Osteosarcoma in children. A study of 125 cases

A study is presented of the aetiology and results of treatment in a group of 125 proven osteosarcomas present in children under fifteen years of age. These cases have been collected from the records of one English and six European treatment centres. There is a slight male preponderance, but the stri...

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Veröffentlicht in:Journal of bone and joint surgery. British volume 1975-08, Vol.57 (3), p.341-345
Hauptverfasser: Price, C H, Zhuber, K, Salzer-Kuntschik, M, Salzer, M, Willert, H G, Immenkamp, M, Groh, P, Matĕjovský, Z, Keyl, W
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container_end_page 345
container_issue 3
container_start_page 341
container_title Journal of bone and joint surgery. British volume
container_volume 57
creator Price, C H
Zhuber, K
Salzer-Kuntschik, M
Salzer, M
Willert, H G
Immenkamp, M
Groh, P
Matĕjovský, Z
Keyl, W
description A study is presented of the aetiology and results of treatment in a group of 125 proven osteosarcomas present in children under fifteen years of age. These cases have been collected from the records of one English and six European treatment centres. There is a slight male preponderance, but the striking aetiological feature is the very high proportion of tumours of the long bones of the limbs (96 per cent). The two and a half and five year disease-free survival rates were respectively 15 and 12 per cent, with a further 9 per cent still living, but under observation for less than two and a half years. Evidence of metastasis after two and a half years is very unusual, but no child with a tumour of an axial or girdle bone lived this length of time. Although the differences in the results of the different methods of treatment employed are not statistically valid, the largest number of long survivors had been treated by early amputation, which method also provided the lowest rate of local tumour recurrences. Reasons are discussed which indicate that prompt ablation is the treatment of choice, perhaps with certain advantages in the light of recent advances in adjuvant treatment. The past situation in connection with childhood osteosarcoma certainly provides strong support for immediate carefully designed clinical trials of the new adjuvant methods cited.
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The two and a half and five year disease-free survival rates were respectively 15 and 12 per cent, with a further 9 per cent still living, but under observation for less than two and a half years. Evidence of metastasis after two and a half years is very unusual, but no child with a tumour of an axial or girdle bone lived this length of time. Although the differences in the results of the different methods of treatment employed are not statistically valid, the largest number of long survivors had been treated by early amputation, which method also provided the lowest rate of local tumour recurrences. Reasons are discussed which indicate that prompt ablation is the treatment of choice, perhaps with certain advantages in the light of recent advances in adjuvant treatment. 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source MEDLINE; Alma/SFX Local Collection
subjects Age Factors
Amputation
Antineoplastic Agents - therapeutic use
Bone Neoplasms - drug therapy
Bone Neoplasms - mortality
Bone Neoplasms - radiotherapy
Bone Neoplasms - surgery
Child
Child, Preschool
Drug Therapy, Combination
England
Europe
Female
Follow-Up Studies
Humans
Infant
Male
Neoplasm Metastasis
Neoplasm Recurrence, Local
Osteosarcoma - diagnostic imaging
Osteosarcoma - drug therapy
Osteosarcoma - mortality
Osteosarcoma - surgery
Prognosis
Radiography
title Osteosarcoma in children. A study of 125 cases
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