DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more

Imatinib Mesylate in Treating Patients With Locally Recurrent or Metastatic Dermatofibrosarcoma Protuberans

Information source: National Cancer Institute (NCI)
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Adult Fibrosarcoma; Dermatofibrosarcoma Protuberans; Recurrent Adult Soft Tissue Sarcoma; Stage IV Adult Soft Tissue Sarcoma

Intervention: imatinib mesylate (Drug); laboratory biomarker analysis (Other)

Phase: Phase 2

Status: Completed

Sponsored by: National Cancer Institute (NCI)

Official(s) and/or principal investigator(s):
Scott Schuetze, Principal Investigator, Affiliation: Southwest Oncology Group


This phase II trial is studying how well imatinib mesylate works in treating patients with locally recurrent or metastatic dermatofibrosarcoma protuberans (DFSP) or transformed fibrosarcomatous DFSP (a type of soft tissue sarcoma). Imatinib mesylate may stop the growth of tumor cells by blocking the enzymes necessary for their growth

Clinical Details

Official title: A Phase II Study of Imatinib (NSC-716051) in Patients With Locally Advanced or Metastatic Dermatofibrosarcoma Protuberans

Study design: Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome:

Response rate (confirmed complete and confirmed partial response)

Progression-free survival

Frequency and severity of toxicity as assessed by NCI CTCAE version 3.0

Relationship between PDGFB and survival

Secondary outcome: Relationship between PDGFB and tumor response to imatinib mesylate

Detailed description: PRIMARY OBJECTIVES: I. To assess the response rate (confirmed complete and confirmed partial response) in patients with locally advanced or metastatic dermatofibrosarcoma protuberans (DFSP) treated with imatinib. II. To estimate the one-year progression-free survival probability in this population when treated with imatinib. III. To evaluate the frequency and severity of toxicities associated with this treatment. IV. To measure the presence of PDGFB gene rearrangement in DFSP detectable by RT-PCR (for COL1A1-PDGFB fusions) and/or FISH (PDGFB rearrangements with unknown partners) and explore relationships between these measures and survival and tumor response in a preliminary manner. V. To investigate in a preliminary fashion the correlation of plasma levels of imatinib after 1 month of treatment with the response of DFSP. VI. To obtain tumor material for additional future correlative studies of the activity of intracellular kinases, cDNA microarray analyses and PDGFB receptor gene sequence analyses. OUTLINE: Patients receive oral imatinib mesylate once daily on days 1-56. Treatment repeats every 56 days for 6 courses in the absence of disease progression or unacceptable toxicity. Patients with documented tumor progression and no serious side effects may continue therapy at a higher dose for another 6 courses. Patients are followed every 6 months for 2 years and then annually for 3 years.


Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.


Inclusion Criteria:

- Patients must have histologically confirmed diagnosis of either dermatofibrosarcoma

protuberans (DFSP) or transformed fibrosarcomatous DFSP; patients with transformed fibrosarcomatous DFSP may have primary, locally recurrent or metastatic disease; patients with DFSP must have locally recurrent or metastatic disease OR primary disease for which complete excision with a wide margin (> 1-2 cm) would result in unacceptable cosmetic disfigurement or functional impairment

- Patients must have measurable disease; x-rays, scans or physical examinations used

for tumor measurement must have been completed within 28 days prior to registration; x-rays, scans or other tests for assessment of non-measurable disease must have been performed within 42 days prior to registration; all disease must be assessed

- Pathology materials must be submitted for review; failure to submit pathology

materials will render the patient ineligible

- Patients must be willing to have blood samples submitted for testing of drug levels;

also, it is strongly recommended that patients submit fresh/frozen tumor tissue that will yield 0. 5 grams (0. 5 cubic centimeters) for molecular correlative studies related to the PDGFR pathway

- Patient must not have had chemotherapy, biologic therapy or investigational agents

for this tumor within 28 days prior to registration

- Patients may have received prior major surgery for this disease; at least 14 days

must have elapsed since the surgery and the patient must have recovered from all side effects associated with surgery; biopsy of dermatofibrosarcoma protuberans is not considered major surgery and a 14-day delay after biopsy is not required

- Prior radiotherapy is allowed, provided at least four weeks have elapsed since the

last treatment, there is evidence of progressive disease within or measurable disease outside of the radiation field, and the patient must have recovered from all associated toxicities at the time of registration

- Patients must have Zubrod performance status of =< 2

- WBC >= 2,000/uL

- ANC >= 1,500/uL

- Platelets >= 100,000/uL

- Serum bilirubin =< 1. 5 x institutional upper limit of normal (IULN)

- Serum transaminase (SGOT or SGPT) must be =< 2. 5 x IULN

- Serum albumin must be >= 2. 5 mg/dl

- Patients must not be taking therapeutic doses of coumadin (Warfarin) at the time of

registration; patients requiring therapeutic anticoagulation may use heparin, low molecular weight heparin or other agents; mini-dose coumadin (1 mg orally every day as prophylaxis is allowed

- Patients with known CNS metastases are not eligible

- Pregnant or nursing women may not participate on this study; there is an unknown but

potential risk for adverse events in nursing infants secondary to treatment of the mother with imatinib; male/female patients of reproductive potential must also agree to employ an effective contraceptive barrier method of birth control throughout the study and for up to 3 months following discontinuation of study drug

- No other prior malignancy is allowed except for the following: adequately treated

basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease-free for 5 years

- All patients must be informed of the investigational nature of this study and must

sign and give written informed consent in accordance with institutional and federal guidelines

- At the time of patients registration, the treating institution's name and ID number

must be provided to the Data Operations Center in Seattle in order to ensure that the current (within 365 days) date of institutional review board approval for this study have been entered into the database

Locations and Contacts

Southwest Oncology Group, San Antonio, Texas 78245, United States
Additional Information

Starting date: May 2004
Last updated: February 27, 2013

Page last updated: August 23, 2015

-- advertisement -- The American Red Cross
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2017