Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster display session

372P - Real-world fusion landscape in advanced Chinese pancreatic cancer using next generation sequecing: A multicenter study

Date

23 Nov 2019

Session

Poster display session

Topics

Targeted Therapy

Tumour Site

Pancreatic Adenocarcinoma

Presenters

Yiyu Shen

Citation

Annals of Oncology (2019) 30 (suppl_9): ix122-ix130. 10.1093/annonc/mdz431

Authors

Y. Shen1, S. Fang2, X. Cai3, Y. Fang4, R. Lin5, Y. Zhang6, J. Li7, X. Liang8, L. Wang9, L. Lin10, L. Zhang11, H. Feng12, S. Lan13, X. Cai14, C. Xu15, W. Wang16, M. Fang16, J. Zhang17

Author affiliations

  • 1 Hepatobiliary Surgery, The Second Affiliated Hospital of Jiaxing Medical College, 314000 - Jiaxing/CN
  • 2 Pathology, Daping Hospital and Research Institute of Surgery, Army Medical University, 400042 - Chongqing/CN
  • 3 Oncology, Sun Yat-sen University Cancer Hospital, 510060 - Guangzhou/CN
  • 4 Oncology, Sir Run Run Shaw Hospital, Zhejiang University, 310016 - Hangzhou/CN
  • 5 Oncology, Fujian Cancer Hospital, 3500014 - Fuzhou/CN
  • 6 Oncology, The Second Affiliated Hospital of Medical College, Xi’an Jiaotong University, 710004 - Xi’an/CN
  • 7 Radiotherapy, Xiamen Cancer Hospital, 361003 - Xiamen/CN
  • 8 Oncology, The Third People’s Hospital of Zhengzhou, 450000 - Zhengzhou/CN
  • 9 Oncology, Baotou Cancer Hospital, 014030 - Baotou/CN
  • 10 Oncology, Peking University International Hospital, 102206 - Beijing/CN
  • 11 Pathology, Daxing Teaching Hospital of Capital Medical University, 102600 - Beijing/CN
  • 12 Oncology, Shanxi Dayi Hospital, Shanxi Academy of Medical Science, 030032 - Taiyuan/CN
  • 13 Oncology, The First Hospital of Jilin University, 130021 - Changchun/CN
  • 14 Oncology, the First Affiliated Hospital of Dalian Medical University, 116011 - Dalian/CN
  • 15 Pathology, Fujian Cancer Hospital, 350014 - Fuzhou/CN
  • 16 Chemotherapy, Zhejiang Cancer Hospital, 310022 - Hangzhou/CN
  • 17 Oncology, The Seven Medical Centre of Chinese PLA General Hospital, 100071 - Beijing/CN

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 372P

Background

The therapeutic targets of pancreatic cancer (PC) are fewer. Cell-free DNA (cfDNA) has been a research hotspot in molecular tumour profiling. In advanced PC patients, malignant abdominal dropsy provides a wealth of tumour cells that can be investigated. The aim of this study is to investigate fusion landscape in advanced PC.

Methods

A multicenter study in China was initiated from Oct. 2016, and PC patients have been enrolled as of Apr. 2019. To determine the fusion frequency in PC, we analysed data from 536 clinical PC cases, each of which had results from next-generation sequencing (NGS)-based 808 genes panel assay, analogous to the index patient.

Results

Of this entire cohort, 24 patients (4.48%) were identified with fusions, including ARID1A-PIGV (1), HSD3BP4-HSD3B1 (1), CDKN2A-MTAP (1), PDE10A-BRAF (1), ETV6-NTRK3 (1), NOTCH1-RABL6 (1), ERRFI1-SLC25A33 (1),BRCA1-PTGES3L (1),MYCN-LINC00299 (1), CREBBP-CDIP1 (1), LPAR5-CHD4 (1), PMS2-ETV1 (1), RPTOR-ASPSCR1 (1), CHD2-SLCO3A1 (1), IDH2-SEMA4B (1), BAIAP2-RPTOR (1), CHEK1-OSBP (1), LRP1-KRT81 (1), TBX3-ACSS3 (1), RAB11FIP1-GPR124 (1), AXIN1-SNX29 (1), PPP2R1A-ZNF415 (1), BCL2L14-ETV6 (1) and BMX-NHS (1). BRAF, NTRK and BRCA1 fusions were seen in 12.50% (3/24) advanced Chinese pancreatic cancer fusion landscape patients. These three patients were diagnosed with pancreatic duct adenocarcinoma. For treatments, the BRAF fusion patient chose vemurafenib, another two patients chose chemotherapy, and this case of BRAF fusion patient responding to vemurafenib was actively being sought thru our database.

Conclusions

Advanced Chinese pancreatic cancer fusion landscape is rich, BRAF and NTRK fusions are rare but potentially druggable in TKIs. Detection of BRAF, NTRK, BRCA1, EGFR, ALK, ROS1, RET and ERBB2 fusions should be part of comprehensive profiling panels to determine TKIs and direct appropriate combination therapeutic strategies.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Yiyu Shen.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.