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

被引:41
作者
Boutsikou, Eftimia [1 ]
Kontakiotis, Theodoros [1 ]
Zarogoulidis, Paul [1 ]
Darwiche, Kaid [2 ]
Eleptheriadou, Ellada [1 ]
Porpodis, Konstantinos [1 ]
Galaktidou, Grammati [3 ]
Sakkas, Leonidas [4 ]
Hohenforst-Schmidt, Wolfgang [5 ]
Tsakiridis, Kosmas [6 ]
Karaiskos, Theodoros [7 ]
Zarogoulidis, Konstantinos [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Pulm, Oncol Unit, G Papanikolaou Gen Hosp, GR-54006 Thessaloniki, Greece
[2] Univ Duisburg Essen, Univ Pulm Dept, Intervent Unit, Ruhrland Klin, Essen, Germany
[3] G Papanikolaou Hosp, Theagenio Anticanc Inst, Res Lab, Thessaloniki, Greece
[4] G Papanikolaou Hosp, Dept Pathol, Thessaloniki, Greece
[5] Univ Wurzburg, Med Clin 2, Hosp Coburg, Coburg, Germany
[6] St Luke Private Hosp, Cardiothorac Surg Dept, Panorama, Greece
[7] Aristotle Univ Thessaloniki, G Papanikolaou Gen Hosp, Cardiothorac Surg Dept, GR-54006 Thessaloniki, Greece
关键词
vascular endothelial growth factor; epidermal growth factor receptor; erlotinib; bevacizumab; non-small cell lung cancer; ENDOTHELIAL GROWTH-FACTOR; PHASE-III TRIAL; FACTOR RECEPTOR; CHEMOTHERAPY; PLACEBO; RECURRENT; EFFICACY;
D O I
10.2147/OTT.S42245
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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/m(2) 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.
引用
收藏
页码:125 / 134
页数:10
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