{"id":29697,"date":"2024-09-16T07:35:00","date_gmt":"2024-09-16T07:35:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4506965_CN06965_0"},"modified":"2024-09-16T07:35:00","modified_gmt":"2024-09-16T07:35:00","slug":"akesos-ivonescimab-plus-chemo-in-first-line-triple-negative-breast-cancer-showed-promising-preliminary-efficacy-and-good-safety-at-esmo-2024","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=29697","title":{"rendered":"Akeso&#8217;s Ivonescimab plus Chemo in First-Line Triple-negative Breast Cancer Showed Promising Preliminary Efficacy and Good Safety at ESMO 2024"},"content":{"rendered":"<div id=\"dvContent\" readability=\"57\">\n<p><span class=\"legendSpanClass\"><span class=\"xn-location\">HONG KONG<\/span><\/span>, <span class=\"legendSpanClass\"><span class=\"xn-chron\">Sept. 16, 2024<\/span><\/span> \/PRNewswire\/ &#8212; At the 2024 European Society for Medical Oncology (ESMO) Conference, Akeso (<span id=\"spanHghltcf32\">9926.HK<\/span>) published the phase 2 results from its ivonescimab in combination with chemotherapy as a first-line (1L) treatment for triple-negative breast cancer (TNBC). The preliminary data, with only a 10-month median follow-up, revealed that the ivonescimab combination regimen demonstrated excellent efficacy and a favorable safety profile in 1L TNBC. Professor Wang Xiaojia from Zhejiang Provincial Cancer Hospital, a co-primary investigator of the study, presented the findings orally at the conference.<\/p>\n<p>As of <span class=\"xn-chron\">May 31, 2024<\/span>, a total of 30 patients with locally advanced unresectable or metastatic TNBC were enrolled. 80% of patients had a PD-L1 combined positive score (CPS) &lt;10, and 60% of patients had previously received taxane-based neoadjuvant or adjuvant therapy (a proportion higher than that observed in similar studies involving targeted drugs).<\/p>\n<p><b>Although the follow-up period is relatively short and the data are not yet mature, the study still demonstrates that the ivonescimab combination regimen demonstrates excellent progression-free survival (PFS) benefits for TNBC patients, with safety consistent with previous<\/b><b> ivonescimab<\/b><b>-related studies.<\/b><\/p>\n<ul type=\"disc\">\n<li>Ivonescimab combination regimen demonstrated high efficacy in tumor response and disease control, with an objective response rate (ORR) of 72.4% and a disease control rate (DCR) of 100%, including a complete response (CR) rate of 6.9%.\n<ul type=\"disc\">\n<li>As of the latest update, five additional patients have achieved partial response (PR) (Among them, four newly&nbsp;evaluable patients all achieved a PR, and one patient who previouly had stable disease also achieved a PR ), leading to an adjusted ORR of approximately 78.8% and DCR of 100%.<\/li>\n<\/ul>\n<\/li>\n<li>Ivonescimab combination regimen showed a promising trend towards improved long-term survival benefits, with a median progression-free survival (PFS) of 9.3 months (6.24 months -NE), and a 6-month PFS rate of 73.3%.<\/li>\n<li>In the PD-L1 CPS\u226510 population, the&nbsp;ORR was 83.3%, and the median PFS was not yet reached.<\/li>\n<li>In the PD-L1 CPS &lt;1 population, the&nbsp;ORR was 86.7%, with a median PFS of 9.3 months (5.26 months-NE).\n<ul type=\"disc\">\n<li>As of the latest update, two additional patients in the PD-L1 CPS &lt;1 group have achieved PR, resulting in an adjusted&nbsp;ORR of 88.2%.<\/li>\n<\/ul>\n<\/li>\n<li>In the PD-L1 CPS &lt;10 population, the&nbsp;ORR was 69.6%, with a median PFS of 9.3 months (5.55 months-NE).\n<ul type=\"disc\">\n<li>As of the latest update, five additional patients in this group have achieved PR, leading to an adjusted&nbsp;ORR of approximately 77.8%.<\/li>\n<\/ul>\n<\/li>\n<li>Ivonescimab combined with chemotherapy as a first-line treatment for TNBC exhibited an acceptable safety profile. The most common treatment-related adverse events (TRAEs) were predominantly grade 1-2 and manageable, consistent with previous studies. There were no TRAEs that led to permanent treatment discontinuation or death.<\/li>\n<\/ul><\/div>\n<p>Source: Akeso, Inc.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>HONG KONG, Sept. 16, 2024 \/PRNewswire\/ &#8212; At the 2024 European Society for Medical Oncology (ESMO) Conference, Akeso (9926.HK) published the phase 2 results from its ivonescimab in combination with chemotherapy as a first-line (1L) treatment for triple-negative breast cancer (TNBC). The preliminary data, with only a 10-month median follow-up, revealed that the ivonescimab combination [&hellip;]<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[20],"tags":[],"class_list":["post-29697","post","type-post","status-publish","format-standard","hentry","category-business-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Akeso&#039;s Ivonescimab plus Chemo in First-Line Triple-negative Breast Cancer Showed Promising Preliminary Efficacy and Good Safety at ESMO 2024 - My Blog<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/transmediavictoria.net.au\/?p=29697\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Akeso&#039;s Ivonescimab plus Chemo in First-Line Triple-negative Breast Cancer Showed Promising Preliminary Efficacy and Good Safety at ESMO 2024 - My Blog\" \/>\n<meta property=\"og:description\" content=\"HONG KONG, Sept. 16, 2024 \/PRNewswire\/ &#8212; At the 2024 European Society for Medical Oncology (ESMO) Conference, Akeso (9926.HK) published the phase 2 results from its ivonescimab in combination with chemotherapy as a first-line (1L) treatment for triple-negative breast cancer (TNBC). 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