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4008 citation(s) found for "Yu, Charles".

A Phase 2 Study of Berzosertib in Combination with Carboplatin compared to Docetaxel with Carboplatin in Metastatic Castration-Resistant Prostate Cancer
Choudhury, Atish D. , Zhong, Caiwei , Xie, Wanling , Kochupurakkal, Bose , Wu, Peter I-Fan , Riaz, Irbaz Bin , Liu, Ruolin , Yang, David D. , Folefac, Edmund , Lee, Daniel , McKay, Rana R. , Pace, Amanda F. , Adalsteinsson, Viktor A. , Kunos, Charles A., Gore, Steven D. , Das, Biswajit , Taplin, Mary‐Ellen , Kochupurakkal, Bose S , Parikh, Mamta , Einstein, David J , Kessler, Elizabeth , Mayer, Tina , McKay, Rana R , Pace, Amanda , Mouw, Kent W , Chen, Li , Adalsteinsson, Viktor A , Van Allen, Eliezer M , Kunos, Charles , Gore, Steven D , Das, Biswasjit , D'Andrea, Alan , Taplin, Mary-Ellen , Shapiro, Geoffrey I , Choudhury, Atish D , Riaz, Irbaz B , Xie, Wanling , Wu, Peter I-Fan , Mouw, Kent W. , D’Andrea, Alan D. , Shapiro, Geoffrey I.

Cancer Research Communications | August 24, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1158/2767-9764.crc-26-0488 | PMID 42636061 Get It

Abstract Purpose: Inhibitors of the Ataxia telangiectasia and Rad3-related (ATR) protein kinase, a critical component of the DNA damage repair response, have synergistic anti-cancer activity with platinum compounds in preclinical models. We therefore conducted a Phase 2 study of the ATR inhibitor berzosertib+carboplatin vs. docetaxel+carboplatin in metastatic castration-resistant prostate cancer. Patients and Methods: Patients previously treated with at least one androgen receptor pathway inhibitor and taxane underwent mandatory biopsy and were randomized 1:1 to receive Arm A (docetaxel 60 mg/m2+carboplatin AUC4 day 1; or carboplatin AUC5 if not a docetaxel candidate) or Arm B (berzosertib 90 mg/m2 days 2,9+carboplatin AUC5 day 1) every 21 days. The primary endpoint was overall response rate (ORR; ≥50% PSA decline or radiographic response). Results: Of 73 randomized patients, 65 received protocol treatment: 34 on Arm A (26 docetaxel+carboplatin; 8 carboplatin alone) and 31 on Arm B. Thirteen patients (38%) in Arm A and 20 (65%) in Arm B had ≥Grade 3 treatment-related adverse events (TrAEs). ORR was 15% in Arm A (5/34; 5/26[19%] with docetaxel+carboplatin) and 0% in Arm B (0/31). At interim analysis after 65 of planned 130 patients were treated, enrollment was halted due to futility. Homologous recombination repair deficiency status from tissue and blood did not correlate with clinical outcomes, but ATM-deficiency or high levels of phoshpo-KAP1 detected in tissue was associated with clinical benefit across both arms of the trial. Conclusions: Berzosertib+carboplatin demonstrated lower ORR and more frequent ≥grade 3 TrAEs compared to docetaxel+carboplatin in this heavily pre-treated, biomarker-unselected population. NCT03517969
Epidemiologic Study of Transfusion-Related Alpha-Gal Syndrome
Kaufman, Richard M., Hoen, Anne G., Khan, Jenna, Knudson, C. Michael, Romero, Andres E. Mindiola, Mo, Allison , Takanashi, Minoko , Collaborative, UPTICK Study Group; for the Biomedical Excellence for Safer Transfusion (BEST), Cardigan, Rebecca, Stanworth, Simon J., Commins, Scott P. , Scherer, Emily A., Davenport, Robertson D., Afraz, Sajjad, Andrews, Jennifer , Casey, John, Sullivan, Jensyn Cone , Cousins, Clara C. , Giorgi, Valeria De , Delaney, Meghan, DelBaugh, Regina M. , Gilstad, Colleen W. , Gofton, Alexander , Hill, Kate, Hogan, Keenan , Humbrecht, Catherine , Ikeda, Kazuhiko, Javanbakht, Ayda, Juskewitch, Justin E, Wojtowicz, Monique M. Menzies, Miller, Maureen J., Mills, Georgia, Nelson, Anna C. , Pauly, Marie C., Poisson, Jessica , Raval, Jay S., Samy, Nikitha, Sato, Tomohiko, Takeda, Yoshinori , Thibodeaux, Suzanne R. , Nunen, Sheryl van, Virk, Mrigender S., West-Mitchell, Kamille, Yamanouchi, Jun, Yoshihara, Satoshi, Zheng, X. Long, Ziman, Alyssa, Cone Sullivan, Jensyn , Kaufman, Richard Max , Hoen, Anne Gatewood , Knudson, Charles Michael , Metcalf, Ryan A. , Schäfer, Richard , Dunbar, Nancy M. , Cardigan, Rebecca A. , Stanworth, Simon J., Scherer, Emily A. , Cervinski, Mark A , Arai, Yasuyuki , Brugnara, Carlo , Allen, Elizabeth S. , Aurich, Konstanze , Casey, John , Cohn, Claudia S. , Crowe, Elizabeth P , Delaney, Meghan , Hendrickson, Jeanne E. , Hill, Kate, Ikeda, Kazuhiko , Jacquot, Cyril , Javanbakht, Ayda , Juskewitch, Justin E. , Lu, Wen , Wojtowicz, Monique Menzies , Miller, Maureen J. , Nelson, Anna , Pagano, Monica B. , Pauly, Marie-Christin , Saifee, Nabiha H , Sato, Tomohiko, Takeda, Yoshinori, Tiberghien, Pierre , Nunen, Sheryl van, Virk, Mrigender , Wood, Erica M , Yoshihara, Satoshi , Zheng, X. Long, Ziman, Alyssa

JAMA Internal Medicine | August 24, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1001/jamainternmed.2026.3983 | PMID 42636004 Get It

Importance Recent case reports suggest that B antigen–containing blood products may be associated with anaphylactic transfusion reactions in recipients with preformed immunoglobulin E to galactose- α -1,3-galactose (alpha-gal). Objective To test the association of local alpha-gal syndrome (AGS) prevalence and allergic transfusion reaction (ATR) in patients with blood type O. Design, Setting, and Participants In this international, multicenter, retrospective cohort study at academic medical centers, sites were assigned to AGS high- or low-prevalence clusters based on the known geographic distribution of AGS. Data were collected on platelet or plasma transfusions and ATRs during 2020 to 2024. Consecutive patients receiving platelet or plasma transfusions were included. Exposures Patients with blood type O who received B or AB units and patients with blood type O who received O units (reference group) in AGS high- and low-prevalence clusters were compared. Main Outcomes and Measures Before data collection, the hypothesis was that if transfusion-related alpha-gal syndrome (TRAGS) is a true clinical entity, excess ATRs to group B or AB units would be detected in AGS high-prevalence regions exclusively. The main measure was the overall risk ratio (RR) for ATRs to B or AB plasma or platelets in AGS high- vs low-prevalence clusters. Results In total, 558 823 platelet and plasma transfusions at 40 sites in 5 countries were analyzed, of which ATRs occurred in 1744 transfusions (0.3%). In the US AGS high-prevalence cluster (9 sites), significantly more ATRs of any severity occurred among patients with blood type O who received B or AB units vs patients with blood type O who received O units (overall RR, 3.93; 95% CI, 2.96-5.21; P < .001). In contrast, in the primary analysis of the AGS low-prevalence cluster (15 sites), excess ATRs to B or AB units were not detected. In subgroup analyses among patients with blood type O receiving B units, the RR for moderate to severe ATRs was 9.14 (95% CI, 5.39-15.52; P < .001) in the AGS high-prevalence cluster vs 2.15 (95% CI, 1.34-3.47; P = .002) in the AGS low-prevalence cluster. Outside the US, a signal consistent with TRAGS was not detected. Conclusions and Relevance This cohort study provides provocative epidemiologic evidence that TRAGS may be a unique manifestation of AGS and a previously unrecognized risk associated with transfusion. In AGS high-prevalence regions, blood collectors and hospital transfusion services should consider approaches to preventing severe ATRs from B or AB plasma or platelet units.
Multicenter Evaluation of Noise Levels and Staff Perceptions Across Laser Technologies During Holmium Laser Enucleation of the Prostate: A Prostate Enucleation Collaborative Initiative
Wu, Jessica , Dalkin, Benjamin, Kuravi, Satvik, Cohen, A. , Klose, Charles , Qualkenbush, Eric , Baird, Bryce , Stern, Karen , De, Smita , Klett, Dane, Kahn, Amanda E. , Dalkin, Benjamin , Cohen, Adam , Qualkenbush, Eric , Baird, Bryce A , Stern, Karen L , De, Smita , Jain, Rajat , Quarrier, Scott O , Dora, Chandler D , Jain, Rajat , Dora, Chandler

Lasers in Surgery and Medicine | August 24, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1002/lsm.70197 | PMID 42635390 Get It

ABSTRACT Introduction Operating room (OR) noise during holmium laser enucleation of the prostate (HoLEP), particularly from laser activation, may impair surgical workflow and staff performance. Methods 84 HoLEP procedures were recorded at three academic institutions between June 2024 and January 2026. Laser platforms included Lumenis Moses 2.0, Quanta Litho 150, Quanta Magneto, and Dornier Thulio. Sound measurements were obtained using a standardized smartphone‐based system during three phases: laser‐off (baseline), idle (not firing), and active lasing. Acoustic metrics included average sound level (LAeq), peak sound level (Lcpeak), and sound levels exceeded for 10%, 50%, and 90% of the recording time (L10, L50, and L90). Background noise correction was performed using baseline measurements to account for ambient noise and isolate laser‐related sound. OR staff completed a validated survey assessing perceived noise burden (0–10 scale). Results Background‐corrected noise during active lasing differed significantly by platform. Litho demonstrated lower mean noise levels compared to Thulio for LAeq (60.6 vs. 68.2 dB, p = 0.023) and L10 (61.5 vs. 70.6 dB, p = 0.023), while Moses had higher LAeq compared to Litho (63.1 vs. 60.6 dB, p = 0.043). Overall, Litho had the lowest noise levels, whereas Thulio had the highest. Survey responses paralleled these findings. Litho was associated with lower perceived overall effort (2.1 ± 0.9), while Moses demonstrated higher overall effort (3.6 ± 1.2) for communication and concentration (Figure 2). Significant pairwise differences were observed between Moses and Litho (all p < 0.05). Trends were consistent across sites. Conclusions Noise levels during HoLEP varied by laser technology and correlated with differences in perceived communication and cognitive effort. Litho demonstrated the lowest acoustic burden, while Moses and Thulio had higher noise exposure. These findings highlight the impact of laser selection on the OR environment and intraoperative team performance.
Heterozygous truncating variants in BICC1 are a novel cause of autosomal-dominant tubulointerstitial kidney disease
Eylath, Naomi S, Alyea-Herman, Piper, Meyersiek, Julia, Colombo, Dan A., Rennke, Helmut G. , Guleserian, Ava J, Adams, Victoria W, Bianchi, Giada , Maillard, Arnaud , Bergmann, Carsten , Lecker, Stewart H. , Astley, Megan , Taylor, Abigail, Martin, Lauren M. , Means, Sydney, Weller, Nelson, Kmochová, Tereza , Svojšová, Klára , Pavlovičová, Lea , Yang, Hana , Kmoch, Stanislav, Czarnecki, Peter G. , Bianchi, Giada , Eylath, Naomi, Kidd, Kendrah , Colombo, Dan A., Faguer, Stanislas , Izzi, Claudia , Astley, Megan E , Taylor, Abbigail , Martin, Lauren, Sanchez, Antonio, Hodaňová, Kateřina , Stránecký, Viktor , Hartmannová, Hana , Sikora, Jakub , Harris, Peter C. , Kmoch, Stanislav , Bleyer, Anthony J. , Živná, Martina

No container title available | August 24, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.64898/2026.08.20.26360556 Get It

Introduction: Autosomal-dominant tubulointerstitial kidney disease (ADTKD) is characterized by chronic kidney disease (CKD) with an average age of end-stage renal disease (ESRD) of approximately 45 years, bland urinary sediment, the absence of proteinuria and autosomal dominant inheritance. While several causative genes have been found, there remain families in whom no molecular diagnosis has been identified (ADTKD-NMD). Methods: We identified BICC1 truncating variants in several families with ADTKD-NMD in the Wake Forest Rare Inherited Kidney Disease Registry and then screened families in our database and other referred families for BICC1 truncating variants. We performed segregation analysis and characterized affected individuals for clinical and histopathologic phenotypes. We analyzed oligomer formation of BICC1 mutants with wild-type BICC1-, ANKS3- and ANKS6 proteins through co-immunoprecipitation and Western blotting, and we tested for posttranscriptional regulation of the BICC1 target mRNA, Dand5, in a Luciferase reporter assay. Results: We found 6 heterozygous truncating mutations in BICC1 segregating with the ADTKD phenotype in 8 independent pedigrees worldwide. Affected individuals developed kidney failure in the 6th to 7th decade of life that was characterized pathologically by tubular atrophy and interstitial fibrosis. The truncated gene products localized to cytoplasmic bodies and demonstrated various degrees of self-association or binding to the known interaction partners, ANKS3 and ANKS6. While the wild-type BICC1 gene product acts as a posttranscriptional repressor of target mRNAs, all truncation variants exhibited increased expression of substrate mRNA. Conclusions: Truncating variants in BICC1 are a novel cause of ADTKD, segregating with the disease phenotype and upregulating BICC1 target gene expression through a dominant-negative- or a gain-of-function mode of action.
Case Study in Education: Improving Resident Didactic Training
Charles, Rohan , Turner, Lindsey E , Cole, Channon E Cordes, Barlow, Jonathan D. , Ryssman, Daniel, Vlasak, M.D. Alexander, Turner, Norman S. , Cordes Cole, Channon E, Vlasak, Alexander , Barlow, Jonathan D , Ryssman, Daniel B., Vlasak, Alexander

JBJS Open Access | August 18, 2026 | Volume: 11 | Issue: 3 | Pages: No page available

10.2106/jbjs.oa.26.00095 | PMID 42598316 Get It

Introduction: Flipped classroom models, which use active, case-based discussion, have shown promise across graduate medical education. Previous literature demonstrates that transitioning to a flipped classroom model resulted in significant increases in overall Orthopaedic In-Training Examination (OITE) scores. This observational study retrospectively compares foot and ankle OITE scores for orthopaedic surgery residents before and after implementation of a flipped classroom curriculum. Methods: This retrospective study reviewed OITE scores for orthopaedic residents, comparing a lecture-based curriculum (n = 49) to a flipped classroom curriculum (n = 61). Residents who started their second year in July 2020 or later were defined as treated. The curriculum is given to the postgraduate year-2 (PGY2) residents only. Percentage of correct foot and ankle questions (F&A) were analyzed via mixed-effects models using random-subject intercepts. Fixed effects included PGY, overall performance on other sections, and flipped classroom status. All statistical analyses were performed in R version 4.4.1. Results: Residents in the flipped classroom cohort demonstrated a statistically significant increase in F&A questions answered correctly. The average increase was 7% (95% confidence interval: 4%, 10%; p < 0.001). This improvement trend became clearly visible in PGY3 and grew stronger in senior residents. Specifically, PGY3 residents improved their mean percentage correct from 62.26% to 66.07% (p = 0.16). PGY4 residents improved from 69.16% to 74.83% (p = 0.013), and PGY5 residents improved from 69.03% to 75.53% (p = 0.006). Historically, approximately 75% of traditional PGY5 residents scored lower on the F&A section than on the rest of the examination. Conversely, in the flipped classroom group, approximately 75% of PGY4 and PGY5 residents scored higher on the F&A section compared with other sections Discussion: The implementation of a flipped classroom model was associated with a statistically significant improvement in resident performance on the F&A section of the OITE. The educational benefits of this curriculum appear cumulative over the course of residency, with the most substantial performance gains realized by senior residents in their fourth and fifth years of training. Level of Evidence: Level III , Observational Study. See Instructions for Authors for a complete description of levels of evidence.
SADA-12 MALNUTRITION AS THE CANARY IN THE COAL MINE: NUTRITIONAL STATUS AND ITS ASSOCIATION WITH SURVIVAL IN PATIENTS WITH METASTATIC SPINE DISEASE
Versteeg, Anne L, Charest-Morin, Raphaële , Ramos, Rafael De La Garza, Laufer, I., Teixeira, William G J, Gassbarrini, Alessandro, Fehlings, Michael , Chou, Dean , Gokaslan, Ziya L, Netzer, Cordula, Luzzati, Alessandro, Verlaan, Jorrit-Jan, Goldshlager, Tony, Shin, John, O’Toole, John E, Sciubba, Daniel M. , Bettegowda, Chetan, Weber, Michael H, Mesfin, Addisu, Kawahara, Norio , Patel, Shalin S, Disch, Alexander C. , Reynolds, J., Dea, Nicholas, Sahgal, Arjun, Rhines, Laurence, Fisher, Charles G, Tumor, AO Spine Knowledge Forum, Goodwin, C Rory, Johnson, Eli , Versteeg, Anne , Ramos, Rafael De la Garza , Laufer, Ilya , Teixeira, William Gemio Jacobsen , Barzilai, Ori , Gasbarrini, Alessandro , Luzzati, Alessandro , Verlaan, Jorrit‐Jan , Goldschlager, Tony , Shin, John, Bettegowda, Chetan , Clarke, Michelle J. , Mesfin, Addisu , Reynolds, Jeremy , Lazáry, Áron , Boriani, Stefano , Dea, Nicolas , Rhines, Laurence D. , Fisher, Charles

Neuro-Oncology Advances | August 7, 2026 | Volume: 8 | Issue: Supplement_6 | Pages: No page available

10.1093/noajnl/vdag161.110 Get It

Abstract Introduction Patients with metastatic spine disease (MSD) present with varying degrees of systemic illness and frailty. Given the palliative intent of surgery and radiation treatment for MSD, treatment risks must be judiciously weighed against potential benefits. We sought to examine the impact of peroperative nutritional status as measured by the PG-SGA on survival in patients undergoing surgery and radiation for MSD. Methods This study involved an international, multicenter prospective, observational registry of patients with MSD: AO Knowledge Forum Tumor’s Metastatic Tumor Research and Outcomes Network (MTRON). Variables including baseline demographics, oncologic data, adverse events (medical adverse events and surgical complications), length of stay, and nutritional status were prospectively collected. The Patient-Generated Subjective Global Assessment (PG-SGA) was used to evaluate nutritional status. Results A total of 589 patients were included in this study; 469 (80%) of whom underwent surgery and radiation and 120 (20%) of whom underwent radiation alone. The majority of patients (362, 61%) were classified as well nourished, however, 68 patients (12%) were classified as severely malnourished. Among patients that underwent surgery and radiation, the median overall survival of well nourished patients was 491 days compared to 117 days in the severely malnourished patients (p &lt; 0.001). A multivariate analysis demonstrated severe malnourishment and ECOG performance status of 3 or 4 were associated with worse overall survival. Conclusion Malnutrition as measured by the PG-SGA demonstrated to be significantly and independently associated with perioperative survival in patients with MSD. Further studies that investigate optimal pre-treatment optimization for patients with MSD in order to mitigate morbidity and mortality risk are essential.
SADA-14 WHEN COMPLICATIONS MATTER: THE IMPACT OF POSTOPERATIVE ADVERSE EVENTS ON SURVIVAL AND QUALITY OF LIFE IN METASTATIC SPINE DISEASE
Hardigan, Andrew, Griffoni, Christina, Noli, Luigi Emanuele, Monetta, Annalisa , Disch, Alexander, Gokaslan, Ziya L, Fehlings, Michael G, Verlaan, Jorrit-Jan, Chou, Dean , Rhines, Laurence, Shin, John, Teixeira, William G J, Sciubba, Daniel M. , Bettegowda, Chetan, Charest-Morin, Raphaële , Weber, Michael H, O’Toole, John E, Netzer, Cordula, Mesfin, Addisu, Mummaneni, Praveen V., Dea, Nicholas, Reynolds, J., Sahgal, Arjun, Fisher, Charles G, Gasbarrini, Alessandro, Tumor, AO Spine Knowledge Forum, Goodwin, C Rory, Hardigan, Andrew A. , Bròdano, Giovanni Barbanti , Salamanna, Francesca , Lazáry, Áron , Fehlings, Michael G. , Verlaan, Jorrit‐Jan , Rhines, Laurence D. , Teixeira, William Gemio Jacobsen , Bettegowda, Chetan , Boriani, Stefano , Goldschlager, Tony , Clarke, Michelle J. , Mesfin, Addisu , Mummaneni, Praveen V. , Dea, Nicolas , Reynolds, Jeremy , Fisher, Charles, Gasbarrini, Alessandro

Neuro-Oncology Advances | August 7, 2026 | Volume: 8 | Issue: Supplement_6 | Pages: No page available

10.1093/noajnl/vdag161.112 Get It

Abstract Introduction As the incidence of metastatic spine disease (MSD) increases, treatments to manage refractory pain, pathologic vertebral body fractures, and spinal cord compression are becoming increasingly common. Given the palliative nature of surgical intervention used to achieve tumor control and thus mitigate loss of neurologic function and compromised ambulatory function, it is essential to mitigate the risk of such procedures. Methods The AO Spine Knowledge Forum Tumor’s Metastatic Tumor Research and Outcomes Network (MTRON), an international, prospective registry for patients with spinal metastases, was used for this query. Prospective collection included baseline health and demographic information, oncologic data (including Spinal Instability Neoplastic Score (SINS) score and Bilksy epidural compression classification), and baseline functional status (preoperative American Spinal Injury Association (ASIA) and ECOG scores). Health related quality of life (HRQoL) data included Spine Oncology Study Group Outcomes Questionnaire (SOSGOQ2.0) and Euro-QoL measures. Surgery related adverse events (AE’s) were collected using the Spine Adverse Events Severity (SAVES V2) framework. Kaplan-Meir curves were used to assess survival. Results The cohort consisted of 1267 patients, 701 male (55.3%). A total of 245 (19.3%) experienced at least one postoperative AE, the majority of which were considered minor (grade 3 or less). Among the most common were deep wound infections (3.2%), wound dehiscence (2.5%), and urinary infections (2.4%). A multivariate analysis demonstrated that age, smoking status, ECOG performance, prior radiotherapy, presence of multiple metastases at other sites, and multiple spine metastases were significant risk factors for a postoperative AE. Postoperative AE’s (p = 0.049) and major postoperative AE’s (p = 0.0038) were found to be related to survival as well as a significant change in HRQoL scores (p &lt; 0.001). Conclusion Postoperative AE’s are extremely relevant to the care of patients with MSD and impact both HRQoL and survival.
SUPC-01 USE OF THE SELECTIVE PLASMA KALLIKREIN INHIBITOR RZ402 FOR STABILIZATION OF CEREBRAL EDEMA RELATED TO METASTATIC MELANOMA – RESULTS OF A SINGLE PATIENT PROTOCOL
Sener, Ugur, Schultz, Sydney, Galloway, Taylor , Brickley, Vince, Mason, Charles, Huebert, Carey, Headlee, Amy, Burns, Terry, Yan, Elizabeth, Neth, Bryan, Caron, Samantha, Hood, Davelyn , Breit, Jeff, Sener, Uğur , Huebert, Carey, Neth, Bryan J. , Caron, Samantha

Neuro-Oncology Advances | August 7, 2026 | Volume: 8 | Issue: Supplement_6 | Pages: No page available

10.1093/noajnl/vdag161.096 Get It

Abstract Background Peritumoral brain edema (PTBE) is a frequent complication of CNS tumors and radiation therapy (RT). PTBE is primarily treated with corticosteroids, but prolonged use is associated with severe toxicities including myopathy and immunosuppression. Bevacizumab, an alternative treatment, is not recommended in patients with thromboembolic events and intracerebral hemorrhage. Plasma kallikrein is a key driver of tumor-related edema. By targeting this pathogenic enzyme, the orally delivered inhibitor, RZ402, may provide therapeutic value by controlling edema and decreasing corticosteroid use. Methods In this single-patient investigational new drug protocol, we report results from use of RZ402 for treatment of cerebral edema related to metastatic melanoma and RT. Results A 74-year-old man with BRAF-wildtype melanoma had a right frontal and basal ganglia hemorrhagic metastasis not amenable to resection, treated with stereotactic RT (30 Gy, 5 fractions), followed by ipilimumab and nivolumab. MRI obtained 5 months after RT showed increased edema associated with midline shift. After 12 weeks of treatment with high-dose dexamethasone (16 mg daily), edema remained persistent and patient was unable to tolerate dose reduction below 4 mg daily. Course was complicated by a pulmonary embolus prompting initiation of anticoagulation, leading to deferral of bevacizumab. Patient was treated with RZ402, which was tolerated well with no reported toxicities. Dexamethasone was discontinued over 4 weeks. Follow up imaging 6 weeks after RZ402 initiation and off dexamethasone demonstrated stability without rebound edema. Patient did experience adrenal insufficiency characterized by severe fatigue, managed with low-dose prednisone. RZ402 was discontinued after 8 weeks of treatment with patient remaining clinically stable. Conclusion Despite persistent edema after prolonged use of corticosteroids, the selective plasma kallikrein inhibitor RZ402 was associated with radiographic stabilization and discontinuation of dexamethasone for this patient. These findings support prospective evaluation of RZ402 in treatment of symptomatic cerebral edema related to CNS tumors.
Delayed C5 palsy following thoracolumbar deformity surgery: a case report
Barré, Alyssa , Mechas, Charles A. , Alhankawi, Ahmad, Sarraj, Mohamed , Arunmaithurai, Gokul, Nassr, Ahmad, Mechas, Charles-Antoine , Alhankawi, Ahmad R. , Nassr, Ahmad

Annals of Medicine & Surgery | August 6, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1097/ms9.0000000000005375 | PMID 42725161 Get It

Background: C5 palsy is a known complication following decompressive cervical spine surgery, most often attributed to factors such as foraminal stenosis, cord drift, or traction. While its incidence after cervical procedures is well-documented, C5 palsy occurring after thoracolumbar deformity surgery has not been previously described. Case: A 70-year-old woman with a prior C2-T4 posterior cervical spinal fusion underwent thoracolumbar deformity correction with T4-pelvis fusion. Two months postoperatively, she developed sudden right deltoid and biceps weakness. Laboratory and imaging workups ruled out other pathological causes, and electromyography confirmed a new C5 palsy. She was treated with physical therapy and electrical stimulation and achieved complete recovery by 6 months post-thoracolumbar surgery. Conclusion: This case describes isolated delayed C5 palsy following thoracolumbar deformity surgery in a patient with prior cervical spine fusion 2 years earlier. Potential contributing factors include global alignment changes, altered neural tension, and intrinsic anatomic fragility of the C5 nerve root. This presentation expands the clinical context of postoperative C5 palsy and highlights the importance of monitoring for cervical neurologic deficits, even in the absence of cervical intervention. Level of Evidence: 5 – Case Report
Gene variants associated with pediatric-onset erythromelalgia: Mendelian and rare-variant association analyses
Yonas, Matthew C., Ocay, Don Daniel , Fernandes, Melissa, Groussis, Nicole, Halpin, Meghan , Wilder, Robert T., Berde, Charles B. , Genetti, Casie A. , Lobo, Kimberly , Wilder, Robert T., Yu, Timothy W. , Brownstein, Catherine A.

PAIN Reports | August 6, 2026 | Volume: 11 | Issue: 5 | Pages: No page available

10.1097/pr9.0000000000001465 | PMID 42559536 Get It

Abstract Introduction: Erythromelalgia is a descriptive term for burning pain and erythema in distal extremities, often worsened by heat and improved by cold. Inherited erythromelalgia has been primarily linked to gain-of-function variants in SCN9A , encoding voltage-gated sodium channel NaV1.7. However, approximately 65% to 85% of patients with erythromelalgia do not have pathogenic SCN9A variants. Objectives: The objective of this study was to uncover and assess gene variants potentially associated with pediatric-onset erythromelalgia. Methods: With IRB approval and informed consent, probands and families with erythromelalgia underwent next-generation sequencing. A list of genes of interest was produced based on Mendelian inheritance models. Selected gene candidates were assessed using the Sequence Kernel Association Test-Optimal (SKAT-O). Results: Sixty-two probands with erythromelalgia and their relatives were included in Mendelian analysis, which identified variants in PR domain zinc finger protein 12 ( PRDM12 ) and dihydropyrimidinase-like protein 2 ( DPYSL2 ). In a targeted 12-gene rare-variant set analysis using SKAT-O, zinc finger homeobox protein 2 ( ZFHX2 ) showed evidence of association ( P = 6.9 × 10 −4 ), surpassing Bonferroni correction for 12 tests (α = 4.17 × 10 −3 ), whereas KIF1B showed only a nominal association signal ( P = 0.03) that did not survive multiple-testing correction. Conclusion: Genes associated with both increased and decreased pain sensitivity are of considerable interest for elucidating pain mechanisms and analgesic development. As rare variants in PRDM12 and DPYSL2 were identified in a pediatric erythromelalgia cohort and a gene-based rare-variant association signal for ZFHX2 was identified, replication and functional validation are needed.