骨肉瘤
医学
化疗
肿瘤科
辅助化疗
内科学
佐剂
作者
Michael P. Link,Jonathan J. Shuster,Allen M. Goorin,Angela W. Miser,William H. Meyer,J. E. Kingston,Jean B. Belasco,Andrew T. Baker,Alberto G. Ayala,Teresa J. Vietti
出处
期刊:Springer eBooks
[Springer Nature]
日期:1988-01-01
卷期号:: 283-290
被引量:4
标识
DOI:10.1007/978-94-009-2691-2_44
摘要
The prognosis for children with osteosarcoma has improved dramatically over the past 15 years. Prior to 1970, fewer than 20% of patients with osteosarcoma treated only with surgery of the primary tumor survived 5 years (1,2), and it was inferred from the experience at multiple institutions that at least 80% of patients presenting without overt metastatic disease, in fact, had microscopic subclinical metastases at the time of diagnosis. Today, projected 5-year survivals of 60–80% are reported from a number of treatment centers. This improvement in prognosis for more recently diagnosed patients with osteosarcoma had been attributed to the administration of adjuvant chemotherapy after surgery which apparently was effective in eradicating micrometastatic disease.
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