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Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer

BACKGROUND: Bevacizumab and erlotinib have been demonstrated to prolong overall survival in patients with non-squamous non-small cell lung cancer (NSCLC). We designed a four-arm Phase III trial to evaluate the efficacy and toxicity of the combination of docetaxel, carboplatin, bevacizumab, and erlot...

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Autores principales: Boutsikou, Eftimia, Kontakiotis, Theodoros, Zarogoulidis, Paul, Darwiche, Kaid, Eleptheriadou, Ellada, Porpodis, Konstantinos, Galaktidou, Grammati, Sakkas, Leonidas, Hohenforst-Schmidt, Wolfgang, Tsakiridis, Kosmas, Karaiskos, Theodoros, Zarogoulidis, Konstantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589083/
https://www.ncbi.nlm.nih.gov/pubmed/23467839
http://dx.doi.org/10.2147/OTT.S42245
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author Boutsikou, Eftimia
Kontakiotis, Theodoros
Zarogoulidis, Paul
Darwiche, Kaid
Eleptheriadou, Ellada
Porpodis, Konstantinos
Galaktidou, Grammati
Sakkas, Leonidas
Hohenforst-Schmidt, Wolfgang
Tsakiridis, Kosmas
Karaiskos, Theodoros
Zarogoulidis, Konstantinos
author_facet Boutsikou, Eftimia
Kontakiotis, Theodoros
Zarogoulidis, Paul
Darwiche, Kaid
Eleptheriadou, Ellada
Porpodis, Konstantinos
Galaktidou, Grammati
Sakkas, Leonidas
Hohenforst-Schmidt, Wolfgang
Tsakiridis, Kosmas
Karaiskos, Theodoros
Zarogoulidis, Konstantinos
author_sort Boutsikou, Eftimia
collection PubMed
description BACKGROUND: Bevacizumab and erlotinib have been demonstrated to prolong overall survival in patients with non-squamous non-small cell lung cancer (NSCLC). We designed a four-arm Phase III trial to evaluate the efficacy and toxicity of the combination of docetaxel, carboplatin, bevacizumab, and erlotinib in the first-line treatment of patients with NSCLC. METHODS: A total of 229 patients with stage IIIb/IV non-squamous NSCLC were treated with two cycles of carboplatin (area under the concentration-time curve 5.5) and docetaxel 100 mg/m2 as chemotherapy. After completion of two treatment cycles, patients were evaluated for response and divided into four groups: 61/229 continued with four more cycles of chemotherapy (control group), 52/229 received chemotherapy plus erlotinib 150 mg daily, 56/229 received chemotherapy plus bevacizumab 7.5 mg/kg, and 60/229 were treated with the combination of chemotherapy, erlotinib, and bevacizumab until disease progression. The primary endpoint was overall survival. RESULTS: Over 4 years of follow-up, there was no statistically significant difference in survival and time to progression between the four treatment groups. After two cycles of chemotherapy, responders and nonresponders were divided according to their response in order to examine the role of initial response as an independent factor in survival and response when a biological agent is combined with chemotherapy. Nonresponders, who received additional therapy with bevacizumab or combination therapy, had a survival benefit [657 days (95% confidence interval 349–970) and 681 days (95% confidence interval 315–912), respectively], which was statistically significant compared with continuation of cytotoxic chemotherapy (P < 0.001). The combination therapy had a safety profile comparable with that of bevacizumab and erlotinib taken individually. CONCLUSION: Administration of bevacizumab and erlotinib in combination with first-line chemotherapy, followed by bevacizumab and erlotinib monotherapy as maintenance, showed promising results in patients with NSCLC, with reduced toxicity as compared with chemotherapy alone, but did not translate into longer overall survival.
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spelling pubmed-35890832013-03-06 Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer Boutsikou, Eftimia Kontakiotis, Theodoros Zarogoulidis, Paul Darwiche, Kaid Eleptheriadou, Ellada Porpodis, Konstantinos Galaktidou, Grammati Sakkas, Leonidas Hohenforst-Schmidt, Wolfgang Tsakiridis, Kosmas Karaiskos, Theodoros Zarogoulidis, Konstantinos Onco Targets Ther Original Research BACKGROUND: Bevacizumab and erlotinib have been demonstrated to prolong overall survival in patients with non-squamous non-small cell lung cancer (NSCLC). We designed a four-arm Phase III trial to evaluate the efficacy and toxicity of the combination of docetaxel, carboplatin, bevacizumab, and erlotinib in the first-line treatment of patients with NSCLC. METHODS: A total of 229 patients with stage IIIb/IV non-squamous NSCLC were treated with two cycles of carboplatin (area under the concentration-time curve 5.5) and docetaxel 100 mg/m2 as chemotherapy. After completion of two treatment cycles, patients were evaluated for response and divided into four groups: 61/229 continued with four more cycles of chemotherapy (control group), 52/229 received chemotherapy plus erlotinib 150 mg daily, 56/229 received chemotherapy plus bevacizumab 7.5 mg/kg, and 60/229 were treated with the combination of chemotherapy, erlotinib, and bevacizumab until disease progression. The primary endpoint was overall survival. RESULTS: Over 4 years of follow-up, there was no statistically significant difference in survival and time to progression between the four treatment groups. After two cycles of chemotherapy, responders and nonresponders were divided according to their response in order to examine the role of initial response as an independent factor in survival and response when a biological agent is combined with chemotherapy. Nonresponders, who received additional therapy with bevacizumab or combination therapy, had a survival benefit [657 days (95% confidence interval 349–970) and 681 days (95% confidence interval 315–912), respectively], which was statistically significant compared with continuation of cytotoxic chemotherapy (P < 0.001). The combination therapy had a safety profile comparable with that of bevacizumab and erlotinib taken individually. CONCLUSION: Administration of bevacizumab and erlotinib in combination with first-line chemotherapy, followed by bevacizumab and erlotinib monotherapy as maintenance, showed promising results in patients with NSCLC, with reduced toxicity as compared with chemotherapy alone, but did not translate into longer overall survival. Dove Medical Press 2013-03-01 /pmc/articles/PMC3589083/ /pubmed/23467839 http://dx.doi.org/10.2147/OTT.S42245 Text en © 2013 Boutsikou et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Boutsikou, Eftimia
Kontakiotis, Theodoros
Zarogoulidis, Paul
Darwiche, Kaid
Eleptheriadou, Ellada
Porpodis, Konstantinos
Galaktidou, Grammati
Sakkas, Leonidas
Hohenforst-Schmidt, Wolfgang
Tsakiridis, Kosmas
Karaiskos, Theodoros
Zarogoulidis, Konstantinos
Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer
title Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer
title_full Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer
title_fullStr Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer
title_full_unstemmed Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer
title_short Docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer
title_sort docetaxel-carboplatin in combination with erlotinib and/or bevacizumab in patients with non-small cell lung cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589083/
https://www.ncbi.nlm.nih.gov/pubmed/23467839
http://dx.doi.org/10.2147/OTT.S42245
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