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Stories of progress, inspiration, and information in overcoming osteosarcoma.

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New Data Commons Encourages Osteosarcoma Research

Bringing together clinical, genomic, and imaging data in a user-friendly format, the Osteosarcoma Explorer is designed to accelerate osteosarcoma research and encourage new contributions to the field.

Research relies on data. And thanks to advanced technologies, including next-generation sequencing, digital pathology, and electronic health records, data is being generated at an ever-increasing rate. While most of the data on osteosarcoma is publicly available, it takes specific computational expertise for researchers to analyze data appropriately and generate hypotheses based on the research data. Even data drawn from the same patients is spread between different research projects, making it challenging to draw connections.

While the data challenge affects all disease types, it is even more problematic for rare diseases such as osteosarcoma, simply because there is less data to begin with and fewer experts who know how to use complex data. Despite being the most common bone cancer affecting children, osteosarcoma is much rarer than other childhood cancers like leukemia; about 1,000 new cases of osteosarcoma are diagnosed in the U.S. each year.

Centralizing Osteosarcoma Data

Chand Khanna, DVM, PhD, strategic advisory board chair at the Osteosarcoma Institute, came up with an idea to address the data challenge more than a decade ago when he was chair of the QuadW Childhood Sarcoma Biostatistics and Annotation Office (CSBAO) of the Children’s Oncology Group (COG). (QuadW Foundation is the organization that founded OSI.) Dr. Khanna envisioned a centralized repository where osteosarcoma data would live and be accessible to researchers everywhere. There was just one issue.

“What I had imagined could not proceed because the technology did not exist at the time,” Dr. Khanna says.

Years later, Brian Crompton, MD, a pediatric oncologist at Boston Children’s Hospital and the Research Co-Director of the Solid Tumor Center at Dana-Farber Cancer Institute, took over as chair of the CSBAO and revived Dr. Khanna’s idea.

“The goal was to enable clinical researchers to explore connections between biomarkers and clinical outcomes, and allow those in biological labs, who may not be computationally skilled, to easily navigate and analyze the data to form new hypotheses,” Dr. Crompton says. “We wanted to build a tool that layers a user-friendly graphical interface on top of complex scientific and clinical data to make it accessible for those who are not technologically savvy.”

This time, the capability was there, thanks to work being done at The University of Texas Southwestern Medical Center (UTSW). Dr. Crompton partnered with Yang Xie, PhD, Professor and Associate Dean for data sciences at UTSW to build a data commons that would serve up ready-to-use data to researchers.

“It was a big project that required a lot of collaboration,” Dr. Xie says. “We needed to first collect data, curate it, and then develop a way to link different types of data together. From the beginning, we knew it needed to be presented in a user-friendly way.”

The project took more than three years to complete. While initial funding came from UTSW and QuadW, Dr. Xie was able to secure additional funding from the Cancer Prevention and Research Institute of Texas (CPRIT), allowing the team to develop and implement the cutting-edge data science technology to develop the data integration and online analytics infrastructure.

Introducing the Osteosarcoma Explorer

The Osteosarcoma Explorer (OSE) launched in 2021 and contains data from over 570 osteosarcoma cases, including clinical, genomic, and imaging data. Designed to be accessible to researchers of all backgrounds, the OSE makes it easy to search for and download various types of osteosarcoma research data.

Dr. Crompton explains: “For example, if you are a biologist who thinks the expression of gene XYZ might predict an aggressive form of osteosarcoma, you could go into the data commons to identify the samples with high XYZ gene expression and see if those patients had a worse outcome than patients with low XYZ gene expression. That would give you a hypothesis you could then test.”

“There are many other researchers who want to ask these questions but do not have the computational expertise to search the raw data on their own. The OSE makes this data accessible to any type of scientist.” — Brian Crompton, MD

Although some high-tech labs could potentially search the raw genomic data for such an association, “there are many other researchers who want to ask these questions but do not have the computational expertise to search the raw data on their own,” Dr. Crompton says. “The OSE makes this data accessible to any type of scientist.” Using the OSE, any investigator can instantly search the data for potential links with clinical features, including outcome, that can then be further tested in well-designed experiments, saving researchers time and money finding a plausible hypotheses to test.

Getting the Word Out

Dr. Khanna says he feels strongly that the OSE will not only make it easier for osteosarcoma researchers to do their work but will also expand the number of physicians and scientists studying osteosarcoma.

“For a long time, we have had the same number of researchers doing this work,” he says. “But now, with the OSE, so many more people will have access to osteosarcoma data.”

To help get the word out about the OSE, Donghan Yang, PhD, director of the UT Southwestern Biostatistics and Data Science Core, and collaborators wrote a research article that was published in JCO Clinical Cancer Informatics in November 2023.

“It is definitely a nice milestone,” he says. “We are hoping the article will help us garner more attention and attract even more data contributors and users. Our data science approach to harmonize and integrate data of different types from various sources also sets an example for other rare diseases.”

Dr. Xie says future plans for the OSE include expanding the amount of data it contains as well as expanding the types of data included. Ultimately, the team hopes the OSE will benefit osteosarcoma patients.

“Our long-term goals for the project,” Dr. Crompton says, “are to find new therapies, develop better risk stratified treatment approaches, and improve outcomes.”

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