Abstract
Many patients presenting with soft tissue sarcoma have a poor prognosis as a consequence of the tendency of these tumours to invade extensively, recur locally, and metastasize hematogenously early in the course of the disease. Nevertheless most patients present without clinically evident metastases, and gains in survival will derive from improved local control and the elimination of micrometastases. Effective combination therapy utilizing surgery and radiotherapy has improved the functional outcome without compromizing local control of the primary tumor, particularly in soft tissue sarcomas of the extremities. Métastases, however, occur in up to half of the cases, even with adequate local control [1–3]. This chapter will update studies reviewed in the last volume of this series and discuss new relevant information and topics.
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Mertens, W.C., Bramwell, V.H.C. (1991). Adjuvant Chemotherapy for Soft Tissue Sarcomas. In: Pinedo, H.M., Verweij, J., Suit, H.D. (eds) Soft Tissue Sarcomas: New Developments in the Multidisciplinary Approach to Treatment. Cancer Treatment and Research, vol 56. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3896-7_8
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DOI: https://doi.org/10.1007/978-1-4615-3896-7_8
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