环球中医药
環毬中醫藥
배구중의약
GLOBAL TCM
2013年
z2期
111-112
,共2页
江河%司勇锋%覃扬达%张政%黄波%陆锦龙%翁敬锦
江河%司勇鋒%覃颺達%張政%黃波%陸錦龍%翁敬錦
강하%사용봉%담양체%장정%황파%륙금룡%옹경금
重组人血管内皮抑素/恩度%鼻咽癌%放化疗%抗肿瘤血管形成
重組人血管內皮抑素/恩度%鼻嚥癌%放化療%抗腫瘤血管形成
중조인혈관내피억소/은도%비인암%방화료%항종류혈관형성
Recombinant human endostatin /Endostar%Nasopharyngeal carcinoma%Radiotherapy and chemotherapy%Antiangiogenesis
目的:探讨恩度(重组人血管内皮抑制素)联合放化疗治疗鼻咽癌的有效性和安全性。方法经病理组织学确诊为中晚期鼻咽癌患者60例(Ⅲ期和Ⅳa期),按肿瘤分期进行配对处理后分为:试验组:同步放化疗+恩度治疗30例,对照组:同步放化疗30例。放疗:采用加速器6MVX线常规分割放疗,每周5次,每次2Gy,先面颈联合野加中下颈切线野放疗至36~38Gy,随后改为耳前野加全颈切线野或小面颈联合野加下颈切线野,鼻咽部总剂量为70~78 Gy/7~8周,颈部根治量为60~68 Gy ,预防量为50~56 Gy。化疗:在放疗第1周及第4周配合化疗,化疗方案为卡铂50 mg/m2,d1-5,氟脲嘧啶500 mg/m2,d1-5。化疗期间常规给予止吐、水化、利尿等。其中恩度15 mg加入生理盐水500 ml中静脉滴注,第1~14天连续给药,14天为一个疗程,住院期间给予两个疗程。按照RECIST 标准评价近期疗效,按照NCICTC3.0版标准评价毒性反应。放化疗结束后3个月依据影像学检查评价疗效。结果本组60例均可评价客观疗效,其中治疗组CR 12例,PR16例,SD 1例,PD1例,即客观有效率(RR)为93.3%(28/30),疾病控制率(DCR)为96.7%(29/30);对照组CR 11例,PR15例,SD2例,PD2例,即客观有效率(RR)为86.7%(26/30),疾病控制率(DCR)为93.3%(28/30)。其中治疗组的2年局部无复发生存率、无远处转移生存率、总生存率分别为100%、96.7%、100%,对照组2年局部无复发生存率、无远处转移生存率、总生存率分别为100%、93.3%、100%。两组毒副反应比较无明显差异。结论恩度联合同步放化疗治疗鼻咽癌具有良好的局部控制率,毒性较低,安全性及耐受性比较好,可能对减少鼻咽癌远处转移,延长患者生存时间有一定的作用。
目的:探討恩度(重組人血管內皮抑製素)聯閤放化療治療鼻嚥癌的有效性和安全性。方法經病理組織學確診為中晚期鼻嚥癌患者60例(Ⅲ期和Ⅳa期),按腫瘤分期進行配對處理後分為:試驗組:同步放化療+恩度治療30例,對照組:同步放化療30例。放療:採用加速器6MVX線常規分割放療,每週5次,每次2Gy,先麵頸聯閤野加中下頸切線野放療至36~38Gy,隨後改為耳前野加全頸切線野或小麵頸聯閤野加下頸切線野,鼻嚥部總劑量為70~78 Gy/7~8週,頸部根治量為60~68 Gy ,預防量為50~56 Gy。化療:在放療第1週及第4週配閤化療,化療方案為卡鉑50 mg/m2,d1-5,氟脲嘧啶500 mg/m2,d1-5。化療期間常規給予止吐、水化、利尿等。其中恩度15 mg加入生理鹽水500 ml中靜脈滴註,第1~14天連續給藥,14天為一箇療程,住院期間給予兩箇療程。按照RECIST 標準評價近期療效,按照NCICTC3.0版標準評價毒性反應。放化療結束後3箇月依據影像學檢查評價療效。結果本組60例均可評價客觀療效,其中治療組CR 12例,PR16例,SD 1例,PD1例,即客觀有效率(RR)為93.3%(28/30),疾病控製率(DCR)為96.7%(29/30);對照組CR 11例,PR15例,SD2例,PD2例,即客觀有效率(RR)為86.7%(26/30),疾病控製率(DCR)為93.3%(28/30)。其中治療組的2年跼部無複髮生存率、無遠處轉移生存率、總生存率分彆為100%、96.7%、100%,對照組2年跼部無複髮生存率、無遠處轉移生存率、總生存率分彆為100%、93.3%、100%。兩組毒副反應比較無明顯差異。結論恩度聯閤同步放化療治療鼻嚥癌具有良好的跼部控製率,毒性較低,安全性及耐受性比較好,可能對減少鼻嚥癌遠處轉移,延長患者生存時間有一定的作用。
목적:탐토은도(중조인혈관내피억제소)연합방화료치료비인암적유효성화안전성。방법경병리조직학학진위중만기비인암환자60례(Ⅲ기화Ⅳa기),안종류분기진행배대처리후분위:시험조:동보방화료+은도치료30례,대조조:동보방화료30례。방료:채용가속기6MVX선상규분할방료,매주5차,매차2Gy,선면경연합야가중하경절선야방료지36~38Gy,수후개위이전야가전경절선야혹소면경연합야가하경절선야,비인부총제량위70~78 Gy/7~8주,경부근치량위60~68 Gy ,예방량위50~56 Gy。화료:재방료제1주급제4주배합화료,화료방안위잡박50 mg/m2,d1-5,불뇨밀정500 mg/m2,d1-5。화료기간상규급여지토、수화、이뇨등。기중은도15 mg가입생리염수500 ml중정맥적주,제1~14천련속급약,14천위일개료정,주원기간급여량개료정。안조RECIST 표준평개근기료효,안조NCICTC3.0판표준평개독성반응。방화료결속후3개월의거영상학검사평개료효。결과본조60례균가평개객관료효,기중치료조CR 12례,PR16례,SD 1례,PD1례,즉객관유효솔(RR)위93.3%(28/30),질병공제솔(DCR)위96.7%(29/30);대조조CR 11례,PR15례,SD2례,PD2례,즉객관유효솔(RR)위86.7%(26/30),질병공제솔(DCR)위93.3%(28/30)。기중치료조적2년국부무복발생존솔、무원처전이생존솔、총생존솔분별위100%、96.7%、100%,대조조2년국부무복발생존솔、무원처전이생존솔、총생존솔분별위100%、93.3%、100%。량조독부반응비교무명현차이。결론은도연합동보방화료치료비인암구유량호적국부공제솔,독성교저,안전성급내수성비교호,가능대감소비인암원처전이,연장환자생존시간유일정적작용。
Objective To discuss efficacy and safety of Endostar (Recombinant Human-- Endostatin Injection ) ;combined with the radio-therapy and chemotherapy in the treatment of nasopharyngeal carcinoma .Methods According to the tumor stage ,60 patients with advanced naso-pharyngeal carcinoma (stage Ⅲ and stage Ⅳa) confirmed by histopathology ,were divided into the two groups ,the experimental group has imple-mented in the concurrent chemoradiotherapy combined with Endostar ,the control group carries on the concurrent chemoradiotherapy .Radiation the accelerator 6 MV X-ray conventional radiotherapy ,5 times a week ,each time 2Gy ,first facial-cervical field and the lower neck tangential radio-therapy to 36 ~ 38 Gy ,then the preauricular boost whole neck tangential or facet joint under the neck neck boost tangent field ,total dose naso-pharynx was 70 ~ 78 Gy /7 to 8 weeks ,radical neck is 60 ~ 68Gy ,prevent quantity is 50 ~ 56 Gy .Chemotherapy at first weeks and 4 weeks of radiotherapy combined with chemotherapy ,chemotherapy of carboplatin 50 mg/m2 D1-5 ,5-FU ,500 mg/m2 ,d1-5. During chemotherapy given conventional antiemetic ,hydration ,diuresis .The Endostar 15 mg added 500 ml saline intravenously ,first ~ 14 days continuous administration , 14 days for a course of treatment ,the hospital to give two courses .Efficacy was evaluated according to RECIST standard ,evaluation of toxicity in accordance with the NCICTC3.0 standard .Chemotherapy after the end of March based on the imaging effect evaluation .Results The group of 60 patients could be evaluated objectively the curative effect ,12 cases ,group CR for which PR16 cases ,SD 1 cases ,PD1 cases ,namely the Objective response rate (RR) was 93.3% (28 /30) ,disease control rate (DCR) was 96.7% (29 /30);the control group CR 11 cases ,PR15 cases ,SD2 ca-ses ,PD2 cases ,namely Objective effective rate (RR) was 86.7% (26 /30) ,disease control rate (DCR) was 93.3% (28 /30) .The treatment group 2 years local recurrence-free survival ,distant metastasis-free survival ,overall survival rates were 100% ,96.7% ,100% ,2 years of local re-currence-free survival ,distant metastasis-free survival ,overall survival rates were 100% ,93.3% ,100% in the control group .No significant difference was found between the adverse reaction of two groups .Conclusion Endostar combined with concurrent radiotherapy and chemotherapy in the treatment of nasopharyngeal carcinoma with good local control rate ,low toxicity ,safety and tolerability of relatively good ,may be to reduce distant metastasis of nasopharyngeal carcinoma ,have certain effect to prolong the survival time of patients .