Journal of Clinical Oncology, Vol 16, 3628-3633, Copyright © 1998 by American Society of Clinical Oncology
Ifosfamide-containing chemotherapy in Ewing's sarcoma: The Second United Kingdom Children's Cancer Study Group and the Medical Research Council Ewing's Tumor Study
A Craft, S Cotterill, A Malcolm, D Spooner, R Grimer, R Souhami, J Imeson and I Lewis
United Kingdom Children's Cancer Study Group and the Medical Research Council Bone Sarcoma Working Party. a.w.craft@ncl.ac.uk
PURPOSE: To investigate the possibility that the substitution of ifosfamide
for cyclophosphamide therapy for Ewing's sarcoma will improve survival over
that seen in the first United Kingdom Children's Cancer Study Group
(UKCCSG) Ewing's tumor study (ET-1). PATIENTS AND METHODS: Between 1987 and
1993,243 patients (138 men or boys) were entered onto the study. The median
age was 13.5 years (range, 1.5 to 27 years). The median follow-up was 58
months. Chemotherapy included four courses of vincristine 2 mg/m2;
ifosfamide 9 g/m2; and doxorubicin 60 mg/m2 administered every 3 weeks.
Treatment of the primary tumor was with surgery and/or radiotherapy
followed by ifosfamide 6 g/m2; doxorubicin 60 mg/m2; and vincristine 2
mg/m2; with actinomycin D 1.5 mg/m2 substituted for doxorubicin after a
total dose of 420 mg/m2. RESULTS: Two hundred one patients had no
metastases. One hundred eighteen patients had tumors of the axial skeleton
and 125 patients had limb primary tumors. The major toxicities were
hematologic and infective, but there were no toxic deaths. The overall
survival rate was 62% (95% confidence interval [CI], 56 to 69) and
relapse-free survival (RFS) 56% (95% CI, 49 to 62). For those with no
metastases at diagnosis, the RFS rate was 62% and for those with
metastases, 23%. Multivariate analysis showed age and site to have a
significant effect on RFS. Pelvic sites had the worst RFS rate of 41%;
other axial sites, 55%; and extremity tumors, 73%. Age younger than 10
years had an RFS rate of 86% versus 55% for older patients. The local
relapse rate for axial tumors was 20% and for limb primary tumors was 2.4%.
CONCLUSION: The 5-year survival rate of 62% is improved compared with the
44% survival rate achieved in ET-1. This is probably caused by the use of
higher doses of ifosfamide compared with relatively low doses of
cyclophosphamide in ET-1.
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|
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|
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|

|
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11(1):
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|
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|

|
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|
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14(11):
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|
 |
|

|
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|
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|
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|

|
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|
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|
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|

|
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|
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|
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|
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|
|