Title:
Ewing's sarcoma: A combined approach in the management

dc.contributor.authorG.C. Pant
dc.contributor.authorB. Sanyal
dc.contributor.authorK. Sahni
dc.contributor.authorS.M. Tuli
dc.contributor.authorT.P. Srivastava
dc.date.accessioned2026-02-09T10:24:34Z
dc.date.issued1981
dc.description.abstractTwenty-seven histologically confirmed cases of localised Ewing's sarcoma were treated by two different regimes. Radiotherapy alone was used in 13 cases and a combination of chemotherapy and radiotherapy in 14. Single agent chemotherapy (cyclophosphamide) was given sequentially in nine patients and cyclophosphamide and actinomycin-D in five. There is a significant difference in the response to these different regimes. Only 69.2% of patients treated by radiotherapy alone were disease-free, for a median period of 10.4 months and metastases were noticed in 53.8% of cases. The disease-free survival in patients treated by combination therapy (radiotherapy and chemotherapy) was 18.4 months and metastases were seen in only 42.9%. However, no metastases were seen in patients who received cyclophosphamide and actinomycin-D, during a period of 14 months and only one patient showed residual disease. It is concluded that the addition of cyclophosphamide alone is not adequate in the management of Ewing's sarcoma. Actinomycin-D in addition to cyclophosphamide has improved the disease-free survival period significantly. The optimum dose of radiotherapy and its combination with other chemotherapeutic agents needs further trials to find the best and most suitable schedule. © 1981 Royal College of Radiologists.
dc.identifier.doi10.1016/S0009-9260(81)80309-1
dc.identifier.issn99260
dc.identifier.urihttps://doi.org/10.1016/S0009-9260(81)80309-1
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/58244
dc.titleEwing's sarcoma: A combined approach in the management
dc.typePublication
dspace.entity.typeArticle

Files

Collections