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. Author manuscript; available in PMC: 2020 Aug 19.
Published in final edited form as: Mod Pathol. 2019 Aug 2;33(1):38–46. doi: 10.1038/s41379-019-0324-7

Table 3.

Sensitivity and specificity of pan-Trk immunohistochemistry for detecting NTRK fusions

Sensitivity
NTRK1 96.2% (26/27)
NTRK2   100% (5/5)
NTRK3 79.4% (27/34)
Sensitivity Specificity

Total 87.9% (58/66) 81.1% (257/317)
Colon 87.5% (7/8)  100% (25/25)
Lung 87.5% (7/8)  100% (24/24)
Thyroid 81.8% (9/11)  100% (27/27)
Salivary 88.9% (8/9)    52% (13/25)
Breast    80% (4/5) 82.1% (23/28)
Inflammatory myofibroblastic tumor  100% (3/3)  100% (5/5)
Sarcoma    80% (8/10) 74.4% (29/39)
Pancreas            (0/0)a  100% (20/20)
Appendix  100% (1/1)  100% (1/1)
Cholangio  100% (2/2)  100% (19/19)
Glioma  100% (6/6) 20.8% (5/24)
Melanoma  100% (3/3)  100% (17/17)
Neuroendocrine            (0/0)a 88.9% (8/9)
Small round cell tumorb            (0/0) 45.8% (11/24)
Otherc            (0/0)  100% (30/30)
a

The NTRK fusion positive pancreatic adenocarcinoma and pancreatic neuroendocrine tumor cases were detected on cytology specimens, and no material remained available for immunohistochemical studies

b

Small round cell tumors included embryonal rhabdomyosarcoma (8), neuroblastoma (5), Ewing sarcoma (5), desmoplastic small round cell tumor (5), and NUT midline carcinoma (1)

c

Other tumor types included prostatic adenocarcinoma (9), high-grade serous ovarian carcinoma (7), endometrioid adenocarcinoma (4), ampullary carcinoma (2), esophageal adenocarcinoma (2), esophageal squamous cell carcinoma (1), uterine perivascular epithelioid cell tumor (1), histiocytosis (1), myoepithelial carcinoma (1), granular cell tumor (1), and cancer of unknown primary (1)