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1.
Clin. transl. oncol. (Print) ; 23(5): 922-930, mayo 2021. tab, ilus
Article in English | IBECS | ID: ibc-221232

ABSTRACT

Soft-tissue sarcomas constitute an uncommon and heterogeneous group of tumors of mesenchymal origin. Diagnosis, treatment, and management should be performed by an expert multidisciplinary team. MRI/CT of the primary tumor and biopsy is mandatory before any treatment. Wide surgical resection with tumor-free tissue margin is the mainstay for localized disease. Radiotherapy is indicated in large, deep, high-grade tumors, or after marginal resection not suitable for re-excision. Perioperative chemotherapy should be discussed for high-risk sarcomas of the extremities and trunk-wall. In the case of oligometastatic disease, patients should be considered for local therapies. First-line treatment with anthracyclines (or in combination with ifosfamide) is the treatment of choice. Other drugs have shown activity in second-line therapy and in specific histological subtypes but options are limited and thus, a clinical trial should always be discussed (AU)


Subject(s)
Humans , Soft Tissue Neoplasms/diagnosis , Soft Tissue Neoplasms/therapy , Sarcoma/therapy , Sarcoma/diagnosis , Tomography, X-Ray Computed , Magnetic Resonance Imaging , Societies, Medical , Biopsy , Spain
2.
Clin Transl Oncol ; 23(5): 922-930, 2021 May.
Article in English | MEDLINE | ID: mdl-33405052

ABSTRACT

Soft-tissue sarcomas constitute an uncommon and heterogeneous group of tumors of mesenchymal origin. Diagnosis, treatment, and management should be performed by an expert multidisciplinary team. MRI/CT of the primary tumor and biopsy is mandatory before any treatment. Wide surgical resection with tumor-free tissue margin is the mainstay for localized disease. Radiotherapy is indicated in large, deep, high-grade tumors, or after marginal resection not suitable for re-excision. Perioperative chemotherapy should be discussed for high-risk sarcomas of the extremities and trunk-wall. In the case of oligometastatic disease, patients should be considered for local therapies. First-line treatment with anthracyclines (or in combination with ifosfamide) is the treatment of choice. Other drugs have shown activity in second-line therapy and in specific histological subtypes but options are limited and thus, a clinical trial should always be discussed.


Subject(s)
Sarcoma/diagnosis , Sarcoma/therapy , Soft Tissue Neoplasms/diagnosis , Soft Tissue Neoplasms/therapy , Anthracyclines/therapeutic use , Antineoplastic Agents/therapeutic use , Checklist , Chemotherapy, Adjuvant/methods , Dermatofibrosarcoma/therapy , Female , Fibromatosis, Aggressive/genetics , Fibromatosis, Aggressive/therapy , Humans , Magnetic Resonance Imaging , Male , Medical Oncology , Neoadjuvant Therapy/methods , Radiotherapy/methods , Retroperitoneal Neoplasms/therapy , Sarcoma/diagnostic imaging , Sarcoma/pathology , Societies, Medical , Soft Tissue Neoplasms/diagnostic imaging , Soft Tissue Neoplasms/pathology , Solitary Fibrous Tumors/drug therapy , Spain , Tomography, X-Ray Computed , Uterine Neoplasms/therapy
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