ABSTRACT
BACKGROUND: The optimal duration of first-line chemotherapy for patients with advanced gastric cancer is unknown. Diverse clinical trials have proposed different strategies including limited treatment, maintenance of some drugs, or treatment until progression. METHOD: The sample comprises patients from the AGAMENON multicenter registry without progression after second evaluation of response. The objective was to explore the optimal duration of first-line chemotherapy. A frailty multi-state model was conducted. RESULTS: 415 patients were divided into three strata: discontinuation of platinum and maintenance with fluoropyrimidine until progression (30%, n = 123), complete treatment withdrawal prior to progression (52%, n = 216), and full treatment until progression (18%, n = 76). The hazard of tumor progression decreased by 19% per month with the full treatment regimen. However, we found no evidence that fluoropyrimidine maintenance (hazard ratio [HR] 1.07, confidence interval [CI] 95%, 0.69-1.65) worsened progression-free survival (PFS) with respect to treatment until progression. Predictive factors for PFS were ECOG performance status, ≥ 3 metastatic sites, prior tumor response, and bone metastases. Toxicity grade 3/4 was more common in those who continued the full treatment until progression vs fluoropyrimidine maintenance (16% vs 6%). CONCLUSION: The longer duration of the full initial regimen exerted a protective effect on the patients of this registry. Platinum discontinuation followed by fluoropyrimidine maintenance yields comparable efficacy to treatment up to PD, with a lower rate of serious adverse events.
Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Registries , Stomach Neoplasms/drug therapy , Adult , Aged , Aged, 80 and over , Clinical Decision-Making , Female , Humans , Maintenance Chemotherapy , Male , Middle Aged , Platinum/administration & dosage , Platinum/adverse effects , Progression-Free Survival , Pyrimidines/administration & dosage , Pyrimidines/adverse effects , Stomach Neoplasms/mortality , Stomach Neoplasms/pathology , Survival Rate , Time Factors , Young AdultABSTRACT
The in vitro leishmanicidal activity and cytotoxicity of pyrazole-containing macrocyclic polyamines 1-4 was assayed on Leishmania infantum and Leishmania braziliensis species. Compounds 1-4 were more active and less toxic than glucantime and both infection rates and ultrastructural alterations confirmed that 1 and 2 were highly leishmanicidal and induced extensive parasite cell damage. Modifications in the excretion products of parasites treated with 1-3 were also consistent with substantial cytoplasm alterations. Compound 2 was highlighted as a potent inhibitor of Fe-SOD in both species, whereas its effect on human CuZn-SOD was poor. Molecular modelling suggested that 2 could deactivate Fe-SOD due to a sterically favoured enhanced ability to interact with the H-bonding net that supports the enzyme`s antioxidant features.
Subject(s)
Antiprotozoal Agents/pharmacology , Leishmania braziliensis/drug effects , Leishmania infantum/drug effects , Leishmaniasis/drug therapy , Pyrazoles/pharmacology , Superoxide Dismutase/drug effects , Animals , Antiprotozoal Agents/chemistry , Cell Line , Cell Survival/drug effects , Erythrocytes/drug effects , Female , Humans , Leishmania braziliensis/enzymology , Leishmania braziliensis/ultrastructure , Leishmania infantum/enzymology , Leishmania infantum/ultrastructure , Leishmaniasis/parasitology , Macrocyclic Compounds/chemistry , Macrocyclic Compounds/pharmacology , Macrophages/drug effects , Mice, Inbred BALB C , Microscopy, Electron, Transmission , Models, Molecular , Polyamines/chemistry , Polyamines/pharmacology , Protozoan Proteins/drug effects , Protozoan Proteins/metabolism , Pyrazoles/chemistry , Superoxide Dismutase/metabolismABSTRACT
West Nile virus (WNV) first emerged in the US in 1999 and has since spread across the Americas. Here, we report the continued expansion of WNV to the British Virgin Islands following its emergence in a flock of free-roaming flamingos. Histologic review of a single chick revealed lesions consistent with WNV infection, subsequently confirmed with PCR, immunohistochemistry and in situ hybridization. Full genome analysis revealed 99% sequence homology to strains circulating in the US over the past decade. This study highlights the need for rapid necropsy of wild bird carcasses to fully understand the impact of WNV on wild populations.
Subject(s)
Bird Diseases/epidemiology , Bird Diseases/virology , Culex/virology , Disease Outbreaks/veterinary , Insect Vectors/virology , West Nile Fever/epidemiology , West Nile virus/isolation & purification , Animals , Animals, Wild/virology , Bird Diseases/transmission , Birds/virology , Bites and Stings/virology , British Virgin Islands , Immunohistochemistry , In Situ Hybridization , Polymerase Chain Reaction , West Nile Fever/transmission , West Nile Fever/virology , West Nile virus/geneticsABSTRACT
Bats are reservoirs for a wide range of human pathogens including Nipah, Hendra, rabies, Ebola, Marburg and severe acute respiratory syndrome coronavirus (CoV). The recent implication of a novel beta (ß)-CoV as the cause of fatal respiratory disease in the Middle East emphasizes the importance of surveillance for CoVs that have potential to move from bats into the human population. In a screen of 606 bats from 42 different species in Campeche, Chiapas and Mexico City we identified 13 distinct CoVs. Nine were alpha (α)-CoVs; four were ß-CoVs. Twelve were novel. Analyses of these viruses in the context of their hosts and ecological habitat indicated that host species is a strong selective driver in CoV evolution, even in allopatric populations separated by significant geographical distance; and that a single species/genus of bat can contain multiple CoVs. A ß-CoV with 96.5â% amino acid identity to the ß-CoV associated with human disease in the Middle East was found in a Nyctinomops laticaudatus bat, suggesting that efforts to identify the viral reservoir should include surveillance of the bat families Molossidae/Vespertilionidae, or the closely related Nycteridae/Emballonuridae. While it is important to investigate unknown viral diversity in bats, it is also important to remember that the majority of viruses they carry will not pose any clinical risk, and bats should not be stigmatized ubiquitously as significant threats to public health.
Subject(s)
Chiroptera/virology , Coronavirus Infections/veterinary , Coronavirus/isolation & purification , Genetic Variation , Animals , Base Sequence , Coronavirus/classification , Coronavirus/genetics , Coronavirus Infections/epidemiology , Coronavirus Infections/transmission , Coronavirus Infections/virology , DNA, Complementary/chemistry , DNA, Complementary/genetics , Disease Reservoirs , Ecosystem , Humans , Mexico/epidemiology , Molecular Sequence Data , Phylogeny , Public Health , RNA, Viral/genetics , Sequence Analysis, DNA , ZoonosesABSTRACT
A hypertension detection and control program sponsored by the Pan-American Health Organization and the World Health Organization (PAHO/WHO) was carried out in an urban health district of Havana City, Cuba. A baseline (initial) survey was conducted on a random sample of the population (greater than or equal to 15 years of age) to assess the problem of hypertension in that community. Subsequently, we extended the program in the same area by taking the blood pressure of as many people as we could, and a health education program on hypertension was developed and implemented. All hypertensive persons were treated. We surveyed about 90% of the adult population (29,640) over a 5-year period. We then conducted a final survey on a second random sample of the population to assess the effect of the program. The response rate to the letter of invitation to visit the hypertension clinic was 50%; 30% of the recall appointments were missed, and the dropout rate was 18.6%. Seventy percent of the hypertensive persons had Stage I disease (PAHO/WHO) with normal electrocardiograms. Before the program, 15.7% of the total number of hypertensive persons surveyed in the area had the disease under good control, and this increased to 31% after the program. Mortality due to cerebrovascular disease was reduced from 11/10,000/yr to 7/10,000/yr, whereas mortality caused by myocardial infarction did not change.