皖南医学院学报
皖南醫學院學報
환남의학원학보
ACTA ACADEMIAE MEDICINAE WANNAN
2015年
2期
136-139,140
,共5页
培美曲塞%厄洛替尼%癌,非小细胞肺%药物治疗
培美麯塞%阨洛替尼%癌,非小細胞肺%藥物治療
배미곡새%액락체니%암,비소세포폐%약물치료
pemetrexed%erlotinib%carcinoma%non-small cell lung%medication
目的:比较培美曲塞与厄洛替尼单药治疗一线化疗进展的晚期非小细胞肺癌的疗效、不良反应、生活质量及生存期,为晚期非小细胞肺癌的二线用药提供参考。方法:回顾性分析我科2011年3月~2013年10月门诊或住院收治的经病理组织学或细胞学检查证实为晚期非小细胞肺癌且经含铂类药物为一线标准化疗方案治疗失败的患者90例。其中培美曲塞组46例、厄洛替尼组44例。培美曲塞组采用500 mg/m2静滴,21 d一个周期。厄洛替尼组患者餐后2 h口服厄洛替尼150 mg/d。评价两组患者的临床疗效、无进展生存时间( PFS)、中位生存时间( MST)、不良反应和生活质量。结果:两组患者治疗有效率、疾病控制率、中位PFS、MST相比差异无统计学意义( P>0.05)。培美曲塞组主要不良反应是骨髓抑制和胃肠道反应,厄洛替尼主要不良反应是皮疹和腹泻,两组不良反应发生率比较差异有统计学意义( P<0.05)。厄洛替尼组在改善患者综合生活质量方面效果明显,优于培美曲塞组( P<0.05)。结论:培美曲塞和厄洛替尼单药二线治疗晚期非小细胞肺癌的疗效相似,不良反应各异,两者均能改善患者生活质量,但是厄洛替尼改善更明显。
目的:比較培美麯塞與阨洛替尼單藥治療一線化療進展的晚期非小細胞肺癌的療效、不良反應、生活質量及生存期,為晚期非小細胞肺癌的二線用藥提供參攷。方法:迴顧性分析我科2011年3月~2013年10月門診或住院收治的經病理組織學或細胞學檢查證實為晚期非小細胞肺癌且經含鉑類藥物為一線標準化療方案治療失敗的患者90例。其中培美麯塞組46例、阨洛替尼組44例。培美麯塞組採用500 mg/m2靜滴,21 d一箇週期。阨洛替尼組患者餐後2 h口服阨洛替尼150 mg/d。評價兩組患者的臨床療效、無進展生存時間( PFS)、中位生存時間( MST)、不良反應和生活質量。結果:兩組患者治療有效率、疾病控製率、中位PFS、MST相比差異無統計學意義( P>0.05)。培美麯塞組主要不良反應是骨髓抑製和胃腸道反應,阨洛替尼主要不良反應是皮疹和腹瀉,兩組不良反應髮生率比較差異有統計學意義( P<0.05)。阨洛替尼組在改善患者綜閤生活質量方麵效果明顯,優于培美麯塞組( P<0.05)。結論:培美麯塞和阨洛替尼單藥二線治療晚期非小細胞肺癌的療效相似,不良反應各異,兩者均能改善患者生活質量,但是阨洛替尼改善更明顯。
목적:비교배미곡새여액락체니단약치료일선화료진전적만기비소세포폐암적료효、불량반응、생활질량급생존기,위만기비소세포폐암적이선용약제공삼고。방법:회고성분석아과2011년3월~2013년10월문진혹주원수치적경병리조직학혹세포학검사증실위만기비소세포폐암차경함박류약물위일선표준화료방안치료실패적환자90례。기중배미곡새조46례、액락체니조44례。배미곡새조채용500 mg/m2정적,21 d일개주기。액락체니조환자찬후2 h구복액락체니150 mg/d。평개량조환자적림상료효、무진전생존시간( PFS)、중위생존시간( MST)、불량반응화생활질량。결과:량조환자치료유효솔、질병공제솔、중위PFS、MST상비차이무통계학의의( P>0.05)。배미곡새조주요불량반응시골수억제화위장도반응,액락체니주요불량반응시피진화복사,량조불량반응발생솔비교차이유통계학의의( P<0.05)。액락체니조재개선환자종합생활질량방면효과명현,우우배미곡새조( P<0.05)。결론:배미곡새화액락체니단약이선치료만기비소세포폐암적료효상사,불량반응각이,량자균능개선환자생활질량,단시액락체니개선경명현。
Objective:To evaluate the clinical efficacy,toxicity,quality of life and the median progression-free survival (PFS) using pemetrexed and erlo-tinib as second line medication for advanced non-small cell lung cancer ( NSCLC) .Methods:The clinical outcomes were retrospectively examined in 90 patients confirmed as NSCLC by histopathology or cytological examination ,who failed to respond to first-line of platinum-based regimen chemotherapy and underwent second line treatment with pemetrexed(n=46) or erlotinib(n=44) on outpatient or hospitalization basis between March 2011 and October 2013 in our department.Group pemetrexed received intravenous administration of pemetrexed in dose of 500 mg/m2 for 21 days as a chemotherapy epi-sodes,and group erlotinib were given oral erlotinib in dose of 150 mg/d by postprandial 2 hour.The two groups were assessed regarding the efficacy,pro-gression-free survival time (PFS),median survival time (MST),incidence of toxicity and life quality.Results:The two groups were not significant pertain-ing to effective rate,disease control rate,median PFS and MST(P>0.05).The adverse effects in group pemetrexed were associated with bone marrow sup-pression and gastrointestinal reactions;and erlotinib,development of skin rash and diarrhea,which was statistically different(P<0.05).Erlotinib had bet-ter improved the quality of life for patients than pemetrexed(P<0.05).Conclusion:Although pemetrexed and erlotinib as second line therapy for NSCLC may lead to similar effects and improvement of the quality of life for patients ,yet the adverse effects vary to a certain degree and erlotinib has better out-comes of life quality.