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Comprehensive clinical sequencing opens door to the promise of precision medicine

St. Jude Children's Research Hospital study highlights the power of comprehensive whole genome, whole exome and RNA sequencing to better understand and treat each patient's cancer

Comprehensive clinical sequencing opens door to the promise of precision medicine
2021-07-23
(Press-News.org) St. Jude Children's Research Hospital investigators have demonstrated that comprehensive genomic sequencing of all pediatric cancer patients is feasible and essential to capitalize on the lifesaving potential of precision medicine. Results from the St. Jude Genomes for Kids study appear online today in the journal Cancer Discovery.

Whole genome and whole exome sequencing of germline DNA was offered to all 309 patients who enrolled in the study. Whole genome, whole exome and RNA sequencing of tumor DNA was carried out for the 253 patients for whom adequate tumor samples were available.

Overall, 86% of patients had at least one clinically significant variation in tumor or germline DNA. Those included variants related to diagnosis, prognosis, therapy or cancer predisposition. Researchers estimated that 1 in 5 patients had clinically relevant mutations that would have gone undetected using standard sequencing methods.

"Some of the most clinically relevant findings were only possible because the study combined whole genome sequencing with whole exome and RNA sequencing," said Jinghui Zhang, Ph.D., St. Jude Department of Computational Biology chair and co-corresponding author of the study.

Every tumor is unique. Every patient is unique. Comprehensive clinical sequencing that includes whole genome, whole exome and RNA sequencing is not widely available. But as the technology becomes less expensive and accessible to more patients, researchers said comprehensive sequencing will become an important addition to pediatric cancer care.

"We want to change the thinking in the field," said David Wheeler, Ph.D., St. Jude Precision Genomics team director and a co-author of the study. "We showed the potential to use genomic data at the patient level. Even in common pediatric cancers, every tumor is unique, every patient is unique.

"This study showed the feasibility of identifying tumor vulnerabilities and learning to exploit them to improve patient care," he said.

Tumor sequencing guided the change in treatment for 12 of the 78 study patients for whom standard of care was unsuccessful. In four of the 12 patients, the changes stabilized disease and extended patient lives. Another patient, one with acute myeloid leukemia, went into remission and was cured by blood stem cell transplantation.

"Through the comprehensive genomic testing in this study, we were able to clearly identify tumor variations that could be treated with targeted agents, opening doors for how oncologists manage their patients," said co-corresponding author Kim Nichols, M.D., St. Jude Cancer Predisposition Division director.

Additional findings and details Genomes for Kids enrolled patients between August 2015 and March 2017. Eighteen percent of patients carried germline variations in one of 156 known, cancer-predisposition genes. Almost two-thirds of the germline variations identified would not have been detected based on current screening guidelines. Next steps Genomes for Kids helped launch the hospital's clinical genomics program, which has enrolled about 2,700 cancer patients to date.

Meanwhile, data generated through the Genomes for Kids study are available at no cost to the international research community. By sharing the data, St. Jude aims to speed advances in understanding and treatment of pediatric cancer. The data are available in St. Jude Cloud.

"Even the most treatable cancers are not curable in all patients. For example, relapse remains the leading cause of death for the most common childhood cancer, acute lymphoblastic leukemia," Nichols said. "Being able to understand and predict which patients will respond to treatment and which won't requires collecting comprehensive genomic data on all patients."

INFORMATION:

Authors and funding 2Co-first authors are Wheeler, Scott Newman, Joy Nakitandwe, Chimene Kesserwan and Elizabeth Azzato, all formerly of St. Jude. James R. Downing and David Ellison of St. Jude are co-senior authors. The other authors are Michael Rusch, Sheila Shurtleff, Dale Hedges, Kayla Hamilton, Scott Foy, Michael Edmonson, Andrew Thrasher, Armita Bahrami, Brent Orr, Jeffery Klco, Jiali Gu, Lynn Harrison, Lu Wang, Michael Clay, Annastasia Ouma, Antonina Silkov, Yanling Liu, Zhaojie Zhang, Yu Liu, Samuel Brady, Xin Zhou, Ti-Cheng Chang, Manjusha Pande, Eric Davis, Jared Becksfort, Aman Patel, Mark Wilkinson, Delaram Rahbarinia, Manish Kubal, Jamie Maciaszek, Victor Pastor, Jay Knight, Alexander Gout, Jian Wang, Zhaohui Gu, Charles Mullighan, Rose McGee, Emily Quinn, Regina Nuccio, Roya Mostafavi, Elise Gerhardt, Leslie Taylor, Jessica Valdez, Stacy Hines-Dowell, Alberto Pappo, Giles Robinson, Liza-Marie Johnson and Ching-Hon Pui, all of St. Jude.

The research was funded in part by National Cancer Institute grants (CA216354, CA216391) and ALSAC, the St. Jude fundraising and awareness organization.


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Comprehensive clinical sequencing opens door to the promise of precision medicine

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[Press-News.org] Comprehensive clinical sequencing opens door to the promise of precision medicine
St. Jude Children's Research Hospital study highlights the power of comprehensive whole genome, whole exome and RNA sequencing to better understand and treat each patient's cancer