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. Author manuscript; available in PMC: 2024 Dec 1.
Published in final edited form as: Cancer. 2023 Sep 28;129(23):3772–3782. doi: 10.1002/cncr.35036

Table 1.

Demographic and clinical characteristics

Characteristic N = 36
Age, median (range), years 41 (19-70)
Sex, n (%)
  Male 19 (53)
  Female 17 (47)
Race, n (%)
  White 20 (56)
  Asian 12 (33)
  Other 4 (11)
ECOG performance status, n (%)
  0 14 (39)
  1 17 (47)
  2 5 (14)
Disease status at enrollment, n (%)
  Locally advanced 7 (19)
  Metastatic 29 (81)
Years since initial diagnosis, median (range) 1.1 (0.0-13.0)
NTRK gene fusion, n (%)
  NTRK1 19 (53)
  NTRK2 1 (3)
  NTRK3 16 (44)
Subtype, n (%)
  Bone sarcoma
    Chondrosarcoma 1 (3)
    NOS 1 (3)
  Gastrointestinal stromal tumors 4 (11)
  Soft tissue sarcoma
    NOS 8 (22)
    Malignant peripheral nerve sheath tumor 6 (17)
    Spindle cell sarcoma 4 (11)
    Epithelioid spindle sarcoma 3 (8)
    Inflammatory myofibroblastic tumor 2 (6)
    Myopericytoma 2 (6)
    Stromal tumor 2 (6)
    Dedifferentiated liposarcoma 1 (3)
    Fibrosarcoma 1 (3)
    Synovial sarcoma 1 (3)
Prior therapies, n (%)a
   Surgery 31 (86)
   Radiotherapy 21 (58)
   Systemic therapy 25 (69)
Number of prior systemic therapies, n (%)
  0 10 (28)
  1 12 (33)b
  2 7 (19)
  ≥3 7 (19)
Best response to prior therapy, n (%)
  Complete response 1 (4)
  Stable disease 5 (20)
  Progressive disease 7 (28)
  Otherc 11 (44)

ECOG, Eastern Cooperative Oncology Group; NOS, not otherwise specified; NTRK, neurotrophic tyrosine receptor kinase.

a

Patients may have received more than 1 type of prior therapy.

b

One patient who reported “No” to prior systemic therapies had the number of prior systemic therapies actually reported as “1”.

c

Other includes unknown and not evaluable.