Sarcoma
Conditions
Brief summary
The yearly incidence of soft-tissue sarcomas(STS) in the USA is roughly 11,280 cases, and metastatic STS have a median overall survival of about 12 months. After the standard 1st line chemotherapy with doxorubicin, the only a few treatment option is available. Recently, pemetrexed, a novel multitargeted antifolate, has shown modest activity as a single agent lung cancer and mesothelioma. In patients with refractory STS, pemetrexed is well tolerated and moderately effective. Based on the background, investigators planned to conduct the phase II trial of pemetrexed in combination with cisplatin for metastatic/recurred soft-tissue sarcomas.
Interventions
Pemetrexed 500mg/m2, Intravenous, Q 3weeks. Cisplatin 75mg/m2, Intravenous, Q 3weeks. Combination administration : up to 6cycles After 6 cycle, pemetrexed alone is administered.
Sponsors
Yonsei University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Histologically confirmed advanced bone and soft tissue sarcoma with prior chemotherapy including anthracycline or ifosfamide 2. Measurable or evaluable disease (RECIST 1.1.) 3. Age ≥19 years 4. ECOG performance status of 0-2 5. Adequate laboratory findings * Absolute neutrophil count (ANC) ≥ 1500 /µL * Platelet count ≥ 75,000/ µL * Serum creatinine \< 1.5 x upper limit of normal (ULN) * AST (SGOT) and ALT (SGPT) \< 3 x upper limit of normal (ULN) * Total bilirubin \<1.5 x upper limit of normal (ULN) 6. more than 3 months of expected survival 7. Provision of written informed consent prior to any study procedure
Exclusion criteria
1. Patient who has had chemotherapy, radiotherapy, or biological therapy within 2 weeks prior to entering the study' 2. Patient is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the study. 3. Resectable lung metastases 4. Uncontrolled or active CNS metastasis and/or carcinomatous meningitis 5. Other co-existing malignancies or malignancies diagnosed within the last 3 years with the exception of basal cell carcinoma, thyroid cancer or cervical cancer in situ. 6. Uncontrolled medical conditions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| progression free rate | 12 weeks |
Secondary
| Measure | Time frame |
|---|---|
| adverse event | every 3 weeks |
Countries
South Korea
Outcome results
None listed