30+ years of experience
500+ CRS+HIPEC procedures
International multidisciplinary committee

Life expectancy in soft tissue sarcomas: prognostic factors

11/28/2024 · Dr. François Quenet

Life expectancy in soft tissue sarcomas: prognostic factors

Life expectancy in soft tissue sarcomas

Life expectancy in soft tissue sarcomas depends on many prognostic factors. With appropriate treatment at specialised centres, survival rates have improved in recent decades.

Main prognostic factors

Complete resection (R0): Negative margins are the most important prognostic factor. R0: 5-year survival 50-70%. R1/R2: 10-30%

Histological grade: Low grade: 70-85% at 5 years. High grade: 30-50%

Tumour size: <5cm: better prognosis. >10cm: worse prognosis. >20cm: requires specialised surgery

Depth: Superficial: better than deep/retroperitoneal

Histological subtype: Well-differentiated liposarcoma: very good. Leiomyosarcoma, pleomorphic: worse

Age: <60 years: better than >60 years

Location: Limbs: better. Retroperitoneum/abdomen: worse

Survival by stage

Stage I (low grade, small): 5-year survival: 80-90%

Stage II (small high grade or large low grade): 60-75%

Stage III (large high grade): 50-65%

Stage IV (metastatic): 15-30%

Survival by subtype

Well-differentiated liposarcoma: >90% at 10 years if resection is complete

Myxoid liposarcoma: 70-80% at 5 years

Dedifferentiated/pleomorphic liposarcoma: 30-50% at 5 years

Leiomyosarcoma: 40-60% at 5 years

Undifferentiated pleomorphic sarcoma: 30-50% at 5 years

GIST: With imatinib: 70-85% at 5 years in resectable cases

The importance of a specialised centre

Patients treated at specialised centres have 20-30% higher survival than in general hospitals. See how to choose a centre.

At Quenet Torrent Institute: R0 resection rate >85%, perioperative mortality <2%, 5-year survival similar to that published by international high-volume centres.

Treatments that improve survival

R0 surgery: The main treatment. It includes vascular resections if necessary

Radiotherapy: Preoperative or intraoperative radiotherapy improves local control. See intraoperative radiotherapy

Chemotherapy: Anthracyclines + ifosfamide in high grade

Targeted therapies: Imatinib for GIST, pazopanib in advanced sarcomas

Recurrences

Local recurrence: 20-40% of cases. Further surgery can offer a new chance of cure if resectable

Lung metastases: 30-50% of high-grade sarcomas. Pulmonary metastasectomy can prolong survival

Do you have a sarcoma? The team's experience affects the success of surgery. At Quenet Torrent Institute we treat complex sarcomas. Request a second opinion.

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