Skip to content
← Soft Tissue Sarcoma

FOR PATIENTS · SOURCE READING

Targeted therapy

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

Source updated: June 2, 2023 · Captured 2026-09-09.

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

Context: Treatment Option Overview

Targeted therapy is a type of treatment that uses drugs or other substances to identify and attack specific cancer cells. There are different types of targeted therapy. These include:

Source links and citations

Tyrosine kinase inhibitor therapy: These inhibitors block signals that cancer cells need to grow and divide. Some tyrosine kinase inhibitors also have angiogenesis inhibitor effects. Tyrosine kinase inhibitors used to treat soft tissue sarcoma include pazopanib, imatinib, sunitinib, and regorafenib. New types of tyrosine kinase inhibitors are being studied, including cediranib and larotrectinib.

Source links and citations

Histone methyltransferase inhibitor therapy: This therapy may help keep cancer cells from growing. Tazemetostat is a type of histone methyltransferase inhibitor therapy used to treat soft tissue sarcoma.

Source links and citations

For more information, see Drugs Approved for Soft Tissue Sarcoma.

Source links and citations

Preserved source evidence · Independent clinical review pending · Not medical advice