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1.
ESMO Open ; 7(4): 100519, 2022 08.
Article in English | MEDLINE | ID: mdl-35759854

ABSTRACT

BACKGROUND: Gastroesophageal adenocarcinoma is a major contributor to global disease burden with poor prognosis even in resectable, regionally limited stages. Feasible prognostic tools are crucial to improve patient management, yet scarce. PATIENTS AND METHODS: Disease-related symptoms, patient, tumour, treatment as well as laboratory parameters at initial diagnosis and overall survival (OS) of patients with stage II and III gastroesophageal adenocarcinoma, who were treated between 1990 and 2020 at the Medical University of Vienna, were evaluated in a cross-validation model to develop a feasible risk prediction score. RESULTS: In total, 628 patients were included in this single-centre analysis. The final score ranked from 0 to 10 and included the factors sex (female +1), age, years (30-59 +1, >60 +2), underweight classified by body mass index (+2), location of the tumour (stomach +1), stage (III +2), stenosis in endoscopy (+1) and weight loss (+1). The score was grouped into low- (0-3), medium- (4-6) and high-risk (7+) subgroups. The median OS were 70.3 [95% confidence interval (CI) 51.2-111.8], 23.4 (95% CI 21.2-26.7) and 12.6 (7.0-16.1) months, respectively. The 1-year survival probabilities were 0.88 (95% CI 0.83-0.93), 0.75 (95% CI 0.70-0.79) and 0.54 (95% CI 0.39-0.74), whereas the 5-year survival probabilities were 0.57 (95% CI 0.49-0.66), 0.24 (95% CI 0.20-0.28) and 0.09 (95% CI 0.03-0.28), respectively. CONCLUSIONS: The VIennese risk prediction score for Oesophagogastric Localized Adenocarcinoma (VIOLA) risk prediction score poses a feasible tool for the estimation of OS in patients with regionally limited gastroesophageal adenocarcinoma and, thus, may improve patient management in clinical routine. Prospective analyses should be carried out to confirm our findings.


Subject(s)
Adenocarcinoma , Stomach Neoplasms , Viola , Female , Humans , Prognosis , Prospective Studies
2.
J Environ Manage ; 109: 189-99, 2012 Oct 30.
Article in English | MEDLINE | ID: mdl-22819600

ABSTRACT

As the scientific community has highlighted the plight of freshwater species, there have been increasing calls for protected area (PA) designation and management specific to the conservation of aquatic species and ecosystems. In this study we examined PA management in one relatively well-resourced (high levels of financial and technical resources) part of the world: the Tennessee and Cumberland River Basins, USA. We asked managers their perceptions about the current status of freshwater ecosystems within PAs, the sources of stress that are degrading freshwater ecosystem integrity, the degree to which PAs address these stressors, and the availability of technical, human, and financial resources for management activities that benefit freshwater ecosystems and the species they support. Managers generally perceive that freshwater ecosystems within PAs are under low levels of stress, with less than half reporting any alteration to ecosystem integrity, and very few reporting alterations at medium or high levels. Most PAs have fewer resources dedicated to freshwater conservation and management than to other activities, and some PAs completely lack resources for freshwater management. We recommend a review of every PA's goals and objectives and any needed updates to include the conservation of freshwater ecosystems. We also recommend an analysis to determine the most pressing stressors to aquatic life within each PA, stemming from sources both from within and outside of a PA's boundaries, and that this information be used to guide future management. Finally, we suggest that management resources be prioritized for PAs that include large portions of the catchments of their freshwater systems; that can address the dominant sources of stress within the PA; or that contain representative ecosystems, species assemblages or populations of rare, endemic, and threatened species.


Subject(s)
Conservation of Natural Resources/methods , Fresh Water/analysis , Rivers , Tennessee
3.
Inorg Chem ; 40(20): 5106-16, 2001 Sep 24.
Article in English | MEDLINE | ID: mdl-11559067

ABSTRACT

Reaction of LnI2 (Ln = Sm, Yb) with two equivalents of NaTp(Me2) or reduction of Eu(Tp(Me2))2OTf gives good yields of the highly insoluble homoleptic Ln(II) complexes, Ln(Tp(Me2))2 (Ln = Sm (1a), Yb (2a), Eu (3a)). Use of the additionally 4-ethyl substituted Tp(Me2,4Et) ligand produces the analogous, but soluble Ln(Tp(Me2,4Et))2 (1-3b) complexes. Soluble compounds are also obtained with the Tp(Ph) and Tp(Tn) ligands (Tn = thienyl), Ln(Tp(Ph))2 (Ln = Sm, 1c; Yb, 2c) and Ln(Tp(Tn))2 (Ln = Sm, 1d; Yb, 2d). To provide benchmark parameters for structural comparison the series of Sm(Tp(Me2))2X complexes (X = F, 1e; Cl, 1f; Br, 1g; I, 1h; BPh4, 1j) were prepared either via oxidation of the Sm(Tp(Me2))2 or salt metathesis from SmX3 (X = Cl, Br, I). The solid-state structures of 1-3a, 1b, 1-2c and 1e, 1f, 1h, and 1j were determined by single-crystal X-ray diffraction. The homoleptic bis-Tp complexes are all six-coordinate with trigonal antiprismatic geometries, planes of the kappa(3)-Tp ligands are parallel to one another. In the series of Sm(Tp(Me2))2X complexes the structure changes from seven-coordinate molecular compounds, with intact Sm-X bonds, for X = F, Cl, to six-coordinate ionic structures [Sm(Tp(Me2))2]X (X = I, BPh4), suitable crystals of the bromide compound could not be obtained. The dependence of the structures on the size of X is understandable in terms of the interplay between the size of the cleft that the [Sm(Tp(Me2))2](+) fragment can make available and the donor ability of the anionic group toward the hard Sm(III) center.

4.
Angew Chem Int Ed Engl ; 38(15): 2233-2237, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10425494

ABSTRACT

Divalent and solvent-free: the ytterbium hydrido complex 1 was obtained by the hydrogenolysis of [(Tp(tBu,Me))Yb(CH(2)SiMe(3))(thf)]. The steric demand of the bulky hydrotris(3-tert-butyl-5-methylpyrazolyl)borate ligand, Tp(tBu,Me), is sufficient to stabilize the dimer, yet facile room-temperature reactions with amines, alkynes, diynes, and CO indicate a rich chemistry of 1.

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