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Disulfiram Plus Arsenic Trioxide In Patients With Metastatic Melanoma and at Least One Prior Systemic Therapy

This study has been terminated.
(Halted because of slow accrual and lack of study funding)
Sponsor:
Information provided by (Responsible Party):
Chao Family Comprehensive Cancer Center, University of California, Irvine
ClinicalTrials.gov Identifier:
NCT00571116
First received: December 6, 2007
Last updated: April 3, 2013
Last verified: April 2013

December 6, 2007
April 3, 2013
September 2006
August 2012   (final data collection date for primary outcome measure)
Tolerability of disulfiram in combination with arsenic trioxide [ Time Frame: Up to 6 years ] [ Designated as safety issue: Yes ]
Evaluate the tolerability of disulfiram and arsenic trioxide administration as a therapeutic combination [ Time Frame: 5 years ] [ Designated as safety issue: Yes ]
Complete list of historical versions of study NCT00571116 on ClinicalTrials.gov Archive Site
Response rate (complete or partial response) [ Time Frame: Up to 6 years ] [ Designated as safety issue: No ]
Will be calculated as percentage of the study population. Data will be summarized in tabular form for publication.
Determine the response rate (complete and partial responses) and time to progression [ Time Frame: 5 years ] [ Designated as safety issue: Yes ]
Not Provided
Not Provided
 
Disulfiram Plus Arsenic Trioxide In Patients With Metastatic Melanoma and at Least One Prior Systemic Therapy
Evaluation of Disulfiram Plus Arsenic Trioxide In Patients With Metastatic Melanoma and at Least One Prior Systemic Therapy (Phase 1b)

This phase I trial is studying the side effects and best dose of arsenic trioxide when given together with disulfiram in treating patients with metastatic and progressive melanoma. Drugs used in chemotherapy, such as disulfiram and arsenic trioxide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

PRIMARY OBJECTIVES:

I. Evaluate the tolerability of disulfiram and arsenic trioxide administration as a therapeutic combination. (Phase IB)

SECONDARY OBJECTIVES:

l. Determine the response rate (complete and partial responses) and time to progression of previously treated patients with metastatic malignant melanoma when treated with disulfiram plus Arsenic Trioxide. (Phase II)

OUTLINE: This is a dose-escalation study of arsenic trioxide.

Patients receive disulfiram orally (PO) twice daily and arsenic trioxide intravenously (IV) over 1-2 hours on Monday through Friday, alternating two weeks on treatment followed by two weeks off treatment. Courses repeat every 12 weeks in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 3 months for 2 years and then every 6 months thereafter.

Interventional
Phase 1
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Metastatic Melanoma
  • Drug: Disulfiram
    Given PO
    Other Names:
    • Antabuse
    • 25953
    • 97-77-8
    • bis(diethylthiocarbamoyl) disulfide
    • DS
    • tetraethylthioperoxydicarbonic diamide
    • tetraethylthiuram disulfide
    • Teturamin
    • TTD
  • Drug: Arsenic trioxide
    Given IV
    Other Names:
    • TRISENOX
    • 1327-53-3
    • 57974
    • 706363
    • Arsenic (III) Oxide
    • Arsenic Sesquioxide
    • Arsenous Acid
    • Arsenous Acid Anhydride
    • Arsenous Oxide
    • AS2O3
    • White Arsenic
Experimental: Disulfiram and arsenic trioxide
Patients receive disulfiram PO twice daily and arsenic trioxide IV over 1-2 hours on Monday through Friday, alternating two weeks on treatment followed by two weeks off treatment. Courses repeat every 12 weeks in the absence of disease progression or unacceptable toxicity.
Interventions:
  • Drug: Disulfiram
  • Drug: Arsenic trioxide
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
15
August 2012
August 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Subjects must have bidimensionally measurable disease. All measurable lesions must be assessed (by physical examination, CT scan, radionuclide scan or plain X-ray) within 28 days prior to registration. Non-measurable sites must be assessed within 42 days prior to registration. The subject's disease status must be completely assessed and reported.
  • All subjects must undergo a CT of abdomen and chest within 28 days prior to registration.
  • All subjects must undergo either a CT or MRI of the brain within 28 days of registration. Subjects with asymptomatic brain metastasis are eligible for this protocol but their metastasis must be clinically stable and asymptomatic. Subjects with Central Nervous System (CNS) metastasis must have been evaluated by neurosurgery prior to entry to confirm that they are a candidate for this trial. Treatment of symptomatic CNS metastasis that is required before protocol entry.
  • Subjects must have progressed based on Response Evaluation Criteria in Solid Tumors (RECIST) criteria after at least one prior systemic therapy (chemotherapy, biologic/immunotherapy, or a combination regimen) for metastatic disease. This includes development of any new lesion or a 20% increase in the sum of the subject's measurable disease compared to their previous nadir. New CNS metastasis could be the reason for disease progression, but they must be stable clinically and satisfy criteria delineated in section 5.4. Prior systemic therapy must have been completed at least 28 days before registration.
  • Subjects may have received prior biologic or immunotherapy given in an adjuvant fashion. Prior adjuvant therapy must have been completed at least 28 days prior to registration
  • Subjects may have received prior radiation therapy. If all known sites of disease have been previously radiated, there must be objective evidence of progression for the subject to be eligible. Radiation therapy must have been completed at least 28 days before registration.
  • Subjects may have received prior surgery. Prior surgery must have been completed at least 28 days before registration.
  • Performance status must be 0-2 according to Southwest Oncology Group Criteria

Performance Status:

GRADE SCALE

0 Fully active; able to carry on all pre-disease activities without restriction.

  1. Restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature, e.g., light housework, office work.
  2. Ambulatory and capable of all self care but unable to carry out any work activities. Up and about more than 50% of waking hours.
  3. Capable of only limited self care; confined to bed or chair more than 50% of waking hours.
  4. Completely disabled. Cannot carry on any self care. Totally confined to bed or chair.
  5. Dead

    • Subjects must have a normal ECG, without evidence of congestive heart failure.

      1. Normal heart rate (less than 100 per minute)
      2. Normal sinus rhythm
      3. Normal interval from the beginning of the Q wave to the termination of the S wave, representing the time for ventricular depolarization (QRS) interval
      4. Subjects with QT prolongation > 500msec on their ECG will be considered ineligible.

        Exclusion Criteria:

    • Pregnant or nursing women are not eligible to participate in this trial because the safe use of this drug in pregnancy has not been established.
    • Subjects with severe myocardial disease or coronary occlusion, psychoses, and hypersensitivity to disulfiram or other thiuram derivatives used in pesticides and rubber vulcanization are excluded from the study.
    • Subjects who can not abstain from alcohol intake during the entire duration of this protocol are not qualified for this study.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00571116
UCI 06-08, 2006-5033, NCI-2010-00338
Yes
Chao Family Comprehensive Cancer Center, University of California, Irvine
University of California, Irvine
Not Provided
Principal Investigator: John P Fruehauf, M.D. PhD Chao Family Comprehensive Cancer Center
University of California, Irvine
April 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP