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. 2017 Apr 5;8(24):39254–39267. doi: 10.18632/oncotarget.16845

Table 3. Actionable alteration by sarcoma subtype.

Histology (patients) No reportable alteration, n (%) Patients had alteration(s), but none actionable, n (%) Patients with approved drug(s) in the disease available, n (%) (on-label) Patients with approved drug(s) in another disease available, n (%) (off-label) Patients with experimental treatment options (clinical trials), n (%) Patients with pre-clinical treatment options, n(%)
LEIOMYOSARCOMA 1 10 3 6 8 7
DEDIFFERENTIATED LIPOSARCOMA 0 0 11 10 10
OSTEOSARCOMA 1 6 1 2 4 4
WELL DIFFERENTIATED LIPOSARCOMA 0 1 7 7 7
CARCINOSARCOMA 0 3 5 6 6
RHABDOMYOSARCOMA 1 1 2 5 5
GASTROINTESTINAL STROMAL TUMOR 1 3 3 4 4
SPINDLE CELL SARCOMA 1 1 2 4 3
SYNOVIAL SARCOMA 1 2 0 1 1 1
ALVEOLAR SOFT PART SARCOMA 1 1 0 1 1 1
CHONDROSARCOMA 1 1 0 0 2 1
CHORDOMA 1 0 1 2 2
CLEAR CELL SARCOMA 3 0 0 0 0
EWING SARCOMA 2 0 1 1 1
UNCLASSIFIED 1 0 1 2 2
ALVEOLAR RHABDOMYOSARCOMA 2 0 0 0 0 0
FIBROSARCOMA 2 0 0 0 0
BRAIN GLIOSARCOMA 0 0 1 1 1
DESMOPLASTIC SMALL ROUND CELL TUMOR 0 0 1 1 1
PLEOMORPHIC SARCOMA 0 1 1 1 1
MALIGNANT PERIPHERAL NERVE SHEATH TUMOR 1 0 0 0 0
MYXOID LIPOSARCOMA 0 0 0 1 1
7 33 14 46 61 58
6.86% 32.35% 13.73% 45.10% 59.80% 56.86%