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zenodo16/100

Dataset related to article "The role of stereotactic body radiation therapy and its integration with systemic therapies in metastatic kidney cancer: a multicenter study on behalf of the AIRO (Italian Association of Radiotherapy and Clinical Oncology) genitourinary study group "

<p>This record contains raw data related to article &ldquo;The role of stereotactic body radiation therapy and its integration with systemic therapies in metastatic kidney cancer: a multicenter study on behalf of the AIRO (Italian Association of Radiotherapy and Clinical Oncology) genitourinary study group&quot;</p> <p>Although systemic therapy represents the standard of care for polymetastatic kidney cancer, stereotactic body radiation therapy (SBRT) may play a relevant role in the oligometastatic setting. We conducted a multicenter study including oligometastatic kidney cancer treated with SBRT. We retrospectively analyzed 207 patients who underwent 245 SBRT treatments on 385 lesions, including 165 (42.9%) oligorecurrent (OR) and 220 (57.1%) oligoprogressive (OP) lesions. Most common sites were lung (30.9%) for OR group, and bone (32.7%) for OP group. Among 78 (31.8%) patients receiving concomitant systemic therapy, sunitinib (61.5%) and pazopanib (15.4%) were the most common for OR patients, while sunitinib (49.2%) and nivolumab (20.0%) for OP patients. End points were local control (LC), progression free survival (PFS), overall survival (OS), time to next systemic therapy (TTNS) and toxicity. Median follow-up was 18.6 months. 1, 2 and 3-year LC rates were 89.4%, 80.1% and 76.6% in OR patients, and 82.7%, 76.9% and 64.3% in those with OP, respectively. LC for OP group was influenced by clear cell histology (p = 0.000), total number of lesions (p = 0.004), systemic therapy during SBRT (p = 0.012), and SBRT dose (p = 0.012). Median PFS was 37.9 months. 1, 2- and 3-year OS was 92.7%, 86.4% and 81.8%, respectively. Median TTNS was 15.8 months for OR patients, and 13.9 months for OP patients. No grade 3 or higher toxicities were reported for both groups. SBRT may be considered an effective safe option in the multidisciplinary management of both OR and OP metastases from kidney cancer.</p> <p>&nbsp;</p>

restrictedJan 2022View details →
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Link to dataset related to article "Liquid Biopsy in the Clinical Management of High-Grade Serous Epithelial Ovarian Cancer-Current Use and Future Opportunities "

<p>This record contains raw data related to article &ldquo;&quot;Liquid Biopsy in the Clinical Management of High-Grade Serous Epithelial Ovarian Cancer-Current Use and Future Opportunities&quot;</p> <p>The lack of a sensitive and specific biomarker and the limits relating to the single primary tumor sampling make it difficult to monitor high-grade serous epithelial ovarian cancer (HGS-EOC) over time and to capture those alterations that are potentially useful in guiding clinical decisions. To overcome these issues, liquid biopsy has emerged as a very promising tool for HGS-EOC. The analysis of circulating tumor DNA appears to be feasible and studies assessing specific pathogenic mutations (i.e., <em>TP53</em>) or copy number alterations have shown a sufficient degree of sensitivity and specificity to be realistically used to monitor the effectiveness of antitumor therapy. Liquid biopsy can also provide potential important information on the mechanisms of sensitivity and resistance, e.g., by the determination of the reversion of <em>BRCA</em> mutations. Perspective studies are needed to test whether the application of liquid biopsy will significantly improve HGS-EOC management and patients&#39; survival.</p> <p>&nbsp;</p>

restrictedJan 2022View details →
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Dataset related to article "High prevalence of multidrug-resistant bacteria in patients with pyogenic liver abscess following liver cancer loco-regional treatments"

<p>This record contains raw data related to article &ldquo;High prevalence of multidrug-resistant bacteria in patients with pyogenic liver abscess following liver cancer loco-regional treatments&quot;</p> <p>Liver abscess is a rare condition, associated with significant in-hospital mortality. Because of improved diagnostic yield and standardized treatment strategies, mortality has been reduced from 70% to 6% in the last decades.<sup><a href="https://onlinelibrary.wiley.com/doi/10.1111/liv.14933#liv14933-bib-0001">1</a>, <a href="https://onlinelibrary.wiley.com/doi/10.1111/liv.14933#liv14933-bib-0002">2</a></sup></p> <p>The aetiology of pyogenic liver abscess (PLA) varies according to geographical areas and is relevant to tailor treatment strategies; in Western countries, 80% of PLA are bacterial with <em>Escherichia coli</em>, other Enterobacteriaceae and anaerobes being the most common microorganisms. In Asia, <em>Klebsiella</em> <em>pneumoniae</em> has emerged as the most common pathogen in the last two decades, with up to 81.1% of cases reported in Taiwan.<sup><a href="https://onlinelibrary.wiley.com/doi/10.1111/liv.14933#liv14933-bib-0003">3</a>, <a href="https://onlinelibrary.wiley.com/doi/10.1111/liv.14933#liv14933-bib-0004">4</a></sup> Interestingly, increasing frequencies of PLA from <em>K</em>. <em>pneumonia</em> have also been observed in Europe and the United States.<sup><a href="https://onlinelibrary.wiley.com/doi/10.1111/liv.14933#liv14933-bib-0005">5</a></sup></p> <p>The most common risk factors for PLA include primary liver tumour and metastases, loco-regional liver procedures and liver cysts.</p> <p>The treatment of PLA with antibiotic therapy, percutaneous drainage and management of the underlying cause is the current standard of care; however, the recommended antibiotic regimen and the optimal duration of treatment remain uncertain.</p> <p>Yin et al<sup><a href="https://onlinelibrary.wiley.com/doi/10.1111/liv.14933#liv14933-bib-0006">6</a></sup> reported in a retrospective study the management of 1572 patients with PLA in China. The most identified microorganism was <em>K. pneumoniae</em> (85.6%), with an overall mortality of 4.5% following abscess drainage and antibiotic therapy. Prognosis was associated with length of hospitalization, fever, pleural effusion and development of multiple organ dysfunction.</p> <p>Given the increase in incidence of multi-drug resistant (MDR) infections in the western world and the differences in aetiology of PLA between geographical areas, we analysed the aetiology and mortality of PLA in our centre, focusing on the prevalence and factors associated with MDR bacterial infections</p> <p>&nbsp;</p>

restrictedJan 2022View details →
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Dataset related to the article: "Cyclooxygenase-2 Glycosylation Is Affected by Peroxynitrite in Endothelial Cells: Impact on Enzyme Activity and Degradation"

<p>This record containsraw data related to the article: &quot;Cyclooxygenase-2 Glycosylation Is Affected by Peroxynitrite in Endothelial Cells: Impact on Enzyme Activity and Degradation&quot;</p> <p>Abstract: The exposure of human endothelial cells to 3-morpholinosydnonimine (SIN-1) induced the<br> expression of cyclooxygenase-2 (COX-2) in a dose- and time-dependent manner. Interestingly, after a<br> prolonged incubation (&gt;8 h) several proteoforms were visualized by Western blot, corresponding<br> to different states of glycosylation of the protein. This effect was specific for SIN-1 that generates<br> peroxynitrite and it was not detected with other nitric oxide-donors. Metabolic labeling experiments<br> using 35S or cycloheximide suggested that the formation of hypoglycosylated COX-2 was dependent<br> on de novo synthesis of the protein rather than the deglycosylation of the native protein. Moreover,<br> SIN-1 reduced the activity of the hexokinase, the enzyme responsible for the first step of glycolysis.<br> The hypoglycosylated COX-2 induced by SIN-1 showed a reduced capacity to generate prostaglandins<br> and the activity was only partially recovered after immunoprecipitation. Finally, hypoglycosylated<br> COX-2 showed a more rapid rate of degradation compared to COX-2 induced by IL-1a&nbsp;and an<br> alteration in the localization with an accumulation mainly detected in the nuclear membrane. Our<br> results have important implication to understand the effect of peroxynitrite on COX-2 expression<br> and activity, and they may help to identify new pharmacological tools direct to increase COX-2<br> degradation or to inhibit its activity.</p>

restrictedJan 2022View details →
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Dataset related to article "Pancreatic ductal adenocarcinoma and invasive intraductal papillary mucinous tumor: Different prognostic factors for different overall survival"

<p>Dataset related to article &quot;Pancreatic ductal adenocarcinoma and invasive intraductal papillary mucinous tumor: Different prognostic factors for different overall survival &quot;</p> <p>&nbsp;</p> <p>Abstract</p> <p><strong>Background:&nbsp;</strong>It is unclear whether invasive intraductal papillary mucinous neoplasm (IPMN) has different clinical and prognostic characteristics, beyond histological factors, when compared to pancreatic ductal adenocarcinoma (PDAC).</p> <p><strong>Aims:&nbsp;</strong>compare prognostic features of resected PDAC and invasive IPMN METHODS: A retrospective study of patients resected for PDAC or invasive IPMN realized at Humanitas Cancer Center&#39;s Pancreatic Surgery Unit, Milan, Italy, between 2010 and 2016. Data recorded included patient demographics, onset symptoms, preoperative health status, tumor features, histology and surgical characteristics. Overall survival was estimated using Kaplan-Meier and prognostic factors for survival were assessed by multivariate Cox regression.</p> <p><strong>Results:&nbsp;</strong>A total of 332 patients were included (PDAC, n = 289; invasive IPMN, n = 43). Patients with invasive IPMN had better overall survival than PDAC patients (median: 76.6 versus 25.6 months; 5-year OS rate: 65.4% vs. 14.2%; p &lt; 0.001). PDAC histology was associated with a significantly higher risk of death than IPMN (hazard ratio 1.815, 95% CI: 1.02, 3.24; p = 0.044). Survival was also worse with PDAC in early-stage disease (IA-IB-IIA, N0). In multivariate analysis, independent predictors of worse survival included perineural invasion, preoperative ASA physical status &ge;3 and pain at diagnosis.</p> <p><strong>Conclusions:&nbsp;</strong>Patients with IPMN had a better prognosis than PDAC patients, regardless of disease stage.</p>

restrictedJan 2022View details →
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Dataset related to article "Hepatic and Extrahepatic Colorectal Metastases Have Discordant Responses to Systemic Therapy. Pathology Data from Patients Undergoing Simultaneous Resection of Multiple Tumor Sites"

<p>This record contains raw data related to article &quot;Hepatic and Extrahepatic Colorectal Metastases Have Discordant Responses to Systemic Therapy. Pathology Data from Patients Undergoing Simultaneous Resection of Multiple Tumor Sites&quot;</p> <p><strong>Background: </strong> Systemic therapy is the standard treatment for patients with hepatic and extrahepatic colorectal metastases. It is assumed to have the same effectiveness on all disease foci, independent of the involved organ. The present study aims to compare the response rates of hepatic and extrahepatic metastases to systemic therapy.</p> <p><strong>Methods: </strong> All consecutive patients undergoing simultaneous resection of hepatic and extrahepatic metastases from colorectal cancer after oxaliplatin- and/or irinotecan-based preoperative chemotherapy were analyzed. All specimens were reviewed. Pathological response to chemotherapy was classified according to tumor regression grade (TRG).</p> <p><strong>Results: </strong> We analyzed 45 patients undergoing resection of 134 hepatic and 72 extrahepatic metastases. Lung and lymph node metastases had lower response rates to chemotherapy than liver metastases (TRG 4-5 95% and 100% vs. 67%, <em>p</em> = 0.008, and <em>p</em> = 0.006). Peritoneal metastases had a higher pathological response rate than liver metastases (TRG 1-3 66% vs. 33%, <em>p</em> &lt; 0.001) and non-hepatic non-peritoneal metastases (3%, <em>p</em> &lt; 0.001). Metastases site was an independent predictor of pathological response to systemic therapy.</p> <p><strong>Conclusions: </strong> Response to chemotherapy of distant metastases from colorectal cancer varies in different organs. Systemic treatment is highly effective for peritoneal metastases, more so than liver metastases, while it has a very poor impact on lung and lymph node metastases.</p>

restrictedJan 2022View details →
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Dataset related to article "Re-irradiation for recurrent high grade glioma (HGG) patients: Results of a single arm prospective phase 2 study"

<p>This record contains raw data related to article &ldquo;Re-irradiation for recurrent high grade glioma (HGG) patients: Results of a single arm prospective phase 2 study&quot;</p> <p><strong>Background and purpose: </strong> Standard of care for recurrent high grade glioma (HGG) is missing. Several treatment options have been investigated including re-irradiation (re-RT). Results are promising but provided by retrospective studies. We designed a single arm prospective phase II study aiming to evaluate efficacy, and toxicity of re-irradiation.</p> <p><strong>Materials and methods: </strong> Adults patients with good performance status, HGG diagnosis reclassified according to the new 2021 fifth edition WHO CNS classification, an interval time (IT) from previous RT &ge; 6 months were included. Outcome was evaluated by MRI imaging at 1 month, and every 3 months thereafter. Toxicities were evaluated in terms of radionecrosis occurrence, and neurocognitive status.</p> <p><strong>Results: </strong> Ninety recurrent HGG patients were treated, 11 oligodendroglioma grade 3, 18 astrocytoma grade 3 and 4, and 61 glioblastoma grade 4. The median age was 54 years, and majority had KPS 90-100. The median IT between first-RT and re-RT was 24 months. Re-surgery has been performed in 56.6%, and chemotherapy in 53.3%. The median follow up time was 64 months; median overall survival (OS) time,1,2,3-year OS rates were 17 months (95%CI 14-19), 66.7%&plusmn;4.9, 32.6%&plusmn;5.0, and 22.2 &plusmn; 4.7. Prognostic factors impacting on survival were age (p = 0.0154), IT between first RT and re-RT (p = 0.0051), glioma grade (p = 0.0090), and IDH status (p = 0.0001). Radionecrosis grade 2-3 occurred in 9 (10%) patients; neurocognitive functions remained stable until disease progression.</p> <p><strong>Conclusion: </strong> Re-RT proved to be a safe and feasible treatment option with low toxicity. Younger patients with grade 3 IDH mutated gliomas, and a longer IT had the better outcome.</p>

restrictedFeb 2022View details →
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Dataset related to article "Extended Pleurectomy/Decortication for Malignant Pleural Mesothelioma: Humanitas's Experience"

<p>This record contains raw data related to article &ldquo;Extended Pleurectomy/Decortication for Malignant Pleural Mesothelioma: Humanitas&#39;s Experience&quot;</p> <p><strong>Background: </strong> We analysed a series of malignant pleural mesothelioma (MPM) patients who consecutively underwent extended Pleurectomy/Decortication (eP/D) in a centre with a high level of thoracic surgery experience (IRCCS Humanitas Research Hospital) to explore postoperative morbidity and mortality, pattern of recurrence and survival.</p> <p><strong>Methods: </strong> A retrospective analysis was performed on MPM patients underwent eP/D in our centre from 2010 to 2021. All patients were identified from our departmental database. Postoperative complications were scored according to Clavien-Dindo criteria. Survival analysis was performed by the Kaplan-Meier methods and Cox multivariable analysis.</p> <p><strong>Results: </strong> Eighty-five patients underwent extended pleurectomy decortication (eP/D) during study period. Macroscopical residual disease (R2) was reported in one case. A neoadjuvant chemotherapy regiment was administrated in 88% of the surgical cohort. A complete trimodality treatment including induction with platinum agents and pemetrexed, radical cytoreductive surgery and volumetric modulated arc therapy technology (VMAT) could be administered in 63 patients (74%). Postoperative morbidity rate was 54.11%, major complications (defined as Clavien-Dindo &ge; 3) were reported in 11 patients (12.9%). Thirty-day mortality and 90-day mortality were, respectively, 2.35% and 3.53%. Median disease-free and overall survival were, respectively, 13.7 and 25.5 months. The occurrence of major complications (Clavien-Dindo &ge; 3), operative time, pT3-T4, pathological node involvement (pN+) were prognostic factors associated with worse survival.</p> <p><strong>Conclusions: </strong> In our experience, eP/D is a well-tolerated procedure with acceptable mortality and morbidity, allowing for the administration of trimodality regimens in most patients. eP/D offered in a multimodality treatment setting have satisfactory long term oncological results. To obtain best oncological results the goal of surgery should be macroscopic complete resection in carefully selected patients (clinical N0).</p>

restrictedFeb 2022View details →
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Dataset related to article "Impact of Antibiotic Therapy and Metabolic Parameters in Non-Small Cell Lung Cancer Patients Receiving Checkpoint Inhibitors"

<p>This record contains raw data related to article &ldquo;Impact of Antibiotic Therapy and Metabolic Parameters in Non-Small Cell Lung Cancer Patients Receiving Checkpoint Inhibitors&quot;</p> <p><strong>Introduction: </strong> In the current study, we aimed to assess the impact of antibiotics (ATB) and metabolic parameters on clinical outcome of non-small cell lung carcinoma (NSCLC) patients treated with immune checkpoint inhibitors (ICI).</p> <p><strong>Methods: </strong> Data from fifty NSCLC patients referred for ICI between December 2015 and May 2019 were analyzed. All patients underwent 18F-fluorodeoxyglucose positron emission tomography computed tomography (18F-FDG PET/CT) and contrast-enhanced CT at baseline and for response assessment after 6-8 weeks. Patients who received ATB within 1 month before or after the first dose of ICI were compared with those who did not. Response assessment according to iRECIST and EORTC was evaluated, as well as progression-free survival (PFS) and overall survival (OS). For semi-quantitative parameters, we computed metabolic tumor volume (MTV), total lesion glycolysis (TLG) and their variations (∆).</p> <p><strong>Results: </strong> Twenty NSCLC cases of 50 (40%) had received ATB. Patients receiving ATB had a higher number of metastases (<em>p</em> = 0.046), and were associated with an elevated tumor burden, expressed by TLG (687 vs. 235.3, <em>p</em> = 0.007) and MTV (125.6 vs. 40.6, <em>p</em> = 0.002), compared to no-ATB patients. According to iRECIST, progressive disease rate was significantly higher for ATB group (64.7% vs. 27.6%, <em>p</em> = 0.029). Likewise, PFS was shorter for ATB compared to no-ATB (median 4.1 vs. 12.4 months, <em>p</em> = 0.004), while no difference for OS was detected. On multivariate analysis, the effect of ATB remained significant for poor PFS along with performance status (ECOG &ge; 1), and ∆SUVmax.</p> <p><strong>Conclusions: </strong> ATB therapy seems to be associated with a worse treatment response, PFS, and higher metabolic tumor burden in NSCLC patients treated with ICI.</p>

restrictedFeb 2022View details →
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Dataset related to article "Uncommon single and compound EGFR mutations: clinical outcomes of a heterogeneous subgroup of NSCLC "

<p>This record contains raw data related to article &ldquo;Uncommon single and compound EGFR mutations: clinical outcomes of a heterogeneous subgroup of NSCLC&quot;</p> <p>Molecular characterization of non-small-cell lung cancer (NSCLC) is essential to define the correct therapeutic algorithm in metastatic disease. Approximately 90% of epidermal growth factor receptor (EGFR) mutations are usually associated with sensitivity to EGFR tyrosine kinase inhibitors (TKIs). The remaining 10% defines a small, extremely heterogeneous subgroup of mutations, with a varied profile of sensitivity and response to target therapies.This retrospective observational study includes 47 patients affected by metastatic NSCLC harboring uncommon EGFR mutations (single or compound mutation). Patients were treated with EGFR-targeting TKIs or platinum-based chemotherapy as first-line treatment.Median OS resulted longer in the compound mutation group when compared to single rare mutations (33.6 vs 12 months; P = 0.473); a similar result was observed for PFS (16 vs 7.6 months; P = 0.281), although statistical significance was not reached. ORR, PFS and OS resulted similar for patients treated with first-line EGFR TKIs or chemotherapy. No difference in terms of PFS and OS was found according to the TKI administered.Compound mutations seem to be a good prognostic indicator for OS; they are also predictive of response to 1st and 2nd generation EGFR TKIs, as well as exon 19 insertions and mutations in codon 719 of exon 18. For mutations in exon 18 (not in codon 719) and exon 20 insertions, chemotherapy seems the most effective available option. The addition of immunotherapy to chemotherapy could change this approach in the next future.</p>

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Dataset related to article "NKG2A expression identifies a subset of human Vδ2 T cells exerting the highest antitumor effector functions"

<p>This record contains data related to article &quot;NKG2A expression identifies a subset of human V&delta;2 T cells exerting the highest antitumor effector functions&quot;</p> <p>&nbsp;</p> <p>Human V&delta;2 cells are innate-like &gamma;&delta; T effectors performing potent immune surveillance against tumors. The constitutive expression of NKG2A identifies a subset of V&delta;2 T cells licensed with an intrinsic hyper-responsiveness against cancer. Indeed, the transcriptomic profiles of NKG2A+&nbsp;and NKG2A-&nbsp;cells characterize two distinct &quot;intralineages&quot; of V&delta;2 T lymphocytes that appear early during development, keep their phenotypes, and show self-renewal capabilities in adult life. The hyper-responsiveness of NKG2A+&nbsp;V&delta;2 T cells is counterbalanced by the inhibitory signaling delivered by human leukocyte antigen E (HLA-E) expressed on malignant cells as a tumor-escape mechanism. However, either masking or knocking out NKG2A restores the capacity of V&delta;2 T cells to exert the highest effector functions even against HLA-E+&nbsp;tumors. This is highly relevant in the clinic, as the different degrees of engagement of the NKG2A-HLA-E checkpoint in hepatocellular carcinoma, glioblastoma, and non-small cell lung cancer directly impact patients&#39; overall survival. These findings open avenues for developing combined cellular and immunologic anticancer therapies.</p>

restrictedFeb 2022View details →
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Dataset related to article "Charlson comorbidity index and G8 in older old adult(≥80 years) hepatocellular carcinoma patients treated with stereotactic body radiotherapy "

<p>This record contains raw data related to article &ldquo;Charlson comorbidity index and G8 in older old adult(&ge;80 years) hepatocellular carcinoma patients treated with stereotactic body radiotherapy&quot;</p> <p><strong>Introduction: </strong> Hepatocellular Carcinoma (HCC) is characterized, in Western countries, by higher incidence and mortality rates in the older adult population. In frail patients, limited therapeutic resources are available due to limited expected benefit concerning the risk of treatment-related toxicity. The aim of our study is to evaluate the role of Stereotactic Body Radiotherapy (SBRT) in the clinical management of older old adults (age &ge; 80 years) HCC patients and to identify predictors of efficacy and toxicity.</p> <p><strong>Material and methods: </strong> Clinical and treatment-related data of older old adults HCC patients treated with SBRT at our institution were retrospectively reviewed. Statistical analysis was carried out to identify variables correlated with impaired outcome and toxicity.</p> <p><strong>Results: </strong> Forty-two patients were included, accounting for 63 treated tumors. Median age was 85 (range 80-91) years. Median Charlson Comorbidity Index (CCI) and G8 scores were 10 (range 7-16) and 11 (range 8-14), respectively. SBRT was administered to a median BED10 of 103 Gy10. Median follow-up interval was 11 (range 3-40) months. Two years Local Control (LC), Progression-Free Survival (PFS), and Overall Survival (OS) were 93%, 31%, and 43%, respectively. Acute toxicity occurred in 28% (n = 13) of treatments. A G8 score &gt; 10 was associated with improved survival (p = 0.045), while a CCI &ge;10 was correlated with increased acute toxicity (p = 0.021).</p> <p><strong>Conclusions: </strong> SBRT is a safe and effective option in older old adults HCC patients. A comprehensive geriatric assessment (CGA) is advised before treatment decisions to select optimal candidates for SBRT.</p>

restrictedFeb 2022View details →
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Dataset related to article "Gamma Knife Radiosurgery for the Treatment of Trigeminal Neuralgia in Patients with Multiple Sclerosis: A Single-Center Retrospective Study and Literature Review" "

<p>This record contains raw data related to article &ldquo;Gamma Knife Radiosurgery for the Treatment of Trigeminal Neuralgia in Patients with Multiple Sclerosis: A Single-Center Retrospective Study and Literature Review&quot;</p> <p><strong>Objective: </strong> Trigeminal neuralgia (TN) in patients with multiple sclerosis (MS) is a challenging condition to manage that is treated with Gamma Knife radiosurgery (GKRS). The aim of this report is to assess the safety, efficacy, and durability of GKRS for the treatment of TN in patients with MS. Our findings are compared with those of the existing literature and discussed.</p> <p><strong>Methods: </strong> We retrospectively reviewed all patients at our institution who underwent GKRS for the treatment of TN secondary to MS and had 1 or more years of follow-up. Preoperative and postoperative pain intensities and facial numbness were evaluated with the Barrow Neurological Institute scores. Durability of successful pain relief was statistically evaluated with Kaplan-Meier analysis. The prognostic role of perioperative factors was investigated and analyzed using Cox proportional hazards regression.</p> <p><strong>Results: </strong> There were 29 patients with MS-TN who underwent GKRS at our institution. Two patients underwent bilateral treatment. Four patients underwent repeat GKRS for pain recurrence. The median period of follow-up assessment was 33 months. Rates of reasonable pain reduction at 1, 3, and 5 years were 70%, 57%, and 57% respectively. All patients who underwent repeat GKRS had durable pain reduction. No prognostic factor for successful pain reduction was found.</p> <p><strong>Conclusions: </strong> Our study shows that GKRS for the treatment of TN secondary to MS is a safe and effective procedure in controlling pain in the short term but often fails to provide long-term pain control. GKRS can be safely repeated to prolong the time of pain reduction.</p>

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Dataset related to article "Duplications disrupt chromatin architecture and rewire GPR101-enhancer communication in X-linked acrogigantism"

<p>This record contains raw data related to article &ldquo;Duplications disrupt chromatin architecture and rewire GPR101-enhancer communication in X-linked acrogigantism&quot;</p> <p>X-linked acrogigantism (X-LAG) is the most severe form of pituitary gigantism and is characterized by aggressive growth hormone (GH)- secreting pituitary tumors that occur in early childhood. X-LAG is associated with chromosome Xq26.3 duplications (the X-LAG locus typically includes VGLL1, CD40LG, ARHGEF6, RBMX, and GPR101) that lead to massive pituitary tumoral expression of GPR101, a novel regulator of GH secretion. The mechanism by which the duplications lead to marked pituitary misexpression of GPR101 alone was previously unclear. Using Hi-C and 4C-seq, we characterized the normal chromatin structure at the X-LAG locus.We showed that GPR101 is located within a topologically associating domain (TAD) delineated by a tissue-invariant border that separates it from centromeric genes and regulatory sequences. Next, using 4C-seq with GPR101, RBMX, and VGLL1 viewpoints, we showed that the duplications in multiple X-LAG-affected individuals led to ectopic interactions that crossed the invariant TAD border, indicating the existence of a similar and consistent mechanism of neo-TAD formation in X-LAG.We then identified several pituitary active cis-regulatory elements (CREs) within the neo-TAD and demonstrated in vitro that one of them significantly enhanced reporter gene expression. At the same time, we showed that the GPR101 promoter permits the incorporation of new regulatory information. Our results indicate that X-LAG is a TADopathy of the endocrine system in which Xq26.3 duplications disrupt the local chromatin architecture forming a neo-TAD. Rewiring GPR101- enhancer interaction within the new regulatory unit is likely to cause the high levels of aberrant expression of GPR101 in pituitary tumors caused by X-LAG.</p>

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DATASET RELATED TO ARTICLE "SEX INFLUENCES ON THE NEUROCOGNITIVE OUTCOME OF PRETERM CHILDREN"

<p>VISUOAL-COGNITIVE, PERI-NATAL AND DEMOGRAPHIC DATA OF HEALTHY CHILDREN BORN PRETERM AND CONTROLS&nbsp;</p>

restrictedFeb 2022View details →
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Dataset related to article " RELEVANCE OF NEUROPHYSIOLOGICAL ASSESSMENT IN A CASE OF EPILEPSIA PARTIALIS CONTINUA CAUSED BY ANAPLASTIC LARGE CELL LYMPHOMA"

<p>THE DATASET CONTAINS THE MEG IMAGING OF MOVEMENT-RELATED ACTIVITY AND THE DATA FOR THE COHERENCE ANALYSIS</p> <p>&nbsp;</p>

restrictedFeb 2022View details →
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dataset related to article "Chronic cluster headache: A study of the telencephalic and cerebellar cortical thickness"

<p>xls dataset describing clinical and neuroimaging characteristics of patients involved in the study mentioned at title</p>

restrictedFeb 2022View details →
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Dataset related to article "Cognitive and behavioral associated changes in manifest Huntington disease A retrospective cross-sectional study"

<p>.xls dataset containing clinical and neuropsychological data of HD patients included in the study described at title by Fondazione Besta</p>

restrictedMar 2022View details →
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Dataset related to article "Quantitative Muscle MRI Protocol as Possible Biomarker in Becker Muscular Dystrophy"

<p>The database contains descriptive tables with clinical scores and quantitative MRI parameters values extracted from the thigh and the calf of the subjects involve in the study. A comparison table with the statistical correlation is also reported.</p>

restrictedMar 2022View details →
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dataset relate to article "A hypothesis for the role of axon demyelination in seizure generation"

<p>Dataset contains raw data underlying figures 1,2 and 3 included in the publication mentioned at title</p>

restrictedMar 2022View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

ScienceDex for faculty

Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.