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阿斯利康攜重磅研究,創(chuàng)連續(xù)七年亮相美國臨床腫瘤學(xué)會(huì)(ASCO)全體大會(huì)紀(jì)錄,進(jìn)一步彰顯重新定義乳腺癌治療和改變胃癌治療結(jié)局的雄心

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:

  • SERENA-6 評(píng)估了Camizestrant與廣泛獲批的細(xì)胞周期蛋白依賴性激酶(CDK)4/6抑制劑聯(lián)合,用于一線治療激素受體(HR)陽性、HER2陰性且腫瘤出現(xiàn)ESR1突變的晚期乳腺癌患者的III期臨床研究(Plenary #LBA4)。Camizestrant是在研的新一代選擇性雌激素受體降解劑(SERD)和完全ER拮抗劑。這是首個(gè)在一線治療中取得陽性結(jié)果的新一代口服SERD藥物III期臨床研究,也是Camizestrant的首個(gè)III期陽性結(jié)果。
  • MATTERHORN:評(píng)估了度伐利尤單抗聯(lián)合FLOT化療作為可切除的早期和局部晚期的胃和胃食管結(jié)合部腺癌(GEJ)患者圍手術(shù)期治療方案的III期研究(Plenary #LBA5)。
  • DESTINY-Breast09:評(píng)估德曲妥珠單抗聯(lián)合帕妥珠單抗用于一線治療HER2陽性轉(zhuǎn)移性乳腺癌患者治療獲益的III期研究(口頭報(bào)告摘要#LBA1008)。
  • DESTINY-Gastric04 評(píng)估了德曲妥珠單抗用于二線治療HER2陽性不可切除和/或轉(zhuǎn)移性胃和胃食管結(jié)合部腺癌患者的治療獲益的III期研究(#LBA4002)。
  • NeoADAURA:奧希替尼聯(lián)合或不聯(lián)合化療作為新輔助治療用于可切除的早期EGFR突變非小細(xì)胞肺癌(NSCLC)的III期臨床研究(口頭報(bào)告摘要#8001)。
  • TROPION-Lung02:Datroway聯(lián)合帕博利珠單抗的聯(lián)合或不聯(lián)合鉑類一線化療治療無驅(qū)動(dòng)基因突變的晚期非小細(xì)胞肺癌的Ib期臨床研究結(jié)果,基于計(jì)算病理學(xué)生物標(biāo)志物分析(口頭報(bào)告摘要#8501)。
  • KOMET:評(píng)估司美替尼治療伴有癥狀性、無法手術(shù)的叢狀神經(jīng)纖維瘤的1型神經(jīng)纖維瘤病成人患者的III期臨床研究(快速口頭摘要#3014)。

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 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。

 

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