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Active intelligence prompt Pediatric cancer: surface high-value therapeutic signals across pediatric oncology literature.
PEDIATRIC CANCER RESEARCH INTELLIGENCE

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.

39,079 Papers indexed
1,440 Papers AI scored
39,079 Ranked papers
100.0% Coverage
PATIENT-FRIENDLY SUMMARY

CHIP-AML22: a complex clinical trial in de novo pediatric AML patients, including a gemtuzumab ozogamicin randomization and targeted therapy with quizartinib in eligible subgroups, within the NOPHO-DB-SHIP consortium.

For education only—not personal medical advice.

LIVE PEDIATRIC ONCOLOGY INTELLIGENCE
↑ Therapeutic signals emerging ↑ New pediatric cancer papers ingested ↑ Cross-paper convergence detected ↑ Human relevance scores updating ↑ Overlooked treatment paths surfacing
TOP PEDIATRIC CANCER SIGNALS

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LATEST PEDIATRIC CANCER PAPERS

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Last ingest 2026-10-09 09:15 AM
1 Efficacy of second-line therapeutic strategies in patients with chronic nonbacterial osteomyelitis refractory to NSAIDs: A systematic review. Anales de pediatria — Oct 09, 2026 2 [68Ga]Ga-SSO120 PET/CT Imaging in Pediatric Patients with Neuroblastoma: Biodistribution and Whole-Body Radiation Dosimetry. Journal of nuclear medicine : official publication, Society of Nuclear Medicine — Oct 09, 2026 3 The Impact of Older Age at Diagnosis on Wilms Tumor Characteristics and Patient Outcomes: A Children's Oncology Group Study. Journal of the National Comprehensive Cancer Network : JNCCN — Oct 09, 2026 4 Spatial omics resolves adrenergic and mesenchymal cell states in neuroblastoma. Cancer cell — Oct 09, 2026 5 Prognostic Impact of Telomere Maintenance Mechanisms in Neuroblastoma. Journal of clinical oncology : official journal of the American Society of Clinical Oncology — Oct 09, 2026 6 Socioeconomic status and longitudinal neurocognitive outcomes following childhood brain tumour diagnosis: a Swedish national population-based cohort study. Neuro-oncology — Oct 09, 2026 7 Efficacy and Safety of Alectinib in Pediatric and Adult Patients with ALK-Altered Advanced Solid Tumors: a phase II TACKLE Trial (NCCH1712/MK003). Clinical cancer research : an official journal of the American Association for Cancer Research — Oct 09, 2026 8 Insights from a Multi-Country Survey: Healthcare Providers' Perspectives on the Management of Adults with Neurofibromatosis Type 1 and Plexiform Neurofibroma. Neurology and therapy — Oct 09, 2026
PEDIATRIC CANCER RESEARCH TERMINAL

All ranked pediatric cancer papers

39079 results
C
Construction of nomogram for the clinical outcome for pediatric acute lymphoblastic leukemia patients.
PMID 42675673 Published: 2026-08-28 Ingested: 2026-09-03 09:15 AM Medicine
AI 33.50
Standard 64.0
Final 50.28
AI Summary

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.

Why It Matters

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.

C
Ewing sarcoma of the mandible in a child-reconstruction using a chondrocostal graft.
PMID 42670436 Published: 2026-08-30 Ingested: 2026-09-02 09:15 AM Journal of surgical case reports
AI 40.30
Standard 58.4
Final 50.26
AI Summary

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.

Why It Matters

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.

C
AI 42.60
Standard 56.5
Final 50.25
AI Summary

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.

Why It Matters

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.

B
Age-stratified hormonal profiles in adolescent and young adult PCOS/PMOS: higher mid-adolescent AMH largely unexplained by BMI.
PMID 42620613 Published: 2026-08-05 Ingested: 2026-08-22 09:15 AM Frontiers in endocrinology
AI 24.80
Standard 71.0
Final 50.21
AI Summary

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.

Why It Matters

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.

C
AI 26.60
Standard 69.5
Final 50.20
AI Summary

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.

Why It Matters

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.

C
Implementation of a National Pediatric Cancer Registry in Ethiopia: A systems ("A3") thinking approach.
PMID 42616722 Published: 2026-08-19 Ingested: 2026-08-21 09:15 AM PloS one
AI 42.60
Standard 56.4
Final 50.19
AI Summary

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.

Why It Matters

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.

C
Comparison of clinical characteristics between children and adults with adrenal mass.
PMID 42645631 Published: 2026-08-23 Ingested: 2026-08-28 09:15 AM Discover oncology
AI 28.30
Standard 68.0
Final 50.14
AI Summary

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.

Why It Matters

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.

C
Does Current United Kingdom Childhood Cancer Research Address the James Lind Alliance Children's Cancer Priority Setting Partnership Priorities? A Grant Mapping Study.
PMID 42649119 Published: 2026-10-01 Ingested: 2026-08-28 09:15 AM Health expectations : an international journal of public participation in health care and health policy
AI 35.20
Standard 62.3
Final 50.11
AI Summary

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.

Why It Matters

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.

C
Long-term outcomes and prognostic factors in pediatric Wilms tumor: a 47-year single-center experience.
PMID 42777193 Published: 2026-09-11 Ingested: 2026-09-25 09:15 AM The Turkish journal of pediatrics
AI 30.50
Standard 66.0
Final 50.03
AI Summary

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.

Why It Matters

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.

C
Usefulness of virtual reality application in pediatric urology.
PMID 42573818 Published: 2026-08-10 Ingested: 2026-08-17 12:23 AM Pediatric surgery international
AI 31.80
Standard 64.9
Final 50.01
AI Summary

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.

Why It Matters

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.

C
AI 27.70
Standard 68.2
Final 49.98
AI Summary

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.

Why It Matters

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.

C
Incidence, Risk Factors and Management of Adverse Events in Contemporary Real-World Care of Children with Juvenile Idiopathic Arthritis.
PMID 42734227 Published: 2026-09-14 Ingested: 2026-09-16 09:15 AM Arthritis care & research
AI 29.50
Standard 66.72
Final 49.97
AI Summary

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.

Why It Matters

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.

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AI-assisted research information

Neurocompute uses AI to summarize scientific papers, interpret research signals, and suggest relevant reference links. AI-generated content can be incomplete, misleading, or wrong, and generated links may be irrelevant or unavailable.

Our reviewed outputs have performed strongly to date, but past accuracy is not a guarantee. Verify summaries, scores, claims, and links against the original publication before relying on them.

This platform is for research and education only. It does not provide medical advice, diagnosis, treatment recommendations, or clinical guidance.

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