医学综述
醫學綜述
의학종술
MEDICAL RECAPITULATE
2015年
10期
1883-1885
,共3页
食管癌%多西他赛%奥沙利铂%疗效%不良反应
食管癌%多西他賽%奧沙利鉑%療效%不良反應
식관암%다서타새%오사리박%료효%불량반응
Esophageal cancer%Docetaxel%Oxaliplatin%Efficacy%Adverse reactions
目的:评估多西他赛联合奥沙利铂治疗晚期食管癌的疗效及不良反应。方法选择2010年3月至2013年3月荆州市中心医院收住院、经病理组织学或细胞学及影像学确诊的食管癌晚期患者96例,依据随机数字表法分为对照组和研究组,各48例。两组均给予多西他赛75 mg/m2,对照组联合顺铂80~100 mg/m2,研究组联合奥沙利铂135 mg/m2;每21天化疗1次。比较两组患者的有效率、疾病进展时间( TTP)、中位生存期、Kamofsky评分及不良反应情况。结果两组临床疗效比较差异差异无统计学意义( P>0.05),研究组 Kamofsky评分好转率显著高于对照组(66.7%比43.8%, P<0.05)。研究组中位生存期为(18.2±1.3)个月,TTP为(9.3±0.4)个月,对照组中位生存期为(16.3±1.0)个月,TTP 为(8.7±0.3)个月,两组 TTP、中位生存期比较差异无统计学意义(P >0.05)。研究组血小板减少、腹泻、恶心呕吐及肝损伤、肾损伤明显发生率低于对照组,但神经毒性发生率高于对照组,差异均有统计学意义( P<0.05)。结论多西他赛联合奥沙利铂治疗晚期食管癌临床疗效满意,且肝肾功能、胃肠道及骨髓抑制等不良反应比联用顺铂明显减少,推荐该方案在临床得到合理的应用,并在实际用药中个体化调整奥沙利铂的用药剂量。
目的:評估多西他賽聯閤奧沙利鉑治療晚期食管癌的療效及不良反應。方法選擇2010年3月至2013年3月荊州市中心醫院收住院、經病理組織學或細胞學及影像學確診的食管癌晚期患者96例,依據隨機數字錶法分為對照組和研究組,各48例。兩組均給予多西他賽75 mg/m2,對照組聯閤順鉑80~100 mg/m2,研究組聯閤奧沙利鉑135 mg/m2;每21天化療1次。比較兩組患者的有效率、疾病進展時間( TTP)、中位生存期、Kamofsky評分及不良反應情況。結果兩組臨床療效比較差異差異無統計學意義( P>0.05),研究組 Kamofsky評分好轉率顯著高于對照組(66.7%比43.8%, P<0.05)。研究組中位生存期為(18.2±1.3)箇月,TTP為(9.3±0.4)箇月,對照組中位生存期為(16.3±1.0)箇月,TTP 為(8.7±0.3)箇月,兩組 TTP、中位生存期比較差異無統計學意義(P >0.05)。研究組血小闆減少、腹瀉、噁心嘔吐及肝損傷、腎損傷明顯髮生率低于對照組,但神經毒性髮生率高于對照組,差異均有統計學意義( P<0.05)。結論多西他賽聯閤奧沙利鉑治療晚期食管癌臨床療效滿意,且肝腎功能、胃腸道及骨髓抑製等不良反應比聯用順鉑明顯減少,推薦該方案在臨床得到閤理的應用,併在實際用藥中箇體化調整奧沙利鉑的用藥劑量。
목적:평고다서타새연합오사리박치료만기식관암적료효급불량반응。방법선택2010년3월지2013년3월형주시중심의원수주원、경병리조직학혹세포학급영상학학진적식관암만기환자96례,의거수궤수자표법분위대조조화연구조,각48례。량조균급여다서타새75 mg/m2,대조조연합순박80~100 mg/m2,연구조연합오사리박135 mg/m2;매21천화료1차。비교량조환자적유효솔、질병진전시간( TTP)、중위생존기、Kamofsky평분급불량반응정황。결과량조림상료효비교차이차이무통계학의의( P>0.05),연구조 Kamofsky평분호전솔현저고우대조조(66.7%비43.8%, P<0.05)。연구조중위생존기위(18.2±1.3)개월,TTP위(9.3±0.4)개월,대조조중위생존기위(16.3±1.0)개월,TTP 위(8.7±0.3)개월,량조 TTP、중위생존기비교차이무통계학의의(P >0.05)。연구조혈소판감소、복사、악심구토급간손상、신손상명현발생솔저우대조조,단신경독성발생솔고우대조조,차이균유통계학의의( P<0.05)。결론다서타새연합오사리박치료만기식관암림상료효만의,차간신공능、위장도급골수억제등불량반응비련용순박명현감소,추천해방안재림상득도합리적응용,병재실제용약중개체화조정오사리박적용약제량。
Objective To evaluate the efficacy and adverse reactions of docetaxel combined with oxali-platininpatientswithadvancedesophagealcancer.Methods 96patientswithesophagealcanceradmitted to the Jingzhou Central Hospital from March 2010 to March 2013,hospitalized late stage by histology or cytol-ogy and radiologically confirmed cases,patients were randomly divided into research group and control group, each of 48 cases.Both groups received docetaxel 75 mg/m2 , control group combined with cisplatin 80-100 mg/m2 ,study group combined with oxaliplatin 135 mg/m2 .All patients received chemotherapy once ev-ery 21 d.Both groups of patients in efficacy,disease progression (TTP),the median survival time,Kamofsky score and associated adverse reactions were compared.Results There was no significant difference in effi-ciency( P>0.05) .Kamofsky score improvement rate in the study group was significantly higher than that in control group(66.7% vs 43.8%,P <0.05).The median survival and TTP of study group were (18.2 ± 1.3) months and ( 9.3 ±0.4 ) months, the control group were ( 16.3 ±1.0 ) months and ( 8.7 ± 0.3) months,no statistical significance in two groups (P>0.05).The incidence rates of thrombocytopenia, degree diarrhea, nausea and vomiting, neurotoxicity, liver injury, renal impairment in study group were significantly lower than the control group,neurotoxicity was higher than that of control group(P <0.05). Conclusion Clinical effect of docetaxel combined with oxaliplatin in the treatment of advanced esophageal cancer is satisfactory, and the function of liver and kidney, gastrointestinal and bone marrow suppression and other adverse reactions were reduced than that combined with cisplatin ,it recommend be applied reasonably in clinical,and be closely observed with its possible neurotoxicity by adjusting the dose.