中华耳鼻咽喉头颈外科杂志
中華耳鼻嚥喉頭頸外科雜誌
중화이비인후두경외과잡지
CHINESE JOURNAL OF OTORHINOLARYNGOLOGY HEAD AND NECK SURGERY
2012年
11期
931-936
,共6页
安常明%王铮%韩志楷%李正江%唐平章%马洁
安常明%王錚%韓誌楷%李正江%唐平章%馬潔
안상명%왕쟁%한지해%리정강%당평장%마길
甲状腺肿瘤%肿瘤,实验性%苯磺酸盐类%多柔比星%抗肿瘤药联合化疗方案
甲狀腺腫瘤%腫瘤,實驗性%苯磺痠鹽類%多柔比星%抗腫瘤藥聯閤化療方案
갑상선종류%종류,실험성%분광산염류%다유비성%항종류약연합화료방안
Thyroid neoplasms%Neoplasms experimental%Benzenesulfonates%Doxorubicin%Artineoplastic combined chemotherapy protocols
目的 评估索拉非尼、脂质体阿霉素及两者联合应用治疗甲状腺低分化癌裸鼠移植瘤的疗效.方法 用脂质体阿霉素和索拉非尼治疗甲状腺低分化癌裸鼠皮下移植瘤模型,裸鼠按随机数字法分为7组,为空白对照组、溶剂对照组、单药脂质体阿霉素组、索拉非尼组、低剂量联合组、中剂量联合组和高剂量联合组,观察肿瘤生长情况,评估两种药物的疗效.结果 利用索拉非尼和脂质体阿霉素对甲状腺低分化癌模型进行化疗,空白对照组、溶剂对照组、单药脂质体阿霉素组、索拉非尼组、低剂量联合组、中剂量联合组、高剂量联合组化疗结束后的最终肿瘤体积分别为(1274.13±393.76) mm3、(1060.00±469.05) mm3、(726.76±488.22) mm3、(451.54±97.75) mm3、(518.37±164.44) mm3、(310.51±210.53) mm3和(228.44±129.21) mm3,各组移植瘤最终瘤体质量分别为(1.13 ±0.42)g、(0.91 ±0.39)g、(0.78 ±0.45)g、(0.55 ±0.17)g、(0.52±0.19)g、(0.34±0.21)g和(0.19 ±0.09)g,单药脂质体阿霉素组、索拉非尼组、低剂量联合组、中剂量联合组、高剂量联合组的抑瘤率分别为30.8%、40.8%、42.3%、62.9%和72.6%,高剂量联合组抑瘤率除与中剂量联合组差异无统计学意义外(P =0.357)均高于其余各组,中剂量联合组优于单药脂质体阿霉素组(P=0.001),而与索拉非尼组差异无统计学意义(P =0.192).各治疗组平均瘤体质量均明显低于空白对照组(F=9.985,P<0.05).各治疗组均无荷瘤鼠死亡,高剂量联合组荷瘤鼠体质量在治疗过程中较其余各治疗组有明显减轻(F =14.792,P<0.05).结论 脂质体阿霉素和索拉非尼无论是单药还是联合应用对甲状腺低分化癌移植瘤模型均有明显的抑瘤作用,中剂量联合疗效明显且副作用小.
目的 評估索拉非尼、脂質體阿黴素及兩者聯閤應用治療甲狀腺低分化癌裸鼠移植瘤的療效.方法 用脂質體阿黴素和索拉非尼治療甲狀腺低分化癌裸鼠皮下移植瘤模型,裸鼠按隨機數字法分為7組,為空白對照組、溶劑對照組、單藥脂質體阿黴素組、索拉非尼組、低劑量聯閤組、中劑量聯閤組和高劑量聯閤組,觀察腫瘤生長情況,評估兩種藥物的療效.結果 利用索拉非尼和脂質體阿黴素對甲狀腺低分化癌模型進行化療,空白對照組、溶劑對照組、單藥脂質體阿黴素組、索拉非尼組、低劑量聯閤組、中劑量聯閤組、高劑量聯閤組化療結束後的最終腫瘤體積分彆為(1274.13±393.76) mm3、(1060.00±469.05) mm3、(726.76±488.22) mm3、(451.54±97.75) mm3、(518.37±164.44) mm3、(310.51±210.53) mm3和(228.44±129.21) mm3,各組移植瘤最終瘤體質量分彆為(1.13 ±0.42)g、(0.91 ±0.39)g、(0.78 ±0.45)g、(0.55 ±0.17)g、(0.52±0.19)g、(0.34±0.21)g和(0.19 ±0.09)g,單藥脂質體阿黴素組、索拉非尼組、低劑量聯閤組、中劑量聯閤組、高劑量聯閤組的抑瘤率分彆為30.8%、40.8%、42.3%、62.9%和72.6%,高劑量聯閤組抑瘤率除與中劑量聯閤組差異無統計學意義外(P =0.357)均高于其餘各組,中劑量聯閤組優于單藥脂質體阿黴素組(P=0.001),而與索拉非尼組差異無統計學意義(P =0.192).各治療組平均瘤體質量均明顯低于空白對照組(F=9.985,P<0.05).各治療組均無荷瘤鼠死亡,高劑量聯閤組荷瘤鼠體質量在治療過程中較其餘各治療組有明顯減輕(F =14.792,P<0.05).結論 脂質體阿黴素和索拉非尼無論是單藥還是聯閤應用對甲狀腺低分化癌移植瘤模型均有明顯的抑瘤作用,中劑量聯閤療效明顯且副作用小.
목적 평고색랍비니、지질체아매소급량자연합응용치료갑상선저분화암라서이식류적료효.방법 용지질체아매소화색랍비니치료갑상선저분화암라서피하이식류모형,라서안수궤수자법분위7조,위공백대조조、용제대조조、단약지질체아매소조、색랍비니조、저제량연합조、중제량연합조화고제량연합조,관찰종류생장정황,평고량충약물적료효.결과 이용색랍비니화지질체아매소대갑상선저분화암모형진행화료,공백대조조、용제대조조、단약지질체아매소조、색랍비니조、저제량연합조、중제량연합조、고제량연합조화료결속후적최종종류체적분별위(1274.13±393.76) mm3、(1060.00±469.05) mm3、(726.76±488.22) mm3、(451.54±97.75) mm3、(518.37±164.44) mm3、(310.51±210.53) mm3화(228.44±129.21) mm3,각조이식류최종류체질량분별위(1.13 ±0.42)g、(0.91 ±0.39)g、(0.78 ±0.45)g、(0.55 ±0.17)g、(0.52±0.19)g、(0.34±0.21)g화(0.19 ±0.09)g,단약지질체아매소조、색랍비니조、저제량연합조、중제량연합조、고제량연합조적억류솔분별위30.8%、40.8%、42.3%、62.9%화72.6%,고제량연합조억류솔제여중제량연합조차이무통계학의의외(P =0.357)균고우기여각조,중제량연합조우우단약지질체아매소조(P=0.001),이여색랍비니조차이무통계학의의(P =0.192).각치료조평균류체질량균명현저우공백대조조(F=9.985,P<0.05).각치료조균무하류서사망,고제량연합조하류서체질량재치료과정중교기여각치료조유명현감경(F =14.792,P<0.05).결론 지질체아매소화색랍비니무론시단약환시연합응용대갑상선저분화암이식류모형균유명현적억류작용,중제량연합료효명현차부작용소.
Objective To evaluate the therapeutic effects of sorafenib and liposome doxorubicin on poorly differentiated thyroid carcinoma (PDTC) xenografts in nude mice.Methods Sorafenib and liposome doxorubicin were applied to PDTC xenografts in nude mice.The mice were randomized into seven groups:blank control(A),vehicle control(B),single liposome doxorubicin group(C),single sorafenib group(D),liposome doxorubicin combined with low dose sorafenib group (E),combined group with medium dosage of sorafenib(F),combined group with high-dose of sorafenib(G).The volume,weight and growth inhibition rate of tumours were measured to evaluate the therapeutic effects of the drugs.Results Sorafenib and liposome doxorubicin showed significant antitumor activity in the PDTC xenografts.The mean tumor volumes of seven groups were (1274.13 ± 393.76) mm3 (1060.00 ±469.05)mm3 (726.76 ±488.22)mm3,(451.54 ±97.75) mm3,(518.37 ± 164.44) mm3,(310.51 ± 210.53)mm3,and (228.44 ± 129.21)mm3,respectively.The mean tumor weights of the seven groups were (1.13±0.42) g,(0.91 ± 0.39) g,(0.78 ±0.45)g,(0.55 ±0.17)g,(0.52 ±0.19)g,(0.34 ±0.21)g,and (0.19 ±0.09)g separately.The tumor inhibition rates of group C to G were 30.8%,40.8%,42.3%,62.9%,72.6% separately.Conclusions Sorafenib and liposome doxorubicin,no matter for single agent or in combination,showed significant antitumor activity in the PDTC PDTC xenografts in vivo.The tumour-inhibited effect of single sorafenib is better than that of single liposome doxorubicin.Liposome doxorubicin combined with medium dosage of sorafenib had a better therapeutic effect and less side effects.