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Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients

BACKGROUND: Despite significant benefits of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) treatment in patients with EGFR-mutated NSCLC, access remains limited in Thailand and elsewhere. METHODS: Retrospective analysis of patients with locally advanced/recurrent NSCLC and kno...

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Autores principales: Khiewngam, Khantong, Oranratnachai, Songporn, Kamprerasart, Kaettipong, Kunakorntham, Patratorn, Sanvarinda, Pimtip, Trachu, Narumol, Pimsa, Pongput, Wiwitkeyoonwong, Jirapath, Thamrongjirapat, Thanaporn, Dejthevaporn, Thitiya, Sirachainan, Ekaphop, Reungwetwattana, Thanyanan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989298/
https://www.ncbi.nlm.nih.gov/pubmed/36895484
http://dx.doi.org/10.3389/fonc.2023.1047644
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author Khiewngam, Khantong
Oranratnachai, Songporn
Kamprerasart, Kaettipong
Kunakorntham, Patratorn
Sanvarinda, Pimtip
Trachu, Narumol
Pimsa, Pongput
Wiwitkeyoonwong, Jirapath
Thamrongjirapat, Thanaporn
Dejthevaporn, Thitiya
Sirachainan, Ekaphop
Reungwetwattana, Thanyanan
author_facet Khiewngam, Khantong
Oranratnachai, Songporn
Kamprerasart, Kaettipong
Kunakorntham, Patratorn
Sanvarinda, Pimtip
Trachu, Narumol
Pimsa, Pongput
Wiwitkeyoonwong, Jirapath
Thamrongjirapat, Thanaporn
Dejthevaporn, Thitiya
Sirachainan, Ekaphop
Reungwetwattana, Thanyanan
author_sort Khiewngam, Khantong
collection PubMed
description BACKGROUND: Despite significant benefits of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) treatment in patients with EGFR-mutated NSCLC, access remains limited in Thailand and elsewhere. METHODS: Retrospective analysis of patients with locally advanced/recurrent NSCLC and known EGFR mutation (EGFRm) status treated at Ramathibodi Hospital (2012–2017). Prognostic factors for overall survival (OS), including treatment type and healthcare coverage, were analyzed using Cox regression. RESULTS: Of 750 patients, 56.3% were EGFRm-positive. After first-line therapy (n=646), 29.4% received no subsequent (second-line) treatment. EGFR-TKI-treated EGFRm-positive patients survived significantly longer than EGFRm-negative patients without EGFR-TKIs (median OS [mOS] 36.4 vs. 11.9 months; hazard ratio HR=0.38 [95%CI 0.32–0.46], P<0.001). Cox regression indicated significantly longer OS in patients with comprehensive healthcare coverage that included reimbursement of EGFR-TKIs, versus basic coverage (mOS 27.2 vs. 18.3 months; adjusted HR=0.73 [95%CI 0.59–0.90]). Compared with best supportive care (BSC; reference), EGFR-TKI-treated patients survived significantly longer (mOS 36.5 months; adjusted HR (aHR)=0.26 [95%CI 0.19–0.34]), and versus chemotherapy alone (14.5 months; aHR=0.60 [95%CI 0.47–0.78]). In EGFRm-positive patients (n=422), relative survival benefit of EGFR-TKI treatment remained highly significant (aHR[EGFR-TKI]=0.19 [95%CI 0.12–0.29]; aHR(chemotherapy only)=0.50 [95%CI 0.30–0.85]; reference:BSC), indicating that healthcare coverage (reimbursement) affected treatment choice and survival. CONCLUSION: Our analysis describes EGFRm prevalence and survival benefit of EGFR-TKI therapy for EGFRm-positive NSCLC patients treated from 2012–2017, one of the largest such Thai datasets. Together with research by others, these findings contributed evidence supporting the decision to broaden erlotinib access on healthcare schemes in Thailand from 2021, demonstrating the value of local real-world outcome data for healthcare policy decision-making.
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spelling pubmed-99892982023-03-08 Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients Khiewngam, Khantong Oranratnachai, Songporn Kamprerasart, Kaettipong Kunakorntham, Patratorn Sanvarinda, Pimtip Trachu, Narumol Pimsa, Pongput Wiwitkeyoonwong, Jirapath Thamrongjirapat, Thanaporn Dejthevaporn, Thitiya Sirachainan, Ekaphop Reungwetwattana, Thanyanan Front Oncol Oncology BACKGROUND: Despite significant benefits of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) treatment in patients with EGFR-mutated NSCLC, access remains limited in Thailand and elsewhere. METHODS: Retrospective analysis of patients with locally advanced/recurrent NSCLC and known EGFR mutation (EGFRm) status treated at Ramathibodi Hospital (2012–2017). Prognostic factors for overall survival (OS), including treatment type and healthcare coverage, were analyzed using Cox regression. RESULTS: Of 750 patients, 56.3% were EGFRm-positive. After first-line therapy (n=646), 29.4% received no subsequent (second-line) treatment. EGFR-TKI-treated EGFRm-positive patients survived significantly longer than EGFRm-negative patients without EGFR-TKIs (median OS [mOS] 36.4 vs. 11.9 months; hazard ratio HR=0.38 [95%CI 0.32–0.46], P<0.001). Cox regression indicated significantly longer OS in patients with comprehensive healthcare coverage that included reimbursement of EGFR-TKIs, versus basic coverage (mOS 27.2 vs. 18.3 months; adjusted HR=0.73 [95%CI 0.59–0.90]). Compared with best supportive care (BSC; reference), EGFR-TKI-treated patients survived significantly longer (mOS 36.5 months; adjusted HR (aHR)=0.26 [95%CI 0.19–0.34]), and versus chemotherapy alone (14.5 months; aHR=0.60 [95%CI 0.47–0.78]). In EGFRm-positive patients (n=422), relative survival benefit of EGFR-TKI treatment remained highly significant (aHR[EGFR-TKI]=0.19 [95%CI 0.12–0.29]; aHR(chemotherapy only)=0.50 [95%CI 0.30–0.85]; reference:BSC), indicating that healthcare coverage (reimbursement) affected treatment choice and survival. CONCLUSION: Our analysis describes EGFRm prevalence and survival benefit of EGFR-TKI therapy for EGFRm-positive NSCLC patients treated from 2012–2017, one of the largest such Thai datasets. Together with research by others, these findings contributed evidence supporting the decision to broaden erlotinib access on healthcare schemes in Thailand from 2021, demonstrating the value of local real-world outcome data for healthcare policy decision-making. Frontiers Media S.A. 2023-02-21 /pmc/articles/PMC9989298/ /pubmed/36895484 http://dx.doi.org/10.3389/fonc.2023.1047644 Text en Copyright © 2023 Khiewngam, Oranratnachai, Kamprerasart, Kunakorntham, Sanvarinda, Trachu, Pimsa, Wiwitkeyoonwong, Thamrongjirapat, Dejthevaporn, Sirachainan and Reungwetwattana https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Khiewngam, Khantong
Oranratnachai, Songporn
Kamprerasart, Kaettipong
Kunakorntham, Patratorn
Sanvarinda, Pimtip
Trachu, Narumol
Pimsa, Pongput
Wiwitkeyoonwong, Jirapath
Thamrongjirapat, Thanaporn
Dejthevaporn, Thitiya
Sirachainan, Ekaphop
Reungwetwattana, Thanyanan
Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients
title Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients
title_full Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients
title_fullStr Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients
title_full_unstemmed Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients
title_short Healthcare coverage affects survival of EGFR-mutant Thai lung cancer patients
title_sort healthcare coverage affects survival of egfr-mutant thai lung cancer patients
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989298/
https://www.ncbi.nlm.nih.gov/pubmed/36895484
http://dx.doi.org/10.3389/fonc.2023.1047644
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