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| Name | Class |
|---|---|
| Novartis | INDUSTRY |
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Chemotherapy treatment with docetaxel and gemcitabine is a standard treatment for patients with soft tissue sarcoma. This study is designed to explore whether the addition of tyrosine kinase inhibitor pazopanib enhances the anticancer effect of the chemotherapy drugs.
The Phase I component of this study is designed to determine the maximum tolerated dose of pazopanib when given with docetaxel and gemcitabine. The Phase II component is designed to determine the overall response rate of the combination of docetaxel, gemcitabine and pazopanib prior to surgical resection in patients with soft tissue sarcoma.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| cohort 1 | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Gemcitabine | Drug | 1500 mg/m^2 given days 1 and 15 of every 28 day cycle for a total of 4 cycles |
|
| Measure | Description | Time Frame |
|---|---|---|
| Maximum Tolerated Dose | 1 cycle (28 days) |
| Measure | Description | Time Frame |
|---|---|---|
| Overall response rate | 4 cycles (112 days) |
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Inclusion Criteria:
18 years or older
chemotherapy naive, histologically high grade soft tissue sarcoma that is considered to be operable
tumor greater than 5 cm in longest dimension
life expectancy of at least 6 months
Zubrod performance status of 0-2
signed informed consent
adequate bone marrow function defined by:
adequate hepatic function defined by:
adequate renal function defined by:
1. serum creatinine <1.5 x ULN
negative pregnancy test for women of child bearing potential
willingness to use effective contraception while on treatment and for 3 months thereafter
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Fletcher Allen Health Care | Burlington | Vermont | 05401 | United States |
| Type | Date | Date Unknown |
|---|---|---|
| Release | Mar 10, 2017 | |
| Reset | Apr 20, 2017 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Mar 10, 2017 | Apr 20, 2017 |
| ID | Term |
|---|---|
| D012509 | Sarcoma |
| ID | Term |
|---|---|
| D018204 | Neoplasms, Connective and Soft Tissue |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| D000093542 | Gemcitabine |
| D000077143 | Docetaxel |
| C516667 | pazopanib |
| ID | Term |
|---|---|
| D006571 | Heterocyclic Compounds |
| D003841 | Deoxycytidine |
| D003562 | Cytidine |
| D011741 | Pyrimidine Nucleosides |
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| Docetaxel | Drug | 50 mg/m^2 on days 1 and 15 of each 28 day cycle for a total of 4 cycles |
|
|
| Pazopanib | Drug | Starting dose of 400 mg/day starting 72 hours after docetaxel/gemcitabine administration for 10 days (days 4-13 and 18-27) of each 28 day cycle for a total of 4 cycles. Dose will be increased by 200 mg/day for each cohort until the maximum tolerated dose is identified. |
|
|
| D011743 |
| Pyrimidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D043823 | Taxoids |
| D043822 | Cyclodecanes |
| D003516 | Cycloparaffins |
| D006840 | Hydrocarbons, Alicyclic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D004224 | Diterpenes |
| D013729 | Terpenes |