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Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer

INTRODUCTION: Previous studies have shown interference between epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors and chemotherapy in the cell cycle, thus reducing efficacy. In this randomised controlled trial we investigated whether intercalated erlotinib with chemotherapy was super...

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Autores principales: Gijtenbeek, Rolof G.P., van der Noort, Vincent, Aerts, Joachim G.J.V., Staal-van den Brekel, Jeske A., Smit, Egbert F., Krouwels, Frans H., Wilschut, Frank A., Hiltermann, T. Jeroen N., Timens, Wim, Schuuring, Ed, Janssen, Joost D.J., Goosens, Martijn, van den Berg, Paul M., de Langen, A. Joop, Stigt, Jos A., van den Borne, Ben E.E.M., Groen, Harry J.M., van Geffen, Wouter H., van der Wekken, Anthonie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574558/
https://www.ncbi.nlm.nih.gov/pubmed/36267895
http://dx.doi.org/10.1183/23120541.00239-2022
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author Gijtenbeek, Rolof G.P.
van der Noort, Vincent
Aerts, Joachim G.J.V.
Staal-van den Brekel, Jeske A.
Smit, Egbert F.
Krouwels, Frans H.
Wilschut, Frank A.
Hiltermann, T. Jeroen N.
Timens, Wim
Schuuring, Ed
Janssen, Joost D.J.
Goosens, Martijn
van den Berg, Paul M.
de Langen, A. Joop
Stigt, Jos A.
van den Borne, Ben E.E.M.
Groen, Harry J.M.
van Geffen, Wouter H.
van der Wekken, Anthonie J.
author_facet Gijtenbeek, Rolof G.P.
van der Noort, Vincent
Aerts, Joachim G.J.V.
Staal-van den Brekel, Jeske A.
Smit, Egbert F.
Krouwels, Frans H.
Wilschut, Frank A.
Hiltermann, T. Jeroen N.
Timens, Wim
Schuuring, Ed
Janssen, Joost D.J.
Goosens, Martijn
van den Berg, Paul M.
de Langen, A. Joop
Stigt, Jos A.
van den Borne, Ben E.E.M.
Groen, Harry J.M.
van Geffen, Wouter H.
van der Wekken, Anthonie J.
author_sort Gijtenbeek, Rolof G.P.
collection PubMed
description INTRODUCTION: Previous studies have shown interference between epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors and chemotherapy in the cell cycle, thus reducing efficacy. In this randomised controlled trial we investigated whether intercalated erlotinib with chemotherapy was superior compared to erlotinib alone in untreated advanced EGFR-mutated nonsmall cell lung cancer (NSCLC). MATERIALS AND METHODS: Treatment-naïve patients with an activating EGFR mutation, ECOG performance score of 0–3 and adequate organ function were randomly assigned 1:1 to either four cycles of cisplatin-pemetrexed with intercalated erlotinib (day 2–16 out of 21 days per cycle) followed by pemetrexed and erlotinib maintenance (CPE) or erlotinib monotherapy. The primary end-point was progression-free survival (PFS). Secondary end-points were overall survival, objective response rate (ORR) and toxicity. RESULTS: Between April 2014 and September 2016, 22 patients were randomised equally into both arms; the study was stopped due to slow accrual. Median follow-up was 64 months. Median PFS was 13.7 months (95% CI 5.2–18.8) for CPE and 10.3 months (95% CI 7.1–15.5; hazard ratio (HR) 0.62, 95% CI 0.25–1.57) for erlotinib monotherapy; when compensating for number of days receiving erlotinib, PFS of the CPE arm was superior (HR 0.24, 95% CI 0.07–0.83; p=0.02). ORR was 64% for CPE versus 55% for erlotinib monotherapy. Median overall survival was 31.7 months (95% CI 21.8–61.9 months) for CPE compared to 17.2 months (95% CI 11.5–45.5 months) for erlotinib monotherapy (HR 0.58, 95% CI 0.22–1.41 months). Patients treated with CPE had higher rates of treatment-related fatigue, anorexia, weight loss and renal toxicity. CONCLUSION: Intercalating erlotinib with cisplatin-pemetrexed provides a longer PFS compared to erlotinib alone in EGFR-mutated NSCLC at the expense of more toxicity.
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spelling pubmed-95745582022-10-19 Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer Gijtenbeek, Rolof G.P. van der Noort, Vincent Aerts, Joachim G.J.V. Staal-van den Brekel, Jeske A. Smit, Egbert F. Krouwels, Frans H. Wilschut, Frank A. Hiltermann, T. Jeroen N. Timens, Wim Schuuring, Ed Janssen, Joost D.J. Goosens, Martijn van den Berg, Paul M. de Langen, A. Joop Stigt, Jos A. van den Borne, Ben E.E.M. Groen, Harry J.M. van Geffen, Wouter H. van der Wekken, Anthonie J. ERJ Open Res Original Research Articles INTRODUCTION: Previous studies have shown interference between epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors and chemotherapy in the cell cycle, thus reducing efficacy. In this randomised controlled trial we investigated whether intercalated erlotinib with chemotherapy was superior compared to erlotinib alone in untreated advanced EGFR-mutated nonsmall cell lung cancer (NSCLC). MATERIALS AND METHODS: Treatment-naïve patients with an activating EGFR mutation, ECOG performance score of 0–3 and adequate organ function were randomly assigned 1:1 to either four cycles of cisplatin-pemetrexed with intercalated erlotinib (day 2–16 out of 21 days per cycle) followed by pemetrexed and erlotinib maintenance (CPE) or erlotinib monotherapy. The primary end-point was progression-free survival (PFS). Secondary end-points were overall survival, objective response rate (ORR) and toxicity. RESULTS: Between April 2014 and September 2016, 22 patients were randomised equally into both arms; the study was stopped due to slow accrual. Median follow-up was 64 months. Median PFS was 13.7 months (95% CI 5.2–18.8) for CPE and 10.3 months (95% CI 7.1–15.5; hazard ratio (HR) 0.62, 95% CI 0.25–1.57) for erlotinib monotherapy; when compensating for number of days receiving erlotinib, PFS of the CPE arm was superior (HR 0.24, 95% CI 0.07–0.83; p=0.02). ORR was 64% for CPE versus 55% for erlotinib monotherapy. Median overall survival was 31.7 months (95% CI 21.8–61.9 months) for CPE compared to 17.2 months (95% CI 11.5–45.5 months) for erlotinib monotherapy (HR 0.58, 95% CI 0.22–1.41 months). Patients treated with CPE had higher rates of treatment-related fatigue, anorexia, weight loss and renal toxicity. CONCLUSION: Intercalating erlotinib with cisplatin-pemetrexed provides a longer PFS compared to erlotinib alone in EGFR-mutated NSCLC at the expense of more toxicity. European Respiratory Society 2022-10-17 /pmc/articles/PMC9574558/ /pubmed/36267895 http://dx.doi.org/10.1183/23120541.00239-2022 Text en Copyright ©The authors 2022 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Research Articles
Gijtenbeek, Rolof G.P.
van der Noort, Vincent
Aerts, Joachim G.J.V.
Staal-van den Brekel, Jeske A.
Smit, Egbert F.
Krouwels, Frans H.
Wilschut, Frank A.
Hiltermann, T. Jeroen N.
Timens, Wim
Schuuring, Ed
Janssen, Joost D.J.
Goosens, Martijn
van den Berg, Paul M.
de Langen, A. Joop
Stigt, Jos A.
van den Borne, Ben E.E.M.
Groen, Harry J.M.
van Geffen, Wouter H.
van der Wekken, Anthonie J.
Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer
title Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer
title_full Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer
title_fullStr Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer
title_full_unstemmed Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer
title_short Randomised controlled trial of first-line tyrosine-kinase inhibitor (TKI) versus intercalated TKI with chemotherapy for EGFR-mutated nonsmall cell lung cancer
title_sort randomised controlled trial of first-line tyrosine-kinase inhibitor (tki) versus intercalated tki with chemotherapy for egfr-mutated nonsmall cell lung cancer
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574558/
https://www.ncbi.nlm.nih.gov/pubmed/36267895
http://dx.doi.org/10.1183/23120541.00239-2022
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