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The influence of chemotherapy on the prognosis of rhabdomyosarcoma

✍ Scribed by Ortega, Jorge A. ;Rivard, Georges E. ;Isaacs, Hart ;Hittle, Robert E. ;Hays, Daniel M. ;Pike, Malcolm C. ;Karon, Myron R.


Book ID
102524970
Publisher
John Wiley and Sons
Year
1975
Tongue
English
Weight
393 KB
Volume
1
Category
Article
ISSN
0098-1532

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✦ Synopsis


Abstract

A study of 77 consecutive cases of childhood rhabdomyosarcoma treated initially at the Children's Hospital of Los Angeles from 1950 to 1972 demonstrated an impressive improvement in survival of patients when intensive chemotherapy was combined with surgery and radiation therapy. The major improvement in survival occurred in Stage II and Stage III disease. Eight out of 9 patients with a primary lesion of the lower extremities developed intra‐abdominal disease. A general approach for treatment of Stage II, III, and IV rhabdomyosarcoma is proposed which involves intensive chemotherapy, following biopsy, as the principle treatment, with radiation and surgery used as adjuvants.


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