A grade PMID 42321916
View analysis →Finding therapies hidden in 39,079 pediatric cancer papers.
Neurocompute scores pediatric oncology literature, surfaces overlooked therapeutic signals, and turns fragmented childhood cancer research into a living discovery terminal.
Ranked Discovery Journal Articles
A grade PMID 42690647
View analysis →A grade PMID 42372741
View analysis →A grade PMID 42216567
View analysis →A grade PMID 41916649
View analysis →A grade PMID 42382416
View analysis →A grade PMID 42150584
View analysis →B grade PMID 42748428
View analysis →A grade PMID 41756844
View analysis →A grade PMID 42765973
View analysis →A grade PMID 42362103
View analysis →A grade PMID 42101908
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All ranked pediatric cancer papers
Using SEER data from 13,869 pediatric ALL patients diagnosed between 2000 and 2019, the study developed a nomogram based on age, race, and radiotherapy that showed moderate-to-good discrimination for 1-, 3-, and 5-year overall survival in training and validation cohorts.
The evidence supports prognostic risk estimation rather than a treatment effect; it may be inferred that validated risk predictions could help clinicians identify patients needing closer assessment or treatment-planning review, but the record does not show that nomogram-guided care improves survival or that radiotherapy itself is beneficial or harmful.
This case report describes a 14-year-old boy with mandibular Ewing sarcoma treated with chemotherapy, hemimandibulectomy, and immediate titanium plate–stabilized chondrocostal graft reconstruction, with satisfactory function and facial symmetry and no recurrence reported at 6 months.
The reported case provides preliminary evidence that chondrocostal autografting can achieve short-term mandibular reconstruction after Ewing sarcoma resection in a growing child; it may offer a growth-compatible reconstructive option, but comparative durability, safety, oncologic compatibility, and effects on craniofacial growth remain untested.
This four-patient pediatric case series describes variable imaging features and pathological confirmation of splenic SANT after partial splenectomy, with uneventful recovery and no recurrence or metastasis over 52–132 months.
The observed benign pathology and long recurrence-free follow-up support SANT as an indolent lesion in these resected cases; the proposal that biopsy-confirmed selected cases could be safely observed to avoid splenic surgery is an inference that was not tested and requires prospective validation.
This single-center retrospective cohort of 878 included patients with clinician-assigned PCOS/PMOS reports that AMH and several other hormonal markers peaked at ages 16–17, with the AMH difference persisting after BMI adjustment and across selected PCOS phenotypes.
The evidence supports age-dependent interpretation of hormonal profiles within PCOS/PMOS, particularly AMH; it does not test a therapy, and any use of these findings to guide diagnosis, monitoring, or treatment selection remains inferential.
This methodological study culturally adapted the Walsh Family Resilience Questionnaire for Korea and found acceptable reliability and validity among 323 parents of children with childhood cancer, spina bifida, or Down syndrome, with reduced measurement precision at very high resilience levels.
Evidence: the WFRQ-K can measure family resilience strengths and needs in Korean families of children with chronic illness. Inference: if prospectively linked to targeted family-support interventions and patient or caregiver outcomes, it could help select supportive care and monitor benefit, but this study did not test an intervention or demonstrate improved clinical outcomes.
The paper reports a collaborative systems-based implementation process that identified workflow deficiencies, developed site-specific standard operating procedures, and launched Ethiopia’s first hospital-based pediatric cancer registry across five cancer centers.
The reported evidence supports feasibility of national registry implementation, not a therapeutic intervention; indirectly, the resulting standardized data infrastructure could enable future identification of care gaps, outcome disparities, treatment patterns, and targets for quality improvement, but no improvement in treatment or survival is demonstrated here.
This retrospective two-institution cohort found that pediatric adrenal masses differed substantially from adult masses, with hematoma, neuroblastoma, and ganglioneuroblastoma predominating in children and lower surgery and minimally invasive surgery rates among pediatric patients.
The study provides descriptive evidence that age-specific adrenal-mass profiles and management patterns differ; it may be inferred that pediatric-specific diagnostic and surgical triage pathways could improve treatment selection or avoid unnecessary intervention, but no therapeutic strategy or outcome benefit was tested.
This retrospective mapping of 452 UK-funded childhood cancer studies from 2020 to July 2025 found that most research and funding focused on effective, less toxic treatments, while five stakeholder-defined priorities received no funding, including improving children's hospital experience.
The study provides no direct therapeutic evidence; it supports the inference that redirecting some research funding toward neglected priorities could generate interventions that improve treatment experience, supportive care, or outcomes, but whether such reallocation would produce effective therapies remains untested.
This 104-patient, single-center retrospective study found substantially improved Wilms tumor survival in 2006–2025 versus 1978–2005, with treatment era and metastatic disease at diagnosis independently associated with poorer survival.
Evidence: survival improved across treatment eras, while metastatic disease identified a higher-risk group; inference: studying era-specific changes in multimodal care and intensifying or refining treatment strategies for metastatic disease could reveal opportunities to improve outcomes, but this record does not identify or test a specific therapeutic intervention.
In a one-year observational series, 20 selected children with complex pediatric urologic anatomy—including one with bilateral Wilms tumor—received CT/MRI-derived VR reconstructions that three surgeons rated as useful mainly for teaching, counselling, anatomical delineation, and surgical planning.
Evidence: VR reconstruction was used clinically as an adjunct and received moderately favorable subjective usefulness ratings with high inter-rater agreement. Inference: better visualization could improve planning for anatomically complex pediatric urologic or oncologic surgery, but this record does not demonstrate improved operative, cancer, safety, cost, or patient outcomes.
This single-center retrospective cohort of 142 HIV-negative adults with drug-resistant tuberculosis found higher early sputum-culture conversion with linezolid plus bedaquiline or delamanid-containing regimens than with linezolid regimens containing neither drug, alongside reported QT-related discontinuations and linezolid toxicity.
The record supports further prospective study of linezolid–delamanid–clofazimine–cycloserine and linezolid–bedaquiline regimens for drug-resistant tuberculosis; any relevance to pediatric patients or children receiving cancer therapy is purely inferential and is not evaluated here.
In a prospective Canadian registry cohort of 964 children with newly diagnosed juvenile idiopathic arthritis, actionable adverse events were common but mostly mild and associated primarily with NSAID and methotrexate use, while serious events were uncommon.
The evidence supports closer adverse-event monitoring and toxicity-management strategies for children receiving methotrexate or NSAIDs for JIA; it only suggests, rather than establishes, that biologic DMARD-based treatment could reduce overall adverse-event risk because treatment selection and other confounding may explain the observational association.