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...

Full description

Bibliographic Details
Main Authors: Venkata Pradeep Babu Koyyala, Ullas Batra, Parveen Jain, Mansi Sharma, Pankaj Goyal, Pavani Medisetty, Ankush Jajodia, Udip Dilip Maheshwari
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Lung India
Subjects:
Online Access:http://www.lungindia.com/article.asp?issn=0970-2113;year=2018;volume=35;issue=5;spage=390;epage=394;aulast=Babu
id doaj-319ccc369cfb45b895f9104d81cb5a2b
record_format Article
spelling doaj-319ccc369cfb45b895f9104d81cb5a2b2020-11-24T22:38:24ZengWolters Kluwer Medknow PublicationsLung India0970-21130974-598X2018-01-0135539039410.4103/lungindia.lungindia_451_17Frequency 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 hospitalVenkata Pradeep Babu KoyyalaUllas BatraParveen JainMansi SharmaPankaj GoyalPavani MedisettyAnkush JajodiaUdip Dilip MaheshwariAim: 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.http://www.lungindia.com/article.asp?issn=0970-2113;year=2018;volume=35;issue=5;spage=390;epage=394;aulast=BabuEpidermal growth factor receptor mutationnonsmall cell lung cancerosimertinibT790M mutation
collection DOAJ
language English
format Article
sources DOAJ
author Venkata Pradeep Babu Koyyala
Ullas Batra
Parveen Jain
Mansi Sharma
Pankaj Goyal
Pavani Medisetty
Ankush Jajodia
Udip Dilip Maheshwari
spellingShingle Venkata Pradeep Babu Koyyala
Ullas Batra
Parveen Jain
Mansi Sharma
Pankaj Goyal
Pavani Medisetty
Ankush Jajodia
Udip Dilip Maheshwari
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
Lung India
Epidermal growth factor receptor mutation
nonsmall cell lung cancer
osimertinib
T790M mutation
author_facet Venkata Pradeep Babu Koyyala
Ullas Batra
Parveen Jain
Mansi Sharma
Pankaj Goyal
Pavani Medisetty
Ankush Jajodia
Udip Dilip Maheshwari
author_sort Venkata Pradeep Babu Koyyala
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_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_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_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
publisher Wolters Kluwer Medknow Publications
series Lung India
issn 0970-2113
0974-598X
publishDate 2018-01-01
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.
topic Epidermal growth factor receptor mutation
nonsmall cell lung cancer
osimertinib
T790M mutation
url http://www.lungindia.com/article.asp?issn=0970-2113;year=2018;volume=35;issue=5;spage=390;epage=394;aulast=Babu
work_keys_str_mv AT venkatapradeepbabukoyyala frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT ullasbatra frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT parveenjain frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT mansisharma frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT pankajgoyal frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT pavanimedisetty frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT ankushjajodia frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
AT udipdilipmaheshwari frequencyoft790mmutationsafterprogressiononepidermalgrowthfactorreceptortyrosinekinaseinhibitorinmetastaticnonsmallcelllungcancerinindianpatientsrealtimedatafromtertiarycancerhospital
_version_ 1725713248410402816