Alternate Title
Basic Trial Information
Objectives
Entry Criteria
Expected Enrollment
Outcomes
Outline
Trial Contact Information
Registry Information

Alternate Title

Vinblastine, Celecoxib, and Combination Chemotherapy in Treating Patients With Newly-Diagnosed Metastatic Ewing's Sarcoma Family of Tumors

Basic Trial Information

Phase	Type	Status	Age	Sponsor	Protocol IDs
Phase II	Treatment	Closed	50 and under (at diagnosis)	NCI	COG-AEWS02P1 AEWS02P1, NCT00061893

Objectives

1. Determine the feasibility and safety of low-dose vinblastine and celecoxib in combination with standard multiagent chemotherapy in patients with newly diagnosed metastatic Ewing's sarcoma family of tumors.
2. Determine the event-free survival of patients treated with this regimen.
3. Determine the pharmacokinetics of this regimen in these patients.

Entry Criteria

Disease Characteristics:

• Newly diagnosed Ewing's sarcoma family of tumors of the bone or soft tissues
  • Paraspinal tumors of extra-dural origin and Askin's tumor of the chest wall are eligible



• Metastatic disease, defined by the following criteria:
  • Lesions are discontinuous from the primary tumor, are not regional lymph nodes, and do not share a body cavity with the primary tumor
  • A single pulmonary or pleural nodule greater than 1 cm OR multiple nodules greater than 0.5 cm are considered evidence of pulmonary or pleural metastases (unless there is another clear medical explanation for these lesions)
  • Contralateral pleural effusions are considered metastatic disease



• No CNS involvement

Prior/Concurrent Therapy:

Biologic therapy

• No prior bone marrow or stem cell transplantation

Chemotherapy

• No prior chemotherapy

Endocrine therapy

• Not specified

Radiotherapy

• No prior radiotherapy

Surgery

• Not specified

Other

• No other concurrent nonsteroidal anti-inflammatory medications, including salicylates
• No concurrent dexrazoxane unless approved by the study investigator

Patient Characteristics:

Age

• 50 and under (at diagnosis)

Performance status

• Lansky 50-100% (under 17 years of age)
• Karnofsky 50-100% (age 17 and over)
  • Patients whose performance status is affected by a pathological fracture are allowed provided they are able to undergo treatment

Life expectancy

• Not specified

Hematopoietic

• Not specified

Hepatic

• Bilirubin no greater than 1.5 times upper limit of normal (ULN)
• AST or ALT less than 5 times ULN

Renal

• Creatinine adjusted according to age as follows*:
  • No greater than 0.4 mg/dL (≤ 5 months)
  • No greater than 0.5 mg/dL (6 months -11 months)
  • No greater than 0.6 mg/dL (1 year-23 months)
  • No greater than 0.8 mg/dL (2 years-5 years)
  • No greater than 1.0 mg/dL (6 years-9 years)
  • No greater than 1.2 mg/dL (10 years-12 years)
  • No greater than 1.4 mg/dL (13 years and over [female])
  • No greater than 1.5 mg/dL (13 years to 15 years [male])
  • No greater than 1.7 mg/dL (16 years and over [male])

  OR

• Creatinine clearance or radioisotope glomerular filtration rate at least 70 mL/min*

 [Note: *Unless these values are related to renal insufficiency secondary to tumor involvement that is expected to improve once the tumor mass is smaller (e.g., pelvic mass causing obstructive hydronephrosis)]

Cardiovascular

• Shortening fraction at least 27% by echocardiogram

  OR

• Ejection fraction at least 50% by MUGA

Other

• Not pregnant or nursing
• Fertile patients must use effective contraception
• Body surface area at least 0.4 m²
• No allergy to sulfa
• No aspirin hypersensitivity
• No asthma triad (asthma with nasal polyps, and urticaria)
• No other prior cancer, including nonmelanoma skin cancer

Expected Enrollment

A total of 6-36 patients will be accrued for this study within 1.17 years.

Outcomes

Feasibility as measured by toxicity at study completion

Event-free survival at 1 to 2 years following study completion

Outline

This is a pilot, multicenter study.

• Induction therapy: Patients receive the following alternating regimens:
  • VAC (courses 1 and 3): Patients receive vincristine IV and cyclophosphamide IV over 1 hour on day 1 and doxorubicin IV continuously on days 1 and 2 of weeks 1 and 7.
  
  
  
  • IE (courses 2 and 4): Patients receive ifosfamide IV over 1 hour and etoposide IV over 1-2 hours on days 1-5 of weeks 4 and 10.

    Patients also receive filgrastim (G-CSF) subcutaneously (SC) beginning 24-48 hours after the last dose of chemotherapy and continuing until blood counts recover.

  
  
  

  Treatment repeats every 21 days for a total of 4 courses in the absence of disease progression or unacceptable toxicity.




• Local control and consolidation therapy: Beginning on week 13, patients are assigned to 1 of 4 regimens based on disease status.
  • Regimen A (surgery only): Patients who respond to induction chemotherapy undergo surgery on week 13. Patients then begin consolidation therapy on week 15 with the following alternating regimens:
    • VAC (courses 5, 7, and 9): Patients receive VAC on weeks 15, 21, and 27.
    
    
    
    • IE (courses 6, 8, 10, 12, and 14): Patients receive IE on weeks 18, 24, 30, 36, and 42.
    
    
    
    • VC (courses 11 and 13): Patients receive vincristine IV and cyclophosphamide IV over 1 hour on weeks 33 and 39.
    
    
    
  
  
  
  • Regimen B (radiotherapy only): Patients with unresectable lesions undergo radiotherapy once daily 5 days a week for up to approximately 6 weeks beginning on week 13. Patients also receive consolidation therapy beginning on week 13, with the following alternating regimens:
    • VAC (courses 5, 9, and 11): Patients receive VAC on weeks 13, 25, and 31.
    
    
    
    • IE (courses 6, 8, 10, 12, and 14): Patients receive IE on weeks 16, 22, 28, 34, and 40.
    
    
    
    • VC (courses 7 and 13): Patients receive VC on weeks 19 and 37.
    
    
    
  
  
  
  • Regimen C (surgery and radiotherapy): Patients who respond to induction chemotherapy undergo surgery on week 13. Patients who have inadequate margins after surgery undergo radiotherapy (as in regimen B) beginning on week 15. Patients also receive consolidation therapy, beginning on week 15, with the following alternating regimens:
    • VAC (courses 5, 9, and 11): Patients receive VAC on weeks 15, 27, and 33.
    
    
    
    • IE (courses 6, 8, 10, 12, and 14): Patients receive IE on weeks 18, 24, 30, 36, and 42.
    
    
    
    • VC (courses 7 and 13): Patients receive VC on weeks 21 and 39.
    
    
    
  
  
  
  • Regimen D (preoperative radiotherapy): Patients with bulky lesions who do not have a good clinical and radiographic response to induction therapy begin consolidation therapy on week 13 with VAC (course 5) and undergo concurrent radiotherapy as in regimen B. Patients then receive IE on weeks 16 and 19 for courses 6 and 7. Patients undergo surgery on week 22. Patients continue consolidation therapy with the following alternating regimens:
    • VAC (courses 8 and 9): Patients receive VAC on weeks 24 and 27.
    
    
    
    • IE (courses 10, 12, and 14): Patients receive IE on weeks 30, 36, and 42.
    
    
    
    • VC (courses 11 and 13): Patients receive VC on weeks 33 and 39.
    
    
    
  
  
  

  Patients receive G-CSF SC (as in induction therapy) during all consolidation courses.

  Consolidation therapy continues for 10 courses in the absence of disease progression or unacceptable toxicity.




• Vinblastine and celecoxib therapy: Throughout induction, local control, and consolidation therapies, patients also receive vinblastine IV 3 times a week (twice a week during the weeks that vincristine is given) and oral celecoxib twice daily, beginning on day 1 of course 1 and continuing until the completion of course 14.*

   [Note: *To assess for safety, the first 6 patients enrolled receive vinblastine only during courses 1 and 2 and celecoxib is then added for all subsequent courses.]

Patients are followed every 3 months for 3 years and then every 6 months for 2 years.

Trial Contact Information

Trial Lead Organizations

Children's Oncology Group

Judy Felgenhauer, MD, PS, Protocol chair		Ph: 509-474-2777; 800-442-8534

Registry Information
Official Title		A Pilot Study of Low-Dose Antiangiogenic Chemotherapy in Combination with Standard Multiagent Chemotherapy for Patients with Newly Diagnosed Metastatic Ewing Sarcoma Family of Tumors
Trial Start Date		2004-04-23
Trial Completion Date		2009-06-29 (estimated)
Registered in ClinicalTrials.gov		NCT00061893
Date Submitted to PDQ		2003-04-09
Information Last Verified		2008-10-23
NCI Grant/Contract Number		CA98543