山东医药
山東醫藥
산동의약
Shandong Medical Journal
2015年
37期
1-3
,共3页
魏崴%张洁霞%蓝玉宏%李勇生%钟标%黎佩建%白力
魏崴%張潔霞%藍玉宏%李勇生%鐘標%黎珮建%白力
위외%장길하%람옥굉%리용생%종표%려패건%백력
肺肿瘤%吉非替尼%癌胚抗原
肺腫瘤%吉非替尼%癌胚抗原
폐종류%길비체니%암배항원
carcinoma,non-small-cell lung%gefitinib%carcinoembryonic antigen
目的:观察非小细胞肺癌(NSCLC)患者经吉非替尼治疗后血清癌胚抗原(CEA)水平的变化,并探讨其临床意义。方法共纳入40例NSCLC患者,临床分期Ⅲ~Ⅳ期,给予吉非替尼联合基础放疗进行治疗,若发现肿瘤进展或不能耐受的毒性反应则停止,治疗后,患者按照RECIST 1.1(2009年颁布的实体瘤疗效评价标准)标准被分为控制组和非控制组,采集患者清晨外周血,利用电化学发光免疫法测定血清CEA。将治疗前患者分为高CEA组( CEA>30μg/L)和低CEA组( CEA≤30μg/L),两组一直随访到2014年6月,记录随访过程中的不良反应及无疾病进展生存率(PFS)。结果治疗前控制组和非控制组之间CEA水平无统计学差异(P>0.05),治疗后两组均下降,以控制组为著( P均<0.01);高CEA组和低CEA组之间不良反应无统计学差异( P>0.05);高CEA组9、12个月的无疾病进展生存期较低CEA组长(P<0.01)。结论吉非替尼治疗后,NSCLC患者血清CEA水平下降;血清CEA水平可作为预测吉非替尼治疗NSCLC的疗效及患者预后的生物学标记。
目的:觀察非小細胞肺癌(NSCLC)患者經吉非替尼治療後血清癌胚抗原(CEA)水平的變化,併探討其臨床意義。方法共納入40例NSCLC患者,臨床分期Ⅲ~Ⅳ期,給予吉非替尼聯閤基礎放療進行治療,若髮現腫瘤進展或不能耐受的毒性反應則停止,治療後,患者按照RECIST 1.1(2009年頒佈的實體瘤療效評價標準)標準被分為控製組和非控製組,採集患者清晨外週血,利用電化學髮光免疫法測定血清CEA。將治療前患者分為高CEA組( CEA>30μg/L)和低CEA組( CEA≤30μg/L),兩組一直隨訪到2014年6月,記錄隨訪過程中的不良反應及無疾病進展生存率(PFS)。結果治療前控製組和非控製組之間CEA水平無統計學差異(P>0.05),治療後兩組均下降,以控製組為著( P均<0.01);高CEA組和低CEA組之間不良反應無統計學差異( P>0.05);高CEA組9、12箇月的無疾病進展生存期較低CEA組長(P<0.01)。結論吉非替尼治療後,NSCLC患者血清CEA水平下降;血清CEA水平可作為預測吉非替尼治療NSCLC的療效及患者預後的生物學標記。
목적:관찰비소세포폐암(NSCLC)환자경길비체니치료후혈청암배항원(CEA)수평적변화,병탐토기림상의의。방법공납입40례NSCLC환자,림상분기Ⅲ~Ⅳ기,급여길비체니연합기출방료진행치료,약발현종류진전혹불능내수적독성반응칙정지,치료후,환자안조RECIST 1.1(2009년반포적실체류료효평개표준)표준피분위공제조화비공제조,채집환자청신외주혈,이용전화학발광면역법측정혈청CEA。장치료전환자분위고CEA조( CEA>30μg/L)화저CEA조( CEA≤30μg/L),량조일직수방도2014년6월,기록수방과정중적불량반응급무질병진전생존솔(PFS)。결과치료전공제조화비공제조지간CEA수평무통계학차이(P>0.05),치료후량조균하강,이공제조위저( P균<0.01);고CEA조화저CEA조지간불량반응무통계학차이( P>0.05);고CEA조9、12개월적무질병진전생존기교저CEA조장(P<0.01)。결론길비체니치료후,NSCLC환자혈청CEA수평하강;혈청CEA수평가작위예측길비체니치료NSCLC적료효급환자예후적생물학표기。
Objective To observe the changes in levels of serum carcinoembryonic antigen ( CEA) in patients before and after gefitinib treatment of non-small-cell lung cancer ( NSCLC) and to investigate the clinical significance .Methods Forty patients with NSCLC in clinical stage of Ⅲ~Ⅳwere treated with gefitinib and radiotherapy , and we stopped if the tumor progression or toxicity reaction were found in patients .After treatment , all patients were divided into the control group and non-control group according to RECIST1.1 (Response Evaluation Criteria in Solid Tumors in 2009).The periph-eral blood was collected in the morning to detect the serum CEA by electro-chemiluminescence immunoassay ( ECLIA ) . Before treatment , the patients were divided into the high CEA group ( CEA>30 μg/L) and low CEA group ( CEA ≤30μg/L) .Two groups were followed up to December , 2012 .The adverse reactions and progression free survival ( PFS) were recorded .Results There was no difference in CEA levels before treatment between the control group and non -control group(P>0.05),but the levels of CEA in the control group decreased more after treatment than that of the non -control group (all P<0.01).No difference was found in the adverse reaction between the high CEA group and the low CEA group (P>0.05), but the PFS at 9 months and 12 months was higher in the high CEA group than that in the low CEA group (P<0.01).Conclusion The serum CEA level is decreased in NSCLC patients after treatment of gefitinib , which can be-come the biological marker in predicting the efficacy and prognosis .