Decitabine and Valproic Acid in Treating Patients With Non-Small Cell Lung Cancer

• ClinicalTrials.gov Identifier: NCT00084981
• Recruitment Status: Completed
• First Posted: June 11, 2004
• Last Update Posted: September 30, 2013
• Sponsor: National Cancer Institute (NCI)
• Information provided by (Responsible Party): National Cancer Institute (NCI)

Tracking Information

• First Submitted Date: June 10, 2004
• First Posted Date: June 11, 2004
• Last Update Posted Date: September 30, 2013
• Study Start Date: April 2004
• Actual Primary Completion Date: February 2013 (Final data collection date for primary outcome measure)
• Current Primary Outcome Measures (submitted: December 13, 2012): MTD, defined as dose in which fewer than 1/3 or 2/6 patients experience DLT [ Time Frame: 28 days ]
• Original Primary Outcome Measures: Not Provided
• Current Secondary Outcome Measures: Not Provided
• Original Secondary Outcome Measures: Not Provided
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Decitabine and Valproic Acid in Treating Patients With Non-Small Cell Lung Cancer
• Official Title: A Phase I Study of Decitabine in Combination With Valproic Acid in Patients With Non-Small Cell Lung Cancer
• Brief Summary: This phase I trial is studying the side effects and best dose of decitabine and valproic acid in treating patients with non-small cell lung cancer. Drugs used in chemotherapy, such as decitabine and valproic acid, work in different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells.

Detailed Description

PRIMARY OBJECTIVES:

I. Determine the safety and tolerability of decitabine and valproic acid in patients with non-small cell lung cancer.

II. Determine the recommended phase II dose of this regimen in these patients.

SECONDARY OBJECTIVES:

I. Determine the ability of this regimen to lead to biological changes in tumor and surrogate tissues in these patients, including hypomethylation of target genes known to be methylated in NSCLC (CDKN2, APC, BMP3B, CDH1 and RASSF1A) in biopsy specimens and surrogate tissues (peripheral blood mononuclear cells [PBMC] and plasma/serum DNA); acetylation and methylation changes in histones from tumor and surrogate tissues (PBMC and oral epithelial cells); inhibition of histone deacetylase (HDAC) activity in peripheral blood; pharmacokinetic analysis of Decitabine and Valproic Acid; DNA methyltransferase 1 (DNMT1) protein loss in PBMC and buccal cells; response of hemoglobin F in patients with non-hematologic conditions to DNMT and HDAC inhibition; and preliminary evidence of antitumor activity in non-small cell lung cancer.

OUTLINE: This is a dose-escalation study.

Patients receive decitabine IV over 1 hour on days 1-10 and oral valproic acid three times daily on days 5-21. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of decitabine and valproic acid until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. After the MTD is determined, an additional 6 patients are treated at that dose.

• Study Type: Interventional
• Study Phase: Phase 1
• Study Design: Allocation: N/A; Intervention Model: Single Group Assignment; Masking: None (Open Label); Primary Purpose: Treatment

Condition

• Recurrent Non-small Cell Lung Cancer
• Stage IV Non-small Cell Lung Cancer

Intervention

• Drug: decitabine
  Given IV
  Other Names:

  • 5-aza-dCyd
  • 5AZA
  • DAC
• Drug: valproic acid
  Given PO
  Other Names:

  • Alti-Valproic
  • Depakene
  • Novo-Valproic
  • VA
• Other: pharmacological study
  Correlative studies
  Other Name: pharmacological studies
• Other: laboratory biomarker analysis
  Correlative studies

Study Arms

Experimental: Treatment (decitabine, valproic acid)

Patients receive decitabine IV over 1 hour on days 1-10 and oral valproic acid three times daily on days 5-21. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of decitabine and valproic acid until the MTD is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. After the MTD is determined, an additional 6 patients are treated at that dose.

Interventions:

• Drug: decitabine
• Drug: valproic acid
• Other: pharmacological study
• Other: laboratory biomarker analysis

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: November 8, 2006): 25
• Original Enrollment: Not Provided
• Study Completion Date: Not Provided
• Actual Primary Completion Date: February 2013 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Histologically or cytologically confirmed non-small cell lung cancer
• Tumor accessible to biopsy by bronchoscopy, through surface biopsy (e.g., skin punch biopsy for skin/subcutaneous metastasis) or through CT scan guidance
• Not eligible for curative surgery, chemotherapy, radiotherapy, or multimodality treatment options

• No uncontrolled brain metastases

  • Controlled brain metastases allowed provided patient has no neurologic deterioration when off steroids; has completed prior radiotherapy or other treatments; has fully recovered from prior treatment; and does not require anticonvulsants
• Performance status - ECOG 0-2
• Performance status - Karnofsky 60-100%
• More than 12 weeks
• Absolute neutrophil count > 1,500/mm^3
• Platelet count > 100,000/mm^3
• WBC > 3,000/mm^3
• AST and ALT =< 2.5 times upper limit of normal (ULN)
• Bilirubin =< 1.5 times ULN
• Creatinine =< 1.5 times ULN
• Creatinine clearance >= 60 mL/min
• No symptomatic congestive heart failure
• No unstable angina pectoris
• No cardiac arrhythmia
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No prior allergic reaction to compounds of similar chemical or biological composition to decitabine, valproic acid, or other study agents
• No other concurrent uncontrolled illness
• No ongoing or active infection requiring antibiotics
• No history of seizures requiring anticonvulsants
• No medical problem that would preclude study participation
• No psychiatric illness or social situation that would preclude study compliance
• No other active malignancy except non-melanoma skin cancer or carcinoma in situ of the cervix
• No concurrent prophylactic growth factors (e.g., filgrastim [G-CSF] or epoetin alfa)
• No more than 3 prior chemotherapy regimens
• More than 3 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered

• Prior definitive radiotherapy to the chest allowed

  • Clinical (radiographic or other) evidence of tumor progression for previously irradiated indicator lesion in the chest
• More than 2 weeks since prior radiotherapy and recovered
• No concurrent palliative radiotherapy
• Prior curative or palliative intent surgery allowed
• At least 2 weeks since prior surgery and recovered
• At least 4 weeks since prior photodynamic therapy
• No concurrent combination antiretroviral therapy for HIV-positive patients
• No other concurrent anticancer agents or therapies
• No other concurrent investigational agents

• No concurrent administration of any of the following medications:

  • Aspirin

    • Chronic low-dose (=< 81 mg/day) aspirin allowed
  • Felbamate
  • Rifampin
  • Amitriptyline
  • Nortriptyline
  • Carbamazepine
  • Clonazepam
  • Diazepam
  • Ethosuximide
  • Lamotrigine
  • Phenobarbital
  • Barbiturates
  • Primidone
  • Phenytoin
  • Zidovudine
• No concurrent divalproex sodium
• Concurrent gabapentin for neuropathic pain allowed

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: United States

Administrative Information

• NCT Number: NCT00084981
• Other Study ID Numbers: NCI-2012-01451; NCI-2012-01451 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) ); NCI-6237; OSU-2003C0087; OSU-0346; CDR0000367115; OSU 0346 ( Other Identifier: Ohio State University Medical Center ); 6237 ( Other Identifier: CTEP ); U01CA076576 ( U.S. NIH Grant/Contract )
• Has Data Monitoring Committee: Not Provided
• U.S. FDA-regulated Product: Not Provided
• IPD Sharing Statement: Not Provided
• Current Responsible Party: National Cancer Institute (NCI)
• Original Responsible Party: Not Provided
• Current Study Sponsor: National Cancer Institute (NCI)
• Original Study Sponsor: Ohio State University Comprehensive Cancer Center
• Collaborators: Not Provided

Investigators

• Principal Investigator: Gregory Otterson; Ohio State University

• PRS Account: National Cancer Institute (NCI)
• Verification Date: September 2013