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 in | Journal of thoracic oncology Vol. 11; no. 3; pp. 380 - 390 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.03.2016
Copyright by the International Association for the Study of Lung Cancer |
Subjects | |
Online Access | Get full text |
ISSN | 1556-0864 1556-1380 1556-1380 |
DOI | 10.1016/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. |
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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 |
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