Genetic Marker Predicts Early Relapse in Pediatric ALL
|
By LabMedica International staff writers Posted on 24 Dec 2018 |

Image: Bone marrow aspirate smear from a patient with acute lymphoblastic leukemia reveals increased blasts which are small to medium in size with high nuclear-to-cytoplasmic ratios, round to irregular nuclei, smooth chromatin, and scant basophilic agranular cytoplasm (Photo courtesy of Karen M. Chisholm MD, PhD).
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer; however, treatment has improved dramatically due to the ability to stratify patients into groups based on risk factors and genetic analysis.
About 15% to 20% of ALL patients who have reached complete remission eventually relapse. ALL relapse is considered one of the major cancer-related causes of death among childhood malignancies. Relapse can occur even in patients with favorable prognostic factors at diagnosis.
Scientists at the Nova Southeastern University (Fort Lauderdale, FL, USA) and their associates discovered that by testing the level of nucleotide excision repair (NER) gene expression, pediatric oncologists can determine the likelihood of early relapse (less than three years) in their acute lymphoblastic leukemia (ALL) patients. This study included two matched diagnosis-relapse paired gene expression datasets of pediatric ALL. The Staal dataset included 41 patients diagnosed with both precursor-B-ALL (n = 27) and T-ALL (n = 14) and treated. The Hogan dataset included 49 treated patients with precursor-B-ALL.
The Affymetrix Human Genome U133 plus 2 array was used to generate both datasets. Data on 51 probes representing 20 NER canonical genes were extracted. Expression data on multiple probes for a single gene were averaged. The expression of the canonical 20 NER genes was examined in matched pediatric samples at the time of diagnosis and relapse of only precursor-B-ALL patients from both datasets. The team classified patients based on the time of recurrence as either early (less than 36 months) or late (equal to or more than 36 month) relapsers, regardless of other prognostic variables.
The scientists reported that gene expression of the NER pathway was significantly increased upon relapse in patients that took three years or greater to relapse, whereas no such change was evident in patients that relapsed in less than three years. Moreover, at diagnosis, the NER gene expression of the early relapsing subpopulation was already significantly elevated over that of the late relapsing group. This pattern was validated by an ‘NER score’ established by averaging the relative expression of the 20 canonical NER genes. The NER score at diagnosis was found to be significantly associated with disease-free survival in precursor-B-ALL.
Jean Latimer, PhD, an associate professor and oncology scientist, said, “Our study found a correlation between high NER expression levels and early relapses of ALL among relapsing patients. Being able to identify patients with the highest risk of early recurrence who are not detectable using present clinical measures and then treating them with a more targeted therapy is crucial to overcoming the cancer.” The study was published on October 30, 2018, in the journal BMC Medical Genomics.
Related Links:
Nova Southeastern University
About 15% to 20% of ALL patients who have reached complete remission eventually relapse. ALL relapse is considered one of the major cancer-related causes of death among childhood malignancies. Relapse can occur even in patients with favorable prognostic factors at diagnosis.
Scientists at the Nova Southeastern University (Fort Lauderdale, FL, USA) and their associates discovered that by testing the level of nucleotide excision repair (NER) gene expression, pediatric oncologists can determine the likelihood of early relapse (less than three years) in their acute lymphoblastic leukemia (ALL) patients. This study included two matched diagnosis-relapse paired gene expression datasets of pediatric ALL. The Staal dataset included 41 patients diagnosed with both precursor-B-ALL (n = 27) and T-ALL (n = 14) and treated. The Hogan dataset included 49 treated patients with precursor-B-ALL.
The Affymetrix Human Genome U133 plus 2 array was used to generate both datasets. Data on 51 probes representing 20 NER canonical genes were extracted. Expression data on multiple probes for a single gene were averaged. The expression of the canonical 20 NER genes was examined in matched pediatric samples at the time of diagnosis and relapse of only precursor-B-ALL patients from both datasets. The team classified patients based on the time of recurrence as either early (less than 36 months) or late (equal to or more than 36 month) relapsers, regardless of other prognostic variables.
The scientists reported that gene expression of the NER pathway was significantly increased upon relapse in patients that took three years or greater to relapse, whereas no such change was evident in patients that relapsed in less than three years. Moreover, at diagnosis, the NER gene expression of the early relapsing subpopulation was already significantly elevated over that of the late relapsing group. This pattern was validated by an ‘NER score’ established by averaging the relative expression of the 20 canonical NER genes. The NER score at diagnosis was found to be significantly associated with disease-free survival in precursor-B-ALL.
Jean Latimer, PhD, an associate professor and oncology scientist, said, “Our study found a correlation between high NER expression levels and early relapses of ALL among relapsing patients. Being able to identify patients with the highest risk of early recurrence who are not detectable using present clinical measures and then treating them with a more targeted therapy is crucial to overcoming the cancer.” The study was published on October 30, 2018, in the journal BMC Medical Genomics.
Related Links:
Nova Southeastern University
Latest Hematology News
- Rapid Cartridge-Based Test Aims to Expand Access to Hemoglobin Disorder Diagnosis
- New Guidelines Aim to Improve AL Amyloidosis Diagnosis
- Automated Hemostasis System Helps Labs of All Sizes Optimize Workflow
- Fast and Easy Test Could Revolutionize Blood Transfusions
- High-Sensitivity Blood Test Improves Assessment of Clotting Risk in Heart Disease Patients
- AI Algorithm Effectively Distinguishes Alpha Thalassemia Subtypes
- MRD Tests Could Predict Survival in Leukemia Patients
- Platelet Activity Blood Test in Middle Age Could Identify Early Alzheimer’s Risk
- Microvesicles Measurement Could Detect Vascular Injury in Sickle Cell Disease Patients
- ADLM’s New Coagulation Testing Guidance to Improve Care for Patients on Blood Thinners
- Viscoelastic Testing Could Improve Treatment of Maternal Hemorrhage
- Pioneering Model Measures Radiation Exposure in Blood for Precise Cancer Treatments
- Platelets Could Improve Early and Minimally Invasive Detection of Cancer
- Portable and Disposable Device Obtains Platelet-Rich Plasma Without Complex Equipment
- Disposable Cartridge-Based Test Delivers Rapid and Accurate CBC Results
- First Point-of-Care Heparin Monitoring Test Provides Results in Under 15 Minutes
Channels
Clinical Chemistry
view channel
New CLIA Status Brings Mass Spectrometry Steroid Testing to Routine Labs
Steroid hormone measurement is a core application of clinical mass spectrometry, which is widely regarded as a diagnostic gold standard. Access to these high-specificity methods has often been constrained... Read more
Study Shows Dual Biomarkers Improve Accuracy of Alzheimer’s Detection
Alzheimer’s disease develops slowly, and biological changes can appear in blood many years before symptoms. While plasma assays for phosphorylated tau offer earlier detection, discerning whether these... Read moreHematology
view channel
Rapid Cartridge-Based Test Aims to Expand Access to Hemoglobin Disorder Diagnosis
Sickle cell disease and beta thalassemia are hemoglobin disorders that often require referral to specialized laboratories for definitive diagnosis, delaying results for patients and clinicians.... Read more
New Guidelines Aim to Improve AL Amyloidosis Diagnosis
Light chain (AL) amyloidosis is a rare, life-threatening bone marrow disorder in which abnormal amyloid proteins accumulate in organs. Approximately 3,260 people in the United States are diagnosed... Read moreImmunology
view channel
FDA Approval Expands Use of PD-L1 Companion Diagnostic in Esophageal and GEJ Carcinomas
Esophageal and gastroesophageal junction carcinomas (GEJ) have a poor prognosis, with approximately 16,250 deaths in the United States in 2025 and a five-year relative survival of 21.9%.... Read more
Study Identifies Inflammatory Pathway Driving Immunotherapy Resistance in Bladder Cancer
Bladder cancer remains a prevalent malignancy with variable responses to immune checkpoint inhibitors. Clinicians often observe elevated C-reactive protein and interleukin-6 in affected patients, yet the... Read moreMicrobiology
view channel
WHO Endorses Rapid Point-of-Care Testing to Improve TB Detection
Tuberculosis (TB) remains a leading infectious killer, with more than 3,300 deaths and 29,000 new illnesses every day. Diagnostic delays and dependence on centralized laboratory networks continue to impede... Read more
Breath Analysis Approach Offers Rapid Detection of Bacterial Infection
Accurate and rapid identification of bacterial infections remains challenging in acute care, where delays can hinder timely, targeted therapy. Infectious diseases are a major cause of mortality worldwide,... Read more
Study Highlights Accuracy Gaps in Consumer Gut Microbiome Kits
Direct-to-consumer gut microbiome kits promise personalized insights by profiling fecal bacteria and generating health readouts, but their analytical accuracy remains uncertain. A new study shows that... Read more
WHO Recommends Near POC Tests, Tongue Swabs and Sputum Pooling for TB Diagnosis
Tuberculosis (TB) remains one of the world’s leading infectious disease killers, yet millions of cases go undiagnosed or are detected too late. Barriers such as reliance on sputum samples, limited laboratory... Read morePathology
view channel
Biopsy-Based Gene Test Predicts Recurrence Risk in Lung Adenocarcinoma
Lung cancer is the leading cause of cancer death, killing more people in the United States than breast, prostate, and colon cancers combined. In lung adenocarcinoma (LUAD), tumors that invade nearby blood... Read more
AI-Powered Tool to Transform Dermatopathology Workflow
Skin cancer accounts for the largest number of cancer diagnoses in the United States, placing sustained pressure on pathology services. Diagnostic interpretation can be variable for challenging melanocytic... Read moreTechnology
view channel
Rapid Biosensor Detects Drug Sensitivity in Breast Tumors
Chemotherapy selection for breast cancer is challenged by heterogeneous tumor responses. Conventional chemosensitivity assays can be slow, require large sample volumes, and struggle with complex biological... Read more
Online Tool Supports Family Screening for Inherited Cancer Risk
Genetic test results in oncology often have implications for relatives who may share inherited cancer risk. Many health systems lack structured processes to help patients alert family members, limiting... Read moreIndustry
view channel
Integrated DNA Technologies Expands into Clinical Diagnostics
Integrated DNA Technologies (IDT; Coralville, Iowa, USA) has announced the launch of Archer FUSIONPlex-HT Dx and VARIANTPlex-HT Dx. This launch marks the company’s first in vitro diagnostic (IVD) offerings... Read more








