Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer
Treatment of advanced stage lung cancer is changing rapidly. With the new found knowledge on molecular targets such as the epidermal growth factor receptor (EGFR), effective therapy is now available in a selected population with the target mutation. Single-agent epidermal growth factor receptor tyro...
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Series: | Therapeutic Advances in Medical Oncology |
Online Access: | https://doi.org/10.1177/1758834012440015 |
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doaj-bf0671bd964d45f1a7f0d5c9a43447572020-11-25T02:50:10ZengSAGE PublishingTherapeutic Advances in Medical Oncology1758-83401758-83592012-07-01410.1177/1758834012440015Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancerLinda LeungTony S.K. MokHerbert LoongTreatment of advanced stage lung cancer is changing rapidly. With the new found knowledge on molecular targets such as the epidermal growth factor receptor (EGFR), effective therapy is now available in a selected population with the target mutation. Single-agent epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) is a standard first-line therapy for patients with activating-EGFR mutation such as base-pair deletion in exon 19 or point mutation at exon 21. At the same time, this class of drugs may be combined with chemotherapy. Studies on the concurrent combination of chemotherapy and EGFR-TKI confirmed a lack of efficacy. A phase II study on sequential intercalated combination has demonstrated an improvement in progression-free survival (PFS), but this needs to be validated by the ongoing phase III study. The third approach is to combine EGFR-TKI as maintenance therapy after tumour response or stable disease to cytotoxic chemotherapy. Two phase III studies have shown improvement in PFS, but the use of biomarkers for the selection of maintenance therapy remains debatable. Cetuximab is a monoclonal antibody against EGFR and its combination with chemotherapy was shown to improve overall survival in an unselected population. A new biomarker using the H-score will help to select patients for this combination.https://doi.org/10.1177/1758834012440015 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Linda Leung Tony S.K. Mok Herbert Loong |
spellingShingle |
Linda Leung Tony S.K. Mok Herbert Loong Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer Therapeutic Advances in Medical Oncology |
author_facet |
Linda Leung Tony S.K. Mok Herbert Loong |
author_sort |
Linda Leung |
title |
Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer |
title_short |
Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer |
title_full |
Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer |
title_fullStr |
Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer |
title_full_unstemmed |
Combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer |
title_sort |
combining chemotherapy with epidermal growth factor receptor inhibition in advanced non-small cell lung cancer |
publisher |
SAGE Publishing |
series |
Therapeutic Advances in Medical Oncology |
issn |
1758-8340 1758-8359 |
publishDate |
2012-07-01 |
description |
Treatment of advanced stage lung cancer is changing rapidly. With the new found knowledge on molecular targets such as the epidermal growth factor receptor (EGFR), effective therapy is now available in a selected population with the target mutation. Single-agent epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) is a standard first-line therapy for patients with activating-EGFR mutation such as base-pair deletion in exon 19 or point mutation at exon 21. At the same time, this class of drugs may be combined with chemotherapy. Studies on the concurrent combination of chemotherapy and EGFR-TKI confirmed a lack of efficacy. A phase II study on sequential intercalated combination has demonstrated an improvement in progression-free survival (PFS), but this needs to be validated by the ongoing phase III study. The third approach is to combine EGFR-TKI as maintenance therapy after tumour response or stable disease to cytotoxic chemotherapy. Two phase III studies have shown improvement in PFS, but the use of biomarkers for the selection of maintenance therapy remains debatable. Cetuximab is a monoclonal antibody against EGFR and its combination with chemotherapy was shown to improve overall survival in an unselected population. A new biomarker using the H-score will help to select patients for this combination. |
url |
https://doi.org/10.1177/1758834012440015 |
work_keys_str_mv |
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