![肿瘤药物治疗方案及综合评价](https://wfqqreader-1252317822.image.myqcloud.com/cover/13/43604013/b_43604013.jpg)
HER2阳性乳腺癌二线治疗
方案Ⅰ 拉帕替尼联合卡培他滨vs卡培他滨
![](https://epubservercos.yuewen.com/B8A9D8/22919013101368106/epubprivate/OEBPS/Images/T154_297_1341_2007_1633_147992.jpg?sign=1739611185-vwUKpbLserAHgwKhJTIxvtLf4XX2wi4c-0-3b61739dcc8e6aef11356eeaa95c6020)
方案评价
![](https://epubservercos.yuewen.com/B8A9D8/22919013101368106/epubprivate/OEBPS/Images/T154_287_1733_2038_2831_148448.jpg?sign=1739611185-KMgfom5WE0D4RGEcuEBPypK4LDMyT3i1-0-e44a2a5f903359e93c78d59c5571f74b)
续表
![](https://epubservercos.yuewen.com/B8A9D8/22919013101368106/epubprivate/OEBPS/Images/T155_238_343_1952_1049_94899.jpg?sign=1739611185-XdlzG8WH3KWVnY4q66qrjC7yAOj1lIHH-0-c3c75c0492887e4124678f5464224eda)
点评
本研究为一项Ⅲ期随机对照研究,评估HER2阳性晚期乳腺癌患者在蒽环、紫杉类化疗和曲妥珠单抗治疗失败后,卡培他滨单纯化疗与拉帕替尼联合卡培他滨的疗效。结果显示,联合拉帕替尼的方案较卡培他滨单药更有效,PFS延长。基于本项研究结果,拉帕替尼被批准用于蒽环、紫杉类化疗和曲妥珠单抗治疗失败后HER2阳性晚期乳腺癌的二线治疗。拉帕替尼主要的不良事件包括腹泻和皮疹。
(安 欣 史艳侠)
参考文献
[1] CAMERON D,CASEY M,PRESS M,et al.A phaseⅢ randomized comparison of lapatinib plus capecitabine versus capecitabine alone in women with advanced breast cancer that has progressed on trastuzumab:updated efficacy and biomarker analyses.Breast Cancer Res Treat,2008,112(3):533-543.
方案Ⅱ TDM-1 vs拉帕替尼联合卡培他滨
![](https://epubservercos.yuewen.com/B8A9D8/22919013101368106/epubprivate/OEBPS/Images/T155_238_2326_1952_2694_147993.jpg?sign=1739611185-ssrwaWBHW3oKNB52oL7vSKppIIELRWhi-0-f72e10ff1dc4866c054c9848830fe39e)
方案评价
![](https://epubservercos.yuewen.com/B8A9D8/22919013101368106/epubprivate/OEBPS/Images/T156_287_349_2018_2121_148453.jpg?sign=1739611185-dubJO3AaQ4WDAceyXMxdVOaPTSI99JXO-0-0c1475bcac3dfd41962c5ab62954d82b)
点评
该研究入组患者为既往接受过曲妥珠单抗和紫杉类药物化疗的晚期HER2阳性乳腺癌。在中期分析时观察到TDM-1组具有生存优势,因此允许拉帕替尼联合卡培他滨组交叉至TDM-1组,结果仍显示TDM-1能显著延长患者的生存。在总体不良事件方面,TDM-1组3~4级不良事件发生率更低,最主要的不良事件为血小板下降、转氨酶升高和贫血,而拉帕替尼联合卡培他滨组主要的不良事件为腹泻、手足综合征和呕吐。TDM-1较拉帕替尼联合卡培他滨方案优效低毒,因此被推荐用于曲妥珠单抗失败的晚期HER2阳性乳腺癌的新的标准二线方案。
(安 欣 史艳侠)
参考文献
[1] DIÉRAS V,MILES D,VERMA S,et al.Trastuzumab emtansine versus capecitabine plus lapatinib in patients with previously treated HER2-positive advanced breast cancer(EMILIA):a descriptive analysis of final overall survival results from a randomised,open-label,phase 3 trial.Lancet Oncol,2017,18(6):732-742.