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第四届世界抗体药物偶联物峰会:2012 年 2 月 29 日-3 月 1 日,德国法兰克福。

Fourth World Antibody-Drug Conjugate Summit: February 29-March 1, 2012, Frankfurt, Germany.

机构信息

Centre d'Immunologie Pierre Fabre, Saint-Julien-en-Genevois, France.

出版信息

MAbs. 2012 Nov-Dec;4(6):637-47. doi: 10.4161/mabs.21697. Epub 2012 Aug 22.

Abstract

The 4th World Antibody Drug Conjugate (WADC) Summit, organized by Hanson Wade was held on February 29‑March 1, 2012 in Frankfurt, Germany, which was also the location for the Antibody Drug Conjugate Summit Europe held in February 2011. During the one year between these meetings, antibody drug conjugates (ADCs) have confirmed their technological maturity and their clinical efficacy in oncology. Brentuximab vedotin (ADCETRIS (TM) ) gained approval by the US Food and Drug Administration in August 2011 and trastuzumab emtansine (T-DM1) confirmed impressive clinical efficacy responses in a large cohort of breast cancer patients. During the 4th WADC meeting, antibody-maytansinoid conjugates were showcased by representatives of ImmunoGen (T-DM1, SAR3419, lorvotuzumab mertansine/IMGN801, IMGN529 and IMG853) and Biotest (BT-062). Data on antibody-auristatin conjugates were presented by scientists and clinicians from Seattle Genetics and Takeda (brentuximab vedotin), Pfizer (5T4-MMAF), Agensys/Astella (AGS-16M8F), Progenics (PSMA-ADC) and Genmab (anti-TF ADCs). Alternative payloads such as calicheamicins and duocarmycin used for preparation of ADCs were discussed by Pfizer and Synthon representatives, respectively. In addition, emerging technologies, including site-directed conjugation (Ambrx), a protein toxin as payload (Viventia), hapten-binding bispecific antibodies (Roche), and use of light activated drugs (Photobiotics), were also presented. Last but not least, progresses in solving Chemistry Manufacturing and Control, and pharmacokinetic issues were addressed by scientists from Genentech, Pfizer, Novartis and Pierre Fabre.

摘要

第四届世界抗体药物偶联物(WADC)峰会由 Hanson Wade 组织,于 2012 年 2 月 29 日至 3 月 1 日在德国法兰克福举行,这也是 2011 年 2 月举行的抗体药物偶联物峰会欧洲会议的举办地。在这两次会议之间的一年中,抗体药物偶联物(ADC)已证实其在肿瘤学领域的技术成熟度和临床疗效。Brentuximab vedotin(ADCETRIS(TM))于 2011 年 8 月获得美国食品和药物管理局的批准,曲妥珠单抗emtansine(T-DM1)在一大群乳腺癌患者中证实了令人印象深刻的临床疗效反应。在第四届 WADC 会议上,ImmunoGen(T-DM1、SAR3419、lorvotuzumab mertansine/IMGN801、IMGN529 和 IMG853)和 Biotest(BT-062)的代表展示了抗体-美坦辛偶联物。西雅图遗传学公司和武田(Brentuximab vedotin)、辉瑞(5T4-MMAF)、Agensys/Astella(AGS-16M8F)、Progenics(PSMA-ADC)和 Genmab(抗 TF ADCs)的科学家和临床医生介绍了抗体-auristatin 偶联物的数据。辉瑞和 Synthon 的代表分别讨论了用于制备 ADC 的替代有效载荷,如 calicheamicins 和 duocarmycin。此外,还介绍了新兴技术,包括定点偶联(Ambrx)、作为有效载荷的蛋白毒素(Viventia)、半抗原结合双特异性抗体(罗氏)和使用光激活药物(Photobiotics)。最后但同样重要的是,Genentech、辉瑞、诺华和皮埃尔·法伯的科学家们解决了化学制造和控制以及药代动力学问题的进展。

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