Implementation of a low-activation Au-In-Cd decoupler into the J-PARC 1 MW short pulsed spallation neutron source

A silver-indium-cadmium (Ag-In-Cd, or AIC) alloy with a 1 eV high neutron cut-off energy was originaly developed as a decoupler to provide a narrow neutron pulse width with a short tail for the J-PARC 1-MW short-pulsed spallation neutron source. As a result of later studies, gold (Au) was chosen as a substitute for Ag for the production of spare decoupled moderators and reflector in order to reduce residual radioactivity thus easing handling and disposal of the spent moderator and reflector. The decoupler material Au-In-Cd (AuIC) was therefore investigated and developed. To implement it into an actual moderator-reflector assembly many critical engineering issues needed to be resolved with regard to large-sized bonding between AuIC and aluminum alloy A5083 by the hot isostatic pressing process (HIP). The HIP process for AuIC and aluminum was investigated in terms of surface condition, size, and heat capacity. Implementation of an AuIC decoupler into a spare reflector assembly was successfuly achieved and will result in a remarkable reduction of radioactivity compared to AIC without sacrificing neutronic performance

Immunohistochemical investigation of prognostic biomarkers in resected colorectal liver metastases : A systematic review and meta-analysis

Background: Many studies have investigated the prognostic role of biomarkers in colorectal liver metastases (CRLM). However, no biomarker has been established in routine clinical practice. The aim of this study was to scrutinize the current literature for biomarkers evaluated by immunohistochemistry as prognostic markers in patients with resected CRLM. Methods: A systematic review was performed according to the PRISMA guidelines. Articles were identified in the PubMed database with selected search terms and by cross-references search. The REMARK quality criteria were applied. Markers were included if they reported the prognostic impact of immunohistochemical markers in a multivariable setting in relation to overall survival (OS). A meta-analysis was conducted when more than one original article provided survival data of a marker. Results: In total, 26 biomarkers were identified as independent significant markers for OS in resected CRLM. These biomarkers were found to be involved in multiple oncogenic signalling pathways that control cell growth, apoptosis, angiogenesis and evasion of immune detection. Among these biomarker candidates were Ki-67, EGFR, p53, hTERT, CD34, TSP-1, KISS1, Aurora kinase A and CDX2. CD34 and TSP-1 were reported as significantly associated with survival by more than one study and where therefore pooled in a meta-analysis. Conclusion: A number of independent prognostic biomarkers for resected CRLM were identified. However, most markers were evaluated in a retrospective setting with small patient cohorts, without external validation. Large, prospective, multicentre studies with standardised methods are needed before biomarkers can translated into the clinic