Sarcoma
Conditions
Keywords
localized osteosarcoma
Brief summary
RATIONALE: Drugs used in chemotherapy, such as ifosfamide, methotrexate, cisplatin, and doxorubicin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving it after surgery may kill any tumor cells that remain after surgery. PURPOSE: This clinical trial is studying how well combination chemotherapy works in treating patients undergoing surgery for newly diagnosed high-grade osteosarcoma.
Detailed description
OBJECTIVES: * To evaluate the efficacy of a new induction regimen comprising ifosfamide in combination with high-dose methotrexate, cisplatin, and doxorubicin hydrochloride, in terms of clinical response and pathological response of the tumor, in patients with newly diagnosed high-grade osteosarcoma. * To determine the overall survival and disease-free survival of these patients. * To evaluate the toxicity of this regimen. * To correlate MRI imaging of the primary tumor with histopathologic grading after treatment with this regimen. OUTLINE: This is a multicenter study. * Neoadjuvant chemotherapy (weeks 1-15): Patients receive ifosfamide IV over 1 hour on days 1-5 and 36-40; doxorubicin hydrochloride IV over 18 hours on days 1-3 and 36-38 and IV over 72 hours on days 71-73; high-dose methotrexate IV over 4 hours on days 22, 29, 57, 64, 92, and 99; and cisplatin IV over 4 hours on day 71. * Surgery (week 16): Patients undergo resection of the tumor on day 106. Patients found to have unresectable disease are treated on an alternative protocol unless they have clear clinical and pathologic response to treatment. * Adjuvant chemotherapy (weeks 18-43): Beginning 2 weeks after surgery, patients receive ifosfamide IV over 1 hour on days 120-124, 155-159, 225-229, and 260-264; doxorubicin hydrochloride IV over 18 hours on days 120-122 and 155-157 and IV over 72 hours on days 190-192; high-dose methotrexate IV over 4 hours on days 141, 148, 176, 183, 211, 218, 246, 253, 281, and 288; and cisplatin IV over 4 hours on days 190 and 289. After completion of study therapy, patients are followed every 2 months for 1 year, every 4 months for 2 years, every 6 months for 2 years, and then annually thereafter.
Interventions
DRUGmethotrexate
DRUGcisplatin
DRUGdoxorubicin hydrochloride
DRUGifosfamide
PROCEDUREadjuvant therapy
PROCEDUREneoadjuvant therapy
PROCEDUREtherapeutic conventional surgery
Sponsors
National Cancer Institute (NCI)
Mayo Clinic
Study design
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically confirmed osteosarcoma of the extremity * High-grade (grade III or IV) disease * No low-grade disease (e.g., parosteal or periosteal osteosarcoma) * No secondary osteosarcoma (i.e., tumor occurring in a radiotherapy field designed for a prior tumor) * No Paget's disease * No known metastases PATIENT CHARACTERISTICS: * Total bilirubin \< 2 times normal * AST \< 2 times normal * Alkaline phosphatase \< 2 times normal * Creatinine ≤ 1.5 mg/dL OR creatinine clearance \> 60 mL/min * LVEF ≥ 45% * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * No other prior malignancy except retinoblastoma * Patients with familial retinoblastoma syndrome who develop osteosarcoma unrelated to radiotherapy (e.g., in a primary site in the extremities) are eligible PRIOR CONCURRENT THERAPY: * No prior chemotherapy or radiotherapy * Patients with retinoblastoma may have received radiotherapy to the orbits * At least 28 days since prior initial amputation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Histopathologic response rate | — |
| Clinical response rate | — |
| Toxicity | — |
| Disease-free survival | — |
| Overall survival | — |
Outcome results
None listed