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Soft tissue sarcoma - Rare malignant tumour of the connective tissue
Soft tissue sarcomas are rare malignant tumours of the connective tissue. Find out more about symptoms, diagnosis, treatment options and new approaches such as the TRAPTRAP study.
Add as Preferred SourceThings worth knowing about "Soft tissue sarcoma"
Soft tissue sarcomas are rare malignant tumours of the connective tissue
soft tissue sarcoma is a malignant tumour that arises from the mesenchymal tissue.strong data-start=""201"" data-end=""225"">mesenchymal tissue of the soft tissue - this includes connective, fatty, muscle, nerve, vascular and tendon sheath tissue. This type of tumour is rare, but accounts for around 1% of all malignant tumours in adults. There are over 50 histological subtypes, which can differ greatly in terms of growth, metastasis and response to treatment.
recognised late.
Typical signs are:
- Painless, progressive swelling or lump
- Restriction of movement when joints or nerves are affected
- Pain or discomfort, with increasing spread
- General symptoms such as fatigue, weight loss or fever are rare
sporadically, without a clear cause. Possible risk factors:
- Previous radiotherapy
- Genetic syndromes (e.g. Li-Fraumeni syndrome, neurofibromatosis type 1)
- Chronic inflammation or tissue damage
- CD13 expression, relevant for targeted therapies
- Previous radiotherapy
- Genetic syndromes (e.g. Li-Fraumeni syndrome, neurofibromatosis type 1)
- Chronic inflammation or tissue damage
- CD13 expression, relevant for targeted therapies
- additional therapy with tTF-NGR, a fusion protein that specifically closes tumour-supplying vessels via CD13
Literature references:
- ""Soft tissue sarcomas: ESMO-EURACAN Clinical Practice Guidelines."" Annals of Oncology.
- ""Patient guide for soft tissue sarcomas.""
- ""TRAPTRAP trial - Targeted vascular infarction in soft tissue sarcoma."" Journal of Clinical Oncology.
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