2025-05-22 16:54:00來源:瀏覽量:404
SERENA-6 研究的全體大會(huì)報(bào)告將聚焦用于晚期 HR 陽性乳腺癌一線治療的新一代口服 SERD 藥物 Camizestrant
MATTERHORN 研究的全體大會(huì)報(bào)告將展示英飛凡用于早期胃和胃食管結(jié)合部腺癌的圍手術(shù)期治療方案
DESTINY-Breast09 研究的專場口頭報(bào)告將強(qiáng)調(diào)優(yōu)赫得在 HER2 陽性轉(zhuǎn)移性乳腺癌更前線治療的潛力
上海 2025年5月22日 /美通社/ -- 阿斯利康在2025年5月30日至6月3日召開的美國臨床腫瘤學(xué)會(huì)(ASCO)上,憑借行業(yè)領(lǐng)先的多樣化產(chǎn)品與管線布局的全新研究數(shù)據(jù),進(jìn)一步深化自身讓癌癥不再成為致死主因的雄心。
會(huì)上將有超過80個(gè)摘要公布,其中涵蓋20款已獲得批準(zhǔn)的藥物和潛在新藥,包括兩項(xiàng)重磅研究的全體大會(huì)報(bào)告(plenary presentation),一項(xiàng)特別重磅研究摘要口頭報(bào)告(late-breaking oral abstract session),以及19項(xiàng)口頭報(bào)告。其中亮點(diǎn)包括:
阿斯利康全球執(zhí)行副總裁、全球腫瘤研發(fā)負(fù)責(zé)人高書璨( Susan Galbraith)表示:"本次ASCO大會(huì)上公布的兩項(xiàng)乳腺癌重磅研究數(shù)據(jù)將凸顯我們在以創(chuàng)新藥物和產(chǎn)品管線改變腫瘤治療結(jié)局上所取得的進(jìn)展。SERENA-6是首個(gè)采用循環(huán)腫瘤DNA檢測指導(dǎo)治療方案切換的一項(xiàng)關(guān)鍵III期臨床研究,開創(chuàng)了這一技術(shù)在一線治療中的應(yīng)用,以延緩HR陽性、HER2陰性晚期乳腺癌的疾病進(jìn)展。此外,DESTINY-Breast09研究評(píng)估了德曲妥珠單抗與帕妥珠單抗的聯(lián)合治療方案,這是十年來首次在HER2陽性轉(zhuǎn)移性乳腺癌廣泛患者群體中,證明療效優(yōu)于目前一線治療標(biāo)準(zhǔn)方案的試驗(yàn)。"
阿斯利康全球執(zhí)行副總裁,全球腫瘤研發(fā)負(fù)責(zé)人Dave Fredrickson表示:"MATTERHORN的研究數(shù)據(jù)證明,度伐利尤單抗作為胃和胃食管結(jié)合部腺癌患者圍手術(shù)期的治療方案,是我們將免疫療法遷入癌癥早期階段治療的成功例證,有望實(shí)現(xiàn)早期治愈的可能。這是阿斯利康連續(xù)第七年登上ASCO全體大會(huì),這一非凡的里程碑彰顯出我們在多個(gè)癌腫領(lǐng)域已建立行業(yè)領(lǐng)先的腫瘤產(chǎn)品組合和強(qiáng)大的研發(fā)管線。
阿斯利康與第一三共聯(lián)合開發(fā)和商業(yè)化德曲妥珠單抗與Datroway;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(hào))聯(lián)合開發(fā)和商業(yè)化司美替尼;與和黃醫(yī)藥合作開發(fā)和商業(yè)化賽沃替尼。
阿斯利康在 2025 年 ASCO 大會(huì)期間的重要演講 1
| 主要作者 | 摘要標(biāo)題 | 演示文稿詳情 (CDT) |
| 抗體偶聯(lián)藥物 | ||
| Shitara, K
| Trastuzumab deruxtecan (T- DXd) vs ramucirumab (RAM) + paclitaxel (PTX) in second-line treatment of patients (pts) with human epidermal growth factor receptor 2-positive (HER2+) unresectable/metastatic gastric cancer (GC) or gastroesophageal junction adenocarcinoma (GEJA): Primary analysis of the randomized, phase 3 DESTINY-Gastric04 study. | Abstract #LBA4002 Oral Abstract Session 31 May 2025 3:24pm
|
| Tolaney, SM
| Trastuzumab deruxtecan (T- DXd) + pertuzumab (P) vs taxane + trastuzumab + pertuzumab (THP) for first-line (1L) treatment of patients (pts) with human epidermal growth factor receptor 2–positive (HER2+) advanced/metastatic breast cancer (a/mBC): Interim results from DESTINY-Breast09. | Abstract #LBA1008 Oral Abstract Session 2 June 2025 7:30am
|
| Dent, R
| Exploratory biomarker analysis of trastuzumab deruxtecan (T- DXd) vs physician's choice of chemotherapy (TPC) in HER2- low/-ultralow, hormone receptor-positive (HR+) metastatic breast cancer (mBC) in DESTINY-Breast06 (DB-06). | Abstract #1013 Oral Abstract Session 31 May 2025 3:23pm
|
| Levy, BP
| TROPION-Lung02: Datopotamab deruxtecan (Dato-DXd) plus pembrolizumab (pembro) with or without platinum chemotherapy (Pt-CT) as first- line (1L) therapy for advanced non-small cell lung cancer (aNSCLC). | Abstract #8501 Oral Abstract Session 1 June 2025 8:12am
|
| Waqar, SN
| First-line (1L) datopotamab deruxtecan (Dato-DXd) + rilvegostomig in advanced or metastatic non-small cell lung cancer (a/mNSCLC): Results from TROPION-Lung04 (cohort 5). | Abstract #8521 Poster Session 31 May 2025 1:30pm
|
| 腫瘤驅(qū)動(dòng)因素和耐藥性 | ||
| Turner, NC
| Camizestrant + CDK4/6 inhibitor (CDK4/6i) for the treatment of emergent ESR1 mutations during first-line (1L) endocrine-based therapy (ET) and ahead of disease progression in patients (pts) with HR+/HER2– advanced breast cancer (ABC): Phase 3, double-blind ctDNA-guided SERENA-6 trial. | Abstract #LBA4 Plenary Session 1 June 2025 2:41pm
|
| Lu, S
| Savolitinib (Savo) combined with osimertinib (osi) versus chemotherapy (chemo) in EGFR-mutant (EGFRm) and MET-amplification (METamp) advanced NSCLC after disease progression (PD) on EGFR tyrosine kinase inhibitor (TKI): Results from a randomized phase 3 SACHI study. | Abstract #LBA8505 Oral Abstract Session 1 June 2025 9:48am
|
| Levy, BP
| Efficacy and CNS results from a randomized subset of the phase 2 SAVANNAH study comparing savolitinib (savo) + osimertinib (osi) combination with savo + placebo (PBO). | Abstract #8513 Rapid Oral Abstract Session 2 June 2025 8:06am
|
| Chaft JE
| Neoadjuvant (neoadj) osimertinib (osi) ± chemotherapy (CT) vs CT alone in resectable (R) epidermal growth factor receptor-mutated (EGFRm) NSCLC: NeoADAURA. | Abstract #8001 Oral Abstract Session 2 June 2025 3:12pm
|
| 免疫腫瘤學(xué)與雙特異性抗體 | ||
| Janjigian, YY
| Event-free survival in MATTERHORN: a randomized, phase 3 study of durvalumab plus 5-fluorouracil, leucovorin, oxaliplatin, and docetaxel chemotherapy (FLOT) in resectable gastric/gastroesophageal junction cancer (GC/GEJC). | Abstract #LBA5 Plenary Session 1 June 2025 3:13pm
|
| Powles, T
| Circulating tumor DNA (ctDNA) in patients with muscle-invasive bladder cancer (MIBC) who received perioperative durvalumab (D) in NIAGARA | Abstract #4503 Oral Abstract Session 1 June 2025 10:45am
|
| Reck, M
| Associations of post-surgical MRD status with neoadjuvant ctDNA dynamics, genomic mutations, and clinical outcomes in patients with resectable NSCLC (R-NSCLC) from the phase 3 AEGEAN trial. | Abstract #8009 Rapid Oral Abstract Session 1 June 2025 4:30pm
|
| Barbie, DA
| Clinical and molecular characteristics of early progressors (EPs) and long -term progression-free survivors (LTPs) from the phase 3 ADRIATIC trial of consolidation durvalumab (D) vs placebo (P) after concurrent chemoradiotherapy (cCRT) in limited-stage small-cell lung cancer (LS-SCLC). | Abstract #8014 Rapid Oral Abstract Session 1 June 2025 5:12pm
|
| Mayadev, J
| Ultrasensitive detection and tracking of circulating tumor DNA (ctDNA) and association with relapse and survival in locally advanced cervical cancer (LACC): Phase 3 CALLA trial analyses. | Abstract #5502 Oral Abstract Session 2 June 2025 8:48am
|
| Westin, SN
| Durvalumab plus carboplatin/paclitaxel followed by durvalumab with or without olaparib as first-line treatment for endometrial cancer: Longitudinal changes in circulating tumor DNA. | Abstract #5512 Rapid Oral Abstract Session 3 June 2025 8:30am
|
| Erinjeri, JP
| Outcomes by baseline tumor burden using the 6-and-12 score in EMERALD-1: a phase 3 study of durvalumab (D) ± bevacizumab (B) with transarterial chemoembolization (TACE) in embolization-eligible unresectable hepatocellular carcinoma (uHCC). | Abstract #4083 Poster Session 31 May 2025 9:00am
|
| Cascone, T
| Neoadjuvant durvalumab (D) + chemotherapy (CT) + novel anticancer agents and adjuvant D ± novel agents in resectable non-small-cell lung cancer (NSCLC): Updated outcomes from NeoCOAST-2. | Abstract #8046 Poster Session 31 May 2025 1:30pm
|
| Zhou, J
| First-line rilvegostomig (rilve) plus chemotherapy (CTx) in advanced biliary tract cancer (BTC): Primary analysis of GEMINI-Hepatobiliary substudy 2 Cohort A. | Abstract #4080 Poster Session 31 May 2025 9:00am
|
| Xu, R
| ARTEMIDE-Gastric01: a phase 3 randomized study of rilvegostomig with fluoropyrimidine and trastuzumab deruxtecan (T- DXd) as first-line (1L) treatment for locally advanced or metastatic HER2-positive gastric or gastroesophageal junction cancer (GC/GEJC). | Abstract #TPS4204 Poster Session 31 May 2025 9:00am
|
| Mathias, C
| ARTEMIDE-Lung03: a phase 3, randomized, double-blind, multicenter, global study of rilvegostomig or pembrolizumab in combination with platinum-based chemotherapy as first-line treatment for patients with metastatic non-squamous non- small-cell lung cancer whose tumors express PD-L1. | Abstract #TPS8653 Poster Session 31 May 2025 1:30pm
|
| 細(xì)胞療法 | ||
| Yoo, C
| RHEA-1: First-in-human (FIH) study of AZD9793, a first-in- class CD8-guided T cell- engager (TCE) for glypican-3- positive (GPC3+) advanced or metastatic hepatocellular carcinoma (HCC). | Abstract #TPS4215 Poster Session 31 May 2025 9:00am
|
| Kim, TM
| Safety and Efficacy of AZD0486, a CD19xCD3 T-cell Engager, in Relapsed or Refractory Diffuse Large B-cell Lymphoma. | Abstract #7046 Poster Session 1 June 2025 9:00am
|
| Shadman, M
| TITANium: An open-label, global multicenter Phase 1/2 study of AZD5492, a first-in- class subcutaneous CD8- guided tri-specific T-cell engager (TCE), in patients (pts) with relapsed or refractory (r/r) B-cell malignancies. | Abstract #TPS7091 Poster Session 1 June 2025 9:00am
|
| Le Gouill, S
| SOUNDTRACK-E: A Phase 1/2 Open-label Multicenter Study to Evaluate the Safety and Efficacy of AZD0486 Monotherapy or Combination Therapy in Patients With Mature B-cell Malignancies. | Abstract #TPS7083 Poster Session 1 June 2025 9:00am
|
| 罕見病藥物 | ||
| Chen, AP
| Efficacy and safety of selumetinib in adults with neurofibromatosis type 1 (NF1) and symptomatic, inoperable plexiform neurofibroma (PN): Primary analysis of KOMET (NCT04924608), a Phase 3, international, randomized, placebo-controlled study. | Abstract #3014 Rapid Oral Abstract Session 2 June 2025 8:00am
|
1 阿斯利康在2025年ASCO大會(huì)將公布超過80個(gè)摘要,涵蓋其產(chǎn)品和管線中的分子藥物
關(guān)于阿斯利康腫瘤領(lǐng)域的研究
阿斯利康正引領(lǐng)著腫瘤領(lǐng)域的一場革命,致力提供多元化的腫瘤治療方案,以科學(xué)探索腫瘤領(lǐng)域的復(fù)雜性,發(fā)現(xiàn)、研發(fā)并向患者提供改變生命的藥物。
阿斯利康專注于最具挑戰(zhàn)性的腫瘤疾病,通過持續(xù)不斷的創(chuàng)新,阿斯利康已經(jīng)建立了行業(yè)領(lǐng)先的多元化的產(chǎn)品組合和管線,持續(xù)推動(dòng)醫(yī)療實(shí)踐變革,改變患者體驗(yàn)。
阿斯利康以期重新定義癌癥治療并在未來攻克癌癥。
關(guān)于阿斯利康
阿斯利康(LSE/STO/Nasdaq: AZN)是一家科學(xué)至上的全球生物制藥企業(yè),專注于研發(fā)、生產(chǎn)及營銷處方類藥品,重點(diǎn)關(guān)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(nèi)的生物制藥等領(lǐng)域。阿斯利康全球總部位于英國劍橋,業(yè)務(wù)遍布超過125個(gè)國家,創(chuàng)新藥物惠及全球數(shù)百萬患者。
關(guān)于阿斯利康中國
阿斯利康自1993年進(jìn)入中國以來,專注中國患者需求最迫切的治療領(lǐng)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(chuàng)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(shè)立全球戰(zhàn)略研發(fā)中心,在北京、廣州、杭州、成都、青島設(shè)立區(qū)域總部,在無錫、泰州、青島建立全球生產(chǎn)供應(yīng)基地,向全球70多個(gè)市場輸送優(yōu)質(zhì)創(chuàng)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(yīng)癥,阿斯利康不推薦任何未被批準(zhǔn)的藥品使用。