The influence of fluctuations of the shape degree of freedom in collisions of deformed nuclei with energies between 0.8 and 2.1 GeV/nucleon is analyzed on the basis of an intranuclear cascade simulation for the strongly deformed systems 46Ti+ 46Ti and 166Er+ 166Er. While there is a considerable sensitivity of the global event variables to the orientation for polarized beams and targets, this dependence disappears in the average over all orientations for impact parameter selected and integrated events. The dependence of the nuclear stopping and thermalization on the size of the system under consideration and on the bombarding energy is also investigated.
We present a theoretical description of nuclear collisions which consists of a three-dimensional fluid-dynamical model, a chemical equilibrium breakup calculation for local light fragment (i.e., p, n, d, t, 3He, and 4He) production, and a final thermal evaporation of these particles. The light fragment cross sections and some properties of the heavy target residues are calculated for the asymmetric system Ne+U at 400 MeV/N. The results of the model calculations are compared with recent experimental data. Several observable signatures of the collective hydrodynamical processes are consistent with the present data. An event-by-event analysis of the flow patterns of the various clusters is proposed which can yield deeper insight into the collision dynamics.
The nucleons taking part in heavy ion reaction are considered as a three-component fluid. The first and second components correspond to the nucleons of the target and the projectile, while the thermalized nucleons produced in the course of the collision belong to the third component. Making use of the Boltzmann equation, hydrodynamical equations are derived. An equation of state for anisotropic nuclear matter obtained from a field theoretical model in mean field approximation is applied in a one dimensional version of the three-component fluid model. The speed of thermalization is analyzed and compared to the results of cascade and kinetic models. NUCLEAR REACTIONS Relativistic heavy-ion reactions, hydrodynamic description.
Purpose: Molecular diagnostics including next generation gene sequencing are increasingly used to determine options for individualized therapies in brain tumor patients. We aimed to evaluate the decision-making process of molecular targeted therapies and analyze data on tolerability as well as signals for efficacy.
Methods: Via retrospective analysis, we identified primary brain tumor patients who were treated off-label with a targeted therapy at the University Hospital Frankfurt, Goethe University. We analyzed which types of molecular alterations were utilized to guide molecular off-label therapies and the diagnostic procedures for their assessment during the period from 2008 to 2021. Data on tolerability and outcomes were collected.
Results: 413 off-label therapies were identified with an increasing annual number for the interval after 2016. 37 interventions (9%) were targeted therapies based on molecular markers. Glioma and meningioma were the most frequent entities treated with molecular matched targeted therapies. Rare entities comprised e.g. medulloblastoma and papillary craniopharyngeoma. Molecular targeted approaches included checkpoint inhibitors, inhibitors of mTOR, FGFR, ALK, MET, ROS1, PIK3CA, CDK4/6, BRAF/MEK and PARP. Responses in the first follow-up MRI were partial response (13.5%), stable disease (29.7%) and progressive disease (46.0%). There were no new safety signals. Adverse events with fatal outcome (CTCAE grade 5) were not observed. Only, two patients discontinued treatment due to side effects. Median progression-free and overall survival were 9.1/18 months in patients with at least stable disease, and 1.8/3.6 months in those with progressive disease at the first follow-up MRI.
Conclusion: A broad range of actionable alterations was targeted with available molecular therapeutics.
However, efficacy was largely observed in entities with paradigmatic oncogenic drivers, in particular with BRAF mutations. Further research on biomarker-informed molecular matched therapies is urgently necessary.
This paper reports on Monte Carlo simulation results for future measurements of the moduli of time-like proton electromagnetic form factors, |GE | and |GM|, using the ¯pp → μ+μ− reaction at PANDA (FAIR). The electromagnetic form factors are fundamental quantities parameterizing the electric and magnetic structure of hadrons. This work estimates the statistical and total accuracy with which the form factors can be measured at PANDA, using an analysis of simulated data within the PandaRoot software framework. The most crucial background channel is ¯pp → π+π−,due to the very similar behavior of muons and pions in the detector. The suppression factors are evaluated for this and all other relevant background channels at different values of antiproton beam momentum. The signal/background separation is based on a multivariate analysis, using the Boosted Decision Trees method. An expected background subtraction is included in this study, based on realistic angular distribuations of the background contribution. Systematic uncertainties are considered and the relative total uncertainties of the form factor measurements are presented.