肿瘤基础与临床
腫瘤基礎與臨床
종류기출여림상
JOURNAL OF BASIC AND CLINICAL ONCOLOGY
2014年
5期
397-399
,共3页
李绮云%李太东%陈思现%陈永锋%林王美
李綺雲%李太東%陳思現%陳永鋒%林王美
리기운%리태동%진사현%진영봉%림왕미
晚期肝细胞癌%恩度%吉西他滨
晚期肝細胞癌%恩度%吉西他濱
만기간세포암%은도%길서타빈
advanced hepatocellular cancer%endostar%gemcitabine
目的:观察恩度联合吉西他滨治疗晚期肝细胞癌的近期疗效和安全性。方法57例晚期肝细胞癌患者随机分为2组,治疗组29例给予恩度联合吉西他滨治疗,对照组28例仅给予吉西他滨治疗,2组患者均至少接受2周期的化疗,然后评价近期疗效和毒副反应。结果治疗组有效率为51.7%,高于对照组的25.0%(P<0.05);临床获益率为82.8%,高于对照组的57.1%(P<0.05);中位肿瘤进展时间分别为6.5个月和3.5个月(P<0.05)。2组患者治疗后生活质量评分均有所提高,以治疗组提高更明显(P<0.05)。2组患者治疗后血清AFP、CA19-9水平均有不同程度下降,以治疗组下降较为明显( P<0.05)。2组患者治疗后中、重度毒副反应发生率相近(P>0.05)。结论恩度联合吉西他滨治疗晚期肝细胞癌安全有效,值得临床推广应用。
目的:觀察恩度聯閤吉西他濱治療晚期肝細胞癌的近期療效和安全性。方法57例晚期肝細胞癌患者隨機分為2組,治療組29例給予恩度聯閤吉西他濱治療,對照組28例僅給予吉西他濱治療,2組患者均至少接受2週期的化療,然後評價近期療效和毒副反應。結果治療組有效率為51.7%,高于對照組的25.0%(P<0.05);臨床穫益率為82.8%,高于對照組的57.1%(P<0.05);中位腫瘤進展時間分彆為6.5箇月和3.5箇月(P<0.05)。2組患者治療後生活質量評分均有所提高,以治療組提高更明顯(P<0.05)。2組患者治療後血清AFP、CA19-9水平均有不同程度下降,以治療組下降較為明顯( P<0.05)。2組患者治療後中、重度毒副反應髮生率相近(P>0.05)。結論恩度聯閤吉西他濱治療晚期肝細胞癌安全有效,值得臨床推廣應用。
목적:관찰은도연합길서타빈치료만기간세포암적근기료효화안전성。방법57례만기간세포암환자수궤분위2조,치료조29례급여은도연합길서타빈치료,대조조28례부급여길서타빈치료,2조환자균지소접수2주기적화료,연후평개근기료효화독부반응。결과치료조유효솔위51.7%,고우대조조적25.0%(P<0.05);림상획익솔위82.8%,고우대조조적57.1%(P<0.05);중위종류진전시간분별위6.5개월화3.5개월(P<0.05)。2조환자치료후생활질량평분균유소제고,이치료조제고경명현(P<0.05)。2조환자치료후혈청AFP、CA19-9수평균유불동정도하강,이치료조하강교위명현( P<0.05)。2조환자치료후중、중도독부반응발생솔상근(P>0.05)。결론은도연합길서타빈치료만기간세포암안전유효,치득림상추엄응용。
Objective Toinvestigatetheshort-termeffectsandsafetyofendostarcombinedwithgemcitabinein thetreatmentofadvancedhepatocellularcarcinoma.Methods Fifty-sevenpatientswithadvancedhepatocellular carcinoma were randomly divided into two groups,29 patients of the treatment group received endostar plus gemcit-abine,and 28 patients of the control group received gemcitabine only. All the patients received at least 2 cycles of chemotherapy,andtheshort-termeffectsandtoxicitieswereobserved.Results Theresponseratewas51.7%in the treatment group,and was 25. 0% in the control group(P<0. 05). The clinical benefit rate was 82. 8% in the treatment group,and was 57. 1% in the control group(P<0. 05). The median tumor to progression time was 6. 5 months in the treatment group,and was 3. 5 months in the control group(P<0. 05). The scores of quality of life in the two groups were both increased,and the increasing rate in the treatment group was significantly higher than that in the control group(P<0. 05). The serum levels of AFP and CA19-9 in the two groups were decreased significant-ly after the treatment,and the decreasing degree in treatment group was higher than that in the control group( P<0. 05). There were no significant statistical differences in the incidence of moderate-severe toxicities between the twogroups.Conclusion Endostarcombinedwithgemcitabineiseffeetiveandsafeinthetreatmentofadvanced hepatocellular carcinoma.