肿瘤药学
腫瘤藥學
종류약학
ANTI-TUMOR PHARMACY
2013年
4期
274-277
,共4页
王家祺%梁永%欧阳征%刘超%欧阳松%唐红宇
王傢祺%樑永%歐暘徵%劉超%歐暘鬆%唐紅宇
왕가기%량영%구양정%류초%구양송%당홍우
贝伐单抗%替莫唑胺%胶质母细胞瘤%临床疗效
貝伐單抗%替莫唑胺%膠質母細胞瘤%臨床療效
패벌단항%체막서알%효질모세포류%림상료효
Bevacizumab%Temozolomide%Glioblastoma
目的观察贝伐单抗联合替莫唑胺治疗胶质母细胞瘤的临床疗效。方法选择2011年5月至2012年7月在我院肿瘤科住院治疗的54例胶质母细胞瘤患者并将其随机分成对照组和治疗组,每组27例患者。对照组给予替莫唑胺治疗,治疗组给予贝伐单抗联合替莫唑胺治疗。治疗后,评价和比较两组患者的临床疗效及不良反应的发生情况。结果治疗6个月后,治疗组和对照组的疾病有效率(RR)分别为37%和26%,治疗组显著高于对照组(P=0.047);治疗组和对照组的疾病控制率(DCR)分别为77.8%和63%,治疗组显著高于对照组(P=0.01);治疗12个月后,治疗组和对照组的 RR 分别为30.8%和16.7%,治疗组显著高于对照组(P=0.01);治疗组和对照组的 DCR 分别为65.4%和37.5%,治疗组显著高于对照组(P<0.0001);两组的不良反应的发生情况相互比较,差异无统计学意义(P>0.05)。结论贝伐单抗联合替莫唑胺治疗胶质母细胞瘤临床疗效较单用替莫唑胺更好,值得临床推广。
目的觀察貝伐單抗聯閤替莫唑胺治療膠質母細胞瘤的臨床療效。方法選擇2011年5月至2012年7月在我院腫瘤科住院治療的54例膠質母細胞瘤患者併將其隨機分成對照組和治療組,每組27例患者。對照組給予替莫唑胺治療,治療組給予貝伐單抗聯閤替莫唑胺治療。治療後,評價和比較兩組患者的臨床療效及不良反應的髮生情況。結果治療6箇月後,治療組和對照組的疾病有效率(RR)分彆為37%和26%,治療組顯著高于對照組(P=0.047);治療組和對照組的疾病控製率(DCR)分彆為77.8%和63%,治療組顯著高于對照組(P=0.01);治療12箇月後,治療組和對照組的 RR 分彆為30.8%和16.7%,治療組顯著高于對照組(P=0.01);治療組和對照組的 DCR 分彆為65.4%和37.5%,治療組顯著高于對照組(P<0.0001);兩組的不良反應的髮生情況相互比較,差異無統計學意義(P>0.05)。結論貝伐單抗聯閤替莫唑胺治療膠質母細胞瘤臨床療效較單用替莫唑胺更好,值得臨床推廣。
목적관찰패벌단항연합체막서알치료효질모세포류적림상료효。방법선택2011년5월지2012년7월재아원종류과주원치료적54례효질모세포류환자병장기수궤분성대조조화치료조,매조27례환자。대조조급여체막서알치료,치료조급여패벌단항연합체막서알치료。치료후,평개화비교량조환자적림상료효급불량반응적발생정황。결과치료6개월후,치료조화대조조적질병유효솔(RR)분별위37%화26%,치료조현저고우대조조(P=0.047);치료조화대조조적질병공제솔(DCR)분별위77.8%화63%,치료조현저고우대조조(P=0.01);치료12개월후,치료조화대조조적 RR 분별위30.8%화16.7%,치료조현저고우대조조(P=0.01);치료조화대조조적 DCR 분별위65.4%화37.5%,치료조현저고우대조조(P<0.0001);량조적불량반응적발생정황상호비교,차이무통계학의의(P>0.05)。결론패벌단항연합체막서알치료효질모세포류림상료효교단용체막서알경호,치득림상추엄。
Objective To explore the curative effects of bevacizumab integrated with temozolomide in the treatment of glioblastoma. Methods Fifty-four patients with glioblastoma admitted in our oncology department between May 2011 and July 2012 were randomly divided into two groups, 27 cases in each group. The control group was treated with temozolomide while the treatment group was treated with bevacizumab integrated with temozolomide. The therapeutic effect and adverse reactions were observed and compared between two groups after treatment. Results After 6 months’treatment, the RR was 37% in the treatment group but 26% in the control group, which was significantly higher in the treatment group (P=0.047); the DCR was 77.8% in the treatment group but 63% in the control group, which was significantly higher in the treatment group (P=0.01). After 12 months’treatment, the RR was 30.8% and 16.7% respectively in the treatment group and control group, also sig-nificantly higher in the treatment group(P=0.01); the DCR in the treatment group and control group were 65.4% and 37.5%respectively, also significantly higher in the treatment group (P<0.0001). However, there was no statistical difference in the side effects between the two groups (P>0.05). Conclusion The bevacizumab integrated with temozolomide in the treatment of glioblastoma had better curative effect than temozolomide alone. It was worthy of being popularized.