(L to R) co-corresponding authors Jinghui Zhang, PhD, St. Jude Department of Computational Biology, and Sara Federico, MD, St. Jude Department of Oncology, Division of Solid Tumor director.
St. Jude Children’s Research Hospital scientists report the first successful treatment of a pediatric patient with high-risk refractory neuroblastoma using a targeted therapy guided by clinical genomics. Poly (ADP-ribose) polymerase (PARP) inhibition successfully exploited an identified genetic vulnerability in the patient’s cancer. The vulnerability was a mutation in the BARD1 gene, causing a defect in a DNA damage repair pathway. PARP inhibition, in combination with chemotherapeutics, exploited the cancer’s DNA damage repair defect, eventually leading to the malignancy’s destruction. The report was published today in The New England Journal of Medicine.
“At the time the patient came to St. Jude, multiple therapies had failed them,” said co-corresponding author Sara Federico, MD, St. Jude Department of Oncology, Division of Solid Tumor director. “Once we identified their specific BARD1 mutation, we were able to give them targeted therapy and eradicate their cancer. We were thrilled to see a dramatic clinical response. The patient has been off therapy for more than two years now. This treatment regimen may be successfully used for other patients with BARD1 mutations in the future.”
Refractory neuroblastoma, which resists frontline conventional treatment, is a high-risk disease with a poor prognosis. The St. Jude team used germline DNA and RNA sequencing to look for new vulnerabilities in the patient’s cancer that could be targeted therapeutically. Analyzing the data led to identifying BARD1 as driver mutation in this patient’s cancer.
“Understanding the genetic basis of an individual cancer, in this patient the complete loss of BARD1 in the tumor, led to the impressive clinical outcomes observed after PARP inhibition,” said co-corresponding author Jinghui Zhang, PhD, Endowed Chair of Bioinformatics, St. Jude Department of Computational Biology. “This case report demonstrates the potential impact of multi-omics analysis of RNA and DNA in the clinical setting. Such computational analysis is critical to assess target vulnerability and pediatric patient eligibility for precision treatments such as PARP inhibition.”
After uncovering BARD1’s involvement, the oncologists adapted treatment to PARP inhibitor talazoparib in combination with irinotecan. Talazoparib is already Food and Drug Administration approved for use in different indications adults. The pediatric patient has been off therapy for over two and a half years with no detectable disease, making this the first report of a neuroblastoma patient with a BARD1 mutation successfully treated with PARP inhibition. This provides rationale for future treatments to target vulnerabilities in DNA damage response genes in solid tumors.
Authors and funding
The report’s co-first authors are Margaret Cupit-Link and Kohei Hagiwara, of St. Jude. The report’s other authors are Matthew Nagy and Eytan Ruppin, National Cancer Institute, and Selene Koo, Brent Orr, and John Easton, St. Jude.
The work was supported by grants from the National Cancer Institute (NCI) (R01CA216391 and P30 CA21765) and ALSAC, the fundraising and awareness organization of St. Jude.
St. Jude Children's Research Hospital
St. Jude Children's Research Hospital is leading the way the world understands, treats and cures childhood cancer, sickle cell disease, and other life-threatening disorders. It is the only National Cancer Institute-designated Comprehensive Cancer Center devoted solely to children. Treatments developed at St. Jude have helped push the overall childhood cancer survival rate from 20% to 80% since the hospital opened more than 60 years ago. St. Jude shares the breakthroughs it makes to help doctors and researchers at local hospitals and cancer centers around the world improve the quality of treatment and care for even more children. To learn more, visit stjude.org, read St. Jude Progress, a digital magazine, and follow St. Jude on social media at @stjuderesearch.