肿瘤基础与临床
腫瘤基礎與臨床
종류기출여림상
JOURNAL OF BASIC AND CLINICAL ONCOLOGY
2014年
3期
232-233,234
,共3页
非小细胞肺癌%厄洛替尼%培美曲塞%维持治疗
非小細胞肺癌%阨洛替尼%培美麯塞%維持治療
비소세포폐암%액락체니%배미곡새%유지치료
non-small cell lung cancer%erlotinib%pemetrexed%maintenance therapy
目的:比较观察厄洛替尼与培美曲塞在晚期非小细胞肺癌( NSCLC)维持治疗中的疗效及毒副反应。方法纳入72例晚期NSCLC患者,一线治疗均给予含铂双药标准一线方案化疗,能顺利完成4周期化疗且病情得到控制者共42例,然后随机均分为2组,分别给予厄洛替尼及培美曲塞维持治疗,比较观察2组的生存情况和毒副反应。结果厄洛替尼组、培美曲塞组的中位无进展生存时间分别为5.8个月、5.5个月,差异无统计学意义( P﹥0.05)。厄洛替尼组主要毒副反应为皮疹和腹泻,培美曲塞组主要毒副反应为消化道反应和血液学毒性,2组骨髓抑制、恶心呕吐、皮疹发生率比较差异有统计学意义( P﹤0.05)。结论厄洛替尼与培美曲塞作为维持治疗方法治疗晚期NSCLC在延长生存期方面作用相似,但厄洛替尼的毒副反应更轻,患者更易于耐受。
目的:比較觀察阨洛替尼與培美麯塞在晚期非小細胞肺癌( NSCLC)維持治療中的療效及毒副反應。方法納入72例晚期NSCLC患者,一線治療均給予含鉑雙藥標準一線方案化療,能順利完成4週期化療且病情得到控製者共42例,然後隨機均分為2組,分彆給予阨洛替尼及培美麯塞維持治療,比較觀察2組的生存情況和毒副反應。結果阨洛替尼組、培美麯塞組的中位無進展生存時間分彆為5.8箇月、5.5箇月,差異無統計學意義( P﹥0.05)。阨洛替尼組主要毒副反應為皮疹和腹瀉,培美麯塞組主要毒副反應為消化道反應和血液學毒性,2組骨髓抑製、噁心嘔吐、皮疹髮生率比較差異有統計學意義( P﹤0.05)。結論阨洛替尼與培美麯塞作為維持治療方法治療晚期NSCLC在延長生存期方麵作用相似,但阨洛替尼的毒副反應更輕,患者更易于耐受。
목적:비교관찰액락체니여배미곡새재만기비소세포폐암( NSCLC)유지치료중적료효급독부반응。방법납입72례만기NSCLC환자,일선치료균급여함박쌍약표준일선방안화료,능순리완성4주기화료차병정득도공제자공42례,연후수궤균분위2조,분별급여액락체니급배미곡새유지치료,비교관찰2조적생존정황화독부반응。결과액락체니조、배미곡새조적중위무진전생존시간분별위5.8개월、5.5개월,차이무통계학의의( P﹥0.05)。액락체니조주요독부반응위피진화복사,배미곡새조주요독부반응위소화도반응화혈액학독성,2조골수억제、악심구토、피진발생솔비교차이유통계학의의( P﹤0.05)。결론액락체니여배미곡새작위유지치료방법치료만기NSCLC재연장생존기방면작용상사,단액락체니적독부반응경경,환자경역우내수。
Objective To compare the efficacy and toxicities between erlotinib and pemetrexed for in the mainte-nance therapy of advanced non-small cell lung cancer( NSCLC ). Methods Seventy-two patients with advanced NSCLC were treated with platinum-based double standard regimen as the first-line drug regimen. 42 patients with disease control after 4 cycles of chemotherapy,was divided into two groups,were given erlotinib and pemetrexed for maintenance therapy separately,the survival and toxicities of the two groups were compared. Results The median progression-free survival time of the erlotinib group was 5. 8 months,and was 5. 5 months of the pemetrexed group (P﹥0. 05). The major toxicities of erlotinib were rash and diarrhea,those of pemetrexed were gastrointestinal reac-tion and haematological toxicities,there were statistically significant differences in the incidence of marrow depres-sion,nausea and vomiting,rash showed between the two groups(P﹤0. 05). Conclusion The survival of erlotinib and pemetrexed is similar in the maintenance treatment of advanced NSCLC,but the toxicities of erlotinib are milder than pemetrexed.