DHEA in Synovial Sarcoma Patients

NCT02683148 | Terminated Phase 1 DMC FDA Drug

• 1 other identifier: 201603100
• Study Type: interventional
• Target: 11
• Locations: 1 country
• Sites: 1

Brief Summary

DHEA is a natural allosteric inhibitor of glucose-6-phosphate dehydrogenase (G6PD). G6PD is a key regulatory enzyme for the survival of synovial sarcoma. The investigators postulate that they can inhibit the production of NADPH in synovial sarcoma and cause cell death by using a naturally occurring G6PD inhibitor.

Conditions

Synovial Sarcoma; Sarcoma, Synovial

Outcome Measures

Primary Outcomes (2)

• Maximum tolerated dose (MTD) of DHEA (Phase I only)

  * MTD is defined as the dose level immediately below the dose level at which 2 patients of a cohort (of 2 to 6 patients) experience dose-limiting toxicity during the first cycle. Dose escalations will proceed until the MTD has been reached. * Dose-limiting toxicities are defined as one of the following events occurring during the 1st cycle of treatment thought to be possibly, probably, or definitely related to treatment: * Grade 3 or greater liver function test abnormalities * Grade 3 or greater psychiatric disorder * Quality of life (QOL) alteration (change in score of 30%)

  Completion of cycle 1 for all phase I patients (estimated to be 2 years)

• Progression-free rate (complete response + partial response + stable disease) (Phase II only)

  * Complete response (CR): disappearance of all target lesions, any pathological lymph nodes (whether target or non-target) must have reduction inf short axis to \<10mm, disappearance of all non-target lesions and normalization of tumor marker level. * Partial response (PR): at least a 30% decrease in the sum of the diameters of target lesions, taking as reference the baseline sum diameters. * Stable disease (SD): neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease, taking as reference the smallest sum diaters while on study

  Up to 5 years

Secondary Outcomes (2)

• Rate of progression-free survival (PFS) (Phase II only)

  3 months

• Toxicity of DHEA as measured by grade and frequency of adverse events

  30 days after completion of treatment (estimated to be 7 months)

Study Arms (4)

Arm 1: DHEA Dose Level 1

EXPERIMENTAL

-DHEA is an oral supplement which will be administered on an outpatient basis at the prescribed dose daily on a 28-day cycle.

Drug: DHEA; Other: FACT-67 validated survey

Arm 2: DHEA Dose Level 2

EXPERIMENTAL

-DHEA is an oral supplement which will be administered on an outpatient basis at the prescribed dose daily on a 28-day cycle.

Drug: DHEA; Other: FACT-67 validated survey

Arm 3: DHEA Dose Level 3

EXPERIMENTAL

-DHEA is an oral supplement which will be administered on an outpatient basis at the prescribed dose daily on a 28-day cycle.

Drug: DHEA; Other: FACT-67 validated survey

Arm 4: DHEA Phase II

EXPERIMENTAL

-DHEA is an oral supplement which will be administered on an outpatient basis at the prescribed dose daily on a 28-day cycle.

Drug: DHEA; Other: FACT-67 validated survey

Interventions

DHEA DRUG

Also known as: Dehydroepiandrosterone

Arm 1: DHEA Dose Level 1; Arm 2: DHEA Dose Level 2; Arm 3: DHEA Dose Level 3; Arm 4: DHEA Phase II

FACT-67 validated survey OTHER

* Baseline, Cycle 1 Day 15, and Day 1 of each cycle beginning with Cycle 2 * 7 questions with answers ranging from 0=Not At All to 4 = Very Much.

Arm 1: DHEA Dose Level 1; Arm 2: DHEA Dose Level 2; Arm 3: DHEA Dose Level 3; Arm 4: DHEA Phase II

Eligibility Criteria

• Age: 16 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Diagnosis of histologically or cytologically confirmed metastatic or non-resectable synovial sarcoma.
• Failed at least one line of chemotherapy. Neoadjuvant and adjuvant chemotherapy count as a prior line of therapy.
• Measurable disease defined as lesions that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 10 mm with CT scan, as ≥ 20 mm by chest x-ray, or ≥ 10 mm with calipers by clinical exam.
• At least 16 years of age.
• ECOG performance status ≤ 2
• Normal bone marrow and organ function as defined below:
• Leukocytes ≥ 3,000/mcL
• Absolute neutrophil count ≥ 1,500/mcl
• Platelets ≥ 50,000/mcl
• Total bilirubin ≤ 1.5 x IULN
• AST(SGOT)/ALT(SGPT) ≤ 3.0 x IULN
• Creatinine ≤ IULN OR Creatinine clearance ≥ 60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal
• Women of childbearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation. Patients using antiestrogens for oral birth control are ineligible. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.
• Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

You may not qualify if:

• A history of other malignancy ≤ 3 years previous with the exception of basal cell or squamous cell carcinoma of the skin which were treated with local resection only or carcinoma in situ of the cervix.
• Currently receiving any other investigational agents.
• Known brain metastases. Patients with known brain metastases must be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.
• A history of allergic reactions attributed to compounds of similar chemical or biologic composition to DHEA or other agents used in the study.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 14 days of study entry.
• Known HIV-positivity on combination antiretroviral therapy because of the potential for pharmacokinetic interactions with DHEA. In addition, these patients are at increased risk of lethal infections when treated with marrow-suppressive therapy. Appropriate studies will be undertaken in patients receiving combination antiretroviral therapy when indicated.
• Known mania-associated psychiatric disorder.
• Known seizure disorder.
• Using corticosteroids or estrogen-based oral birth control.
• Using drugs known to lower or increase levels of DHEA.
• Requires estrogen or testosterone.
• Taking warfarin sodium. Patients on other blood thinners should be monitored for thrombocytopenia.
• Taking a strong inhibitor or inducer of cytochrome P450. Intermediate inhibitors are allowed if deemed medically necessary.

Sponsors & Collaborators

• Washington University School of Medicine: lead

Study Sites (1)

Washington University School of Medicine

St Louis, Missouri, 63110, United States

Location

Related Links

• Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine

MeSH Terms

Conditions

Sarcoma, Synovial

Interventions

Dehydroepiandrosterone

Condition Hierarchy (Ancestors)

Neoplasms, Connective Tissue; Neoplasms, Connective and Soft Tissue; Neoplasms by Histologic Type; Neoplasms; Sarcoma

Intervention Hierarchy (Ancestors)

Androstenols; Androstenes; Androstanes; Steroids; Fused-Ring Compounds; Polycyclic Compounds; 17-Ketosteroids; Ketosteroids; Adrenal Cortex Hormones; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Testosterone Congeners; Gonadal Steroid Hormones; Gonadal Hormones

Study Officials

• Brian A Van Tine, M.D., Ph.D.

  Washington University School of Medicine

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 11, 2016
• First Posted: February 17, 2016
• Study Start: September 13, 2016
• Primary Completion: September 9, 2018
• Study Completion: April 4, 2019
• Last Updated: September 9, 2019

Record last verified: 2019-09

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)