Unite.AI 01月15日
Peter Ellman, President and CEO of Certis Oncology Solutions – Interview Series
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Certis Oncology Solutions 推出CertisOI Assistant,旨在解决肿瘤研究中药物研发失败率高的问题。该工具通过整合全面的肿瘤数据,利用AI算法预测药物反应,并提供用户友好的界面,帮助研究人员更有效地选择临床前模型、识别生物标志物,从而提高药物研发的成功率。CertisOI Assistant 专注于临床前肿瘤研究,特别是PDX和细胞系模型,提供早期药物开发和肿瘤生物学方面的独特见解,通过交互式可视化和数据分析,将复杂数据转化为可操作的见解。

🔬CertisOI Assistant 通过整合患者信息、肿瘤特征、基因图谱和药物反应预测等广泛的肿瘤数据,提供全面的数据分析能力,使得研究人员能够进行更深入的研究。

💡该工具利用AI算法预测药物反应和耐药性,为个性化医疗提供关键信息,并与仅依赖历史数据的工具区分开来。它还支持交互式可视化,如药理学和肿瘤生长研究,使研究人员能够以更具吸引力和信息量的方式探索数据。

🧬CertisOI Assistant 通过结构化的工作流程将原始数据转化为有意义的见解,包括数据查询、分析、可视化以及解释和见解,帮助研究人员做出明智的决策,并支持高度定制化的分析。

🧪该工具还提供了一个虚拟环境来测试和验证与药物疗效、靶点结合和生物标志物发现相关的假设,无需立即进行实验室实验。这有助于研究人员快速改进他们的假设,并专注于最有希望的研究途径。

📊CertisOI Assistant 支持多种癌症模型和数据集,包括PDX和PDX衍生的肿瘤模型,以及癌症细胞系百科全书(CCLE)的数据。该平台算法还利用了来自GDSC、ICGC等其他数据集的数据。

Certis Oncology Solutions, led by Peter Ellman, President and CEO, is a life science technology company dedicated to realizing the promise of precision oncology. The company’s product is Oncology Intelligence® — highly predictive therapeutic response data derived from advanced cancer models. Certis partners with physician-scientists and industry researchers to expand access to precision oncology and address the critical translation gap between preclinical studies and clinical trials.

Can you describe the broader problem in oncology research that the CertisOI Assistant is addressing?

The failure rate of oncology investigational drug candidates is high. It was recently reported that in 2023, 90% of oncology programs ultimately failed. That figure is a remarkable improvement over the historical trend, which hovered around 96% until 2022. Considering the cost of developing drugs, a 90% failure rate is not sustainable. Imagine how patients would benefit if the success rate were even 50%.

CertisOI Assistant immediately addresses two really important issues that contribute to this failure rate:

How does the CertisOI Assistant use AI to improve access to oncology data, and what sets it apart from other AI tools in the field?

The CertisOI Assistant provides advanced data analysis and predictive modeling capabilities through an easy-to-use, natural language interface. It stands out in several ways:

How does the tool transform complex data into actionable insights, especially for researchers working on drug sensitivity or genomic data?

CertisOI Assistant leverages a structured workflow to transform raw data into meaningful insights. It involves querying a comprehensive oncology dataset, analyzing the data, and presenting the results in a clear and interpretable format. Here's how it works:

How does the CertisOI Assistant enhance researchers’ ability to select cancer models, design biomarker strategies, or perform in silico validations?

I covered the first two areas – the cancer model section and biomarker strategy design – at the outset of this interview, so I’ll focus on performing in silico validations. CertisOI Assistant provides a virtual environment to test and validate hypotheses related to drug efficacy, target engagement, and biomarker discovery without the need for immediate laboratory experiments. This allows them to rapidly refine their hypotheses and focus experimental efforts on the most promising avenues.

Here are a few examples:

Can you share examples of how researchers are anticipated to use this tool to improve their workflows or achieve breakthroughs?

The simplest example is preclinical model selection. Every preclinical study begins with the selection of tumor models. CertisOI Assistant takes the manual effort out of this process and brings great precision to selecting the optimal models for any given study.

Another is developing a biomarker strategy. The traditional approach is to hypothesize what biomarker or biomarkers might be linked to the drug's mechanism of action and then test those hypotheses in preclinical studies, which is usually an iterative process. If preclinical data is promising, researchers must validate predictive biomarkers in human clinical trials—and as discussed, the failure rate is high.

The CertisOI Assistant helps researchers identify and validate more precise, predictive gene expression biomarkers earlier in the development process and with less iteration than the traditional workflow—saving time, and money, and improving chances for commercial success.

What kinds of cancer models or datasets does the tool support, and how does this breadth benefit the research community?

The current version of CertisOI gives researchers access to Certis’ rapidly expanding library of PDX and PDX-derived tumor models and the entire Cancer Cell Line Encyclopedia (CCLE) of models. The platform’s algorithms also draw on data from Genomics of Drug Sensitivity in Cancer (GDSC), International Cancer Genome Consortium (ICGC), CI ALMANAC, O’Neil, and other datasets. This holistic approach to data integration allows for a more comprehensive analysis than tools that focus on isolated data types.

The CertisOI Assistant is designed to be user-friendly. How do you ensure that it is accessible to researchers who may not have extensive technical expertise?

Several features make CertisOI Assistant accessible to researchers at all levels:

Collaboration is a key aspect of research. How does the CertisOI Assistant facilitate teamwork among researchers or institutions?

With CertisOI Assistant, researchers from different teams or institutions can access the same dataset and tools, allowing them to work collaboratively on shared projects or research questions. The platform also makes it easy to download and share data queries, results, and insights among team members so everyone involved in a project can contribute effectively.

What are the biggest challenges in scaling AI adoption in cancer research, and how can they be addressed?

Significant challenges include data security, data integration, and trust in AI‐based outcome predictions. I am not an expert on data security or data integration, but great minds are working to solve those challenges. With respect to trusting AI-generated predictions, we need efficient and credible ways to validate those predictions.

Certis has taken a two-pronged approach to this: in silico validation via internal, cross-validation studies, and in vivo validation—performing studies in clinically relevant mouse models to evaluate the accuracy of our platform’s predictions. Over time, these tools will also be validated clinically in human patients—but of course, that will take a great deal of time and money, as well as the willingness to change the current cancer treatment paradigm. The medical and regulatory community will have to stop relying on how things have always been done and embrace the power of computational analyses to inform decisions.

How do you envision tools like the CertisOI Assistant shaping the future of cancer treatment and precision medicine?

Modern medicine doesn’t yet have a great way to match patients to the ideal treatments. Overall, only 10% of cancer patients experience a clinical benefit from treatments matched to tumor DNA mutations. That not only hurts patients’ health, but it also harms them financially. An estimated $2.5 billion —with a B—is wasted on ineffective therapies. It is a very sad fact that 42% of cancer patients fully deplete their assets by the second year of their diagnosis.

Tools like CertisOI Assistant and CertisAI will help us realize the promise of precision medicine—getting people the optimal treatment for their unique form of cancer the first time, every time…. And to democratize access to more effective, personalized care.

Thank you for the great interview, readers who wish to learn more should visit Certis Oncology Solutions.

The post Peter Ellman, President and CEO of Certis Oncology Solutions – Interview Series appeared first on Unite.AI.

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精准肿瘤学 AI 药物研发 生物标志物 临床前模型
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