Scientists identify genes linked to relapse in the most common form of childhood leukemia

Scientists from St. Jude Children’s Research Hospital, Seattle Children’s and the Children’s Oncology Group (COG) have identified novel genetic variations that influence relapse risk in children with standard risk B-cell acute lymphoblastic leukemia (SR B-ALL), the most common childhood cancer. The identification of genomic predictors of relapse in SR B-ALL provides a basis for improved diagnosis, precise tailoring of treatment intensity and potentially the development of novel treatment approaches. The study was published today in the Journal of Clinical Oncology.  

Standard risk ALL has an excellent prognosis, with remission rates over 90%. However, around 15% of patients who achieve remission later experience a relapse. Previous studies examining genomic alterations to predict relapse risk have primarily focused on high-risk ALL subgroups. SR B-ALL represents a larger group of patients and accounts for approximately half of children with ALL that relapse. This study is one of the first to systematically examine genetic factors on a large scale that influence relapse risk in SR B-ALL.  

“ALL, as the most common childhood cancer, is a great success story with over 90% of children cured. But there remains a population of children whose disease is not fully cured, and we’ve not completely understood why that’s the case,” said co-senior author, Charles Mullighan, MBBS (Hons), MSc, MD, St. Jude Comprehensive Cancer Center Deputy Director and Department of Pathology member. “This study focused on that group of poorly understood cases, where we know less about the features that influence the risk of treatment not working and the disease coming back.”  

Identifying genetic variations that modulate risk 

Genomic profiling identifies specific genetic alterations associated with cancer susceptibility, relapse risk and how tumors respond to therapeutics. These studies allow scientists and clinicians to predict how patients are likely to respond to therapy, providing insights that shape the treatment of childhood ALL. Results from this collaborative study demonstrate the importance of genomic profiling in accurately determining patient risk in B-ALL, in conjunction with traditional criteria.  

“We are planning to reduce conventional therapies in the future for children with ALL because we know that many patients can be cured with less therapy,” explained co-senior author, Mignon Loh, MD, leader of Seattle Children’s Cancer and Blood Disorders Center, COG ALL Committee chair emeritus, Seattle Children’s Ben Towne Center for Childhood Cancer Research director, and head of Seattle Children’s Division of Pediatric Hematology, Oncology, Bone Marrow Transplant and Cellular Therapy.  “We want to make sure we accurately identify those children, and because of the special design of the study, this project allowed us to do just that.” 

The scientists conducted genome and transcriptome sequencing on both SR B-ALL samples that relapsed and samples that remained in complete remission in a one:two ratio. They found that ALL subtypes, genetic alterations and patterns of aneuploidy (extra or missing chromosomes) were associated with the risk of relapse and time to relapse. Some B-ALL subtypes, such as hyperdiploid and ETV6::RUNX1 ALL, had a low frequency of relapse, but others including PAX5-altered, TCF3/4::HLF, ETV6::RUNX1-like and BCR::ABL1-like were associated with an increased risk of relapse. Notably, the specific type of genetic changes within those B-ALL subtypes further influenced the risk of relapse. This work demonstrated that genetic variations and cancer subtypes influence relapse risk in SR B-ALL, and patients classified as standard-risk can have tumors with high-risk features.  

“Whole genome sequencing was important to accurately and comprehensively identify these changes, and they could not all have been identified without it,” explained Mullighan. “Children with SR ALL should have their tumor cell genome sequenced upon their initial diagnosis to identify if their tumor cells have these high-risk features, so that their initial therapy intensity can be increased.” 

“Beyond conventional therapies, this information could also be used to develop and explore novel, personalized treatment strategies,” added Loh.  

Authors and Funding  

The study’s co-first authors are Ti-Cheng Chang and Wenan Chen of St. Jude. 

The study’s other authors are Mary Shago, University of Toronto; Karen Rabin, Baylor College of Medicine; Elizabeth Raetz, William Carroll, Perlmutter Cancer Center; Anne Angiolillo, Children’s National Medical Center; Michael Borowitz, John Hopkins University; Michael Burke, Medical College of Wisconsin; Andrew Carroll, University of Alabama at Birmingham; I-Ming Chen, Richard Harvey; University of New Mexico, Albuquerque; Nyla Heerema, The Ohio State University; Jeremy Wang, University of North Carolina at Chapel Hill; Eric Larsen, Maine Children’s Cancer Program; Leonard Mattano, HARP Pharma Consulting; Kelly Maloney, University of Colorado; Nilsa Ramirez, Nationwide Children’s Hospital and The Ohio State University; Wanda Salzer, Uniformed Services University; Cheryl Willman, Mayo Clinic; Naomi Winick, University of Texas Southwestern Medical Center; Brent Wood, University of Southern California; Stephen Hunger, Children’s Hospital of Philadelphia and the University of Pennsylvania; and Chunxu Qu, Zhongshan Chen, Dale Hedges, Abdelrahman Elsayed, Stanley Pounds, Meenakshi Devidas, Cheng Cheng, Pradyuamma Baviskar, Ilaria Iacobucci, Sima Jeha, Ching-Hon Pui, and Gang Wu, St. Jude. 

The study was supported by the National Institutes of Health (R35 CA197695 and CA21765), the Cancer Moonshot (HHSN261201500003I) and ALSAC, the fundraising 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

Seattle Children’s Hospital

Seattle Children’s mission is to provide hope, care and cures to help every child live the healthiest and most fulfilling life possible. Together, Seattle Children’s Hospital, Research Institute and Foundation deliver superior patient care, identify new discoveries and treatments through pediatric research, and raise funds to create better futures for patients. Ranked as one of the top children’s hospitals in the country by U.S. News & World Report, Seattle Children’s serves as the pediatric and adolescent academic medical center for Washington, Alaska, Montana and Idaho – the largest region of any children’s hospital in the country. As one of the nation’s top five pediatric research centers, Seattle Children’s Research Institute is internationally recognized for its work in neurosciences, immunology, cancer, infectious disease, injury prevention and much more. Seattle Children’s Foundation, along with Seattle Children’s Guild Association – the largest all volunteer fundraising network for any hospital in the country – works with our generous community to raise funds for lifesaving care and research. For more information, visit seattlechildrens.org or follow us on X, Facebook, LinkedIn, Instagram or on our On the Pulse blog.