.g., unstable or uncompensated respiratory or cardiac disease)

12. Inability to take oral medications, due to impaired swallowing ability or poor absorption capacity

13. Known glucose-6-phosphate dehydrogenase (G-6PD) deficiency

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Alison Sehgal, MD, MS

OTHER

Sponsor Role: lead

Responsible Party

Alison Sehgal, MD, MS

Assistant Professor of Medicine

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Alison Sehgal, MD

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

Locations

University of Pittsburgh Cancer Institute - Hillman Cancer Center

Pittsburgh, Pennsylvania, United States

Countries

United States

Other Identifiers

14-133

Identifier Type: -

Identifier Source: org_study_id