Literature DB >> 319895

Rhabdomyosarcoma: response with chemotherapy prior to radiation in patients with gross residual disease.

M Tefft, C H Fernandez, T E Moon.   

Abstract

One hundred and ten Group III patients enrolled in the IRS Study have been reviewed. Of these, 39 are fully and 56 are partially evaluable. Combining the data for both groups 77/95 (81%) have shown complete or partial response/no measurable disease and this has been maintained in 53/95 (56%). No patient received premature RT for local progression during the time of pre-radiation chemotherapy. However, 15/95 patients have shown local recurrence or direct extension to neighboring tissues; 13/15 could be reviewed. Only 3/13 have recurred at a time related to the delay in starting radiation. Overall survival for Group III patients is 72%-85% (Regimen F and Regimen E respectively).

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Year:  1977        PMID: 319895     DOI: 10.1002/1097-0142(197702)39:2<665::aid-cncr2820390244>3.0.co;2-b

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  4 in total

1.  The clinical features and prognosis of rhabdomyosarcoma: follow-up studies on pediatric tumors from the Japanese Pediatric Tumor Registry 1971-1980. Part II. Committee of Malignant Tumors, Japanese Society of Pediatric Surgeons.

Authors:  K Nakada
Journal:  Jpn J Surg       Date:  1990-09

2.  Fibrosarcoma of bladder exhibiting endocrine characteristics of phaeochromocytoma.

Authors:  R A Keenan; J D Buchanan
Journal:  J R Soc Med       Date:  1979-08       Impact factor: 5.344

3.  The management of rhabdomyosarcoma in children and young adults.

Authors:  D M Hays
Journal:  World J Surg       Date:  1980-01       Impact factor: 3.352

4.  Local therapy of rhabdomyosarcoma, osteosarcoma and Ewing's sarcoma of children and adolescents.

Authors:  G Prindull; H G Willert; G Notter
Journal:  Eur J Pediatr       Date:  1985-07       Impact factor: 3.183

  4 in total

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