2017
DOI: 10.1051/sicotj/2017010
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Management of soft-tissue sarcomas; treatment strategies, staging, and outcomes

Abstract: Soft-tissue sarcomas (STS) are a rare group of malignant tumors which can affect any age group. For the majority of patients who present with a localized STS, treatment involves a multidisciplinary team decision-making approach ultimately relying on surgical resection with or without adjuvant radiation for successful limb salvage. The goals of treatment are to provide the patient with a functional extremity without local tumor relapse. The purpose of this article is to review the treatment of extremity STS, wi… Show more

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Cited by 34 publications
(36 citation statements)
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“…The acute awareness of one's own mortality further contributed to their subjective levels of distress. Some participants found little comfort in learning more about their illness, perhaps because STS is a rare disease with unknown causes and high morbidity 1,2,12 . These factors might make worries in patients with STS unique in their nature.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The acute awareness of one's own mortality further contributed to their subjective levels of distress. Some participants found little comfort in learning more about their illness, perhaps because STS is a rare disease with unknown causes and high morbidity 1,2,12 . These factors might make worries in patients with STS unique in their nature.…”
Section: Discussionmentioning
confidence: 99%
“…Patients with STS typically undergo a combination of invasive surgery and radiation therapy, which can result in disfigurement, wound complications, or amputation 1,2,12 . While these procedures have a curative intention and are largely limb‐sparing, these medical interventions come with a high burden to patients 9 .…”
Section: Introductionmentioning
confidence: 99%
“…However, chemotherapy for SS remains controversial because it is di cult to conduct a prospective study on the e cacy of neoadjuvant therapy, speci cally for this tumor type. Moreover, several pretreatment characteristics, including the tumor size, age, histologic grade, and tumor depth [6,9,11,[14][15][16], in uence the prognosis of a patient with SS and may have affected the results of previous studies.…”
Section: Introductionmentioning
confidence: 99%
“…Sarcomas comprise a rare, heterogeneous group of malignant neoplasms that frequently arise from the soft tissue structures of the lower extremity . Current sarcoma management practices utilize a multidisciplinary approach combining limb‐sparing surgery and oncologic therapy to achieve local disease control while preserving the function of the limb . Wide surgical resection of soft tissue sarcomas can lead to large, complex defects with exposure of underlying neurovascular structures, tendons, and/or bone.…”
Section: Introductionmentioning
confidence: 99%
“…Wide surgical resection of soft tissue sarcomas can lead to large, complex defects with exposure of underlying neurovascular structures, tendons, and/or bone. Subsequent reconstructive surgery is often required to provide adequate soft tissue coverage and restore limb function . The utilization of a multidisciplinary approach involving orthopedic and plastic surgeons, medical oncologists, and radiation oncologists has led to limb salvage rates of greater than 90% with favorable oncologic and functional outcomes …”
Section: Introductionmentioning
confidence: 99%