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. Author manuscript; available in PMC: 2021 Sep 1.
Published in final edited form as: Cancer. 2020 Jun 18;126(17):3972–3981. doi: 10.1002/cncr.33036

Table 1.

Demographics and clinicopathologic information among HRAS-mutant salivary cancer patients receiving tipifarnib

Characteristic All patients N = 13a
Age at diagnosis (median) 58 (34–75)
Gender
 Female 2 (15)
 Male 11 (85)
ECOG performance status
 0–1 13 (100)
Ethnicity & Race
 White 10 (77)b
 Asian 2 (15)
 Black 1 (8)
Site of Primary Disease
 Parotid gland 12 (92)
 Minor salivary gland 1 (8)
Histologic subtype (high grade)
 Salivary duct carcinoma 4 (31)
 Myoepithelial-epithelial carcinoma 4 (31)
 Mucoepidermoid carcinoma 1 (8)
 Acinic cell carcinoma 1 (8)
 Oncocytic carcinoma 1 (8)
 Adenocarcinoma 1 (8)
 Carcinoma ex pleomorphic adenoma 1 (8)
Initial Disease Stagingc
 Stage I, II 2 (15)
 Stage III, IVA-C 11 (85)d
Initial or Primary Therapy
 Surgery alone 1 (8)
 Surgery + radiation (RT) 6 (46)
 Surgery + chemoradiation (CRT) 4 (31)
 Systemic therapy 2 (15)
Median time to recurrence (in months) 22.0 (4–81)
# of Lines of Prior Therapy for Advanced Disease
 1–2 9 (69)
 3+ 4 (31)
a

parentheses indicate % except for age which represents range;

b

no patients identified as Hispanic;

c

American Joint Committee on Cancer (AJCC) 8th edition Staging (2017);

d

N=2 had metastatic disease at initial presentation; ECOG = Eastern Cooperative Oncology Group