DESTINY-Breast11與DESTINY-Breast05兩項研究入選主席研討會(Presidential Symposium),凸顯德曲妥珠單抗在治療HER2陽性早期乳腺癌中的潛在價值
TROPION-Breast02研究數據將展示德達博妥單抗在轉移性三陰性乳腺癌這一最具侵襲性的乳腺癌分型中的治療潛力
POTOMAC研究的無病生存期數據與MATTERHORN研究的生存期數據將展示度伐利尤單抗在早期膀胱癌與胃癌治療中的獲益
上海2025年10月14日 /美通社/ -- 阿斯利康將于2025年10月17日至21日召開的歐洲腫瘤內科學會(ESMO)年會上,憑借?業領先的多樣化產品與管線布局的全新研究數據,進一步彰顯其重新定義癌癥治療格局的雄心壯志。
本次大會上,阿斯利康將公布逾95項摘要,涵蓋9款已獲得批準藥物及9款潛在新藥,包括2項入選重要主席研討會(Presidential Symposium)的摘要以及26項口頭報告。
其中主要亮點包括:
阿斯利康全球執行副總裁、全球腫瘤研發負責人高書璨(Susan Galbraith)表示:"我們正加速推進多元創新療法管線,以變革乳腺癌患者的治療格局。在本屆ESMO大會上,我們將公布TROPION-Breast02、DESTINY-Breast11和DESTINY-Breast05研究的數據和重要進展。同時,我們也將展示新一代潛在抗腫瘤新藥的數據,包括saruparib聯合新型激素療法用于前列腺癌領域,靶向葉酸受體的抗體偶聯藥物torvu-sam用于卵巢癌領域,以及rilvegostomig用于在非小細胞肺癌領域。"
阿斯利康全球執行副總裁,腫瘤業務負責人Dave Fredrickson表示:"我們業界領先的腫瘤產品組合在本次ESMO持續展現強勁勢頭,首次公布了四項關鍵研究的數據。其中,不僅有德曲妥珠單抗和德達博妥單抗在乳腺癌領域的重大進展,度伐利尤單抗的POTOMAC試驗結果也證明了免疫療法為早期膀胱癌治療帶來的益處,進而闡釋我們的策略——將前沿治療引入癌癥早期這一患者最能夠獲益的階段。"
其他亮點包括:
阿斯利康與第?三共聯合開發和商業化德曲妥珠單抗與德達博妥單抗;與默沙東(默沙東是美國新澤西州羅威市默克公司的公司商號)聯合開發和商業化奧拉帕利;與和黃醫藥合作開發和商業化賽沃替尼。Rilvegostomig是一種靶向PD-1和TIGIT的雙特異性抗體,其中TIGIT部分源自Compugen公司臨床階段的抗TIGIT抗體COM902。
阿斯利康在2025年ESMO年會期間的重要演講[1]
主要作者 |
摘要標題 |
報告詳情(CEST) |
抗體偶聯藥物 |
||
Harbeck, N |
DESTINY-Breast11: neoadjuvant trastuzumab deruxtecan |
Abstract #291O Presidential 1 18 October 2025 4:30 PM |
Geyer, C |
Trastuzumab deruxtecan (T-DXd) vs trastuzumab |
Abstract #LBA1 Presidential 1 18 October 2025 4:52 PM |
Dent, R. |
First-line (1L) datopotamab deruxtecan (Dato-DXd) vs |
Abstract #LBA21 Proffered Paper Session 19 October 2025 9:25 AM |
Loibl, S |
Trastuzumab deruxtecan (T-DXd) + pertuzumab vs taxane |
Abstract #LBA18 Proffered Paper Session 19 October 2025 8:30 AM |
Rha, SY |
Datopotamab deruxtecan (Dato-DXd) + rilvegostomig |
Abstract #3072MO Mini Oral Session 17 October 2025 4:10 PM |
Oaknin, A |
First-in-human study of AZD5335, a folate receptor α |
Abstract #1065MO Mini Oral Session 19 October 2025 10:53 AM |
Schmid, P |
Datopotamab deruxtecan (Dato-DXd) + durvalumab (D) as |
Abstract #555MO Mini Oral Session 20 October 2025 10:50 AM |
Raghav, K |
Trastuzumab deruxtecan (T DXd) in patients (pts) with |
Abstract #737P Poster Session |
Peng, Z |
Trastuzumab deruxtecan (T-DXd) in patients (pts) with |
Abstract #2105P Poster Session |
Shen, L |
Risk of hepatitis B virus reactivation (HBVr) in patients |
Abstract #2175P Poster Session |
Pietrantonio, F |
Trastuzumab deruxtecan (T-DXd) vs ramucirumab (RAM) |
Abstract #2099P Poster Session |
Makker, V |
Trastuzumab deruxtecan (T-DXd) for pretreated patients |
Abstract #957P Poster Session |
Lee, J-Y |
Trastuzumab deruxtecan (T-DXd) in pretreated patients |
Abstract #145P Poster Session |
免疫腫瘤學 |
||
Tabernero, J |
MATTERHORN Phase III trial of Imfinzi (durvalumab) |
Abstract #LBA81 Proffered Paper Session 17 October 2025 2:00 PM |
De Santis, M |
Durvalumab (D) in Combination with Bacillus Calmette- |
Abstract #LBA108 Proffered Paper Session 17 October 2025 2:10 PM |
Larkin, J |
First results from RAMPART: An international phase 3 |
Abstract #LBA93 Proffered Paper Session 18 October 2025 9:20 AM |
Aghajanian, C |
Durvalumab + paclitaxel/carboplatin + bevacizumab |
Abstract #LBA44 Mini Oral Session 19 October 2025 11:31 AM |
Goss, G |
CCTG BR.31: Adjuvant durvalumab (D) in resected non- |
Abstract #LBA68 Mini Oral Session 20 October 2025 3:20 PM |
Heymach, J |
Association of radiomic features ± on-treatment ctDNA |
Abstract #LBA70 Mini Oral Session 20 October 2025 3:50 PM |
Wermke, M |
Tarlatamab with first-line chemoimmunotherapy for |
Abstract #2757O Proffered Paper Session 18 October 2025 8:30 AM |
Loibl, S |
Durvalumab in Combination with Neoadjuvant |
Abstract #292MO Mini Oral Session 19 October 2025 10:15 AM |
Van der Heijden, M |
Health-related quality of life (HRQoL) from the NIAGARA |
Abstract #3069MO Mini Oral Session 17 October 2025 4:00 PM |
Sangro, B |
Pooled efficacy and safety outcomes with tremelimumab |
Abstract #1494P Poster Session |
Westin, S |
Durvalumab plus carboplatin/paclitaxel followed by |
Abstract #1117P Poster Session |
Leal, TA |
Global quantitative assessment of multidisciplinary team |
Abstract #1794P Poster Session |
Reck, M |
Neoadjuvant durvalumab (D) + chemotherapy (CT) |
Abstract #LBA65 Proffered Paper Session 18 October 2025 9:15 AM |
Maruki, Y |
CELEBRATE Study (JCOG2107E): A Multicenter, Open- |
Abstract #1734TiP Poster Session |
Oudard, S |
A phase IIIb, open-label, single-arm, global study of |
Abstract #3133eTiP ePoster Session |
雙特異性抗體 |
||
Chul Cho, B |
Efficacy and Safety of Rilvegostomig, an Anti-PD-1/TIGIT |
Abstract #1853MO Mini Oral Session 20 October 2025 10:25 AM |
Slomovitz, BM |
A randomized Phase 3 study of first-line (1L) trastuzumab |
Abstract #1223TiP Poster Session |
Naidoo, J |
ARTEMIDE-Lung04: A Phase 3, randomised, double-blind, programmed cell death ligand-1 (PD-L1) expression ≥50% |
Abstract #2025TiP Poster Session |
腫瘤驅動因子和耐藥性 |
||
Jänne, PA |
FLAURA2: exploratory overall survival (OS) analysis in |
Abstract #LBA77 Proffered Paper Session 17 October 2025 4:56 PM |
Mayer, E |
Patient-reported outcomes (PROs) from the SERENA-6 |
Abstract #486MO Mini Oral Session 20 October 2025 10:25 AM |
Arriola, E |
Molecular residual disease (MRD) analysis from the |
Abstract #1817MO Mini Oral Session 20 October 2025 2:55 PM |
Park, YH |
Visual symptom questionnaire results from SERENA-6, a |
Abstract #528P Poster Session |
Chu, Q |
SAVANNAH: Safety and tolerability of osimertinib (osi) + |
Abstract #1955P Poster Session |
Rotow, J |
MET testing and treatment (tx) sequencing after |
Abstract #1967P Poster Session |
Yu, Y |
ctDNA analysis in phase 3 SACHI trial: Savolitinib (savo) |
Abstract #1954P Poster Session |
DNA損傷應答 |
||
Azad, AA |
First interim efficacy analysis of the Phase 1/2 PETRANHA |
Abstract #2384MO Mini Oral Session 17 October 2025 2:35 PM |
Fizazi, K |
A Phase 3 study of capivasertib (capi) + abiraterone (abi) |
Abstract #2383O Proffered Paper Session 19 October 2025 11:19 AM |
Rugo, HS |
Capivasertib with fulvestrant as first- and second-line |
Abstract #526P Poster Session |
Gao, Q |
Final overall survival (OS) analysis of L-MOCA: olaparib |
Abstract #1090P Poster Session |
AI驅動的臨床試驗 |
||
Gonuguntla, HK |
Real-World Validation of AI-defined Lung Nodule |
Abstract #2978P Poster Session |
[1]阿斯利康在2025年ESMO年會將公布逾90個摘要,涵蓋其產品和管線中的分子藥物
關于阿斯利康腫瘤領域的研究
阿斯利康正引領著腫瘤領域的?場革命,致力提供多元化的腫瘤治療方案,以科學探索腫瘤領域的復雜性,發現、研發并向患者提供改變生命的藥物。
阿斯利康專注于最具挑戰性的腫瘤疾病,通過持續不斷的創新,阿斯利康已經建立了行業領先的多元化的 產品組合和管線,持續推動醫療實踐變?,改變患者體驗。
阿斯利康以期重新定義癌癥治療并在未來攻克癌癥。
關于阿斯利康
阿斯利康(LSE/STO/Nasdaq: AZN)是?家科學至上的全球生物制藥企業,專注于研發、生產及營銷處方類藥品,重點關注腫瘤、罕見病以及包括心血管腎臟及代謝、呼吸及免疫在內的生物制藥等領域。阿斯利康全球總部位于英國劍橋,業務遍布超過125個國家,創新藥物惠及全球數百萬患者。更多信息,請訪問www.astrazeneca.com。
關于阿斯利康中國
阿斯利康自1993年進入中國以來,專注中國患者需求最迫切的治療領域,包括腫瘤、心血管、腎臟、代謝、呼吸、消化、罕見病、疫苗抗體及自體免疫等,已將40多款創新藥物帶到中國。阿斯利康中國總部位于上海,并在上海和北京設立全球戰略研發中心,在北京、廣州、杭州、成都、青島設立區域總部,在無錫、泰州、青島建立全球生產供應基地,向全球70多個市場輸送優質創新藥品。
聲明:本文研究中涉及的多種藥品用法尚未在中國獲批適應癥,阿斯利康不推薦任何未被批準的藥品使用。