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Daniels, David J.

https://orcid.org/0000-0002-0702-1459

Mayo Clinic

Mayo Clinic

Citations 133

Tranexamic Acid Decreases Blood Transfusion Burden in Open Craniosynostosis Surgery Without Operative Compromise
Lu, Victor M. , Goyal, Anshit , Daniels, David J.

Journal of Craniofacial Surgery | November 3, 2018 | Volume: 30 | Issue: 1 | Pages: 120-126

10.1097/scs.0000000000004875 Get It

Abstract In the surgical management of craniosynostosis, there is a high red blood cell (RBC) transfusion burden due to the small blood volume of the patients combined with significant blood loss that can occur with open surgery (OS). Tranexamic acid (TXA) is an antifibrinolytic which has been shown to decrease such a burden in particular surgeries. The aim of this study was to compare the operative outcomes of craniosynostosis OS which did and did not utilize TXA. Searches of 7 electronic databases from inception to February 2018 were conducted following Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines. There were 206 articles screened against selection criteria for inclusion. Relevant data were extracted and analyzed using meta-analysis of proportions. A total of 9 comparative studies were included for meta-analysis. Compared with the control cohort, craniosynostosis OS utilizing TXA demonstrated significantly lower intraoperative RBC transfusion volumes (mean difference, −8.25 mL/kg; P < 0.001), blood loss (mean difference, −10.96 mL/kg; P < 0.001) and postoperative RBC transfusion incidence (odds ratio, OR, 0.12; P = 0.005). Fresh frozen plasma and crystalloid transfusion, operation time, length of stay, and complications were not significantly different with TXA use. Based on the comparative evidence currently available, TXA significantly decreased RBC transfusion burden during craniosynostosis OS without operative compromise. There is significant heterogeneity in reported TXA regimes in the literature. Future studies that are larger, randomized, and account for these factors will further enhance the authors’ understanding.
Case-based review: atypical teratoid/rhabdoid tumor
Rao, Amulya A. Nageswara , Raghunathan, Aditya , Biegel, Jaclyn A. , Nesvick, Cody L. , Raghunathan, Aditya , Daniels, David J.

Neuro-Oncology Practice | October 5, 2018 | Volume: 6 | Issue: 3 | Pages: 163-178

10.1093/nop/npy037 Get It

AbstractAtypical teratoid/rhabdoid tumor (AT/RT) is a rare CNS cancer that typically occurs in children younger than 3 years of age. Histologically, AT/RTs are embryonal tumors that contain a rhabdoid component as well as areas with primitive neuroectodermal, mesenchymal, and epithelial features. Compared to other CNS tumors of childhood, AT/RTs are characterized by their rapid growth, short symptomatic prodrome, and large size upon presentation, often leading to brain compression and intracranial hypertension requiring urgent intervention. For decades, the mainstay of care has been a combination of maximal safe surgical resection followed by adjuvant chemotherapy and radiotherapy. Despite advances in each of these modalities, the relative paucity of data on these tumors, their inherently aggressive course, and a lack of molecular data have limited advances in treatment over the past 3 decades. Recent large-scale, multicenter interdisciplinary studies, however, have significantly advanced our understanding of the molecular pathogenesis of these tumors. Multiple clinical trials testing molecularly targeted therapies are underway, offering hope for patients with AT/RT and their families.
Novel suprasellar location of desmoplastic infantile astrocytoma and ganglioglioma: a single institution’s experience
Naylor, Ryan M. , Wohl, Anton , Raghunathan, Aditya , Eckel, Laurence J. , Keating, Gesina F. , Raghunathan, Aditya , Daniels, David J.

Journal of Neurosurgery: Pediatrics | July 6, 2018 | Volume: 22 | Issue: 4 | Pages: 397-403

10.3171/2018.4.peds17638 Get It

OBJECTIVEThe aim of this study was to describe the clinical presentation, imaging appearance, and differential outcomes based on tumor location in 7 patients with desmoplastic infantile astrocytoma and desmoplastic infantile gangliogliomas (DIA/DIG).METHODSData of 7 patients with histopathology-proven DIA/DIGs and preoperative imaging were retrospectively reviewed, and age, sex, clinical presentation, imaging characteristics, tumor location, surgical procedure, postoperative morbidity, and overall mortality were recorded.RESULTSTwo subgroups of patients with DIA/DIGs were found to exist based on whether their tumor was located in the cerebral hemispheres or suprasellar region. Nearly all patients presented with rapidly enlarging head circumference regardless of tumor location. However, ocular abnormalities, including nystagmus and preference for downward gaze, were specific for patients with suprasellar disease. These patients experienced significant postoperative complications and had poor long-term outcomes. In contrast, patients with hemispheric tumors underwent more extensive resection than patients with suprasellar tumors, had uneventful postoperative courses, and had no documented long-term comorbidities.CONCLUSIONSPostoperative course and long-term outcome for patients with DIA/DIGs were correlated to the anatomical location and radiographic appearance of their tumor at presentation, despite having histologically and molecularly indistinguishable, WHO grade I tumors.
Author response: H3.3K27M mutant proteins reprogram epigenome by sequestering the PRC2 complex to poised enhancers
Dong, Fang , Gan, Haiyun , Cheng, Liang , Zhou, Hui , Lee, Jeong‐Heon , Sarkaria, Jann N. , Daniels, David J. , Zhang, Zhiguo

No container title available | July 5, 2018 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.7554/elife.36696.031 Get It

Letter: Impact of H3.3 K27M Mutation on Prognosis and Survival of Grade IV Spinal Cord Glioma on the Basis of New 2016 World Health Organization Classification of the Central Nervous System
Lu, Victor M. , Alvi, Mohammed Ali , Alvi, Mohammed A, Daniels, David J. , Alvi, Mohammed Ali

Neurosurgery | July 3, 2018 | Volume: 83 | Issue: 4 | Pages: E193-E194

10.1093/neuros/nyy347 Get It

H3.3K27M mutant proteins reprogram epigenome by sequestering the PRC2 complex to poised enhancers
Dong, Fang , Gan, Haiyun , Cheng, Liang , Lee, Jeong‐Heon , Zhou, Hui , Zhang, Zhiguo , Fang, Dong , Zhang, Zhiguo , Lee, Jeong-Heon , Sarkaria, Jann N. , Daniels, David J.

eLife | June 22, 2018 | Volume: 7 | Issue: No issue available | Pages: No page available

10.7554/elife.36696 Get It

Expression of histone H3.3K27M mutant proteins in human diffuse intrinsic pontine glioma (DIPG) results in a global reduction of tri-methylation of H3K27 (H3K27me3), and paradoxically, H3K27me3 peaks remain at hundreds of genomic loci, a dichotomous change that lacks mechanistic insights. Here, we show that the PRC2 complex is sequestered at poised enhancers, but not at active promoters with high levels of H3.3K27M proteins, thereby contributing to the global reduction of H3K27me3. Moreover, the levels of H3.3K27M proteins are low at the retained H3K27me3 peaks and consequently having minimal effects on the PRC2 activity at these loci. H3K27me3-mediated silencing at specific tumor suppressor genes, including Wilms Tumor 1, promotes proliferation of DIPG cells. These results support a model in which the PRC2 complex is redistributed to poised enhancers in H3.3K27M mutant cells and contributes to tumorigenesis in part by locally enhancing H3K27me3, and hence silencing of tumor suppressor genes.
DIPG-21. EVALUATING THERAPEUTIC VULNERABILITIES IN DIPG USING AURORA KINASE INHIBITOR AS A NOVEL THERAPY
Zhang, Liang , Bender, Andrew T. , Daniels, David J.

Neuro-Oncology | June 21, 2018 | Volume: 20 | Issue: suppl_2 | Pages: i53-i53

10.1093/neuonc/noy059.114 Get It

CRAN-38. CLINICOPATHOLOGIC FEATURES OF SUPRASELLAR AND LATERAL CEREBRAL DESMOPLASTIC INFANTILE ASTROCYTOMA AND GANGLIOGLIOMA
Naylor, Ryan M. , Eckel, Laurence J. , Keating, Gesina F. , Nesvick, Cody L. , Wohl, Anton , Raghunathan, Aditya , Daniels, David J.

Neuro-Oncology | June 21, 2018 | Volume: 20 | Issue: suppl_2 | Pages: i44-i44

10.1093/neuonc/noy059.073 Get It

CRAN-37. MOLECULAR HETEROGENEITY OF SUBEPENDYMAL GIANT CELL ASTROCYTOMAS IN PATIENTS WITH MILD-PHENOTYPE TUBEROUS SCLEROSIS COMPLEX
Rao, Amulya Nageswara, Nesvick, Cody L. , Rao, Amulya A. Nageswara , Raghunathan, Aditya , Daniels, David J.

Neuro-Oncology | June 21, 2018 | Volume: 20 | Issue: suppl_2 | Pages: i44-i44

10.1093/neuonc/noy059.072 Get It

Synchronous Epstein-Barr virus–associated skull base and adrenal smooth-muscle tumors in an 8-year-old girl with recent Epstein-Barr virus infection
Deep, Nicholas L. , Driscoll, Colin L. W., Link, Michael J. , Jentoft, Mark E. , Brown, Desmond , Daniels, David J.

Journal of Neurosurgery: Pediatrics | June 15, 2018 | Volume: 22 | Issue: 3 | Pages: 283-287

10.3171/2018.3.peds17609 Get It

Epstein-Barr virus–associated smooth-muscle tumors are rare tumors seen in immunocompromised patients. Most cases occur in the context of AIDS and organ transplantation, and very rarely in the setting of congenital immunodeficiency, with only 5 case reports of the latter published so far in the literature. The authors report the case of a previously healthy 8-year-old girl with headaches and precocious puberty who was found to have a large skull base lesion. There was a synchronous left adrenal lesion. She underwent resection of the skull base lesion and a left adrenalectomy. Thorough evaluation for immunodeficiency was negative for a known congenital immunodeficiency syndrome. She had a short course of intravenous immunoglobulin and has had no recurrence of disease or new lesions in the 17 months since presentation. Continued surveillance for the development of opportunistic infections and new or recurrent lesions is warranted in this case. Repeat surgery for surgically accessible tumors or chemoradiation would be recommended for any additional lesions.