Literature DB >> 2171439

How curable is relapsed Wilms' tumour? The United Kingdom Children's Cancer Study Group.

J J Groot-Loonen1, C R Pinkerton, P H Morris-Jones, J Pritchard.   

Abstract

Three hundred and eighty one children with Wilms' tumour were treated on the United Kingdom Children's Cancer Study Group WT1 Study (1980/6). Seventy one patients relapsed during or after treatment, which included surgery and chemotherapy, with irradiation depending on stage and histology. Despite treatment with various combinations of chemotherapy, surgery, and radiotherapy there were only 17 survivors. For unfavourable histology, any stage, only two of 20 survive. We conclude that, after relapse, even for patients who have had localised disease and favourable histology, the 'salvage' rate is little more than 50% and for all others the likelihood of cure is very small. Three of 41 children who relapsed less than 12 months from diagnosis survive, compared with 14 of 30 who relapsed later. It is essential that even with this 'good prognosis' tumour initial treatment is optimal and given by centres experienced in management of children's cancer. Furthermore, there is a clear need for additional effective chemotherapeutic agents for relapsed patients.

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Year:  1990        PMID: 2171439      PMCID: PMC1792105          DOI: 10.1136/adc.65.9.968

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  20 in total

1.  Long-term survival following brain metastasis of Wilm's tumor.

Authors:  A M Mohammad; J Meyer; N Hakami
Journal:  J Pediatr       Date:  1977-04       Impact factor: 4.406

2.  Histopathology and prognosis of Wilms tumors: results from the First National Wilms' Tumor Study.

Authors:  J B Beckwith; N F Palmer
Journal:  Cancer       Date:  1978-05       Impact factor: 6.860

3.  Overtreatment of children with Wilms' tumour outside paediatric oncology centres.

Authors:  J Pritchard; C A Stiller; E L Lennox
Journal:  BMJ       Date:  1989-09-30

4.  Partial hepatectomy in metastatic Wilms' tumor.

Authors:  W B Smith; W M Wara; L W Margolis; J H Kushner; A A De Lorimier
Journal:  J Pediatr       Date:  1974-02       Impact factor: 4.406

5.  Factors influencing the cure rate in nephroblastoma. A review of 335 cases.

Authors:  B Jereb; G Eklund
Journal:  Acta Radiol Ther Phys Biol       Date:  1973-04

6.  The treatment of Wilms' tumor: results of the Second National Wilms' Tumor Study.

Authors:  G J D'Angio; A Evans; N Breslow; B Beckwith; H Bishop; V Farewell; W Goodwin; L Leape; N Palmer; L Sinks; W Sutow; M Tefft; J Wolff
Journal:  Cancer       Date:  1981-05-01       Impact factor: 6.860

7.  Survival following brain metastases in wilms' tumor.

Authors:  S K Morgan; M G Buse
Journal:  Pediatrics       Date:  1976-07       Impact factor: 7.124

8.  Late recurrence of Wilms tumor.

Authors:  N Clausen
Journal:  Med Pediatr Oncol       Date:  1982

9.  Prognosis in children with Wilms' tumor metastases prior to or following primary treatment: results from the first National Wilms' Tumor Study (NWTS-1).

Authors:  W W Sutow; N E Breslow; N F Palmer; G J D'Angio; J Takashima
Journal:  Am J Clin Oncol       Date:  1982-08       Impact factor: 2.339

10.  Bleomycin in combination chemotherapy of metastatic Wilms tumor: a late recurrent case, refractory to conventional therapy.

Authors:  T Kisielius; A Bianco; J M Merrill; S G Taylor; W DeWys
Journal:  Med Pediatr Oncol       Date:  1979
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  1 in total

1.  Expression and prognostic relevance of vascular endothelial growth factor (VEGF) and its receptor (FLT-1) in nephroblastoma.

Authors:  M A Ghanem; G J van Steenbrugge; M K Sudaryo; R B Mathoera; J M Nijman; Th H van der Kwast
Journal:  J Clin Pathol       Date:  2003-02       Impact factor: 3.411

  1 in total

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