Phase I Dose-Escalation Study Of Azacitidine In Combination With Temozolomide

A Phase I Dose-Escalation Study Of Azacitidine In Combination With Temozolomide In Patients With Unresectable Or Metastatic Soft Tissue Sarcoma or Malignant Mesothelioma

The purpose of this study is to determine safety and toxicity for the combination of Temozolomide and Azacitidine in the treatment of Advanced Soft Tissue Sarcoma or Malignant Mesothelioma. This is a single-center, open-label, single-arm Phase I dose-escalation trial. Patients will be evaluated with complete history and physical as well as laboratory studies (complete blood count, metabolic panel, liver function tests), biopsy, and imaging of all sites of measurable disease. This study will be conducted over the course of 3 years.

Study Overview

• Status: Completed
• Conditions: Soft Tissue Sarcoma; Mesothelioma
• Intervention / Treatment: Drug: Azacitidine; Drug: Temozolomide

Detailed Description

The primary objective of the study is to determine the clinical and laboratory toxicities as well as acceptability/tolerance of this dose schedule of combined drug treatment with temozolomide and azacitidine.

Secondary objectives include determination of biochemical response to azacitidine as defined as change in methylation status. The investigators will specifically be looking at changes in genome wide methylation patterns as determined by two high-throughput platforms:

1. A single nucleotide polymorphism chip-based method (MSNP) for genome wide epigenetic profiling
2. CpG island promoter arrays will be performed to focus on promoter methylation status.

The investigators will also monitor clinical response, time to progression and overall survival.

• Study Type: Interventional
• Enrollment (Actual): 27
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • New York
    • New York, New York, United States, 10032
      • Columbia University Medical Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Histologically confirmed soft tissue sarcoma or mesothelioma.
• Ineligible for other high priority national or institutional study.
• Non-pregnant, non-lactating.
• Recurrent or progressive disease defined as an increase in size of any existing tumor mass, or the development of new tumor mass or masses, which is not amenable to definitive surgical therapy.
• Measurable disease defined as lesions that can be measured in at least one dimension by physical examination or by means of medical imaging techniques. Ascites and pleural effusions will not be considered measurable disease.
• Prior chemotherapy is allowed with the exception of prior treatment with Temozolomide or Azacitidine. Patients must have received prior 1st line therapy. There is no upper limit to the number of prior therapies received. Prior treatment with an alkylating agent is acceptable.
• Prior radiation therapy is allowed.
• At least 4 weeks since prior chemotherapy or at least 6 weeks since prior radiation therapy.
• Patients may have had another cancer but there must be convincing clinical evidence that the sarcoma is the disease requiring therapeutic intervention. (i.e. Several sarcoma patients have had had a prior cancer [Hodgkin's disease or breast cancer] treated years previously and then developed a clinically active sarcoma.)
• Clinical parameters: Life expectancy > 3 months, Age > 18 years, Performance Karnofsky performance status of greater than or equal to 60%.

• Required initial laboratory data:

  • Absolute neutrophil count > 1,500/mm3
  • Hemoglobin > 10.0 g/dl
  • Platelet count > 100,000/mm3
  • Total Bilirubin < 1.5 times upper limit of normal (ULN) for the laboratory.
  • Transaminases: aspartate aminotransferase (AST) or alanine aminotransferase (ALT) levels must be < 2 x ULN. If there is known hepatic metastasis, transaminases may be < 5 times upper limit of normal.
  • Serum creatinine levels < 1.5 x ULN.
  • Women of child-bearing potential must have a negative serum pregnancy test prior to initiation of treatment.
• Men and women of child-bearing potential must be willing to consent to using effective contraception while on treatment and for a reasonable period thereafter (approximately 3 months).
• Capable of providing written, informed consent. Each patient must be completely aware of the nature of his/her disease process and must willingly give consent after being informed of the procedure to be followed, the experimental nature of the therapy, alternatives, potential benefits, side-effects, risks and discomforts.
• No serious medical or psychiatric illness preventing informed consent or intensive treatment (e.g. serious infection).
• No uncontrolled central nervous system metastases.

Exclusion Criteria:

• Known or suspected hypersensitivity to azacitidine or mannitol
• Pregnant or breast-feeding
• Histology other than soft-tissue sarcoma or mesothelioma
• Active or uncontrolled infection or other serious systemic disease
• Prior treatment with temozolomide or azacitidine
• Pregnant or lactating women
• Uncontrolled central nervous system metastases
• Liver metastases
• Patients will not be excluded if they do not wish to participate in the second biopsy for tissue evaluation
• Subjects who have not had prior chemotherapy.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Treatment; Subjects will receive azacitidine in combination with temozolomide	Drug: Azacitidine; Azacitidine will be delivered sub-cutaneously for 5 days; Other Names: Vidaza; Drug: Temozolomide; Temozolomide will be given starting on day 8 for 5 days at a dose of 200 mg/m2 po qd x 5 days; Other Names: Temodar

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Maximum Tolerated Dose of Temozolomide	Maximum tolerated dose of temozolomide when used in combination with azacitidine	Up to 26 weeks for each dosing cohort
Maximum Tolerated Dose of Azacitidine	Maximum tolerated dose of azacitidine when used in combination with temozolomide	Up to 26 weeks for each dosing cohort

Secondary Outcome Measures

Outcome Measure	Time Frame
Clinical response, time to progression and overall survival.	Study Completion

Collaborators and Investigators

• Sponsor: Columbia University
• Collaborators: Celgene Corporation; Schering-Plough
• Investigators: Principal Investigator: Robert N Taub, MD, Columbia University

Study record dates

Study Major Dates

• Study Start: October 1, 2007
• Primary Completion (Actual): October 1, 2012
• Study Completion (Actual): October 1, 2012

Study Registration Dates

• First Submitted: February 26, 2008
• First Submitted That Met QC Criteria: March 5, 2008
• First Posted (Estimated): March 6, 2008

Study Record Updates

• Last Update Posted (Actual): June 5, 2025
• Last Update Submitted That Met QC Criteria: May 19, 2025
• Last Verified: May 1, 2025

More Information

Terms related to this study

• Keywords: Temozolomide; Temodar; Azacitidine; Mesothelioma; Soft Tissue Sarcoma
• Additional Relevant MeSH Terms: Neoplasms by Site; Neoplasms; Respiratory Tract Diseases; Neoplasms by Histologic Type; Lung Diseases; Neoplasms, Glandular and Epithelial; Respiratory Tract Neoplasms; Thoracic Neoplasms; Lung Neoplasms; Adenoma; Neoplasms, Mesothelial; Pleural Neoplasms; Neoplasms, Connective and Soft Tissue; Mesothelioma, Malignant; Mesothelioma; Sarcoma; Antineoplastic Agents; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Antimetabolites, Antineoplastic; Antimetabolites; Antineoplastic Agents, Alkylating; Alkylating Agents; Temozolomide; Azacitidine
• Other Study ID Numbers: AAAC3255

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO