First-Line Afatinib versus Chemotherapy in Patients with Non–Small Cell Lung Cancer and Common Epidermal Growth Factor Receptor Gene Mutations and Brain Metastases

Metastatic spread to the brain is common in patients with non–small cell lung cancer (NSCLC), but these patients are generally excluded from prospective clinical trials. The studies, phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mu...

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Published inJournal of thoracic oncology Vol. 11; no. 3; pp. 380 - 390
Main Authors Schuler, Martin, Wu, Yi-Long, Hirsh, Vera, O’Byrne, Kenneth, Yamamoto, Nobuyuki, Mok, Tony, Popat, Sanjay, Sequist, Lecia V., Massey, Dan, Zazulina, Victoria, Yang, James C.-H.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2016
Copyright by the International Association for the Study of Lung Cancer
Subjects
Online AccessGet full text
ISSN1556-0864
1556-1380
1556-1380
DOI10.1016/j.jtho.2015.11.014

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Abstract Metastatic spread to the brain is common in patients with non–small cell lung cancer (NSCLC), but these patients are generally excluded from prospective clinical trials. The studies, phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations (LUX-Lung 3) and a randomized, open-label, phase III study of BIBW 2992 versus chemotherapy as first-line treatment for patients with stage IIIB or IV adenocarcinoma of the lung harbouring an EGFR activating mutation (LUX-Lung 6) investigated first-line afatinib versus platinum-based chemotherapy in epidermal growth factor receptor gene (EGFR) mutation-positive patients with NSCLC and included patients with brain metastases; prespecified subgroup analyses are assessed in this article. For both LUX-Lung 3 and LUX-Lung 6, prespecified subgroup analyses of progression-free survival (PFS), overall survival, and objective response rate were undertaken in patients with asymptomatic brain metastases at baseline (n = 35 and n = 46, respectively). Post hoc analyses of clinical outcomes was undertaken in the combined data set (n = 81). In both studies, there was a trend toward improved PFS with afatinib versus chemotherapy in patients with brain metastases (LUX-Lung 3: 11.1 versus 5.4 months, hazard ratio [HR] = 0.54, p = 0.1378; LUX-Lung 6: 8.2 versus 4.7 months, HR = 0.47, p = 0.1060). The magnitude of PFS improvement with afatinib was similar to that observed in patients without brain metastases. In combined analysis, PFS was significantly improved with afatinib versus with chemotherapy in patients with brain metastases (8.2 versus 5.4 months; HR, 0.50; p = 0.0297). Afatinib significantly improved the objective response rate versus chemotherapy in patients with brain metastases. Safety findings were consistent with previous reports. These findings lend support to the clinical activity of afatinib in EGFR mutation–positive patients with NSCLC and asymptomatic brain metastases.
AbstractList Metastatic spread to the brain is common in patients with non-small cell lung cancer (NSCLC), but these patients are generally excluded from prospective clinical trials. The studies, phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations (LUX-Lung 3) and a randomized, open-label, phase III study of BIBW 2992 versus chemotherapy as first-line treatment for patients with stage IIIB or IV adenocarcinoma of the lung harbouring an EGFR activating mutation (LUX-Lung 6) investigated first-line afatinib versus platinum-based chemotherapy in epidermal growth factor receptor gene (EGFR) mutation-positive patients with NSCLC and included patients with brain metastases; prespecified subgroup analyses are assessed in this article.INTRODUCTIONMetastatic spread to the brain is common in patients with non-small cell lung cancer (NSCLC), but these patients are generally excluded from prospective clinical trials. The studies, phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations (LUX-Lung 3) and a randomized, open-label, phase III study of BIBW 2992 versus chemotherapy as first-line treatment for patients with stage IIIB or IV adenocarcinoma of the lung harbouring an EGFR activating mutation (LUX-Lung 6) investigated first-line afatinib versus platinum-based chemotherapy in epidermal growth factor receptor gene (EGFR) mutation-positive patients with NSCLC and included patients with brain metastases; prespecified subgroup analyses are assessed in this article.For both LUX-Lung 3 and LUX-Lung 6, prespecified subgroup analyses of progression-free survival (PFS), overall survival, and objective response rate were undertaken in patients with asymptomatic brain metastases at baseline (n = 35 and n = 46, respectively). Post hoc analyses of clinical outcomes was undertaken in the combined data set (n = 81).METHODSFor both LUX-Lung 3 and LUX-Lung 6, prespecified subgroup analyses of progression-free survival (PFS), overall survival, and objective response rate were undertaken in patients with asymptomatic brain metastases at baseline (n = 35 and n = 46, respectively). Post hoc analyses of clinical outcomes was undertaken in the combined data set (n = 81).In both studies, there was a trend toward improved PFS with afatinib versus chemotherapy in patients with brain metastases (LUX-Lung 3: 11.1 versus 5.4 months, hazard ratio [HR] = 0.54, p = 0.1378; LUX-Lung 6: 8.2 versus 4.7 months, HR = 0.47, p = 0.1060). The magnitude of PFS improvement with afatinib was similar to that observed in patients without brain metastases. In combined analysis, PFS was significantly improved with afatinib versus with chemotherapy in patients with brain metastases (8.2 versus 5.4 months; HR, 0.50; p = 0.0297). Afatinib significantly improved the objective response rate versus chemotherapy in patients with brain metastases. Safety findings were consistent with previous reports.RESULTSIn both studies, there was a trend toward improved PFS with afatinib versus chemotherapy in patients with brain metastases (LUX-Lung 3: 11.1 versus 5.4 months, hazard ratio [HR] = 0.54, p = 0.1378; LUX-Lung 6: 8.2 versus 4.7 months, HR = 0.47, p = 0.1060). The magnitude of PFS improvement with afatinib was similar to that observed in patients without brain metastases. In combined analysis, PFS was significantly improved with afatinib versus with chemotherapy in patients with brain metastases (8.2 versus 5.4 months; HR, 0.50; p = 0.0297). Afatinib significantly improved the objective response rate versus chemotherapy in patients with brain metastases. Safety findings were consistent with previous reports.These findings lend support to the clinical activity of afatinib in EGFR mutation-positive patients with NSCLC and asymptomatic brain metastases.CONCLUSIONSThese findings lend support to the clinical activity of afatinib in EGFR mutation-positive patients with NSCLC and asymptomatic brain metastases.
INTRODUCTION:Metastatic spread to the brain is common in patients with non–small cell lung cancer (NSCLC), but these patients are generally excluded from prospective clinical trials. The studies, phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations (LUX-Lung 3) and a randomized, open-label, phase III study of BIBW 2992 versus chemotherapy as first-line treatment for patients with stage IIIB or IV adenocarcinoma of the lung harbouring an EGFR activating mutation (LUX-Lung 6) investigated first-line afatinib versus platinum-based chemotherapy in epidermal growth factor receptor gene (EGFR) mutation-positive patients with NSCLC and included patients with brain metastases; prespecified subgroup analyses are assessed in this article. METHODS:For both LUX-Lung 3 and LUX-Lung 6, prespecified subgroup analyses of progression-free survival (PFS), overall survival, and objective response rate were undertaken in patients with asymptomatic brain metastases at baseline (n = 35 and n = 46, respectively). Post hoc analyses of clinical outcomes was undertaken in the combined data set (n = 81). RESULTS:In both studies, there was a trend toward improved PFS with afatinib versus chemotherapy in patients with brain metastases (LUX-Lung 311.1 versus 5.4 months, hazard ratio [HR] = 0.54, p = 0.1378; LUX-Lung 68.2 versus 4.7 months, HR = 0.47, p = 0.1060). The magnitude of PFS improvement with afatinib was similar to that observed in patients without brain metastases. In combined analysis, PFS was significantly improved with afatinib versus with chemotherapy in patients with brain metastases (8.2 versus 5.4 months; HR, 0.50; p = 0.0297). Afatinib significantly improved the objective response rate versus chemotherapy in patients with brain metastases. Safety findings were consistent with previous reports. CONCLUSIONS:These findings lend support to the clinical activity of afatinib in EGFR mutation–positive patients with NSCLC and asymptomatic brain metastases.
Metastatic spread to the brain is common in patients with non–small cell lung cancer (NSCLC), but these patients are generally excluded from prospective clinical trials. The studies, phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations (LUX-Lung 3) and a randomized, open-label, phase III study of BIBW 2992 versus chemotherapy as first-line treatment for patients with stage IIIB or IV adenocarcinoma of the lung harbouring an EGFR activating mutation (LUX-Lung 6) investigated first-line afatinib versus platinum-based chemotherapy in epidermal growth factor receptor gene (EGFR) mutation-positive patients with NSCLC and included patients with brain metastases; prespecified subgroup analyses are assessed in this article. For both LUX-Lung 3 and LUX-Lung 6, prespecified subgroup analyses of progression-free survival (PFS), overall survival, and objective response rate were undertaken in patients with asymptomatic brain metastases at baseline (n = 35 and n = 46, respectively). Post hoc analyses of clinical outcomes was undertaken in the combined data set (n = 81). In both studies, there was a trend toward improved PFS with afatinib versus chemotherapy in patients with brain metastases (LUX-Lung 3: 11.1 versus 5.4 months, hazard ratio [HR] = 0.54, p = 0.1378; LUX-Lung 6: 8.2 versus 4.7 months, HR = 0.47, p = 0.1060). The magnitude of PFS improvement with afatinib was similar to that observed in patients without brain metastases. In combined analysis, PFS was significantly improved with afatinib versus with chemotherapy in patients with brain metastases (8.2 versus 5.4 months; HR, 0.50; p = 0.0297). Afatinib significantly improved the objective response rate versus chemotherapy in patients with brain metastases. Safety findings were consistent with previous reports. These findings lend support to the clinical activity of afatinib in EGFR mutation–positive patients with NSCLC and asymptomatic brain metastases.
Author Wu, Yi-Long
Yamamoto, Nobuyuki
Yang, James C.-H.
Mok, Tony
Zazulina, Victoria
Hirsh, Vera
Schuler, Martin
O’Byrne, Kenneth
Massey, Dan
Sequist, Lecia V.
Popat, Sanjay
AuthorAffiliation aWest German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany bGerman Cancer Consortium (DKTK), Heidelberg, Germany cGuangdong Lung Cancer Institute, Guangdong General Hospital, Guangzhou, Peopleʼs Republic of China dGuangdong Academy of Medical Sciences, Guangzhou, Peopleʼs Republic of China eMcGill University Health Centre, Royal Victoria Hospital, Montreal, Quebec, Canada fPrincess Alexandra Hospital and Queensland University of Technology, Brisbane, Australia gWakayama Medical University, Wakayama, Japan hState Key Laboratory of South China, Hong Kong Cancer Institute, The Chinese University of Hong Kong, Hong Kong, Hong Kong iRoyal Marsden Hospital, London, United Kingdom jMassachusetts General Hospital and Harvard Medical School, Boston, Massachusetts kBoehringer Ingelheim Limited, Bracknell, Berkshire, United Kingdom lNational Taiwan University Hospital and National Taiwan University, Taipei, Republic of China
AuthorAffiliation_xml – name: aWest German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany bGerman Cancer Consortium (DKTK), Heidelberg, Germany cGuangdong Lung Cancer Institute, Guangdong General Hospital, Guangzhou, Peopleʼs Republic of China dGuangdong Academy of Medical Sciences, Guangzhou, Peopleʼs Republic of China eMcGill University Health Centre, Royal Victoria Hospital, Montreal, Quebec, Canada fPrincess Alexandra Hospital and Queensland University of Technology, Brisbane, Australia gWakayama Medical University, Wakayama, Japan hState Key Laboratory of South China, Hong Kong Cancer Institute, The Chinese University of Hong Kong, Hong Kong, Hong Kong iRoyal Marsden Hospital, London, United Kingdom jMassachusetts General Hospital and Harvard Medical School, Boston, Massachusetts kBoehringer Ingelheim Limited, Bracknell, Berkshire, United Kingdom lNational Taiwan University Hospital and National Taiwan University, Taipei, Republic of China
Author_xml – sequence: 1
  givenname: Martin
  surname: Schuler
  fullname: Schuler, Martin
  email: Martin.Schuler@uk-essen.de
  organization: West German Cancer Center, University Hospital Essen, University Duisburg-Essen, Essen, Germany
– sequence: 2
  givenname: Yi-Long
  surname: Wu
  fullname: Wu, Yi-Long
  organization: Guangdong Lung Cancer Institute, Guangdong General Hospital, Guangzhou, People's Republic of China
– sequence: 3
  givenname: Vera
  surname: Hirsh
  fullname: Hirsh, Vera
  organization: McGill University Health Centre, Royal Victoria Hospital, Montreal, Quebec, Canada
– sequence: 4
  givenname: Kenneth
  surname: O’Byrne
  fullname: O’Byrne, Kenneth
  organization: Princess Alexandra Hospital and Queensland University of Technology, Brisbane, Australia
– sequence: 5
  givenname: Nobuyuki
  surname: Yamamoto
  fullname: Yamamoto, Nobuyuki
  organization: Wakayama Medical University, Wakayama, Japan
– sequence: 6
  givenname: Tony
  surname: Mok
  fullname: Mok, Tony
  organization: State Key Laboratory of South China, Hong Kong Cancer Institute, The Chinese University of Hong Kong, Hong Kong, Hong Kong
– sequence: 7
  givenname: Sanjay
  surname: Popat
  fullname: Popat, Sanjay
  organization: Royal Marsden Hospital, London, United Kingdom
– sequence: 8
  givenname: Lecia V.
  surname: Sequist
  fullname: Sequist, Lecia V.
  organization: Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts
– sequence: 9
  givenname: Dan
  surname: Massey
  fullname: Massey, Dan
  organization: Boehringer Ingelheim Limited, Bracknell, Berkshire, United Kingdom
– sequence: 10
  givenname: Victoria
  surname: Zazulina
  fullname: Zazulina, Victoria
  organization: Boehringer Ingelheim Limited, Bracknell, Berkshire, United Kingdom
– sequence: 11
  givenname: James C.-H.
  surname: Yang
  fullname: Yang, James C.-H.
  organization: National Taiwan University Hospital and National Taiwan University, Taipei, Republic of China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26823294$$D View this record in MEDLINE/PubMed
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Snippet Metastatic spread to the brain is common in patients with non–small cell lung cancer (NSCLC), but these patients are generally excluded from prospective...
INTRODUCTION:Metastatic spread to the brain is common in patients with non–small cell lung cancer (NSCLC), but these patients are generally excluded from...
Metastatic spread to the brain is common in patients with non-small cell lung cancer (NSCLC), but these patients are generally excluded from prospective...
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SubjectTerms Adult
Afatinib
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Brain metastases
Brain Neoplasms - drug therapy
Brain Neoplasms - enzymology
Brain Neoplasms - genetics
Brain Neoplasms - secondary
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - enzymology
Carcinoma, Non-Small-Cell Lung - genetics
Carcinoma, Non-Small-Cell Lung - pathology
Epidermal growth factor receptor
Female
Humans
Lung Neoplasms - drug therapy
Lung Neoplasms - enzymology
Lung Neoplasms - genetics
Lung Neoplasms - pathology
Male
Middle Aged
Mutation
Neoplasm Metastasis
NSCLC
Organoplatinum Compounds - administration & dosage
Quinazolines - therapeutic use
Receptor, Epidermal Growth Factor - genetics
Treatment Outcome
Title First-Line Afatinib versus Chemotherapy in Patients with Non–Small Cell Lung Cancer and Common Epidermal Growth Factor Receptor Gene Mutations and Brain Metastases
URI https://dx.doi.org/10.1016/j.jtho.2015.11.014
https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=01243894-201603000-00013
https://www.ncbi.nlm.nih.gov/pubmed/26823294
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Volume 11
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