Cargando…

Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital

AIM: The aim of this study is to determine the incidence of T790M mutations after progression on epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKI) and median duration on TKI before progression on TKI. METHODS: Records of Rajiv Gandhi Cancer Institute and Research Centre, of pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Babu Koyyala, Venkata Pradeep, Batra, Ullas, Jain, Parveen, Sharma, Mansi, Goyal, Pankaj, Medisetty, Pavani, Jajodia, Ankush, Maheshwari, Udip Dilip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120311/
https://www.ncbi.nlm.nih.gov/pubmed/30168457
http://dx.doi.org/10.4103/lungindia.lungindia_451_17
_version_ 1783352246894854144
author Babu Koyyala, Venkata Pradeep
Batra, Ullas
Jain, Parveen
Sharma, Mansi
Goyal, Pankaj
Medisetty, Pavani
Jajodia, Ankush
Maheshwari, Udip Dilip
author_facet Babu Koyyala, Venkata Pradeep
Batra, Ullas
Jain, Parveen
Sharma, Mansi
Goyal, Pankaj
Medisetty, Pavani
Jajodia, Ankush
Maheshwari, Udip Dilip
author_sort Babu Koyyala, Venkata Pradeep
collection PubMed
description AIM: The aim of this study is to determine the incidence of T790M mutations after progression on epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKI) and median duration on TKI before progression on TKI. METHODS: Records of Rajiv Gandhi Cancer Institute and Research Centre, of patients who were diagnosed with metastatic adenocarcinoma of the lung and progressed on oral EGFR TKIs and underwent T790M mutation analysis in the last 6 months were retrospectively reviewed. The incidence of T790M positivity, sites of progression, and median duration of TKI treatment before progression was calculated. RESULTS: Among 31 patients, 10 patients have undergone rebiopsy, and 24 patients had undergone liquid biopsy by Droplet Digital polymerase chain reaction (ddPCR), and three patients had undergone both tests. Among all, the rate of T790M positivity was 54.8%. Among these 17 patients positive for T790M, seven patients were positive by biopsy, and 11 patients were positive by ddPCR. Among three patients who underwent both, one was positive by both. The most common site of progression among all patients is pleura, and 10% of patients progressed in brain post-TKI. Median progression-free survival on TKI before progression is 289.7 days, highest being 1290 days, and lowest 45 days. CONCLUSIONS: Exact incidence of T790M mutations after progression on TKI s in Asian population is not exactly known and requires large data, as incidence may be different than reported in the Western population. Rebiopsy and ddPCR help to determine the most common type of resistance after progression on TKI, for which effective targeted therapy is available.
format Online
Article
Text
id pubmed-6120311
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-61203112018-09-07 Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital Babu Koyyala, Venkata Pradeep Batra, Ullas Jain, Parveen Sharma, Mansi Goyal, Pankaj Medisetty, Pavani Jajodia, Ankush Maheshwari, Udip Dilip Lung India Original Article AIM: The aim of this study is to determine the incidence of T790M mutations after progression on epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKI) and median duration on TKI before progression on TKI. METHODS: Records of Rajiv Gandhi Cancer Institute and Research Centre, of patients who were diagnosed with metastatic adenocarcinoma of the lung and progressed on oral EGFR TKIs and underwent T790M mutation analysis in the last 6 months were retrospectively reviewed. The incidence of T790M positivity, sites of progression, and median duration of TKI treatment before progression was calculated. RESULTS: Among 31 patients, 10 patients have undergone rebiopsy, and 24 patients had undergone liquid biopsy by Droplet Digital polymerase chain reaction (ddPCR), and three patients had undergone both tests. Among all, the rate of T790M positivity was 54.8%. Among these 17 patients positive for T790M, seven patients were positive by biopsy, and 11 patients were positive by ddPCR. Among three patients who underwent both, one was positive by both. The most common site of progression among all patients is pleura, and 10% of patients progressed in brain post-TKI. Median progression-free survival on TKI before progression is 289.7 days, highest being 1290 days, and lowest 45 days. CONCLUSIONS: Exact incidence of T790M mutations after progression on TKI s in Asian population is not exactly known and requires large data, as incidence may be different than reported in the Western population. Rebiopsy and ddPCR help to determine the most common type of resistance after progression on TKI, for which effective targeted therapy is available. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6120311/ /pubmed/30168457 http://dx.doi.org/10.4103/lungindia.lungindia_451_17 Text en Copyright: © 2018 Indian Chest Society http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Babu Koyyala, Venkata Pradeep
Batra, Ullas
Jain, Parveen
Sharma, Mansi
Goyal, Pankaj
Medisetty, Pavani
Jajodia, Ankush
Maheshwari, Udip Dilip
Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital
title Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital
title_full Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital
title_fullStr Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital
title_full_unstemmed Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital
title_short Frequency of T790M mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in Indian patients: real-time data from tertiary cancer hospital
title_sort frequency of t790m mutations after progression on epidermal growth factor receptor tyrosine kinase inhibitor in metastatic non-small cell lung cancer in indian patients: real-time data from tertiary cancer hospital
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120311/
https://www.ncbi.nlm.nih.gov/pubmed/30168457
http://dx.doi.org/10.4103/lungindia.lungindia_451_17
work_keys_str_mv AT babukoyyalavenkatapradeep frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT batraullas frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT jainparveen frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT sharmamansi frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT goyalpankaj frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT medisettypavani frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT jajodiaankush frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT maheshwariudipdilip frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital