Cargando…
Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor
A new progression pattern, hyperprogressive disease (HPD), has been recently acknowledged in cancer patients accepted immune checkpoint inhibitors (ICIs). We report a unique case of cervical small cell carcinoma which showed primary resistance to pembrolizumab and was with a rapid radiological progr...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826182/ https://www.ncbi.nlm.nih.gov/pubmed/31802899 http://dx.doi.org/10.2147/OTT.S213436 |
_version_ | 1783465033125068800 |
---|---|
author | Xu, Zihan Chen, Liying Zheng, Linpeng Yang, Qiao Chen, Mingjing Wang, Jianmin Zhu, Guangkuo Chen, Zhengtang Sun, Jianguo |
author_facet | Xu, Zihan Chen, Liying Zheng, Linpeng Yang, Qiao Chen, Mingjing Wang, Jianmin Zhu, Guangkuo Chen, Zhengtang Sun, Jianguo |
author_sort | Xu, Zihan |
collection | PubMed |
description | A new progression pattern, hyperprogressive disease (HPD), has been recently acknowledged in cancer patients accepted immune checkpoint inhibitors (ICIs). We report a unique case of cervical small cell carcinoma which showed primary resistance to pembrolizumab and was with a rapid radiological progression after the initiate of ICIs treatment. However, the detection results of multiple predictive biomarkers suggested that the patient was eligible for ICIs treatment. The whole exome sequencing showed that AKT1 E17K mutation was high (26.316%) in tumor tissue, and dynamic monitoring of circulating tumor DNA indicated that AKT1 E17K mutation rate was increasing successively and highly consistent with tumor growth in peripheral blood. Therefore, the correlation between AKT1 E17K mutation and HPD, and the role of AKT1 E17K mutation in identifying patients who might not benefit from ICIs treatment need to be further studied. |
format | Online Article Text |
id | pubmed-6826182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-68261822019-12-04 Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor Xu, Zihan Chen, Liying Zheng, Linpeng Yang, Qiao Chen, Mingjing Wang, Jianmin Zhu, Guangkuo Chen, Zhengtang Sun, Jianguo Onco Targets Ther Case Report A new progression pattern, hyperprogressive disease (HPD), has been recently acknowledged in cancer patients accepted immune checkpoint inhibitors (ICIs). We report a unique case of cervical small cell carcinoma which showed primary resistance to pembrolizumab and was with a rapid radiological progression after the initiate of ICIs treatment. However, the detection results of multiple predictive biomarkers suggested that the patient was eligible for ICIs treatment. The whole exome sequencing showed that AKT1 E17K mutation was high (26.316%) in tumor tissue, and dynamic monitoring of circulating tumor DNA indicated that AKT1 E17K mutation rate was increasing successively and highly consistent with tumor growth in peripheral blood. Therefore, the correlation between AKT1 E17K mutation and HPD, and the role of AKT1 E17K mutation in identifying patients who might not benefit from ICIs treatment need to be further studied. Dove 2019-10-30 /pmc/articles/PMC6826182/ /pubmed/31802899 http://dx.doi.org/10.2147/OTT.S213436 Text en © 2019 Xu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Report Xu, Zihan Chen, Liying Zheng, Linpeng Yang, Qiao Chen, Mingjing Wang, Jianmin Zhu, Guangkuo Chen, Zhengtang Sun, Jianguo Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor |
title | Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor |
title_full | Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor |
title_fullStr | Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor |
title_full_unstemmed | Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor |
title_short | Hyperprogressive Disease In Cervical Small Cell Carcinoma Treated By Immune Checkpoint Inhibitor |
title_sort | hyperprogressive disease in cervical small cell carcinoma treated by immune checkpoint inhibitor |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826182/ https://www.ncbi.nlm.nih.gov/pubmed/31802899 http://dx.doi.org/10.2147/OTT.S213436 |
work_keys_str_mv | AT xuzihan hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT chenliying hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT zhenglinpeng hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT yangqiao hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT chenmingjing hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT wangjianmin hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT zhuguangkuo hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT chenzhengtang hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor AT sunjianguo hyperprogressivediseaseincervicalsmallcellcarcinomatreatedbyimmunecheckpointinhibitor |