A grade PMID 42321916
View analysis →Finding therapies hidden in 39,000 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
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All ranked pediatric cancer papers
In a single-arm study of 396 Nigerian girls aged 9–14, a bundled, comic book-guided educational intervention was associated with improved HPV knowledge and vaccine safety perception after six weeks, but not with increased class-level vaccine receipt.
The evidence shows improved knowledge and perceived vaccine safety following the bundled intervention; it is reasonable but unproven to hypothesize that culturally tailored comics could support HPV vaccination programs and ultimately cervical cancer prevention, because this study did not demonstrate increased vaccine uptake or cancer-related outcomes.
This 19-year, single-center retrospective study of 42 children with hepatoblastoma reports that chemotherapy was frequently extended or otherwise adapted to surgical timing—particularly before liver transplantation—with reported toxicity rates no higher than historical figures.
The study provides observational evidence that individualized chemotherapy adaptation can bridge selected children to resection or transplantation; it supports, but does not establish, the hypothesis that timing-responsive treatment strategies preserve operability without materially increasing cardiac, renal, or auditory toxicity.
In germline whole-genome data from 2,334 pediatric cancer cases and 3,447 controls, the study found no difference in global transposable-element burden but identified rare insertions enriched in cancer genes among solid-tumor patients, including a subset with measurable RNA effects.
The evidence supports adding transposable-element detection to germline genomic analysis to uncover otherwise missed pediatric cancer-predisposition variants; it is an inference, not demonstrated here, that improved detection could guide surveillance, treatment selection, or family management and thereby improve outcomes.
In a retrospective multi-institutional cohort of 162 children and young adults with relapsed or refractory B-ALL receiving tisagenlecleucel, peripheral blasts at apheresis correlated with inferior 12-month survival but were not independently associated with mortality after accounting for disease burden at infusion.
The evidence indicates that peripheral blasts at apheresis are primarily a readily observable correlate of later disease burden rather than an independent prognostic factor; it can be inferred, but is not demonstrated here, that monitoring or reducing disease burden between apheresis and infusion might improve risk stratification or outcomes.
This two-case report describes short-term tumor responses and acceptable reported tolerability in pediatric relapsed/refractory high-risk neuroblastoma treated with tislelizumab plus anti-GD2 antibody, GM-CSF, and sequential chemotherapy.
The cases provide preliminary evidence that this multi-agent salvage regimen can coincide with clinically meaningful responses; it is only an inference that PD-1 blockade adds benefit to anti-GD2 chemoimmunotherapy because the uncontrolled report cannot separate tislelizumab's effect from those of chemotherapy, anti-GD2 therapy, or GM-CSF.
This prospective 25-center registry analysis of 787 patients—including 18 pediatric patients—reports short hospitalization, preserved functional status, a 12.8% adverse-event rate, and associations of greater ablation extent or smaller lesion volume with improved survival outcomes after laser interstitial thermal therapy for brain tumors.
The registry supports LITT as a clinically deployable cytoreductive approach in selected patients with primary or metastatic brain tumors; it is reasonable to hypothesize, but not established by the small pediatric subgroup or observational design, that pediatric patients with suitably sized and located lesions could obtain similar treatment or recovery benefits.
Single-cell chromatin accessibility profiling of 177,500 cells from 16 diagnostic pediatric AML samples identified relapse-associated inflammatory, innate-immune, and stem-like regulatory states present at diagnosis, with AP-1, RUNX1, SPI1, and ETS factors implicated by motif enrichment.
The evidence supports an association between diagnostic epigenetic priming and later relapse; it is reasonable but unproven to hypothesize that this transcriptional network could enable relapse-risk stratification or reveal intervention targets, as no functional perturbation, prospective validation, or treatment response data are reported.
This case report and systematic review synthesized 24 uncontrolled descriptive studies involving 28 children with supratentorial intraventricular AT/RT, reporting frequent progression, high mortality, and descriptively lower mortality after gross total versus subtotal resection.
The reported clinical evidence suggests that maximal safe resection followed by risk-adapted adjuvant therapy may improve outcomes in this rare AT/RT location, but this is only a hypothesis because the apparent resection-associated survival difference comes from very small, uncontrolled, publication-prone case literature and cannot establish treatment efficacy.
In a 20-year retrospective Qatar cohort of 175 patients with inborn errors of immunity, 23 developed predominantly hematologic malignancies, with early and highly lethal cancers in DNA-repair defects and later cancers that often preceded recognition of antibody deficiencies.
The evidence supports IEI-subtype-associated differences in cancer timing and mortality; as an inference requiring prospective validation, subtype- and age-adapted surveillance—along with evaluation for underlying immunodeficiency when malignancy is a sentinel presentation—could enable earlier recognition and potentially improve outcomes, but no treatment or surveillance intervention was tested.
This cross-sectional assessment of 467 fifth-grade girls in Palau found that 70% had documented consent for HPV vaccination but only 42% had received at least one recorded dose, identifying a substantial consent-to-vaccination gap within the school-based program.
The reported evidence shows a gap between parental consent and recorded vaccine delivery; it is reasonable—but not tested here—to hypothesize that identifying and correcting school outreach, workflow, or documentation failures could increase HPV vaccine coverage and thereby improve long-term cervical cancer prevention.
This narrative review summarizes multifactorial mechanisms of chemotherapy-induced ovarian injury and preclinical strategies targeting follicular apoptosis, primordial-follicle activation, and stromal damage to preserve fertility.
The reviewed preclinical evidence suggests that inhibiting chemotherapy-triggered follicular apoptosis or activation, or protecting ovarian stroma, may preserve ovarian reserve; however, clinical safety, efficacy, and applicability—particularly in children—remain unestablished.
In 20 children with Ph+ ALL receiving oral dasatinib, paired LC-MS/MS measurements showed therapeutic systemic exposure but very low 2-hour CSF concentrations, with a median plasma-to-CSF ratio of 225:1.
The observed low CSF exposure provides direct pharmacokinetic evidence that standard oral dasatinib may inadequately cover the CNS compartment in pediatric Ph+ ALL; it can therefore be hypothesized—but is not demonstrated here—that alternative CNS-directed strategies, dosing approaches, or agents with better CNS penetration could improve CNS disease control.