A grade PMID 42321916
View analysis →Finding therapies hidden in 39,040 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
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All ranked pediatric cancer papers
In an exploratory Japanese school-based intervention, medical student-led HPV education was followed by higher knowledge among some participant groups and self-reported vaccination within two weeks in 10 of 134 previously unvaccinated females and 1 of 114 previously unvaccinated males included in follow-up.
The record provides preliminary evidence that near-peer HPV education is associated with knowledge, intentions, and limited short-term self-reported vaccine uptake; it remains an inference, not a demonstrated causal effect, that this approach could increase durable vaccination coverage and thereby reduce future HPV-associated cancers.
In a cross-sectional comparison of 27 pediatric patients receiving active treatment for hematologic malignancies with an ethnically matched healthy reference population, patients had lower phase angle and handgrip strength despite greater adiposity, with the phase-angle difference persisting after adjustment for waist circumference.
The study provides evidence that direct bioelectrical impedance parameters, particularly phase angle, can detect nutritional and body-composition abnormalities not apparent from adiposity measures alone; it remains an inference requiring prospective validation that phase-angle-guided nutritional assessment or intervention could reduce toxicity or improve treatment outcomes.
This review describes biological, regulatory, commercial, and trial-design barriers in pediatric oncology and advocates mechanism-of-action-based regulation, international alignment, innovative trials, and greater attention to child-specific tumor biology.
The supplied record supports the existence of development barriers and a regulatory shift toward mechanism-of-action-based pediatric evaluation; it is plausible, but not directly demonstrated here, that combining this approach with coordinated global trials could accelerate access to effective therapies for relapsed, refractory, and rare pediatric cancers.
This 10-year retrospective cohort reports 17.6% crude PICU mortality among pediatric cancer patients and identifies older age and invasive mechanical ventilation—IMV OR 9.029 (95% CI 2.921–27.914)—as independent mortality-associated factors.
The evidence supports IMV as a prognostic marker rather than a causal treatment target; it can be hypothesized, but not concluded, that earlier recognition of deterioration and carefully evaluated noninvasive respiratory support strategies might reduce intubation or improve outcomes in selected patients.
This case report describes staged limb-salvage reconstruction in a 10-year-old girl with distal femoral osteosarcoma using a hybrid endoprosthesis–motorised lengthening nail, achieving 6 cm of distraction-generated length and a reported 1-cm residual discrepancy with pain-free activity at latest follow-up.
The reported case supports feasibility of generating native bone length after pediatric osteosarcoma resection through a temporary hybrid endoprosthesis–motorised nail construct; it remains an inference, requiring larger and longer-term studies, that this strategy could preserve bone stock, reduce repeated prosthetic expansions, and improve future revision options compared with conventional expandable prostheses.
A two-round Delphi process involving 39 experts from 22 Spanish hospitals reached consensus on 70 of 87 statements for malignancy screening and surveillance in CVID, while recommending individualized, age-adapted pediatric management rather than direct adoption of adult protocols.
The consensus supports structured risk assessment and surveillance as a feasible approach to earlier malignancy detection in CVID; however, any resulting reduction in cancer morbidity or mortality—especially in children—is an inference not tested in this record.
This retrospective cohort examined ovarian-sparing surgery versus oophorectomy in 30 girls with ovarian lesions ≥8 cm classified as O-RADS 3–4, all of which were benign on histology, although comparative surgical and follow-up outcomes are not reported in the supplied abstract.
The record supports that very large pediatric ovarian masses with non-high-risk imaging classifications can be benign and may be considered for ovarian-sparing management; it remains an inference—not demonstrated by the supplied results—that ovarian-sparing surgery provides equivalent oncologic safety while improving fertility preservation compared with oophorectomy.
This review of 16 studies comprising 1,369 pediatric posterior fossa tumor patients found no statistically significant difference in cerebellar mutism syndrome risk between transvermian and telovelar surgical approaches (pooled OR 1.85, 95% CI 0.95–3.59; p=0.07).
The evidence does not demonstrate that choosing the telovelar rather than transvermian route prevents CMS; as an inference requiring stronger prospective evidence, surgical-route selection might still influence risk because the pooled estimate and wide confidence interval do not exclude a clinically meaningful difference.
In a single-center retrospective cohort of 75 pediatric patients with 76 solitary osteochondromas, surgical excision had a low reported complication rate and no observed recurrence or reoperation over a median 63-month follow-up, while radiographs systematically underestimated intraoperative lesion size.
The reported clinical outcomes support surgical excision as a potentially effective local treatment for appropriately selected symptomatic pediatric osteochondromas; however, any inference that surgery is broadly superior, prevents recurrence, or should be guided by imaging-based size estimates requires prospective comparative evidence.
This retrospective single-center Iranian cohort of 153 infants younger than 6 months reports markedly different five-year overall survival by cancer type, with particularly poor survival among the 17 infants with leukemia compared with those with retinoblastoma or neuroblastoma.
The observed high mortality in infant leukemia provides evidence for a clinically important high-risk subgroup; it can be hypothesized, but was not tested here, that earlier recognition, leukemia-specific risk stratification, and adapted supportive or therapeutic protocols could improve outcomes.
This case report describes complete lesion resolution and sustained remission after off-label adalimumab in a 4-year-old girl with refractory classic juvenile pityriasis rubra pilaris, without severe adverse events reported during the limited observation period.
The case provides preliminary evidence that adalimumab may benefit severe juvenile PRP after conventional treatment failure; inference that TNF-α blockade is responsible for the remission remains unconfirmed because there was no comparator, mechanistic assessment, or larger pediatric cohort.
This population-based Québec study of 2,927 patients aged 0–19 years found that diagnostic intervals varied substantially by cancer type, age, rurality, and period, with shorter intervals for several cancers during 2020–2022.
The evidence identifies geographic, age-related, and cancer-specific differences in diagnostic timeliness; it is reasonable but unproven to infer that identifying and reproducing care-pathway features associated with shorter 2020–2022 intervals could accelerate diagnosis, although the record does not show improved cancer outcomes.