Pemetrexed Versus Erlotinib in the Second-line Treatment of Patients with Advanced-stage Non-squamous NSCLC Harboring Wild-type EGFR Gene

被引:1
作者
Fiala, Ondrej [1 ,4 ]
Pesek, Milos [2 ]
Finek, Jindrich [1 ]
Svaton, Martin [2 ]
Minarik, Marek [5 ,6 ]
Benesova, Lucie [6 ]
Bortlicek, Zbynek [7 ]
Kucera, Radek [3 ]
Topolcan, Ondrej [3 ]
机构
[1] Charles Univ Prague, Med Sch & Teaching Hosp Pilsen, Dept Radiotherapy & Oncol, Prague, Czech Republic
[2] Charles Univ Prague, Med Sch & Teaching Hosp Pilsen, Dept Pneumol, Prague, Czech Republic
[3] Charles Univ Prague, Med Sch & Teaching Hosp Pilsen, Dept Nucl Med, Prague, Czech Republic
[4] Charles Univ Prague, Fac Med Pilsen, Biomed Ctr, Prague, Czech Republic
[5] Charles Univ Prague, Fac Sci, Dept Analyt Chem, Prague, Czech Republic
[6] Genomac Res Inst, Ctr Appl Genom Solid Tumours, Prague, Czech Republic
[7] Masaryk Univ, Fac Med, Inst Biostat & Anal, Brno, Czech Republic
关键词
Pemetrexed; erlotinib; NSCLC; second-line treatment; targeted treatment; chemotherapy; CELL LUNG-CANCER; GROWTH-FACTOR RECEPTOR; OPEN-LABEL; PHASE-III; 1ST-LINE TREATMENT; KRAS MUTATIONS; CHEMOTHERAPY; MULTICENTER; GEFITINIB; HISTOLOGY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Pemetrexed and erlotinib represent different agents commonly used for the second-line treatment of patients with advanced-stage non-small cell lung cancer (NSCLC). Patients and Methods: We analyzed data of 137 patients with advanced-stage non-squamous NSCLC treated with pemetrexed or erlotinib in the second line. All patients harbored a wild-type epidermal growth factor receptor gene. Genetic testing was performed using a combination of denaturing capillary electrophoresis and direct Sanger sequencing. Results: overall response rate and disease control rate in patients treated with pemetrexed was 20.8% and 62.5% vs. 6.3% and 53.2% in patients treated with erlotinib (p=0.022; p=0.358). Median progression-free and overall survival in patients treated with pemetrexed was 1.6 and 11.3 months vs. 1.9 and 11.4 months in patients treated with erlotinib (p=0.470 and p=0.942, respectively). Erlotinib was associated with skin rash and diarrhea; pemetrexed was associated with hematological toxicity and fatigue. Conclusion: A similar efficacy and different, although well-tolerated, toxicity profile of both pemetrexed and erlotinib was shown.
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收藏
页码:447 / 453
页数:7
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