Department of Oral Maxillofacial-Head and Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, China; Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, China; National Clinical Research Center of Stomatology, Shanghai, China.
Department of Oral Maxillofacial-Head and Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, China; School of Stomatology, Weifang Medical University, Weifang, China.
Radiother Oncol. 2021 Nov;164:83-91. doi: 10.1016/j.radonc.2021.09.013. Epub 2021 Sep 25.
Among oral squamous cell carcinoma (OSCC) patients who receive docetaxel, cisplatin, and 5-fluorouracil (TPF) induction chemotherapy, those with a favorable pathological response tend to obtain satisfactory clinical outcomes, while the total population exhibit no survival benefit. Thus, there is an urgent need to improve the therapeutic effect of TPF by applying personalized treatment according to distinct biomarkers.
In the present study, we collected oral rinse samples from 44 OSCC patients enrolled in our prospective multicenter random phase II trial before TPF induction chemotherapy to conduct 16S rRNA gene sequencing and metagenomic analysis. Patients were administrated with two cycles of TPF induction chemotherapy (75 mg/m cisplatin and 75 mg/m docetaxel on day 1 and 750 mg/m fluorouracil from the first to the fifth day), and then divided into responsive and nonresponsive groups according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
In the 16S rRNA gene sequence analysis, Fusobacterium and Mycoplasma were more enriched in the nonresponsive group, while Slackia was more enriched in the responder group at the genus level. In the metagenomic shotgun sequencing analysis, Fusobacterium nucleatum was more enriched in the nonresponsive group. Functional analysis showed that the platinum drug resistance pathway and microRNAs in cancer and RNA degradation pathways were remarkably associated with patient sensitivity to induction chemotherapy.
Our data suggest that the oral microbiome may play an important role in the OSCC patient sensitivity to TPF induction chemotherapy and offer novel potential biomarkers for predicting the response to TPF induction chemotherapy.
在接受多西他赛、顺铂和 5-氟尿嘧啶(TPF)诱导化疗的口腔鳞状细胞癌(OSCC)患者中,病理反应良好的患者往往获得满意的临床结局,而总体人群则无生存获益。因此,迫切需要通过根据不同的生物标志物应用个性化治疗来提高 TPF 的治疗效果。
本研究前瞻性地收集了 44 例接受 TPF 诱导化疗的 OSCC 患者的口腔冲洗样本,进行 16S rRNA 基因测序和宏基因组分析。患者接受两周期 TPF 诱导化疗(第 1 天给予 75mg/m2 顺铂和 75mg/m2 多西他赛,第 1 天至第 5 天给予 750mg/m2 氟尿嘧啶),然后根据实体瘤反应评估标准 1.1(RECIST)将患者分为反应组和无反应组。
在 16S rRNA 基因序列分析中,无反应组中 Fusobacterium 和 Mycoplasma 更为丰富,而反应组中 Slackia 更为丰富。在宏基因组鸟枪法测序分析中,无反应组中 Fusobacterium nucleatum 更为丰富。功能分析表明,铂类药物耐药途径和癌症中的 microRNAs 以及 RNA 降解途径与患者对诱导化疗的敏感性显著相关。
我们的数据表明,口腔微生物组可能在 OSCC 患者对 TPF 诱导化疗的敏感性中发挥重要作用,并为预测 TPF 诱导化疗反应提供了新的潜在生物标志物。