CPI-613 in Treating Patients With Myelodysplastic Syndromes Who Failed Previous Therapy

Previously Treated Myelodysplastic Syndromes Clinical Trial

Official title:

A Pilot Study of CPI-613 in Patients With Myelodysplastic Syndrome Who Have Failed Previous Therapy

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01902381
• Other study ID #: IRB00024007
• Secondary ID: NCI-2013-01312P3
• Status: Terminated
• Phase: Phase 2
• Start date: August 2013
• Est. completion date: November 26, 2018

Study information

• Verified date: June 2021
• Source: Wake Forest University Health Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This pilot clinical trial studies 6, 8-bis (benzylthio) octanoic acid (CPI-613) in treating patients with myelodysplastic syndromes who failed previous therapy. Sometimes when chemotherapy or biological therapy is given, it does not stop the growth of tumor cells. The tumor is said to be resistant to treatment. 6, 8-bis (benzylthio) octanoic acid may interfere with the growth of tumor cells and may be an effective treatment for myelodysplastic syndromes that did not respond to previous therapy.

Description:

PRIMARY OBJECTIVES:

I. To evaluate the safety and anti-cancer activities of CPI-613 in myelodysplastic syndrome (MDS) patients who have failed previous agents (such as decitabine [Dacogen], azacitidine [Vidaza], growth factors or lenalidomide).

OUTLINE:

Patients receive 6, 8-bis (benzylthio) octanoic acid intravenously (IV) over 2 hours on days 1 and 4 of weeks 1-3. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 5 years.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 12
• Est. completion date: November 26, 2018
• Est. primary completion date: November 26, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically or cytologically documented MDS of any risk group that has failed previous therapy (therapy failure is defined as patients who have been sufficiently treated with previous agents without response in the opinion of the treating physician, or whose disease has progressed or relapsed while on a hypomethylating agent)

• Eastern Cooperative Oncology Group (ECOG) performance status of =< 3

• Expected survival > 2 months

• Women of child-bearing potential (i.e., women who are pre-menopausal or not surgically sterile) must use accepted contraceptive methods (abstinence, intrauterine device [IUD], oral contraceptive or double barrier device) during the study, and must have a negative serum or urine pregnancy test within 1 week prior to treatment initiation

• Fertile men must practice effective contraceptive methods during the study, unless documentation of infertility exists

• Patients must have fully recovered from the acute, non-hematological, non-infectious toxicities of any prior treatment with cytotoxic drugs, radiotherapy or other anti-cancer modalities; patients with persisting, non-hematologic, non-infectious toxicities from prior treatment =< grade 2 are eligible, but must be documented as such

• Aspartate aminotransferase (AST/serum glutamic oxaloacetic transaminase [SGOT]) =< 3 x upper normal limit (UNL)

• Alanine aminotransferase (ALT)/serum glutamate pyruvate transaminase (SGPT) =< 3 x UNL (=< 5x ULN if liver metastases present)

• Bilirubin =< 1.5 x UNL

• Serum creatinine =< 1.5 mg/dL or 133 umol/L

• International normalized ratio (or INR) must be < 1.5

• Albumin >= 2.0 g/dL or >= 20 g/L

• Mentally competent, ability to understand and willingness to sign an Institutional Review Board (IRB)-approved written informed consent form

• Have access via central line (e.g., portacath)

Exclusion Criteria:

• Serious medical illness, such as significant cardiac disease (e.g. symptomatic congestive heart failure, unstable angina pectoris, coronary artery disease, myocardial infarction within the past 3 months, uncontrolled cardiac arrhythmia, pericardial disease or New York Heart Association class III or IV), or severe debilitating pulmonary disease, that would potentially increase patients' risk for toxicity

• Patients with active central nervous system (CNS) or epidural tumor

• Any active uncontrolled bleeding or bleeding diathesis (e.g., active peptic ulcer disease)

• Any condition or abnormality which may, in the opinion of the investigator, compromise his or her safety

• Pregnant women, or women of child-bearing potential not using reliable means of contraception

• Fertile men unwilling to practice contraceptive methods during the study period

• Lactating females

• Life expectancy less than 2 months

• Unwilling or unable to follow protocol requirements

• A history of additional risk factors for torsades de pointes (e.g., heart failure, hypokalemia, family history of long QT syndrome, etc.)

• Evidence of active infection or serious infection within the past month

• Requirement for immediate palliative treatment of any kind including surgery

• Prior illicit drug addiction

• Patients with large and recurrent pleural or peritoneal effusions requiring frequent drainage (e.g. weekly)

• Patients with any amount of clinically significant pericardial effusion

• Patients with known human immunodeficiency virus (HIV) infection; (Note: patients with known HIV infection are excluded because patients with an immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy, and because there may be unknown or dangerous drug interactions between CPI-613 and anti-retroviral agents used to treat HIV infections)

• Patients who have received radiotherapy, surgery, treatment with cytotoxic agents (except CPI-613), treatment with biologic agents, immunotherapy, or any other anti-cancer therapy of any kind, or any other standard or investigational treatment for their cancer, or any other investigational agent for any indication, within the past 2 weeks prior to initiation of CPI-613 treatment

• Patients that have received a chemotherapy regimen with stem cell support in the previous 6 months

Related Conditions & MeSH terms

• Myelodysplastic Syndromes
• Preleukemia
• Previously Treated Myelodysplastic Syndromes
• Syndrome

Intervention

Drug:
• 6,8-bis(benzylthio)octanoic acid
Given IV

Locations

Country	Name	City	State
United States	Comprehensive Cancer Center of Wake Forest University	Winston-Salem	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Wake Forest University Health Sciences	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response rate (RR), defined as the combined rate of complete remission (CR), marrow CR, partial remission (PR), or stable disease (SD), as described by Cheson, et al. (2006)	Proportion of RR (along with a 95% confidence interval) of patients who respond will be presented.	Up to 5 years
Secondary	Safety profile of CPI-613, based on evaluation of symptoms, vital signs, ECOG performance status and survival, clinical chemistry, hematology, and coagulation, assessed by National Cancer Institute Common Terminology Criteria for Adverse Events v 4.0	Toxicities will be examined by looking at each toxicity identified by grade.	Up to 1 month post-treatment
Secondary	Progression-free survival (PFS)	Survival curves for PFS using Kaplan-Meier techniques will be estimated. In addition, the 6 month and 1-year PFS rates for these participants will be estimated.	Up to 5 years
Secondary	Overall survival (OS)	Survival curves for OS using Kaplan-Meier techniques will be estimated. In addition, the 6 month and 1-year OS rates for these participants will be estimated.	Up to 5 years
Secondary	Number of patients who achieve a reduction in blood transfusion requirements		Up to 5 years
Secondary	Number of patients who achieve hematologic improvement (HI), as defined by Cheson, et al. (2006)		Up to 5 years