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Paclitaxel in Treating Patients With Locally Advanced or Metastatic Soft Tissue Angiosarcoma or Lymphangiosarcoma That Cannot Be Removed By Surgery

Multicentric Phase II Study Evaluating the Efficacy and Toxicity of Weekly Paclitaxel in Locally Advanced or Metastatic Soft Tissue Angiosarcomas That Cannot be Treated by Surgery

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00217607
Enrollment
30
Registered
2005-09-22
Start date
2005-02-28
Completion date
2012-01-31
Last updated
2016-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcoma

Keywords

adult angiosarcoma, recurrent adult soft tissue sarcoma, stage III adult soft tissue sarcoma, stage IV adult soft tissue sarcoma

Brief summary

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. PURPOSE: This phase II trial is studying how well paclitaxel works in treating patients with locally advanced or metastatic soft tissue angiosarcoma or lymphangiosarcoma that cannot be removed by surgery.

Detailed description

OBJECTIVES: Primary * Determine the 2-month objective response rate in patients with locally advanced or metastatic, unresectable soft tissue angiosarcoma or lymphangiosarcoma treated with paclitaxel. Secondary * Determine the 4- and 6-month response rate in patients treated with this drug. * Determine tolerability of this drug in these patients. * Determine the time to disease progression and overall survival of patients treated with this drug. * Determine the clinical criteria predicting response in patients treated with this drug. * Correlate the efficacy of this drug with the expression of genes involved in angiogenesis regulation in these patients. OUTLINE: This is a multicenter study. Patients receive paclitaxel IV on days 1, 8, and 15. Treatment repeats every 28 days for up to 6 courses. PROJECTED ACCRUAL: A total of 15-30 patients will be accrued for this study.

Interventions

DRUGpaclitaxel

Sponsors

UNICANCER
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed soft tissue angiosarcoma or lymphangiosarcoma * Locally advanced or metastatic disease * Unresectable disease * Angiosarcomas in previously irradiated areas allowed provided disease is clearly progressive * Measurable disease * No Kaposi's sarcoma PATIENT CHARACTERISTICS: Age * 18 to 70 Performance status * WHO 0-2 Life expectancy * Not specified Hematopoietic * Absolute neutrophil count \> 1,500/mm\^3 * Platelet count \> 100,000/mm\^3 Hepatic * Bilirubin \< 3 times upper limit of normal (ULN) * SGOT and SGPT \< 2.5 times ULN * No severe liver failure Renal * Creatinine clearance \> 60 mL/min * No severe kidney failure Cardiovascular * LVEF ≥ 50% Other * Not pregnant or nursing * Fertile patients must use effective contraception * No weight loss ≥ 20% of body weight prior to illness * Patient must be amenable to receiving care during the day * No HIV positivity * No clinical neuropathy * No known allergy to study drug or to any of its components (e.g., Cremophor EL) * No other progressive malignant tumor * No chronic illness (somatic or psychiatric) that would preclude study compliance and follow-up * No psychological, geographical, or social reason that would preclude study follow-up PRIOR CONCURRENT THERAPY: Biologic therapy * Not specified Chemotherapy * No more than 2 prior courses of chemotherapy Endocrine therapy * Not specified Radiotherapy * See Disease Characteristics Surgery * Not specified Other * No other concurrent anticancer therapy * No concurrent participation in another therapeutic investigational study

Design outcomes

Primary

MeasureTime frame
Objective Response Rate2 months

Secondary

MeasureTime frame
Tolerability6 months
Time to progression5 years
Response rate4 months
Clinical criteria predicting response2 months
Correlation of efficacy with the expression of genes involved in the angiogenesis regulation6 months
Overall survival5 years

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026