China Journal of Oral and Maxillofacial Surgery ›› 2018, Vol. 16 ›› Issue (4): 322-327.doi: 10.19438/j.cjoms.2018.04.006

• Original Articles • Previous Articles     Next Articles

TP53 truncating mutation as a predictive biomarker for induction chemotherapy in patients with locally advanced oral squamous cell carcinoma

FU Yong1, MA Jie1, LIU Ying1, TAN Yi-ran1, JU Wu-tong1, SUN Wen-wen1, ZHAO Tong-chao1, WANG Min1, WANG Li-zhen2, LI Jiang2, ZHANG Chen-ping1, ZHANG Zhi-yuan1, ZHONG Lai-ping1   

  1. 1.Department of Oromaxillofacial Head and Neck Oncology,
    2.Department of Oral Pathology, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine; National Clinical Research Center For Oral Diseases; Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology. Shanghai 200011, China;
  • Received:2018-04-18 Revised:2018-07-09 Online:2018-07-20 Published:2018-08-09

Abstract: PURPOSE:To test the status of TP53 mutations in patients with locally advanced oral squamous cell carcinoma (OSCC) and investigate whether or not TP53 truncating mutation could be used as a predictive biomarker to screen patients who would benefit from induction chemotherapy. METHODS: One hundred and one patients with locally advanced OSCC treated in our hospital from 2008 to 2014 were included in this study. Their clinicopathologic information, frozen or formalin-fixed, paraffin-embedded samples of tumor and matched normal samples were collected. Using Ion PGM system, all samples were sequenced with high-throughput technology. Bioinformatics software was used to analyze and interpret the variants. SPSS 23.0 software package was used for statistical analysis. RESULTS: Among 101 patients, there were 74 men and 27 women with a median age of 59 years. The median follow-up time was 34.9 months. There were 102 TP53 non-synonymous mutations (allele frequency ≥3%) in 73 OSCC patients, with an average sequencing depth of 2366-fold in the tumor samples and 2225-fold in the matched normal samples. Compared with 42 patients who did not receive induction chemotherapy, 59 patients who received induction chemotherapy had a seemingly better distant metastasis free survival (P=0.090) while no significant difference in overall survival. Subgroup analysis showed that patients with TP53 truncating mutations could benefit from induction chemotherapy in distant metastasis free survival (P=0.038). CONCLUSIONS: Our study does not find that the patients with locally advanced OSCC could benefit from induction chemotherapy in overall survival, but TP53 truncating mutation could be used as a candidate of predictive biomarker to screen patients who would benefit from induction chemotherapy in distant metastasis free survival.

Key words: Oral squamous cell carcinoma, TP53 truncating mutation, Distant metastasis free survival, Biomarker, Induction chemotherapy

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