中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2014年
30期
2337-2341
,共5页
娄娜娜%杨衿记%严红虹%周清%廖日强%徐崇锐%黄逸生%杨学宁%杨艳
婁娜娜%楊衿記%嚴紅虹%週清%廖日彊%徐崇銳%黃逸生%楊學寧%楊豔
루나나%양금기%엄홍홍%주청%료일강%서숭예%황일생%양학저%양염
腺癌%癌,非小细胞肺%基因,erbB-1%表皮生长因子受体-酪氨酸激酶抑制剂%药物疗法,联合
腺癌%癌,非小細胞肺%基因,erbB-1%錶皮生長因子受體-酪氨痠激酶抑製劑%藥物療法,聯閤
선암%암,비소세포폐%기인,erbB-1%표피생장인자수체-락안산격매억제제%약물요법,연합
Adenocarcinoma%Carcinoma,non-small-cell lung%Genes,erbB-1%Epidermal growth factor receptor-tyrosine kinase inhibitors%Drug therapy,combination
目的 比较分析吉非替尼与紫杉醇联合卡铂治疗晚期肺腺癌患者的临床效果.方法 纳入2006年10月至2007年9月,广东省人民医院收治的年龄≥18岁,未接受过化疗、生物学或免疫学治疗的不吸烟或少吸烟晚期肺腺癌患者,按体能状态(PS)评分、吸烟状况和性别采用动态均衡随机化方法随机纳入吉非替尼组和联合化疗组,吉非替尼组接受一线吉非替尼治疗(250 mg,口服,1次/d),联合化疗组接受化疗[紫杉醇200 mg/m2,静脉滴注,21d为1个周期;卡铂按剂量血药浓度-时间曲线下面积(AUC) =5 mg.ml-1·min-1计算,静脉输注,21 d为1个周期,两药都在每周期的第1天使用].主要终点指标是无进展生存期(PFS),次要终点指标是客观缓解率(ORR)和总生存期(OS).结果 共纳入51例患者,其中吉非替尼组25例,联合化疗组26例;两组中位PFS分别为4.2个月和8.3个月(P =0.422),ORR分别为36.0%和42.3% (P =0.645),中位OS分别为14.4个月和15.0个月(P =0.290).多因素Cox回归分析显示:年龄(P=0.004)、表皮生长因子受体(EGFR)基因突变状态(P =0.012)和后续治疗[含铂化疗,P=0.001;EGFR-酪氨酸激酶抑制剂(TKI),P=0.005]是OS显著的预后影响因素.结论 对于不吸烟或少吸烟的晚期肺腺癌患者,一线吉非替尼治疗与紫杉醇联合卡铂化疗的客观疗效近似.但限于样本量的不足,我们仍然不推荐基于临床因素一线选择吉非替尼治疗晚期非小细胞肺癌.
目的 比較分析吉非替尼與紫杉醇聯閤卡鉑治療晚期肺腺癌患者的臨床效果.方法 納入2006年10月至2007年9月,廣東省人民醫院收治的年齡≥18歲,未接受過化療、生物學或免疫學治療的不吸煙或少吸煙晚期肺腺癌患者,按體能狀態(PS)評分、吸煙狀況和性彆採用動態均衡隨機化方法隨機納入吉非替尼組和聯閤化療組,吉非替尼組接受一線吉非替尼治療(250 mg,口服,1次/d),聯閤化療組接受化療[紫杉醇200 mg/m2,靜脈滴註,21d為1箇週期;卡鉑按劑量血藥濃度-時間麯線下麵積(AUC) =5 mg.ml-1·min-1計算,靜脈輸註,21 d為1箇週期,兩藥都在每週期的第1天使用].主要終點指標是無進展生存期(PFS),次要終點指標是客觀緩解率(ORR)和總生存期(OS).結果 共納入51例患者,其中吉非替尼組25例,聯閤化療組26例;兩組中位PFS分彆為4.2箇月和8.3箇月(P =0.422),ORR分彆為36.0%和42.3% (P =0.645),中位OS分彆為14.4箇月和15.0箇月(P =0.290).多因素Cox迴歸分析顯示:年齡(P=0.004)、錶皮生長因子受體(EGFR)基因突變狀態(P =0.012)和後續治療[含鉑化療,P=0.001;EGFR-酪氨痠激酶抑製劑(TKI),P=0.005]是OS顯著的預後影響因素.結論 對于不吸煙或少吸煙的晚期肺腺癌患者,一線吉非替尼治療與紫杉醇聯閤卡鉑化療的客觀療效近似.但限于樣本量的不足,我們仍然不推薦基于臨床因素一線選擇吉非替尼治療晚期非小細胞肺癌.
목적 비교분석길비체니여자삼순연합잡박치료만기폐선암환자적림상효과.방법 납입2006년10월지2007년9월,광동성인민의원수치적년령≥18세,미접수과화료、생물학혹면역학치료적불흡연혹소흡연만기폐선암환자,안체능상태(PS)평분、흡연상황화성별채용동태균형수궤화방법수궤납입길비체니조화연합화료조,길비체니조접수일선길비체니치료(250 mg,구복,1차/d),연합화료조접수화료[자삼순200 mg/m2,정맥적주,21d위1개주기;잡박안제량혈약농도-시간곡선하면적(AUC) =5 mg.ml-1·min-1계산,정맥수주,21 d위1개주기,량약도재매주기적제1천사용].주요종점지표시무진전생존기(PFS),차요종점지표시객관완해솔(ORR)화총생존기(OS).결과 공납입51례환자,기중길비체니조25례,연합화료조26례;량조중위PFS분별위4.2개월화8.3개월(P =0.422),ORR분별위36.0%화42.3% (P =0.645),중위OS분별위14.4개월화15.0개월(P =0.290).다인소Cox회귀분석현시:년령(P=0.004)、표피생장인자수체(EGFR)기인돌변상태(P =0.012)화후속치료[함박화료,P=0.001;EGFR-락안산격매억제제(TKI),P=0.005]시OS현저적예후영향인소.결론 대우불흡연혹소흡연적만기폐선암환자,일선길비체니치료여자삼순연합잡박화료적객관료효근사.단한우양본량적불족,아문잉연불추천기우림상인소일선선택길비체니치료만기비소세포폐암.
Objective To compare the clinical efficacies of gefitinib versus paclitaxel/carboplatin in patients with advanced pulmonary adenocarcinoma.Methods A total of 51 advanced pulmonary adenocarcinoma patients were recruited from Guangdong General Hospital during October 2006 to September 2007.Eligible patients were ≥ 18 years old,either non-smokers or former light smokers and receiving no prior chemotherapy or biological/immunological therapy.According to performance status,smoking status and gender,they were selected with dynamic equilibrium randomized method 1:1 to receive first-line gefitinib (250 mg/d) in gefitinib arm or carboplatin/paclitaxel (carboplatin,area under the curve 5 mg · ml-1 · min-1,21-day cycle; paclitaxel,200 mg/m2,21-day cycle in chemotherapy ann.The primary endpoint was progression free survival (PFS).And the secondary endpoints were objective response rate (ORR) and overall survival (OS).Results They were randomized into gefitinib arm (n =25) and paclitaxel/carboplatin arm (n =26).The median PFS was 4.2 months in gefitinib arm and 8.3 months in paclitaxeL/carboplatin arm (P =0.422) ; ORR 36.0% in gefitinib arm and 42.3% in paclitaxel/carboplatin arm (P =0.645) ; Median OS 14.4 months in gefitinib arm and 15.0 months in paclitaxel/carboplatin arm (P =0.290).Multifactorial Cox regression analysis showed that age (P =0.004),epidermal growth factor receptor (EGFR) gene mutation status (P =0.012) and subsequent treatments (platinum-based chemotherapy,P =0.001; EGFR-tyrosine kinase inhibitors (TKI),P =0.005) were the significant predictors of OS.Conclusions No significant differences exist in terms of efficacy and survival between first-line gefitinib and paclitaxel/carboplatin for Chinese patients with pulmonary adenocarcinoma who are non-smokers or former light smokers.And age,EGFR gene mutation status and subsequent treatments are significant predictor of OS.However,first-line gefitinib should not be recommended for advanced non-small cell lung cancer (NSCLC) patients only based on clinical factors,due to a very small sample-size in our study.