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Workshop on immunotherapy combinations. Society for immunotherapy of cancer annual meeting Bethesda November 3 2011

机译:免疫疗法联合研讨会。癌症免疫疗法学会年会贝塞斯达2011年11月3日

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摘要

Although recent FDA approvals on ipilimumab and sipuleucel-T represent major milestones, the ultimate success of immunotherapy approaches will likely benefit from appropriate combinations with other immunotherapeutic and/or non-immunotherapeutic approaches. However, implementation of ideal combinations in the clinic may still face formidable challenges in regulatory, drug-availability and intellectual property aspects. The 2011 SITC annual meeting hosted a workshop on combination immunotherapy to discuss: 1) the most promising combinations found in the laboratory; 2) early success of combination immunotherapy in clinical trials; 3) industry perspectives on combination approaches, and 4) relevant regulatory issues. The integrated theme was how to accelerate the implementation of efficacious combined immunotherapies for cancer patients. Rodent animal models are providing many examples of synergistic combinations that typically include more than two agents. However, mouse and human immunology differ in a significant number of mechanisms and hence we might be missing opportunities peculiar to humans. Nonetheless, incisive animal experimentation with deep mechanistic insight remains the best compass that we can use to guide our paths in combinatorial immunotherapy. Combination immunotherapy clinical trials are already in progress and preliminary results are extremely promising. As a key to translate promising combinations into clinic, real and “perceived” business and regulatory hurdles were debated. A formidable step forward would be to be able to test combinations of investigational agents prior to individual approval. Taking together the FDA and the industrial perspective on combinatorial immunotherapy, the audience was left with the clear message that this is by no means an impossible task. The general perception is that the road ahead of us is full of combination clinical trials which hopefully will bring clinical benefit to our cancer patients at a fast pace.
机译:尽管最近FDA对ipilimumab和sipuleucel-T的批准代表了主要的里程碑,但免疫治疗方法的最终成功可能会受益于与其他免疫治疗和/或非免疫治疗方法的适当组合。然而,在诊所中实现理想组合可能仍会在监管,药物利用和知识产权方面面临巨大挑战。 2011年SITC年度会议主办了一次组合免疫疗法研讨会,讨论:1)实验室中发现的最有希望的组合; 2)联合免疫疗法在临床试验中的早期成功; 3)行业对组合方法的看法,以及4)相关监管问题。整体主题是如何加快对癌症患者有效的联合免疫疗法的实施。啮齿动物模型提供了许多协同组合的例子,通常包括两种以上的药物。但是,小鼠和人类的免疫学在许多机制上都存在差异,因此我们可能会错过人类特有的机会。尽管如此,具有深远的机械洞察力的敏锐的动物实验仍然是我们可以用来指导组合免疫疗法道路的最佳指南针。组合免疫疗法临床试验已经在进行中,初步结果非常有希望。作为将有希望的组合转化为临床的关键,人们讨论了实际的和“可感知的”业务和监管障碍。一个巨大的进步将是能够在个人批准之前测试研究人员的组合。结合FDA和组合免疫疗法的工业观点,听众得到了明确的信息:这绝不是不可能的任务。普遍的看法是,我们前面的道路上充满了联合临床试验,有望为我们的癌症患者带来快速的临床收益。

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