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- Publisher Website: 10.1007/s00280-009-1107-5
- Scopus: eid_2-s2.0-77951895524
- PMID: 19680652
- WOS: WOS:000275632400003
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Article: Erlotinib as salvage treatment after failure to first-line Gefitinib in non-small cell lung cancer
Title | Erlotinib as salvage treatment after failure to first-line Gefitinib in non-small cell lung cancer |
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Authors | |
Keywords | Asians Disease control rate Epidermal growth factor receptor tyrosine kinase inhibitors Erlotinib Gefitinib Non-small cell lung cancer |
Issue Date | 2010 |
Publisher | Springer. The Journal's web site is located at http://www.springer.com/medicine/oncology/journal/280 |
Citation | Cancer Chemotherapy and Pharmacology, 2010, v. 65 n. 6, p. 1023-1028 How to Cite? |
Abstract | Purpose Chemotherapy is the mainstay treatment for advanced non-small cell lung cancer (NSCLC). Gefitinib, an epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI), has been recently shown to be effective as a first-line treatment in Asian patients with advanced NSCLC, especially for those with favourable clinical features such as female, non-smoker and adenocarcinoma. However, resistance to gefitinib ensues invariably and there is little evidence as for the effectiveness of subsequent salvage treatment. The purpose of this study is to evaluate the efficacy of erlotinib, another EGFR-TKI, after failed first-line use of gefitinib. Method Retrospective review of NSCLC patients with favourable clinical features who received gefitinib as firstline treatment and subsequent salvage treatment with erlotinib. Results A total of 21 patients with NSCLC were included in the study. Among them, 18 (85.7%) patients had disease control with gefitinib and 12 (57.1%) patients with salvage erlotinib. There was an association between the disease control with gefitinib and erlotinib (p = 0.031). The disease control rate of erlotinib was independent of the chemotherapy use between the two EGFR-TKIs. Conclusion For NSCLC patients with favourable clinical features, erlotinib was effective in those who had prior disease control with first-line gefitinib. © Springer-Verlag 2009. |
Persistent Identifier | http://hdl.handle.net/10722/123997 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.869 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Wong, MK | en_HK |
dc.contributor.author | Lo, AI | en_HK |
dc.contributor.author | Lam, B | en_HK |
dc.contributor.author | Lam, WK | en_HK |
dc.contributor.author | Ip, MS | en_HK |
dc.contributor.author | Ho, JC | en_HK |
dc.date.accessioned | 2010-10-18T06:18:55Z | - |
dc.date.available | 2010-10-18T06:18:55Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Cancer Chemotherapy and Pharmacology, 2010, v. 65 n. 6, p. 1023-1028 | en_HK |
dc.identifier.issn | 0344-5704 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/123997 | - |
dc.description.abstract | Purpose Chemotherapy is the mainstay treatment for advanced non-small cell lung cancer (NSCLC). Gefitinib, an epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI), has been recently shown to be effective as a first-line treatment in Asian patients with advanced NSCLC, especially for those with favourable clinical features such as female, non-smoker and adenocarcinoma. However, resistance to gefitinib ensues invariably and there is little evidence as for the effectiveness of subsequent salvage treatment. The purpose of this study is to evaluate the efficacy of erlotinib, another EGFR-TKI, after failed first-line use of gefitinib. Method Retrospective review of NSCLC patients with favourable clinical features who received gefitinib as firstline treatment and subsequent salvage treatment with erlotinib. Results A total of 21 patients with NSCLC were included in the study. Among them, 18 (85.7%) patients had disease control with gefitinib and 12 (57.1%) patients with salvage erlotinib. There was an association between the disease control with gefitinib and erlotinib (p = 0.031). The disease control rate of erlotinib was independent of the chemotherapy use between the two EGFR-TKIs. Conclusion For NSCLC patients with favourable clinical features, erlotinib was effective in those who had prior disease control with first-line gefitinib. © Springer-Verlag 2009. | en_HK |
dc.language | eng | - |
dc.publisher | Springer. The Journal's web site is located at http://www.springer.com/medicine/oncology/journal/280 | en_HK |
dc.relation.ispartof | Cancer Chemotherapy and Pharmacology | en_HK |
dc.subject | Asians | en_HK |
dc.subject | Disease control rate | en_HK |
dc.subject | Epidermal growth factor receptor tyrosine kinase inhibitors | en_HK |
dc.subject | Erlotinib | en_HK |
dc.subject | Gefitinib | en_HK |
dc.subject | Non-small cell lung cancer | en_HK |
dc.subject.mesh | Aged | - |
dc.subject.mesh | Carcinoma, Non-Small-Cell Lung - drug therapy | - |
dc.subject.mesh | Lung Neoplasms - drug therapy | - |
dc.subject.mesh | Quinazolines - therapeutic use | - |
dc.subject.mesh | Salvage Therapy - methods | - |
dc.title | Erlotinib as salvage treatment after failure to first-line Gefitinib in non-small cell lung cancer | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Ip, MS:msmip@hku.hk | en_HK |
dc.identifier.email | Ho, JC:jhocm@hku.hk | en_HK |
dc.identifier.authority | Ip, MS=rp00347 | en_HK |
dc.identifier.authority | Ho, JC=rp00258 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1007/s00280-009-1107-5 | en_HK |
dc.identifier.pmid | 19680652 | - |
dc.identifier.pmcid | PMC2946542 | - |
dc.identifier.scopus | eid_2-s2.0-77951895524 | en_HK |
dc.identifier.hkuros | 172598 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77951895524&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 65 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 1023 | en_HK |
dc.identifier.epage | 1028 | en_HK |
dc.identifier.eissn | 1432-0843 | en_HK |
dc.identifier.isi | WOS:000275632400003 | - |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Wong, MK=23480818200 | en_HK |
dc.identifier.scopusauthorid | Lo, AI=31767490300 | en_HK |
dc.identifier.scopusauthorid | Lam, B=9246012800 | en_HK |
dc.identifier.scopusauthorid | Lam, WK=35934675100 | en_HK |
dc.identifier.scopusauthorid | Ip, MS=7102423259 | en_HK |
dc.identifier.scopusauthorid | Ho, JC=7402649981 | en_HK |
dc.identifier.citeulike | 5541820 | - |
dc.identifier.issnl | 0344-5704 | - |