Temozolomide and Thalidomide in Treating Patients With Metastatic, Locally Advanced, or Unresectable Leiomyosarcoma

Sarcoma Clinical Trial

Official title:

A Phase II Study of Combination Therapy of a Protracted Oral Schedule of Temozolomide and Thalidomide as First-Line or Subsequent Therapy for Patients With Metastatic, Locally Advanced or Unresectable Leiomyosarcoma

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00033709
• Other study ID #: CDR0000069314
• Secondary ID: CPMC-IRB-14323NC
• Status: Active, not recruiting
• Phase: Phase 2
• First received: April 9, 2002
• Last updated: January 3, 2014
• Start date: March 2002

Study information

• Verified date: May 2005
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Thalidomide may stop the growth of cancer by stopping blood flow to the tumor. Combining temozolomide with thalidomide may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of combining temozolomide with thalidomide in treating patients who have metastatic, locally advanced, or unresectable leiomyosarcoma.

Description:

OBJECTIVES:

• Determine the efficacy of temozolomide and thalidomide in patients with metastatic, locally advanced, or unresectable leiomyosarcoma.

• Determine the time to progression in patients treated with this regimen.

• Determine the overall survival of patients treated with this regimen.

• Determine the clinical and laboratory toxic effects and tolerability of this regimen in these patients.

OUTLINE: Patients receive oral temozolomide once daily for 7 days every other week and oral thalidomide once daily. Treatment continues for up to 26 weeks in the absence of disease progression or unacceptable toxicity.

PROJECTED ACCRUAL: A total of 15-25 patients will be accrued for this study within 7.5-25 months.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed leiomyosarcoma

• Metastatic, locally advanced, or unresectable

• Ineligible for other high priority national or institutional study

• At least 1 unidimensionally measurable lesion documented on radiologic study

• At least 2 cm by 2 cm

• Not previously irradiated unless disease progression at the site is evident

• No brain metastases

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• SWOG 0-2

Life expectancy:

• More than 2 months

Hematopoietic:

• WBC greater than 3,000/mm^3

• Neutrophil count at least 1,500/mm^3

• Platelet count greater than 70,000/mm^3

• Hemoglobin at least 10 g/dL

Hepatic:

• Bilirubin less than upper limit of normal (ULN)

• SGOT or SGPT less than 1.5 times ULN*

• Alkaline phosphatase less than 2 times ULN* NOTE: * Less than 5 times ULN if documented liver disease

Renal:

• Creatinine less than 1.5 times normal OR

• Creatinine clearance greater than 60 mL/min

• BUN less than 1.5 times normal

Other:

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use 2 forms of effective contraception for 4 weeks before, during, and for 4 weeks after study therapy

• No acute infection requiring systemic antibiotics

• No frequent vomiting or medical condition that would preclude intake of oral medication (e.g., partial bowel obstruction)

• No other serious medical or psychiatric illness that would preclude study participation

• No prior malignancy except curatively treated carcinoma in situ of the cervix or skin cancer

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• Not specified

Chemotherapy:

• At least 4 weeks since prior chemotherapy

• No more than 3 prior systemic chemotherapy regimens for metastatic, locally advanced, or unresectable leiomyosarcoma

• Prior dacarbazine allowed

Endocrine therapy:

• Not specified

Radiotherapy:

• See Disease Characteristics

• At least 4 weeks since prior radiotherapy

• No prior radiotherapy to 50% or more of bone marrow

• Concurrent radiotherapy for local control or palliative therapy for painful bony or soft tissue lesion allowed

Surgery:

• At least 4 weeks since prior surgery and recovered

Other:

• Recovered from all prior therapies

• No other concurrent investigational drugs

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

• Leiomyosarcoma
• Sarcoma

Intervention

Drug:
• temozolomide

• thalidomide

Locations

Country	Name	City	State
United States	Herbert Irving Comprehensive Cancer Center at Columbia University	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
Herbert Irving Comprehensive Cancer Center	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Boyar M, Keohan ML, Hesdorffer M, et al.: Phase II study of temozolomide and thalidomide in patients with unresectable or metastatic leiomyosarcoma. [Abstract] J Clin Oncol 23 (Suppl 16): A-9029, 823s, 2005.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response (complete and partial response)			No
Secondary	Time to progression			No
Secondary	Overall survival			No
Secondary	Clinical benefit			No