Dacomitinib and gedatolisib in combination with fractionated radiation in head and neck cancer

被引:8
作者
Wilson, George D. [1 ]
Wilson, Thomas G. [1 ]
Hanna, Alaa [1 ]
Dabjan, Mohamad [1 ]
Buelow, Katie [1 ]
Torma, John [1 ]
Marples, Brian [2 ]
Galoforo, Sandra [1 ]
机构
[1] William Beaumont Hosp, Dept Radiat Oncol, 3811 W Thirteen Mile Rd, Royal Oak, MI 48073 USA
[2] Univ Rochester, Dept Radiat Oncol, Rochester, NY USA
关键词
Head and neck cancer; Radiation; Targeted agents; Xenografts; Growth delay; SQUAMOUS-CELL CARCINOMA; DUAL PI3K/MTOR INHIBITOR; GROWTH-FACTOR RECEPTOR; ANTITUMOR-ACTIVITY; IN-VITRO; TUMOR MICROENVIRONMENT; PI3K INHIBITORS; WILD-TYPE; CETUXIMAB; IRRADIATION;
D O I
10.1016/j.ctro.2020.11.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: There has been little success targeting individual genes in combination with radiation in head and neck cancer. In this study we investigated whether targeting two key pathways simultaneously might be more effective. Materials and methods: We studied the effect of combining dacomitinib (pan-HER, irreversible inhibitor) and gedatolisib (dual PI3K/MTOR inhibitor) with radiation in well characterized, low passage xenograft models of HNSCC in vitro and in vivo. Results: Dacomitinib showed differential growth inhibition in vitro that correlated to EGFR expression whilst gedatolisib was effective in both cell lines. Neither agent radiosensitized the cell lines in vitro. In vivo studies demonstrated that dacomitinib was an effective agent alone and in combination with radiation whilst the addition of gedatolisib did not enhance the effect of these two modalities despite inhibiting phosphorylation of key genes in the PI3K/MTOR pathway. Conclusions: Our results showed that combining two drugs with radiation provided no added benefit compared to the single most active drug. Dacomitinib deserves more investigation as a radiation sensitizing agent in HNSCC. (C) 2020 The Authors. Published by Elsevier B.V. on behalf of European Society for Radiotherapy and Oncology.
引用
收藏
页码:15 / 23
页数:9
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