Bartlettmckinnon5812

The integrated area under the curve of the modified PAGE

model was greater than those of the PAGE-B and mPAGE-B models (0.760 vs 0.714 and 0.716, respectively) in the derivation dataset. The cumulative HCC incidence was significantly higher in the high-risk (modified PAGE-B

score≥24) group than in the intermediate-risk (modified PAGE

-B score 12-24) or low-risk (modified PAGE

-B score<12) group (all P<0.001). Similar results were observed in the validation cohort.

The predictive accuracies of the PAGE-B and mPAGE-B models were validated in Korean patients with CHB receiving AVT. However, the modified PAGE

-B model featuring the addition of LS value showed higher predictability than the PAGE-B and mPAGE-B models.

The predictive accuracies of the PAGE-B and mPAGE-B models were validated in Korean patients with CHB receiving AVT. However, the modified PAGELS -B model featuring the addition of LS value showed higher predictability than the PAGE-B and mPAGE-B models.

Prostate-specific membrane antigen (PSMA)-targeted radionuclide therapy (TRT) has demonstrated efficacy and tolerability with a dose-response effect in phase I/II trials in men with metastatic castration-resistant prostate cancer (mCRPC). The need for positive PSMA imaging before PSMA-TRT to select patients is largely practiced, but its utility is not proven. Given target heterogeneity, developing a biomarker to identify the optimal patient population remains an unmet need. The aim of this study was to assess PSMA uptake by imaging and response to PSMA-TRT.

We performed an analysis of men with mCRPC enrolled in sequential prospective phase I/II trials of PSMA-TRT. Each patient had baseline PSMA imaging by planar

In and/or

Lu SPECT (N = 171) or

Ga-PSMA-11 PET/CT (N = 44), but the results were not used to include/exclude treatment. Semiquantitative imaging scores (IS) on a 0-4 scale were assigned based on PSMA uptake in tumors compared to liver uptake. We compared the≥50% PSA decline response propoSMA-TRT PSA decline with 2 (7.7%) having ≥ 50% PSA declines.

Collectively, the data provide evidence in favor of the hypothesis that patients with high PSMA uptake and high administered radionuclide dose correlate with a higher chance of response.

Collectively, the data provide evidence in favor of the hypothesis that patients with high PSMA uptake and high administered radionuclide dose correlate with a higher chance of response.Identifying ecosystems where biota may be contaminated with hazardous levels of methylmercury (MeHg) is a challenge. One widely used approach for determining site-specific MeHg contamination is to monitor MeHg contamination in sentinel species. Terrestrial shoreline spiders that consume emergent aquatic insects (e.g., midges and mayflies) have been proposed as sentinels of MeHg contamination of aquatic ecosystems. The purpose of the present study was to determine whether a novel sampling technique, collection of spiders from nests of mud dauber wasps (Sphecidae), would be an efficient method for capturing MeHg-contaminated shoreline spiders for use as sentinels in ecological risk assessments. Mud dauber nests were collected near the Clear Fork of the Trinity River in Fort Worth, Texas (USA) on 3 dates from 4 human-made structures. Nests contained 627 unconsumed spiders from 5 families Araneidae, Salticidae, Thomisidae, Oxyopidae, and Theridiidae. Fenebrutinib in vivo Methylmercury concentrations ranged from 12.2 to 56.3 ng/g wet weight in Thomisidae and Araenidae, respectively. Methylmercury concentrations of the spiders were generally low relative to risk thresholds for adult birds, but a few families of spiders could pose a risk to nestlings. Although mud dauber nests have been recognized as a source of spiders for biodiversity studies, the present study is the first to demonstrate the potential use of spiders collected from mud dauber nests for ecotoxicology studies. Environ Toxicol Chem 2021;401335-1340. © 2021 SETAC.A market for bisphenol A (BPA) replacement compounds has emerged as a result of restrictions on the use of BPA. Some of these compounds have been detected in the environment; however, little is known about their toxicological properties. In the present study, an avian in vitro toxicogenomic approach was used to compare the effects of 5 BPA alternatives. Cell viability and mRNA expression were compared in primary embryonic hepatocytes of chicken (CEH) and double-crested cormorant (DCEH) exposed to 4,4'-(propane-2,2-diyl) diphenol (BPA), bis (4-hydroxyphenyl) methane (BPF), bis (3-allyl-4-hydroxyphenyl) sulfone (TGSH), 7-bis (4-hydroxyphenylthio)-3,5-dioxaheptane (DD-70), 2,2-bis (4-hydroxyphenyl) hexafluoropropane (BPAF), and 4-hydroxyphenyl 4-isoprooxyphenylsulfone (BPSIP). Changes in gene expression were determined using 2 polymerase chain reaction (PCR) arrays 1) species-specific ToxChips that contain genes representing toxicologically relevant pathways, and 2) chicken-specific AestroChip that measures estrogen responsive genes. In CEH and DCEH, BPA alternatives TGSH, DD-70, and BPAF were most cytotoxic. Some of the replacement compounds changed the expression of genes related to xenobiotic metabolism, bile acid, and cholesterol regulation. The rank order based on the number of genes altered on the chicken ToxChip array was TGSH > DD-70 > BPAF = BPF > 17β estradiol (E2) > BPSIP > BPA. On the cormorant ToxChip array, BPSIP altered the greatest number of genes. Based on the chicken AestroChip data, BPSIP and BPF were slightly estrogenic. These results suggest that the replacement compounds have comparable or even greater toxicity than BPA and act via different mechanisms. Environ Toxicol Chem 2021;401368-1378. © 2021 Her Majesty the Queen in Right of Canada. Reproduced with the permission of the Minister of Environment and Climate Change Canada.The current Australian and New Zealand default guideline value of 3 µg Cl/L for total residual chlorine in freshwaters is largely based on acute data converted to chronic data using a default acute to chronic ratio of 10, without consideration of chlorine decomposition. Given the rapid decomposition of chlorine, initially as hypochlorite and then as chloramine, it is appropriate to consider a guideline value based on short-term (acute) toxicity rather than one based on longer-term chronic data, as has been recommended for chlorine in marine waters. The literature on the fate of chlorine in drinking water discharged to freshwaters and on the ecotoxicity of total residual chlorine has been reviewed, and on the basis of this, revised default guideline values were derived for both hypochlorite and chloramine in freshwater using a species sensitivity distribution of toxicity data. The values for 95% species protection were 7 and 9 µg Cl/L as total residual chlorine, respectively. The former would apply to any total residual chlorine-containing effluent, but in the case of drinking water where dechlorination has been undertaken, the chloramine-based default guideline value is likely to be more appropriate.