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
View analysis →A grade PMID 42216567
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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
This observational case series characterizes clinical findings and seven pathogenic or likely pathogenic WAS variants in 10 genetically confirmed Moroccan boys, of whom one underwent HSCT with sustained remission while the remainder received supportive therapy.
The record supports molecular testing as a means to confirm WAS and inform counseling and referral, and reports sustained remission after HSCT in one child; it is an untested inference that earlier genetic diagnosis and referral would increase timely access to curative therapy or improve outcomes in resource-limited settings.
This single-centre pilot found that parental distress generally declined between two assessments during a child's active cancer treatment, although clinically significant fatigue, drowsiness, and anxiety remained common at the second assessment.
The study provides evidence that repeated nurse-navigator-led screening can identify persistent caregiver distress; it is an inference, not demonstrated here, that screening linked to timely psychosocial referrals would improve caregiver well-being, treatment participation, or child outcomes.
Using age-specific pediatric head-and-neck phantoms, the study found that PCXMC-20Rotation estimates generally agreed with dosimeter measurements and that dose-area product strongly correlated with modeled effective dose and radiation-induced cancer-death risk during dental CBCT imaging.
The supplied evidence supports DAP as a practical surrogate for estimated radiation dose and modeled risk in the evaluated imaging settings; it is reasonable but unproven to infer that child-specific settings and routine DAP monitoring could reduce unnecessary radiation exposure and thereby lower long-term radiation-associated cancer risk.
The study reports that hnRNPD is upregulated in Wilms tumor datasets and cell lines, promotes proliferation and suppresses apoptosis in vitro, and that p38 MAPK inhibition counteracts the proliferative effect of hnRNPD overexpression.
The supplied evidence supports an hnRNPD-associated, p38 MAPK-dependent proliferative phenotype in Wilms tumor cells; it is therefore reasonable—but still inferential—to hypothesize that inhibiting hnRNPD or downstream p38 MAPK signaling could provide a therapeutic strategy, pending validation in animal models, patient-derived systems, and clinical safety studies.
In a prospective four-center cohort of 327 adult and pediatric patients with suspected myasthenia gravis, cell-based assays—particularly live CBA—showed better diagnostic accuracy and substantially higher specificity for acetylcholine receptor antibodies than ELISA.
Evidence: live and fixed cell-based assays improved diagnostic classification of suspected myasthenia gravis relative to ELISA; inference: more accurate testing could indirectly support appropriate treatment selection and reduce treatment prompted by false-positive results, but no therapeutic intervention, oncology application, or pediatric-specific outcome was evaluated.
This case report describes a 17-year-old with a rare maxillary solitary extramedullary plasmacytoma showing mixed osteolytic-osteosclerotic imaging features, with complete remission and no recurrence at 21 months after 45 Gy radiotherapy.
The reported observation supports radiotherapy as a potentially effective local treatment in this individual; it may also suggest that imaging-pathology correlation can improve treatment selection by distinguishing plasmacytoma from mimicking maxillofacial tumors, but neither efficacy nor diagnostic performance can be generalized from a single case.
In a secondary analysis of 47 bereaved oncology parents, satisfaction with family coping was associated with lower depression, anxiety, and prolonged-grief symptoms during early bereavement but did not predict later mental health after adjustment for baseline symptoms.
The evidence identifies family-coping satisfaction as an early-bereavement correlate of better parental mental health; it is reasonable—but untested—to hypothesize that interventions improving family coping could reduce distress after a child’s cancer death.
Interviews with 20 adolescent-caregiver dyads from one Chinese tertiary hospital identified stalled long-term planning, social closure, and adolescent-caregiver power asymmetry as predicaments in family resilience during adolescent leukaemia.
The study provides descriptive evidence supporting dyadic assessment; it is reasonable but untested to hypothesize that family-centred nursing interventions addressing adolescent illness disclosure, developmental autonomy, and caregiver emotional support could improve family adaptation or resilience.
This scoping review of 39 studies synthesizes direct reports from children aged 6–12 with cancer and characterizes meaning making as a dynamic, developmentally grounded, relational, and socioculturally influenced process.
The review supports the observation that children actively make meaning during cancer; it is reasonable but untested to hypothesize that developmentally and culturally responsive psychosocial, communication, or palliative-care interventions targeting this process could improve coping, participation, or psychosocial-spiritual well-being.
This article reviews histology-specific indications and multidisciplinary integration of metastasectomy for several metastatic pediatric solid tumors, including management of pulmonary and extrapulmonary disease while considering function and late morbidity.
The supplied record supports the clinical premise that metastasectomy should be individualized by histology, treatment response, metastatic site, and systemic treatment context; it can only be inferred—not established from reported comparative outcomes—that this tailoring may improve tumor control while limiting functional loss and late morbidity.
In a retrospective cohort of 32 pediatric patients with papillary thyroid carcinoma, extrathyroidal extension was independently associated with cervical lymph node metastasis after adjustment for T stage and lymphatic invasion.
The reported association supports extrathyroidal extension as a candidate postoperative risk-stratification marker; it may help identify children who warrant closer surveillance, but improved treatment selection or outcomes remain an untested inference.
In a 2013–2023 surgical database study of 241,885 women with breast cancer, patients aged 18–39 underwent mastectomy and metastatic-setting surgery more often than older patients, with similar 30-day complication and mortality rates but a slightly higher reoperation rate.
The evidence supports using these data as a contemporary perioperative benchmark for counseling young adult breast-cancer patients; it only suggests—and does not establish—that more extensive surgery is acceptably safe or improves cancer outcomes in this population.