Disulfiram and Chemotherapy in Treating Patients with Refractory Solid Tumors or Metastatic Pancreatic Cancer
- Cohort 1 (dose escalation): histologic or cytologic proof of any solid tumor that is incurable with no standard therapy that is likely to make a major impact on clinical outcomes
- Cohort 2 (MTD) only: metastatic adenocarcinoma of the pancreas; prior systemic treatment for metastatic disease is allowed
- Cohort 2 (MTD) only: Patient is thought to be a short- or long-term candidate for chemotherapy in the opinion of the treating oncologist
- Absolute neutrophil count (ANC) >= 1500/mm^3 (obtained =< 7 days prior to registration)
- Platelet >= 100,000/ mm^3 (obtained =< 7 days prior to registration)
- Total bilirubin =< 2 x upper limit of normal (ULN) (obtained =< 7 days prior to registration)
- Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) =< 3 x ULN (obtained =< 7 days prior to registration)
- Creatinine =< 1.5 x ULN (obtained =< 7 days prior to registration)
- Hemoglobin >= 9.0 g/dL (obtained =< 7 days prior to registration)
- Cohort 2 (MTD) only: prothrombin time (PT)/international normalized ratio (INR) =< 1.5 x ULN (only if muscle biopsy has not been waived, does not apply to non-Mayo sites that will not be conducting biopsies) (obtained =< 7 days prior to registration)
- Ability to provide written informed consent
- Life expectancy >= 12 weeks
- Cohort 2 (MTD) only: patient willing to undergo muscle biopsies at baseline and after 28 to 35 days of disulfiram/chemotherapy as required by the protocol unless the muscle biopsy has been waived after discussion with the principal investigator (PI); muscle biopsies will not be required at non-Mayo Clinic sites
- Cohort 2 (MTD) only: patient willing to have paraffin-embedded slides of the primary pancreas tumor or metastatic site, if available, sent to Mayo investigators for this study
- For women of childbearing potential only: negative urine or serum pregnancy test done =< 7 days prior to registration
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2
- Able to swallow or have medication administered through a gastrostomy tube (G-tube) and absorb the medication
- Patient willing to complete a medication diary
- Patient agrees to use acceptable form of contraception during the study and for up to 30 days after last study drug dose if female partner is of childbearing potential * Acceptable forms of contraception: ** Latex condom (always used with spermicide) ** Diaphragm (always used with spermicide) ** Cervical cap (always used with spermicide) * Acceptable forms of secondary contraception, when used along with a barrier method: ** Hormonal contraception methods, including pills, patches, rings, or injections except progestin-only containing pills (i.e. “Mini-pill”) ** Tubal ligation ** Partner’s vasectomy ** Intrauterine device (non-progesterone T) ** Vaginal sponge (containing spermicide) * Other acceptable forms: ** 100% commitment to abstinence * Unacceptable forms of contraception for women of childbearing potential: ** Oral contraception containing progestins only ** Intrauterine device (IUD) progesterone T ** Female condom ** Natural family planning (rhythm method) or breastfeeding ** Fertility awareness ** Withdrawal ** Cervical shield
- Known standard therapy for the patient’s disease that is potentially curative
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, including localized infections, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illness/social situations that would limit compliance with study requirements
- Untreated brain metastases
- Any of the following: * Pregnant women * Nursing women This study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown.
- Other concurrent chemotherapy, immunotherapy, radiotherapy, any ancillary therapy considered investigational (utilized for a non-Food and Drug Administration [FDA]-approved indication and in the context of a research investigation) or receiving any other investigational agent which would be considered as a treatment for the primary neoplasm
- Baseline of grade 2 or worse peripheral sensory neuropathy
- Receiving phenytoin
- Unable to abstain from alcohol for the duration of the study
Thief River Falls
I. To determine the maximally tolerated dose (MTD) of the combination of disulfiram and gemcitabine (gemcitabine hydrochloride) in unresectable solid tumor cancer patients (Cohort 1).
I. To describe the adverse event profile associated with this combination of disulfiram and chemotherapy (Cohort 2).
II. To describe changes in muscle area at the L3 level from baseline to 28 to 60 days from the baseline computed tomography (CT) scan in patients treated with disulfiram/chemotherapy and with placebo/chemotherapy (Cohort 2).
III. To describe changes in fist-grip strength from baseline to 28 to 35 days of treatment with disulfiram/gemcitabine and with placebo/chemotherapy (Cohort 2).
IV. To describe overall survival of pancreas cancer patients who disulfiram/chemotherapy or placebo/chemotherapy (Cohort 2).
V. To estimate the response rate per Response Evaluation Criteria in Solid Tumors (RECIST) criteria around 1 month post-treatment in patients who receive disulfiram/chemotherapy and placebo/chemotherapy (Cohort 2).
I. To assess the effect of disulfiram and chemotherapy on the ubiquitin proteasome and autophagy pathways within muscle, as assessed by means of muscle biopsies performed at baseline and after 28 to 35 days of treatment (Cohort 2) (this is for Mayo only patients and can be waived upon permission from the principal investigator [PI]).
OUTLINE: This is a phase I, dose-escalation study of disulfiram.
COHORT I: Patients receive gemcitabine hydrochloride intravenously (IV) over 30 minutes on days 1, 8, and 15 and disulfiram orally (PO) on days 1-28 or days 1-35.
COHORT II: Patients receive chemotherapy at the discretion of the treating oncologist and disulfiram PO on days 1-28 or days 1-35.
After completion of study treatment, patients are followed up at 30 days, and then every 6 months for 3 years.
Trial Phase Phase I
Trial Type Treatment
Mayo Clinic in Rochester
- Primary ID MC1512
- Secondary IDs NCI-2016-00007, 15-003194
- Clinicaltrials.gov ID NCT02671890