TY - JOUR
T1 - Prognostic significance of PD-L1þ and CD8þ immune cells in HPVþ Oropharyngeal squamous cell carcinoma
AU - Solomon, Benjamin
AU - Young, Richard J.
AU - Bressel, Mathias
AU - Urban, Damien
AU - Hendry, Shona
AU - Thai, Alesha
AU - Angel, Christopher
AU - Haddad, Afaf
AU - Kowanetz, Marcin
AU - Fua, Tsien
AU - Corry, June
AU - Fox, Stephen
AU - Rischin, Danny
N1 - Publisher Copyright:
© 2018 American Association for Cancer Research.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Human papilloma virus–positive oropharyngeal squamous cell carcinoma (HPVþ OPSCC) represents a distinct subgroup of head and neck cancers associated with clinical outcomes that are not accurately categorized by existing tumor–node–metastasis-based staging methods. Given the significant impact of immune parameters, such as tumor-infiltrating lymphocytes (TIL) in many cancers, we sought to determine if immunophenotyping tumors can improve categorization of HPVþ OPSCCs for prognostic purposes. In a cohort of 190 patients with HPVþ OPSCC, we quantified and determined the localization of CD8þ TILs, as well as PD-L1–expressing tumor cells (TC) and immune cells (IC). The prognostic significance of these parameters on overall survival (OS) was evaluated, and their contribution to existing prognostic models was determined. High CD8þ TIL abundance (30% on stromal or intratumoral ICs) was seen in 61.3% patients and was associated with improved OS [HR, 0.4; 95% confidence interval (CI), 0.2–0.9; P ¼ 0.017]. Although the expression of PD-L1 on TC was not prognostic, high expression of PD-L1 on 5% of intratumoral ICs was found in 38.5% patients and was significantly associated with improved OS (HR, 0.37; 95% CI, 0.15–0.93; P ¼ 0. 023). Both high intratumoral IC PD-L1 expression and abundant CD8þ TILs in HPVþ OPSCCs identify subgroups of patients with excellent outcomes and provide additional prognostic information beyond existing staging systems.
AB - Human papilloma virus–positive oropharyngeal squamous cell carcinoma (HPVþ OPSCC) represents a distinct subgroup of head and neck cancers associated with clinical outcomes that are not accurately categorized by existing tumor–node–metastasis-based staging methods. Given the significant impact of immune parameters, such as tumor-infiltrating lymphocytes (TIL) in many cancers, we sought to determine if immunophenotyping tumors can improve categorization of HPVþ OPSCCs for prognostic purposes. In a cohort of 190 patients with HPVþ OPSCC, we quantified and determined the localization of CD8þ TILs, as well as PD-L1–expressing tumor cells (TC) and immune cells (IC). The prognostic significance of these parameters on overall survival (OS) was evaluated, and their contribution to existing prognostic models was determined. High CD8þ TIL abundance (30% on stromal or intratumoral ICs) was seen in 61.3% patients and was associated with improved OS [HR, 0.4; 95% confidence interval (CI), 0.2–0.9; P ¼ 0.017]. Although the expression of PD-L1 on TC was not prognostic, high expression of PD-L1 on 5% of intratumoral ICs was found in 38.5% patients and was significantly associated with improved OS (HR, 0.37; 95% CI, 0.15–0.93; P ¼ 0. 023). Both high intratumoral IC PD-L1 expression and abundant CD8þ TILs in HPVþ OPSCCs identify subgroups of patients with excellent outcomes and provide additional prognostic information beyond existing staging systems.
UR - http://www.scopus.com/inward/record.url?scp=85047764959&partnerID=8YFLogxK
U2 - 10.1158/2326-6066.CIR-17-0299
DO - 10.1158/2326-6066.CIR-17-0299
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C2 - 29378694
AN - SCOPUS:85047764959
SN - 2326-6066
VL - 6
SP - 295
EP - 304
JO - Cancer immunology research
JF - Cancer immunology research
IS - 3
ER -