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. Author manuscript; available in PMC: 2020 Sep 1.
Published in final edited form as: Lancet Oncol. 2019 Dec 11;21(2):271–282. doi: 10.1016/S1470-2045(19)30691-6

Table 1:

Baseline characteristics

All patients in NTRK gene fusion-positive efficacy-evaluable population (n=54)
Age, years 58 (48–67)
Sex
 Female 32 (59%)
 Male 22 (41%)
Race
 White 43 (80%)
 Asian 7 (13%)
 Other 4 (7%)
Eastern Cooperative Oncology Group performance status
 0 23 (43%)
 1 25 (46%)
 2 6 (11%)
Previous lines of systemic therapy
 0 20 (37%)
 1 11 (20%)
 2 14 (26%)
 3 4 (7%)
 ≥4 5 (9%)
Previous treatment*
 Chemotherapy 46 (85%)
 Targeted therapy 13 (24%)
 Hormonal therapy 9 (17%)
 Immunotherapy 7 (13%)
CNS metastases at baseline
 Yes 12 (22%)
 No 42 (78%)
Previous radiotherapy to the brain
 Yes 7 (13%)
 No 47 (87%)
Time from end of previous radiotherapy of the brain to first dose of entrectinib
 <2 months 2 (29%)
 2 to <6 months 4 (57%)
 ≥6 months 1 (14%)
Tumour type
 Sarcoma 13 (24%)
 NSCLC 10 (19%)
 Mammary analogue secretory carcinoma (salivary) 7 (13%)
 Breast 6 (11%)
 Thyroid 5 (9%)
 Colorectal 4 (7%)
 Neuroendocrine 3 (6%)
 Pancreatic 3 (6%)
 Gynaecological 2 (4%)
  Ovarian 1 (2%)
  Endometrial 1 (2%)
 Cholangiocarcinoma 1 (2%)

Data are median (IQR) and n (%). NSCLC=non-small-cell lung cancer.

*

Patient might have received multiple or combination therapies, resulting in the sum of previous treatments being >100%.

Patients with baseline CNS metastases.

Subtypes of soft tissue sarcoma included cervical adenosarcoma (n=1), dedifferentiated chondrosarcoma (n=1), endometrial stromal sarcoma (n=1), follicular dendritic cell sarcoma (n=1), gastrointestinal stromal tumour (n=1; wild-type gastrointestinal stromal tumour, succinate dehydrogenase complex subunit B immunohistochemistry—tumour cells retain normal expression), malignant peripheral nerve sheath tumour (n=1), and sarcoma not otherwise specified (n=7).