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← Childhood Soft Tissue Sarcoma

HEALTH PROFESSIONAL · SOURCE READING

Surgery

Source: Childhood Soft Tissue Sarcoma Treatment (PDQ®)–Health Professional Version, National Cancer Institute.

Source updated: April 21, 2025 · Captured 2026-09-09.

Selected source text with whitespace normalised. This Triangle page is not an NCI PDQ summary.

Context: Treatment of Vascular Tumors / Angiosarcoma / Treatment of angiosarcoma

Localized disease can be cured by aggressive surgery. Complete surgical excision appears to be crucial for the long-term survival of patients with angiosarcomas and lymphangiosarcomas, despite evidence of tumor shrinkage in some patients who were treated with local or systemic therapy.[22,26-28] Data on liver transplant for localized angiosarcomas are limited.[29][Level of evidence C1]

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Evidence (surgery):

A review of 222 patients (median age, 62 years; range, 15–90 years) reported the following:[28]

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A review of 222 patients (median age, 62 years; range, 15–90 years) reported the following:[28]

An overall disease-specific survival (DSS) rate of 38% at 5 years.

A review of 222 patients (median age, 62 years; range, 15–90 years) reported the following:[28]

The 5-year DSS rate was 44% in 138 patients with localized, resected tumors but only 16% in 43 patients with metastases at diagnosis.

One case report suggested that liver transplant may contribute to prolonged disease-free survival.[30][Level of evidence C2]

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Publication references

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Preserved source evidence · Not medical advice