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辉瑞公司的抗癌药物组合在晚期研究中提高了总生存率
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brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"media_name":"Reuters","id":"1036604489","head_image":"https://static.tigerbbs.com/443ce19704621c837795676028cec868"},"pubTimestamp":1728557104,"share":"https://www.laohu8.com/m/news/2474492713?lang=&edition=full","pubTime":"2024-10-10 18:45","market":"us","language":"zh","title":"辉瑞公司的抗癌药物组合在晚期研究中提高了总生存率","url":"https://stock-news.laohu8.com/highlight/detail?id=2474492713","media":"Reuters","summary":" 路透10月10日 - 辉瑞 周四称，在一项晚期研究中，其药物Talzenna和Xtandi的组合有助于延长一种晚期前列腺癌患者的生命。辉瑞公司说，与Xtandi单药相比，这种联合用药在转移性抗性前列腺癌 患者的总生存期方面有明显改善，无论是否存在基因突变。据辉瑞公司称，约有10%-20%的前列腺癌患者会在确诊后5到7年内患上mCRPC。辉瑞表示，它计划与全球卫生机构分享研究结果，以便更新Talzenna的标签。","content":"<html><body><p>((自动化翻译由路透提供，请见免责声明 ))</p><p> 路透10月10日 - <a href=\"https://laohu8.com/S/PFE\">辉瑞</a> 周四称，在一项晚期研究中，其药物Talzenna和Xtandi的组合有助于延长一种晚期前列腺癌患者的生命。</p><p>辉瑞公司说，与Xtandi单药相比，这种联合用药在转移性抗性前列腺癌(mCRPC) 患者的总生存期方面有明显改善，无论是否存在基因突变。 </p><p>总生存期是指患者在确诊或开始治疗后的生存时间。</p><p>mCRPC是一种癌症已扩散到身体其他部位的晚期疾病，通常预后较差。据辉瑞公司称，约有10%-20%的前列腺癌患者会在确诊后5到7年内患上mCRPC。 </p><p>Talzenna-Xtandi组合去年获得美国食品药品管理局批准 (link)，用于治疗有一种基因突变的mCRPC患者。</p><p>辉瑞表示，它计划与全球卫生机构分享研究结果，以便更新Talzenna的标签。</p><p>美国食品和药物管理局去年还批准了 (link) <a href=\"https://laohu8.com/S/AZN\">阿斯利康</a>公司的Lynparza与激素疗法阿比特龙联用，治疗有一种基因突变的mCRPC患者。 </p></body></html>","collect":0,"html":"<!DOCTYPE html>\n<html>\n<head>\n<meta http-equiv=\"Content-Type\" content=\"text/html; charset=utf-8\" />\n<meta name=\"viewport\" content=\"width=device-width,initial-scale=1.0,minimum-scale=1.0,maximum-scale=1.0,user-scalable=no\"/>\n<meta name=\"format-detection\" content=\"telephone=no,email=no,address=no\" />\n<title>辉瑞公司的抗癌药物组合在晚期研究中提高了总生存率</title>\n<style type=\"text/css\">\na,abbr,acronym,address,applet,article,aside,audio,b,big,blockquote,body,canvas,caption,center,cite,code,dd,del,details,dfn,div,dl,dt,\nem,embed,fieldset,figcaption,figure,footer,form,h1,h2,h3,h4,h5,h6,header,hgroup,html,i,iframe,img,ins,kbd,label,legend,li,mark,menu,nav,\nobject,ol,output,p,pre,q,ruby,s,samp,section,small,span,strike,strong,sub,summary,sup,table,tbody,td,tfoot,th,thead,time,tr,tt,u,ul,var,video{ font:inherit;margin:0;padding:0;vertical-align:baseline;border:0 }\nbody{ font-size:16px; line-height:1.5; color:#999; background:transparent; }\n.wrapper{ overflow:hidden;word-break:break-all;padding:10px; }\nh1,h2{ font-weight:normal; line-height:1.35; margin-bottom:.6em; }\nh3,h4,h5,h6{ line-height:1.35; margin-bottom:1em; }\nh1{ font-size:24px; }\nh2{ font-size:20px; }\nh3{ font-size:18px; }\nh4{ font-size:16px; }\nh5{ font-size:14px; }\nh6{ font-size:12px; }\np,ul,ol,blockquote,dl,table{ margin:1.2em 0; }\nul,ol{ margin-left:2em; }\nul{ list-style:disc; }\nol{ list-style:decimal; }\nli,li p{ margin:10px 0;}\nimg{ max-width:100%;display:block;margin:0 auto 1em; }\nblockquote{ color:#B5B2B1; border-left:3px solid #aaa; padding:1em; }\nstrong,b{font-weight:bold;}\nem,i{font-style:italic;}\ntable{ width:100%;border-collapse:collapse;border-spacing:1px;margin:1em 0;font-size:.9em; }\nth,td{ padding:5px;text-align:left;border:1px solid #aaa; }\nth{ font-weight:bold;background:#5d5d5d; }\n.symbol-link{font-weight:bold;}\n/* header{ border-bottom:1px solid #494756; } */\n.title{ margin:0 0 8px;line-height:1.3;color:#ddd; }\n.meta {color:#5e5c6d;font-size:13px;margin:0 0 .5em; }\na{text-decoration:none; color:#2a4b87;}\n.meta .head { display: inline-block; overflow: hidden}\n.head .h-thumb { width: 30px; height: 30px; margin: 0; padding: 0; border-radius: 50%; float: left;}\n.head .h-content { margin: 0; padding: 0 0 0 9px; float: left;}\n.head .h-name {font-size: 13px; color: #eee; margin: 0;}\n.head .h-time {font-size: 11px; color: #7E829C; margin: 0;line-height: 11px;}\n.small {font-size: 12.5px; display: inline-block; transform: scale(0.9); -webkit-transform: scale(0.9); transform-origin: left; -webkit-transform-origin: left;}\n.smaller {font-size: 12.5px; display: inline-block; transform: scale(0.8); -webkit-transform: scale(0.8); transform-origin: left; -webkit-transform-origin: left;}\n.bt-text {font-size: 12px;margin: 1.5em 0 0 0}\n.bt-text p {margin: 0}\n</style>\n</head>\n<body>\n<div class=\"wrapper\">\n<header>\n<h2 class=\"title\">\n辉瑞公司的抗癌药物组合在晚期研究中提高了总生存率\n</h2>\n\n<h4 class=\"meta\">\n\n\n<a class=\"head\" href=\"https://laohu8.com/wemedia/1036604489\">\n\n\n<div class=\"h-thumb\" style=\"background-image:url(https://static.tigerbbs.com/443ce19704621c837795676028cec868);background-size:cover;\"></div>\n\n<div class=\"h-content\">\n<p class=\"h-name\">Reuters </p>\n<p class=\"h-time\">2024-10-10 18:45</p>\n</div>\n\n</a>\n\n\n</h4>\n\n</header>\n<article>\n<html><body><p>((自动化翻译由路透提供，请见免责声明 ))</p><p> 路透10月10日 - <a href=\"https://laohu8.com/S/PFE\">辉瑞</a> 周四称，在一项晚期研究中，其药物Talzenna和Xtandi的组合有助于延长一种晚期前列腺癌患者的生命。</p><p>辉瑞公司说，与Xtandi单药相比，这种联合用药在转移性抗性前列腺癌(mCRPC) 患者的总生存期方面有明显改善，无论是否存在基因突变。 </p><p>总生存期是指患者在确诊或开始治疗后的生存时间。</p><p>mCRPC是一种癌症已扩散到身体其他部位的晚期疾病，通常预后较差。据辉瑞公司称，约有10%-20%的前列腺癌患者会在确诊后5到7年内患上mCRPC。 </p><p>Talzenna-Xtandi组合去年获得美国食品药品管理局批准 (link)，用于治疗有一种基因突变的mCRPC患者。</p><p>辉瑞表示，它计划与全球卫生机构分享研究结果，以便更新Talzenna的标签。</p><p>美国食品和药物管理局去年还批准了 (link) <a href=\"https://laohu8.com/S/AZN\">阿斯利康</a>公司的Lynparza与激素疗法阿比特龙联用，治疗有一种基因突变的mCRPC患者。 </p></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"LU1066051498.USD":"HSBC GIF GLOBAL EQUITY VOLATILITY FOCUSED \"AM2\" (USD) INC","BK4534":"瑞士信贷持仓","LU1066053197.SGD":"HSBC GIF GLOBAL EQUITY VOLATILITY FOCUSED \"AM3\" (SGDHDG) INC","BK4533":"AQR资本管理(全球第二大对冲基金)","BK4007":"制药","LU0122379950.USD":"贝莱德世界健康科学A2","IE000M9KFDE8.USD":"NEUBERGER BERMAN US LARGE CAP VALUE \"A\" (USD) ACC","IE0002270589.USD":"LEGG MASON CLEARBRIDGE 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