A Phase 1 Protocol of 5-Azacytidine and Erlotinib in Advanced Solid Tumor Malignancies

NCT ID: NCT00996515

Last Updated: 2013-05-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-06-30
• Study Completion Date: 2011-09-30

Brief Summary

PRIMARY OBJECTIVES:

I. To document the toxicities, and reversibility of toxicities, of this regimen of 5-azacytidine (azacitidine) and erlotinib (erlotinib hydrochloride).

SECONDARY OBJECTIVES:

I. To determine any potential anti-tumor effects, as determined by the objective tumor response (complete and partial responses), clinical benefit (complete and partial responses, and clinical benefit), the time to tumor response, the time to tumor progression, and the overall survival.

Detailed Description

OUTLINE: This is a dose-escalation study.

Patients receive azacitidine intravenously (IV) over 10-40 minutes or subcutaneously (SC) on days 1 and 15, days 1-2 and 15-16, days 1-3 and 15-17, or days 1-4 and 15-18. Patients also receive erlotinib hydrochloride orally (PO) daily on days 1-21. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed for 28 days and then every 3 months for 5 years.

Conditions

Advanced Solid Tumor Malignancies

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cohort 5

Erlotinib 150mg/day PO Day 1-28 and Vidaza 100mg/m2/day SQ Day 1-4 and 15-18

Group Type: EXPERIMENTAL

5-azacytidine, erlotinib

Intervention Type: DRUG

Erlotinib 150 mg PO daily, days 1-8, and 15-22 5-Azacytidine 75 mg/m2/day, IV days 1 and 15

Erlotinib PO and Vidaza IV

Intervention Type: DRUG

Patients enrolled to 1 of 5 cohorts, with varying drug doses and dose scheduling.

Cohort 4

Erlotinib 200 mg/day PO Day 1-28 and Vidaza 75 mg/m2/day SQ 1-4 and 15-18

Group Type: EXPERIMENTAL

5-azacytidine, erlotinib

Intervention Type: DRUG

Erlotinib 150 mg PO daily, days 1-8, and 15-22 5-Azacytidine 75 mg/m2/day, IV days 1 and 15

Erlotinib PO and Vidaza IV

Intervention Type: DRUG

Patients enrolled to 1 of 5 cohorts, with varying drug doses and dose scheduling.

Cohort 3

Erlotinib 150 mg/day PO Day 1-28 and Vidaza 75 mg/m2/day IV Day 1-3 and 15-17

Group Type: EXPERIMENTAL

5-azacytidine, erlotinib

Intervention Type: DRUG

Erlotinib 150 mg PO daily, days 1-8, and 15-22 5-Azacytidine 75 mg/m2/day, IV days 1 and 15

Erlotinib PO and Vidaza IV

Intervention Type: DRUG

Patients enrolled to 1 of 5 cohorts, with varying drug doses and dose scheduling.

Cohort 2

Erlotinib 150 mg/day PO Day 1-28 and Vidaza 75 mg/m2/day IV Day 1-2 and 15-16

Group Type: EXPERIMENTAL

5-azacytidine, erlotinib

Intervention Type: DRUG

Erlotinib 150 mg PO daily, days 1-8, and 15-22 5-Azacytidine 75 mg/m2/day, IV days 1 and 15

Erlotinib PO and Vidaza IV

Intervention Type: DRUG

Patients enrolled to 1 of 5 cohorts, with varying drug doses and dose scheduling.

Cohort 1

Erlotinib 150 mg/day PO Day 1-28 and Vidaza 75 mg/m2/day IV Day 1 and 15

Group Type: EXPERIMENTAL

5-azacytidine, erlotinib

Intervention Type: DRUG

Erlotinib 150 mg PO daily, days 1-8, and 15-22 5-Azacytidine 75 mg/m2/day, IV days 1 and 15

Erlotinib PO and Vidaza IV

Intervention Type: DRUG

Patients enrolled to 1 of 5 cohorts, with varying drug doses and dose scheduling.

Interventions

5-azacytidine, erlotinib

Erlotinib 150 mg PO daily, days 1-8, and 15-22 5-Azacytidine 75 mg/m2/day, IV days 1 and 15

Intervention Type: DRUG

Erlotinib PO and Vidaza IV

Patients enrolled to 1 of 5 cohorts, with varying drug doses and dose scheduling.

Intervention Type: DRUG

Other Intervention Names

Erlotinib :- Tarceva™ (OSI-774); Vidaza (5-azacytidine)

Eligibility Criteria

Inclusion Criteria

• Patients must fulfill all of the following criteria to be eligible for study entry:
• Those who will be eligible will be all patients with non-hematologic neoplasms (lymphomas, leukemias, myeloma, myelodysplasia, or myeloproliferative syndromes) who have disease which has been previously treated and/or for which there is no acceptable standard treatment regimen available, and cannot be treated definitively with either surgery or radiotherapy. All will be appropriate candidates for treatment, and are not candidates for treatment with protocols of higher priority. All patients should have an ECOG/Zubrod/SWOG performance status of <2 at the time of the initiation of therapy, adequate end-organ function, no severe comorbid disease, and ability to provide informed consent.

Other Eligibility Criteria:

• Signed Informed Consent
• ECOG/Zubrod/SWOG Performance Status <2 (Karnofsky Performance Status > 70%)
• Life expectancy > 8 weeks
• Male or female' age >18 years
• Patients of childbearing potential must be using an effective means of contraception.
• Women of childbearing potential must have a negative serum pregnancy test prior to azacitidine treatment.
• Histologic diagnosis of a solid tumor malignancy that is advanced and cannot be treated adequately by radiotherapy or surgery; or metastatic disease
• Baseline laboratory values (bone marrow, renal, hepatic):

• Adequate bone marrow function:
• Absolute neutrophil count >1000/µL
• Platelet count >100'000/µL
• Renal function:
• Serum creatinine < 1.5 x ULN

• Hepatic function:
• Bilirubin <1.5x normal

• Serum glutamic-oxaloacetic transaminase (SGOT) (aspartate aminotransferase [AST]) or serum glutamic-pyruvic transaminase (SGPT) (alanine aminotransferase [ALT]) levels <=2 x ULN
• Serum calcium < 12 mg/dl

Exclusion Criteria

Patients meeting any of the following criteria are ineligible for study entry:

• Pregnant or lactating females
• Myocardial infarction or ischemia within the 6 months before Cycle 0' Day 0
• Uncontrolled' clinically significant dysrhythmia
• Prior radiotherapy to an indicator lesion unless there is objective evidence of tumor growth in that lesion
• Uncontrolled metastatic disease of the central nervous system
• Sensitivity to erlotinib, 5-azacytidine or mannitol
• Advanced hepatic tumors
• Radiotherapy within the 2 weeks before Cycle 1' Day 1
• Surgery within the 2 weeks before Cycle 1' Day 1
• Any co morbid condition that' in the view of the attending physician' renders the patient at high risk from treatment complications

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

New Mexico Cancer Research Alliance

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Julie E Bauman, M.D.

Role: PRINCIPAL_INVESTIGATOR

University of New Mexico Cancer Center

Locations

University of New Mexico Cancer Center

Albuquerque, New Mexico, United States

Countries

United States

Other Identifiers

NCI-2011-02646

Identifier Type: REGISTRY

Identifier Source: secondary_id

INST 0710C

Identifier Type: -

Identifier Source: org_study_id