Gefitinib in Non Small Cell Lung Cancer

Gefitinib is an oral, reversible, tyrosine kinase inhibitor of epidermal growth factor receptor (EGFR) that plays a key role in the biology of non small cell lung cancer (NSCLC). Phase I studies indicated that the recommended dose of gefitinib was 250 mg/day. Rash, diarrhea, and nausea were the most common adverse events. The positive results obtained in early phase 2 clinical trials with gefitinib were not confirmed in large phase 3 trials in unselected patients with advanced NSCLC. The subsequent discovery that the presence of somatic mutations in the kinase domain of EGFR strongly correlates with increased responsiveness to EGFR tyrosine kinase inhibitors prompted phase 2 and 3 trials with gefitinib in the first line-treatment of EGFR-mutated NSCLC. The results of these trials have demonstrated the efficacy of gefitinib that can be now considered as the standard first-line treatment of patients with advanced NSCLC harbouring activating EGFR mutations

Distribution pattern of hepatitis C virus genotypes and correlation with viral load and risk factors in chronic positive patients.

Objective: Hepatitis C virus (HCV) has emerged as a leading cause of chronic hepatitis, liver cirrhosis and hepatocellular carcinoma worldwide. The purpose of this study was to describe the distribution pattern of HCV genotypes in chronic hepatitis patients in the Campania region of southern Italy and estimate their association with risk factors and viral load. Materials and Methods: 404 consecutive HCV ribonucleic acid-positive patients were included in the study. HCV genotyping was carried out by the HCV line probe assay test and viral load estimation by the TaqMan real-time PCR system. Results: The predominant genotype was 1 (63.6%), followed by genotype 2 (29.4%), 3 (6.2%) and 4 (0.8%). Subtype 1b was more frequent in females than in males. Conversely, genotype 3 was more frequent in males. No significant difference was observed in age distribution of HCV genotypes. Surgery and dental therapy were the most frequent risk factors for genotype 1 and intravenous drug abuse and tattooing for genotype 3. Patients with genotype 1 more frequently showed high HCV viral load when compared to those with genotypes 2 and 3. Conclusion: The present study revealed that HCV genotypes 1 and 2 accounted for over 95% of all HCV infections in the Campania region, and genotype 1 was more frequently associated with a higher viral load when compared to genotypes 2 and 3

Open Science for a shared and collaborative knowledge

The conventional model of “Scholarly communication”, based on the publication in "tall access" journals and by preference in high-Impact Factor journals, has distorted over time, if not betrayed, its original vocation, that is to "communicate" science. The year 1665 is often cited, being the year of birth of the Journal des Sçavans in France and of Philosophical Transactions in England, published by Henry Oldenburg to present advances in scientific research to members of the Royal Society. It is the founding date of the first scientific journals and marks the starting point of the privileged circuit for sharing scientific knowledge and encouraging the so-called "Great Conversation" of science. This debate among scientists should be the true essence and the raison d’être of Scholarly Communication. Since then, unfortunately, academic publishing has turned into a real business, "the most profitable obsolete technology in history", dominated by the "Big Five", a cartel of the five publishing groups (Reed Elsevier, Wiley- Blackwell, Springer, Taylor & Francis, Sage) which rank in the highest positions in the international scientific publishing market, both in terms of profit margins (38% of Reed Elsevier's net profit), and the number of articles published every year, with a price spiral in subscription costs that peaked at 402% for the period 1986-2011. Economic barriers are only one of the obstacles that restrict access to research findings. Paradoxically, although huge economic investments are made by the institutions to enable the academic community to do research, much of the scientific literature is actually inaccessible. Jon Tennant remarks: "we spend 1/3 of the total global research budget (£59/175bn) in publishing and communicating results that 99% of people cannot access"

Dynamics of Viral Infection and Evolution of SARS-CoV-2 Variants in the Calabria Area of Southern Italy

In this study, we report on the results of SARS-CoV-2 surveillance performed in an area of Southern Italy for 12 months (from March 2021 to February 2022). To this study, we have sequenced RNA from 609 isolates. We have identified circulating VOCs by Sanger sequencing of the S gene and defined their genotypes by whole-genome NGS sequencing of 157 representative isolates. Our results indicated that B.1 and Alpha were the only circulating lineages in Calabria in March 2021; while Alpha remained the most common variant between April 2021 and May 2021 (90 and 73%, respectively), we observed a concomitant decrease in B.1 cases and appearance of Gamma cases (6 and 21%, respectively); C.36.3 and Delta appeared in June 2021 (6 and 3%, respectively); Delta became dominant in July 2021 while Alpha continued to reduce (46 and 48%, respectively). In August 2021, Delta became the only circulating variant until the end of December 2021. As of January 2022, Omicron emerged and took over Delta (72 and 28%, respectively). No patient carrying Beta, Iota, Mu, or Eta variants was identified in this survey. Among the genomes identified in this study, some were distributed all over Europe (B1_S477N, Alpha_L5F, Delta_T95, Delta_G181V, and Delta_A222V), some were distributed in the majority of Italian regions (B1_S477N, B1_Q675H, Delta_T95I and Delta_A222V), and some were present mainly in Calabria (B1_S477N_T29I, B1_S477N_T29I_E484Q, Alpha_A67S, Alpha_A701S, and Alpha_T724I). Prediction analysis of the effects of mutations on the immune response (i.e., binding to class I MHC and/or recognition of T cells) indicated that T29I in B.1 variant; A701S in Alpha variant; and T19R in Delta variant were predicted to impair binding to class I MHC whereas the mutations A67S identified in Alpha; E484K identified in Gamma; and E156G and ΔF157/R158 identified in Delta were predicted to impair recognition by T cells. In conclusion, we report on the results of SARS-CoV-2 surveillance in Regione Calabria in the period between March 2021 and February 2022, identified variants that were enriched mainly in Calabria, and predicted the effects of identified mutations on host immune response

Burnout among surgeons before and during the SARS-CoV-2 pandemic: an international survey

Background: SARS-CoV-2 pandemic has had many significant impacts within the surgical realm, and surgeons have been obligated to reconsider almost every aspect of daily clinical practice. Methods: This is a cross-sectional study reported in compliance with the CHERRIES guidelines and conducted through an online platform from June 14th to July 15th, 2020. The primary outcome was the burden of burnout during the pandemic indicated by the validated Shirom-Melamed Burnout Measure. Results: Nine hundred fifty-four surgeons completed the survey. The median length of practice was 10 years; 78.2% included were male with a median age of 37 years old, 39.5% were consultants, 68.9% were general surgeons, and 55.7% were affiliated with an academic institution. Overall, there was a significant increase in the mean burnout score during the pandemic; longer years of practice and older age were significantly associated with less burnout. There were significant reductions in the median number of outpatient visits, operated cases, on-call hours, emergency visits, and research work, so, 48.2% of respondents felt that the training resources were insufficient. The majority (81.3%) of respondents reported that their hospitals were included in the management of COVID-19, 66.5% felt their roles had been minimized; 41% were asked to assist in non-surgical medical practices, and 37.6% of respondents were included in COVID-19 management. Conclusions: There was a significant burnout among trainees. Almost all aspects of clinical and research activities were affected with a significant reduction in the volume of research, outpatient clinic visits, surgical procedures, on-call hours, and emergency cases hindering the training. Trial registration: The study was registered on clicaltrials.gov "NCT04433286" on 16/06/2020

Impiego di campioni paraffinati di lesioni cancerose della cervice uterina nella genotipizzazione di HPV

Nello studio del carcinoma della cervice uterina molta rilevanza assumono i papillomavirus umani quali agenti eziologici. Programmi di screening mediante citologia cervicale (Pap test o test di Papanicolau) hanno consentito una drastica riduzione dell’incidenza del cancro alla cervice, grazie soprattutto alla semplicità di prelievo ed al basso costo dell’indagine che consente di lavorare su grandi numeri ed in tempi brevi; tuttavia questo test ha una sensibilità e una specificità limitata, specialmente in casi di basso grado di lesione (low grade). L’uso della biologia molecolare nello studio delle lesioni neoplastiche di vario grado fornisce l’opportunità per una più accurata diagnosi di infezione da HPV. In questo studio sono stati eseguiti test di genotipizzazione in campioni bioptici ottenuti da pazienti affette da carcinoma in situ o carcinoma invasivo. I risultati confermano il ruolo predominante di HPV 16 così come descritto in letteratura internazionale ma appare evidente che il genotipo 18 nella nostra area geografica non ha la rilevanza che viene descritta in altre nazioni. L’impiego di campioni di tessuto fissati e paraffinati, inoltre, offre l’opportunità di compiere indagini retrospettive che possono consentire una più approfondita conoscenza dell’andamento epidemiologico di HPV e del suo effettivo ruolo nella genesi del carcinoma della cervice uterina