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ePoster Display

903P - Analysis of hyper-progression disease-related gene alterations in Chinese patients with non-nasopharyngeal head and neck cancer

Date

16 Sep 2021

Session

ePoster Display

Topics

Tumour Site

Head and Neck Cancers

Presenters

Qining Jiang

Citation

Annals of Oncology (2021) 32 (suppl_5): S786-S817. 10.1016/annonc/annonc704

Authors

Q. Jiang1, H. Zhang2, S. Liu1, X. Shen3, L. Hou1

Author affiliations

  • 1 Head And Neck Surgery, The affiliated cancer hospital of Guizhou medical university, 550004 - Guiyang/CN
  • 2 The Medical Department, 3D Medicines Inc., Shanghai, 201114, PR China, 201114 - Shanghai/CN
  • 3 The Medical Department, 3D Medicines Inc., Shanghai, 201114, PR China, 550004 - Shanghai/CN

Resources

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Abstract 903P

Background

Resistance to immune checkpoint inhibitors (ICI) treatment has been shown in most patients, and some even present hyper-progression disease (HPD). Some researchers previously reported that almost one third of patients with non-nasopharyngeal head and neck cancer (HNC) suffered HPD, but the mechanism is still unclear. Herein, we evaluated some genetic alterations in Chinese HNC patients, which were reported to be associated with HPD in other solid tumors, and analyzed the association between these gene alteration and tumor microenvironment (TME) level or PD-L1 expression level.

Methods

This study queried the data from formalin-fixed paraffin-embedded tissues of 346 HNC patients which underwent a targeted next-generation sequencing assay performed by 3DMed Clinical Laboratory Inc., a College of American Pathologists (CAP) and Clinical Laboratory Improvement Amendments (CLIA) certified laboratory, between January, 2019 and June, 2021 in China.

Results

Among these patients, 54.3% (188/346) were carry at least one gene alteration associated with HPD, including amplification of gene MDM2/4, CCND1, FGF3/4/19, and gene mutation in CDKN2A/2B, DNMT3CA, etc. The ratio of these gene mutation in HNSCC were 1.73% MDM2/4, 22.83% CCND1, 21.97% FGF3/4/19, 28.32% CDKN2A/2B and 4.34% DNMT3CA. In addition, 249 and 233 patients were available for analysis of TMB level and PD-L1 expression level, respectively. However, no significant difference in both tumor mutational burden (TMB) and PD-L1 expression levels were found among patients with or without HPD-associated gene alteration, and patients carry one of these gene alterations (p>0.05).

Conclusions

There are a high proportion of HPD-associated gene alterations in patients with HNC, however, the mechanism of HPD presented in these patients was not related to lower TMB level or PD-L1 expression level.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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