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Poster Display session 2

3739 - Mutational landscapes and tumor mutational burden expression in endometrial cancer


29 Sep 2019


Poster Display session 2


Tumour Site

Endometrial Cancer


Yingli Zhang


Annals of Oncology (2019) 30 (suppl_5): v403-v434. 10.1093/annonc/mdz250


Y. Zhang1, J. Zhang1, Z. Shao1, L. Zhao1, Y. Zhang2, S. Zhang2, S. Zhao3, F. Guo2, F. Pang2, L. Zhang2, X. Dong4, K. Wang3

Author affiliations

  • 1 Department Of Gynecologic Oncology, Zhejiang Cancer Hospital, 310022 - Hangzhou/CN
  • 2 Medical Liaison Department, OrigiMed, 201100 - Shanghai/CN
  • 3 Bioinformatics, OrigiMed, 200135 - Shanghai/CN
  • 4 Clinical Pathology Department, OrigiMed, 201100 - Shanghai/CN


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Abstract 3739


Endometrial cancer (EC) is one of the most common gynaecological tumours. Tumour mutational burden (TMB) has emerged as a promising predictor to evaluate efficacy to immunotherapy in several kinds of solid tumours. However, the relationship between TMB and genetic features of EC remains unclear.


Total 50 EC patients including 41 endometrioid adenocarcinoma, 6 uterine serous adenocarcinoma, 1 uterine clear cell carcinoma, 1 endometrial squamous cell carcinoma and 1 endometrial adenosquamous carcinoma were enrolled in this study. The ECs had been classified as FIGO I (n = 14), II (n = 6), III (n = 12), IV (n = 16) and not available (n = 2). FFPE tumour and matched blood samples were collected from patients for NGS-based targeted panel sequencing (450 genes). Genomic alterations and TMB were assessed.


The 50 patients had a median age of 56 years (range, 32-73 years) with a median TMB of 3.8 muts/Mb (interquartile range (IQR), 1.5-13.7 muts/Mb). We found recurrent mutations, including PTEN (64%), PIK3CA (44%), ARID1A (40%), PIK3R1 (36%), TP53 (32%), CHD4 (20%), and KRAS (20%). FGFR2 mutations were occurred in 7 (14%) patients. The most frequently mutated genes in early-stage (FIGO I and II) were PTEN (85%), ARID1A (50%), PIK3R1 (50%), PIK3CA (40%), LRP1B (30%), and CHD4 (30%), while the most common mutations in advanced-stage (FIGO III and IV) were PTEN (46%), PIK3CA (43%), TP53 (43%), ARID1A (36%), PIK3R1 (29%), and KRAS (21%). We also found that all POLE mutations (5/5) occurred in early-stage. Mutations of PIK3R1, CHD4, CTCF, SETD2, PPP2R1A, NF1, BRCA2, ARID1B and POLE were associated with TMB-high (TMB-H, TMB≥10muts/Mb) (P < 0.05 for all). Importantly, all POLE mutations occurred in EC with TMB-H, including two cases of EC with ultrahigh TMB (TMB > 100 muts/Mb). At least one actionable mutation was identified in 86% (43/50) patients.


PI3K signaling pathway genes, PTEN, PIK3CA and PIK3R1 were most frequently mutated in EC. 26% patients (13/50) had TMB-H. POLE mutations likely occurred in early stage and were related with TMB-H, which may provide potential targets for immunotherapy of EC.

Clinical trial identification

Editorial acknowledgement

This study was supported by National Natural Science Foundation of China (Youth fund project, no. 81602267).

Legal entity responsible for the study

The authors.


National Natural Science Foundation of China (Youth fund project, no. 81602267).


Y. Zhang: Full / Part-time employment: OrigiMed. S. Zhang: Full / Part-time employment: OrigiMed. S. Zhao: Full / Part-time employment: OrigiMed. F. Guo: Full / Part-time employment: OrigiMed. F. Pang: Full / Part-time employment: OrigiMed. L. Zhang: Full / Part-time employment: OrigiMed. X. Dong: Full / Part-time employment: OrigiMed. K. Wang: Full / Part-time employment: OrigiMed. All other authors have declared no conflicts of interest.

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