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Adaptimmune to Present Data From Planned Interim Analysis of Pivotal IGNYTE-ESO Trial With Lete-cel at ASCO; Data Continue to Support Further Development of Sarcoma Franchise

Adaptimmune to Present Data From Planned Interim Analysis of Pivotal IGNYTE-ESO Trial With Lete-cel at ASCO; Data Continue to Support Further Development of Sarcoma Franchise

Adaptimmune將在ASCO會議上展示IGNYTE-ESO關鍵中期分析的數據,Lete-cel在該數據中繼續支持肉瘤業務線的進一步發展。
newsfile ·  06/04 00:00

Overall response rate of 40% consistent across sarcoma indications; median duration of response ~11 months with patients still in response at time of analysis

肉瘤指示下,總體的反應率爲40%;反應持續中位時間約11個月,患者仍處於反應期分析時間。

Interim analysis data reinforces the potential of lete-cel to bolster Adaptimmune's sarcoma franchise by expanding addressable sarcoma patient population

中期分析數據加強了Lete-cel擴大Adaptimmune肉瘤生意的潛力,增加了肉瘤可尋址患者人群。

Full results from the pivotal IGNYTE-ESO trial are expected in late 2024

關鍵的IGNYTE-ESO試驗整體結果將於2024年底公佈。

Philadelphia, Pennsylvania and Oxford, United Kingdom--(Newsfile Corp. - June 3, 2024) - Adaptimmune Therapeutics plc (NASDAQ: ADAP), a company working to redefine the treatment of solid tumor cancers with cell therapy, is presenting data from its pivotal IGNYTE-ESO trial of lete-cel (letetresgene autoleucel), an engineered cell therapy targeting NY-ESO-1, in synovial sarcoma (SyS) and myxoid/round cell liposarcoma (MRCLS) at the American Society of Clinical Oncology's (ASCO) annual meeting. Dr. Sandra D'Angelo of the Memorial Sloan Kettering Cancer Center will present "Lete-cel in patients with synovial sarcoma or myxoid/round cell liposarcoma: Planned interim analysis of the pivotal IGNYTE-ESO trial" in an oral session at 11:30 a.m. CDT, Monday, June 3rd, in Hall D2 as part of the Developmental Therapeutics-Immunotherapy track.

賓夕法尼亞州的費城和英國牛津--(Newsfile Corp. -2024年6月3日) - 正在使用細胞治療重新定義固體腫瘤癌症治療方法的Adaptimmune Therapeutics plc(納斯達克:ADAP)向設計針對SY和MRCLS的Lete-cel(Letetresgene Autoleucel)的關鍵IGNYTE-ESO試驗提供數據,此次試驗數據將在美國臨床腫瘤學會(ASCO)年會上公佈。Memorial Sloan Kettering癌症中心的Sandra D'Angelo博士將於6月3日星期一中部夏令時上午11:30,在Developmental Therapeutics-Immunotherapy環節的D2廳中以口頭報告形式發表題爲“Lete-cel in patients with synovial sarcoma or myxoid/round cell liposarcoma:Planned interim analysis of the pivotal IGNYTE-ESO trial”的演講。

Dennis Williams, PharmD., Senior Vice President, Late-Stage Development, Adaptimmune: "We're encouraged by the findings from the IGNYTE-ESO trial and the potential of our sarcoma franchise. Our lead cell therapy product, afami-cel, targets MAGE-A4 in synovial sarcoma and the ability to now also target the NY-ESO-1 cancer antigen with lete-cel will enable us to reach a greater number of people impacted by advanced sarcomas. We are eager to continue advancing lete-cel to further realise the promise of engineered TCR T-cell therapies for patients and healthcare providers. We look forward to sharing the full results of the IGNYTE-ESO trial in late 2024. We continue to work toward commercializing afami-cel later this year and lete-cel in 2026."

Adaptimmune的晚期開發高級副總裁Dennis Williams藥劑師:“我們對IGNYTE-ESO試驗的發現和我們肉瘤的潛力感到鼓舞。我們的主要細胞治療產品Afami-cel針對SY中的MAGE-A4,現在使用Lete-cel也能夠針對NY-ESO-1癌症抗原,使我們能夠觸及更多受到晚期肉瘤影響的患者。我們渴望繼續推進Lete-cel,以進一步爲患者和醫療保健提供商實現工程TCR T細胞療法的承諾。我們期待在2024年底分享IGNYTE-ESO試驗的全部結果。我們將繼續努力於今年晚些時候商業化Afami-cel,並於2026年推出Lete-cel。”

Dr. Sandra D'Angelo M.D., Sarcoma Medical Oncology, Memorial Sloan Kettering Cancer Center, lead author and presenter: "Data from this planned interim analysis support the potential of lete-cel to serve as a novel therapy for people with advanced or metastatic MRCLS or synovial sarcoma. As the current treatment options in these two indications are significantly limited, both represent a greatly unmet medical need for novel, innovative therapies."

Memorial Sloan Kettering Cancer Center的肉瘤醫學腫瘤科主任Sandra D'Angelo M.D.,主要作者和演講者:“此次計劃中期分析數據支持Lete-cel的潛力,可作爲晚期或轉移性MRCLS或SY患者的新型治療方案。由於這兩種情況下的當前治療選擇受限,因此都代表一種極大未滿足的醫療需求,需要新穎和創新的治療。”

Lete-cel data at ASCO

ASCO的Lete-cel數據

At the planned interim analysis, 18/45 patients who received a single dose of lete-cel had clinical responses (previously reported). The overall response rate (ORR) of 40% was consistent across both SyS and MRCLS, and markedly greater than historical standard of care outcomes in these indications. The primary endpoint success criterion for efficacy was met by the interim analysis 40% ORR. Responses to lete-cel are durable, with the median duration of response (mDOR) at ~11 months, with 9/18 patients censored from mDOR calculation as their responses were ongoing at the time of the interim analysis. The complete primary analyses from IGNYTE-ESO, including more mature duration of response, are currently in progress with a full dataset anticipated in late 2024.

在計劃的中期分析中,接受單次Lete-cel的45名患者中,18名有臨床反應(先前報道過)。 40%的總反應率(ORR)在SY和MRCLS中都保持一致,並且顯着高於這些跡象中歷史標準護理成果。 起效力的主要終點成功標準是中期分析40%ORR。 對Lete-cel的反應是持久的,反應持續中位時間(mDOR)約爲11個月,其中有9名患者因其反應在中期分析時持續而被刪去mDOR計算。 包括更成熟的反應持續時間在內的IGNYTE-ESO的完整主要分析仍在進行中,預計將於2024年底獲得完整數據集。

Given the success of the pivotal IGNYTE-ESO trial, Adaptimmune plans to initiate a rolling Biologics License Application (BLA) submission for lete-cel for the treatment of advanced or metastatic MRCLS and synovial sarcoma during 2025. Lete-cel will allow Adaptimmune to bolster its sarcoma franchise by expanding the addressable patient population to NY-ESO-1 positive MRCLS and synovial sarcoma solid tumors.

鑑於關鍵的IGNYTE-ESO試驗的成功,Adaptimmune計劃於2025年開始滾動提交用於治療晚期或轉移性MRCLS和SY的Lete-cel生物製品許可申請(BLA)。Lete-cel將使Adaptimmune擴大程序能夠尋址NY-ESO-1陽性MRCLS和SY實體瘤患者人群。

About lete-cel

關於Lete-cel

Lete-cel is an engineered TCR T-cell therapy targeting the solid tumor antigen NY-ESO-1. Lete-cel is being investigated for the treatment of synovial sarcoma and myxoid/round cell liposarcoma (MRCLS) in the pivotal IGNYTE-ESO (NCT03967223) trial in patients who received prior anthracycline treatment.

Lete-cel是一種針對固態腫瘤抗原NY-ESO-1的工程TCR T細胞療法。(NCT03967223)試驗正在調查Letetresgene Autoleucel在之前接受蒽環類藥物治療的患者中治療SY和MRCLS領域。

About Synovial Sarcoma

關於Synovial Sarcoma

There are more than 50 different types of soft tissue sarcomas which are categorised by tumors that appear in fat, muscle, nerves, fibrous tissues, blood vessels, or deep skin tissues.1 Synovial sarcoma accounts for approximately 5% to 10% of all soft tissue sarcomas (there are approximately 13,400 new soft tissue cases in the U.S. each year).2 One third of patients with synovial sarcoma will be diagnosed under the age of 30.2 The five-year survival rate for people with metastatic disease is just 20% and most people undergoing standard of care treatment for advanced disease experience recurrence and go through multiple lines of therapy, often exhausting all options.3

一共有50 多種不同的軟組織肉瘤,根據出現在脂肪、肌肉、神經、纖維組織、血管或深部皮膚組織中的腫瘤進行分類。1滑膜肉瘤約佔所有軟組織肉瘤的5%至10%(每年美國大約有13,400例新的軟組織肉瘤病例)。2三分之一的滑膜肉瘤患者將在30歲以下被診斷。轉移性疾病的五年生存率僅爲20%,大多數接受晚期治療的患者經歷復發並經歷多種療法,通常耗盡了所有選擇。2轉移性疾病的五年生存率僅爲20%,大多數接受標準照護治療的晚期患者會出現復發並經歷多個治療方案,通常耗盡所有選擇。3

About Myxoid/round cell liposarcoma (MRCLS)
Myxoid/round cell liposarcoma (MRCLS) is a type of soft tissue sarcoma that is predominantly found in the limbs. MRCLS accounts for approximately 5% to 10% of all soft tissue sarcomas.4 One-third of MRCLS cases will become metastatic with tumors spreading to unusual bone and soft tissue locations. MRCLS commonly presents at an age ranging from 35-55 years and has a poor prognosis because it recurs locally and tends to metastasize quickly and widely. The 5-year survival rate for metastatic MRCLS is only 5%.5

關於Myxoid/round cell liposarcoma(MRCLS)
Myxoid/round cell liposarcoma(MRCLS)是一種主要在四肢中表現的軟組織肉瘤類型。MRCLS約佔所有軟組織肉瘤的5%至10%。4MRCLS病例中有三分之一會轉移,腫瘤會擴散到非常不尋常的骨骼和軟組織部位。MRCLS通常出現在35-55歲之間,預後不良,因爲它會在局部復發並很快廣泛轉移。轉移性MRCLS的5年生存率僅爲5%。5

About Adaptimmune
Adaptimmune is a fully integrated cell therapy company working to redefine how cancer is treated. With its unique engineered T cell receptor (TCR) platform, the Company is developing personalized medicines designed to target and destroy difficult-to-treat solid tumor cancers and to radically improve the patient's cancer treatment experience.

關於Adaptimmune
Adaptimmune是一家完全集成的細胞治療公司,致力於重新定義癌症的治療。通過其獨特的工程T細胞受體(TCR)平台,該公司正在開發旨在針對和摧毀難以治療的實體腫瘤癌症的個性化藥物,並從根本上改善患者的癌症治療體驗。

Forward-Looking Statements
This release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995 (PSLRA). These forward-looking statements involve certain risks and uncertainties. Such risks and uncertainties could cause our actual results to differ materially from those indicated by such forward-looking statements, and include, without limitation: the success, cost and timing of our product development activities and clinical trials and our ability to successfully advance our TCR therapeutic candidates through the regulatory and commercialization processes. For a further description of the risks and uncertainties that could cause our actual results to differ materially from those expressed in these forward-looking statements, as well as risks relating to our business in general, we refer you to our Annual Report on Form 10-K filed with the Securities and Exchange Commission for the year ended 31 December, 2023, our Quarterly Reports on Form 10-Q, Current Reports on Form 8-K, and other filings with the Securities and Exchange Commission. The forward-looking statements contained in this press release speak only as of the date the statements were made and we do not undertake any obligation to update such forward-looking statements to reflect subsequent events or circumstances.

前瞻性聲明
本發佈中包含根據1995年《私人證券訴訟改革法案》(PSLRA)的“前瞻性聲明”。這些前瞻性聲明涉及某些風險和不確定性。這種風險和不確定性可能會導致我們的實際結果與此類前瞻性聲明所示的結果不同,包括但不限於:我們的產品開發活動和臨床試驗的成功、成本和時間以及我們能否成功推進我們的TCR治療候選人通過監管和商業化流程。有關可能導致我們的實際結果與這些前瞻性聲明中所述的結果有所不同的風險和不確定性的進一步描述,以及與我們業務有關的風險,我們轉至《年報10-K》。提交給美國證券交易委員會的年度報告在2023年12月31日結束,我們提交的《10-Q》季度報告、《8-K》現狀報告和向美國證券交易委員會提供的其他文件。本新聞發佈中包含的前瞻性聲明僅適用於聲明發表的日期,我們不承擔任何更新此類前瞻性聲明以反映隨後發生的事件或情況的義務。

Dr. Sandra D'Angelo has financial interests related to Adaptimmune.

Sandra D'Angelo博士與Adaptimmune有相關財務利益。

Adaptimmune Contact

Adaptimmune聯繫方式

Investor Relations
Juli P. Miller, Ph.D. - VP, Corporate Affairs and Investor Relations
T : +1 215 825 9310
M : +1 215 460 8920
Juli.Miller@adaptimmune.com

投資者關係
Juli P. Miller博士-企業事務和投資者關係副總裁
電話:+1 215 825 9310
手機:+1 215 460 8920
電子郵件:Juli.Miller@adaptimmune.com

Media Relations
Dana Lynch, Senior Director of Corporate Communications
M: +1 267 990 1217
Dana.Lynch@adaptimmune.com

媒體關係
Dana Lynch,企業傳播高級總監
手機:+1 267 990 1217
電子郵件:Dana.Lynch@adaptimmune.com

________________________
1. .
2. Synovial Sarcoma - NCI (cancer.gov).
3. Aytekin MN, et al. J Orthop Surg (Hong Kong). 2020;28(2).
4. .
5. .

________________________
1. 。
2. NCI(癌症.gov)的滑膜肉瘤。
3. Aytekin MN等。J Orthop Surg(香港)。2020;28(2)。
4. 。.
5. 。

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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