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2089 Background: Central neurocytomas (CNs) are rare, WHO grade 2 brain tumors that can have relatively high recurrence rates following surgical resection. Owing to the rarity of CNs and limited robust data, the optimal use and timing of radiotherapy (RT) remain undefined, particularly in young adults with low mortality. Tumor proliferation index (Ki-67) may also predict CN recurrence rates, but there is no consensus on its utility in clinical practice. The present collaboration between Northwestern University and the Mayo Clinic describes long-term outcomes of CN as it relates to RT timing and Ki-67 level. Methods: Patients established between 1990-2025 with a tissue diagnosis of CN at Northwestern University and the Mayo Clinic were reviewed. Demographic, treatment, and tumor characteristics (histologic/molecular) were recorded. Recurrence free survival (RFS) and overall survival (OS) were calculated according to the Kaplan Meier-method. Results: Fifty-one patients with CN (51% male, 49% female)--with a median age of 26 years and 9.7 years median follow-up--were included. RFS at 2, 5, and 10 years for the cohort was 79%, 65%, and 59% respectively; OS at 10 years for the cohort was 94%, and no deaths were attributed to uncontrolled CN. Subtotal resection (STR) yielded 2- and 5-year RFS of 74% and 65%, while gross total resection (GTR) yielded 2- and 5-year RFS of 90% and 66%. Median Ki-67 of the cohort was 3%; RFS at 2 and 5 years for Ki-67 <3% was 82% and 76%, compared to 76% and 43% for Ki-67 ≥3% (p<0.02). In patients who underwent resection without adjuvant RT (n=35), those with STR had a 2- and 5-year RFS of 61% and 45%, and those with GTR had a 2- and 5- year RFS of 88% and 61%. Additionally, without adjuvant RT, RFS at 2 and 5 years for Ki-67 <3% was 73% and 64% versus 71% and 24% for Ki-67 ≥3%. Among patients without adjuvant RT and Ki-67 ≥3% (n=14), 2-year RFS was 60% after STR and 78% after GTR. Salvage RT after first recurrence (n=16) had a 5-year RFS of 81%, with a median follow-up of 4.1 years. Conclusions: We report one of the largest cohorts of CN with long-term follow-up. STR and/or Ki-67 ≥3% were associated with shorter RFS. Salvage RT at recurrence achieved durable long-term tumor control, and long-term (~10-year) mortality was low. In appropriately selected patients, observation after resection may be a reasonable initial strategy, with RT reserved for salvage. General cohort characteristics (n=51) with Ki-67 (n=39). Variable Number (%) Median Age (years) 26 (range: 5-57) Gender, Male:Female (M/F) 26:25 (51/49) Subtotal Resection 29 (57) Gross Total Resection 22 (43) Adjuvant Radiotherapy 16 (31) Salvage Radiotherapy 16 (31) No Radiotherapy 19 (38) Ki-67 ≥3 21 (56) Ki-67 <3 18 (44)

Introduction: Evidence suggests that the distal radioulnar joint injury associated with an operatively treated displaced fracture of the distal radius does not benefit from specific treatment after the radius is realigned. To better understand variation in treatment of the distal radioulnar joint we performed a scenario-based experiment presenting radiographs of displaced distal radial fractures accompanied by clinical scenarios with randomized aspects. Methods: In a survey-based experiment, participants of the Science of Variation Group viewed a random subset of five of 10 sets of radiographs showing displaced fractures of the distal radius before and after anterior plate fixation. Each was accompanied by a clinical scenario with trauma energy level, age and gender randomized. Participants indicated their preferred distal radioulnar joint treatment: none, cast immobilization, operative reattachment of ligaments or ulnar styloid fixation, or distal radioulnar joint pinning. Factors associated with any treatment and with reattachment were sought in multivariable regression. Results: Surgeons recommended distal radioulnar joint treatment in 67% (404 of 607) of the scenarios, most commonly cast immobilization in 41% (247 of 607). Recommendation for any distal radioulnar joint treatment was associated with younger patient age, and for reattachment specifically, was associated with younger patient age, high-energy trauma and fracture of the base of the ulnar styloid. Conclusions: The observation of frequent recommendation for distal radioulnar joint treatment, relatively more so for younger patients with higher energy injuries, and some tendency to repair an aligned ulnar styloid base fracture may diverge from existing evidence.

OBJECTIVE Craniopharyngiomas are challenging lesions, and aggressive resections may cause significant postoperative morbidity and mortality. To mitigate morbidity, a potential strategy of subtotal resection (STR) and adjuvant radiation therapy (RT) has been used, but its impact on survival when compared to gross-total resection (GTR) has been under-investigated. Thus, the objective of this study was to analyze short-term mortality between patients undergoing STR ± RT and GTR, and differences in overall survival (OS) between patients undergoing STR, STR + RT, and GTR in a large, nationally representative database. METHODS The authors queried the National Cancer Database for patients diagnosed with craniopharyngioma between 2004 and 2017. Tumor characteristics, treatment strategies, and extent of resection were analyzed. Endpoints were 3-month mortality rate and OS, which were compared between treatment modalities. Firth’s logistic regression was used to analyze 3-month mortality and was adjusted for age, sex, Charlson Comorbidity Index score, histopathological diagnosis, income quartile, insurance payor, and maximal tumor diameter. Differences in survival between treatment modalities were compared with log time-to-event analyses after excluding deaths occurring within 3 months to control for immortal time bias. RESULTS A total of 1460 adult and 390 pediatric patients were included. Adults undergoing STR ± RT had a lower rate of 3-month mortality compared to those undergoing GTR in adjusted analysis (2.8% vs 4.6%, odds ratio 0.42; p = 0.03). Survival curves for the STR + RT and GTR cohorts did not significantly differ (p = 0.198). A strategy of STR alone showed worse OS compared with GTR and STR + RT (p < 0.01). The average follow-up length for adults was 65.5 months. For pediatric patients, 3-month mortality for those undergoing GTR and STR ± RT was similar (0% vs 1%, respectively; p = 0.33). Additionally, compared to GTR, there were no significant differences in OS between STR + RT (p = 0.41) and STR alone (p = 0.44). The average follow-up length for the pediatric cohort was 79 months. CONCLUSIONS STR + RT was associated with a favorable perioperative mortality profile when compared with GTR and provided similar long-term survival outcomes. Therefore, STR + RT may be considered when GTR carries significant risks.

Background The purpose of this study was to assess the clinical benefits of guideline‐directed medical therapy (GDMT) for heart failure (HF) in adults with congenital heart disease and HF with reduced ejection fraction. Methods HF with reduced ejection fraction was defined as stage B/C HF and systemic left ventricular ejection fraction <50%. GDMT score was assessed at baseline encounter (baseline GDMT score) and 1‐year follow‐up. GDMT uptitration was calculated as defined as ∆GDMT score from baseline. Cox regression was used to assess the relationship between HF therapy (baseline and ∆GDMT score) and outcomes (HF hospitalization and mortality). Results Of 778 patients (age 44±16, 480 [62%] males), baseline GDMT score was 2 (1, 3) and ∆GDMT score was 0.62 (95% CI, 0.55–0.69). Of 778, only 258 (33%) had GDMT uptitration (∆GDMT score >0). Higher use of GDMT at baseline (adjusted HR per 1 point increase in GDMT score 0.81, 95% CI, 0.74–0.88, P <0.001), and increased use of GDMT over time (adjusted HR for 1 point increase in ∆GDMT score HR 0.70, 95% CI, 0.61–0.79, P <0.001) were associated with lower risk of HF hospitalization. Higher baseline GDMT score (adjusted HR 0.85, 95% CI, 0.76–0.94, P <0.001), and ∆ GDMT score (adjusted HR 0.82, 95% CI, 0.71–0.94, P <0.000) were also associated with lower mortality. Conclusions GDMT use at baseline and GDMT uptitration were associated with improved outcomes and suggest a dose‐dependent relationship between use of GDMT and risk of adverse outcomes. Furthermore, 67% of patients did not receive GDMT uptitration, suggesting suboptimal therapy, and opportunities for improvement.

ABSTRACT Aim The supply of donor kidneys (living and deceased) has fallen far behind the need, while the number of patients with end stage kidney disease continues to rise, increasing their risk of cardiovascular mortality. Kidney transplant candidates frequently exhibit large artery calcification, a major contributor to cardiovascular death. This study aimed to evaluate the relationship between abdominal arterial calcification (AAC) and survival in patients awaiting kidney transplant. Methods We modified the coronary calcium scoring method (Modified Agatston Method) and applied it to quantify AAC. This retrospective study included all adult patients ( N = 4184) listed for kidney transplant from 2005 to 2023 who had undergone abdominal computed tomography (CT) scans. Patients were categorised into two groups: those who died while on the waiting list (DWL) and those who survived (SWL). Results Among 4184 candidates, 446 (10.7%) died while on the waiting list, and 3738 (89.3%) survived to transplant or study end. Patients in the DWL group had significantly higher AAC scores across all vascular sites. The median total AAC score was 3605.8 (IQR 780.1–9017.3) in the DWL group versus 940.1 (IQR 49.2–4915.0) in the SWL group. Each 1000‐point increase in total AAC was associated with a 5.1% increase in mortality risk (HR 1.051; p < 0.001). An AAC cutoff of > 1769 correlated with reduced 5‐year survival (45.4% vs. 77.4%, p < 0.001). Conclusion AAC scoring on non‐contrast abdominal CT represents a noninvasive biomarker of mortality in kidney transplant waitlist patients and may enhance risk stratification and personalised care.

The European Health Data Space (EHDS) aims to enable both the primary use of health data for direct patient care (EHDS1) and the secondary use of data for research, innovation, and public health (EHDS2). While each pillar is supported by distinct infrastructures—MyHealth@EU for clinical continuity and HealthData@EU for trusted reuse—the lack of seamless integration between them poses significant technical, governance, and legal challenges. Existing standards such as HL7 CDA, HL7 FHIR, OHDSI OMOP, CDISC, EEHRxF, and HealthDCAT-AP, together with IHE integration profiles including XDS, XCA, XCPD, ATNA, and BPPC, provide a robust foundation but remain fragmented across domains. This paper introduces the EHDS Data Continuum, a proposed IHE integration profile designed to bridge EHDS1 and EHDS2 by harmonizing interoperability, data quality, privacy, and governance requirements across the full data lifecycle. By aligning primary and secondary use within a coherent technical and policy framework, the EHDS Data Continuum supports the realization of a trustworthy, interoperable, and citizen-centered European Health Data Space.

BACKGROUND AND OBJECTIVES: Contralateral transfalcine approaches are widely used for interhemispheric/mesial cortical pathologies, even those extending beyond 2 cm lateral from the midline. Nevertheless, the superior limit of contralateral exposure through this approach is not defined. This anatomic study aims to characterize the maximal superior and lateral limits of contralateral exposure using a contralateral transfalcine approach. METHODS: Interhemispheric approaches in the anterior, middle, and posterior-thirds of the interhemispheric fissure were performed in 10 cadaveric head specimens. Rectangular falcine incisions were made and carried maximally superiorly. The contralateral hemisphere was maximally laterally resected from the superior point of visualization down to the level of the corpus callosum. Distances between the most superior point of visualization of the contralateral hemisphere and the superficial point of its cortex and between the midline and the most lateral point of visualization at the level of the corpus callosum were measured and are reported as averages. RESULTS: At the anterior-third of the interhemispheric fissure, the superior point of visualization was 4.8 mm inferior to the cortex. The lateral distance of visualization at the genu of the corpus callosum was 22.9 mm. At the middle-third, the superior point of visualization was 9.7 mm inferior to the cortex. The lateral distance visualized at the body of the corpus callosum was 22.4 mm. At the posterior-third, the superior point visualization of the mesial contralateral hemisphere was 12.6 mm inferior to the cortex. The lateral distance visualized at the splenium of the corpus callosum was 21.3 mm. CONCLUSION: Using the contralateral transfalcine approach, the superior limit of contralateral exposure progressively decreases more posteriorly along the interhemispheric corridor—ranging from 4.8 mm inferior to the cortex in the anterior-third to 12.6 mm inferior to the cortex in the posterior-third. The contralateral optimal view of exposure increases deeper along the interhemispheric corridor.

ABSTRACT Richter transformation of Chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) into classic Hodgkin lymphoma (CHL-RT) is rare and remains incompletely understood. Two histologic subtypes are recognized: type 1 (CLL/SLL with scattered Hodgkin/Reed-Sternberg (HRS) cells) and type 2 (HRS cells within a polymorphous inflammatory background). In this multi-institutional study of 77 patients with CHL-RT (27 type 1 and 50 type 2), we characterized immune evasion markers, PD-L1 / PD-L2 copy number alterations, tumor microenvironment, and performed targeted next-generation sequencing on 37 CLL/SLL samples. HRS cells in CHL-RT displayed immune-evasion phenotypes similar to de novo CHL, though PD-L1 expression was lower in type 1 cases. PD-L1/PD-L2 gain/polysomy were frequent (83.3%). CLL/SLL with CHL-RT harbored increased mutations in XPO1, FBXW7, BIRC3, TRAF3 , and HLA-A versus reference CLL/SLL. Similar mutational profiles, demographics, and survival outcomes support a biological continuum between type 1 and type 2 CHL-RT, with distinct genetic features in CLL/SLL predisposing to CHL transformation. STATEMENT OF SIGNIFICANCE Classic Hodgkin lymphoma-type Richter transformation arises from convergent Hodgkin-like immune evasion on a genetically primed CLL/SLL background. Through integrated genomic and tumor microenvironment analyses in a large multicenter cohort, we establish this as a biologically coherent entity and provide rationale for PD-L1/PD-L2-directed therapeutic strategies.