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Chad Tang, MD, The University of Texas MD Anderson Cancer Center, discusses the unmet needs for patients with oligometastatic prostate cancer. There have been randomized trials for oligometastatic prostate cancer, including STOMP (NCT01558427) and ORIOLE (NCT02680587), which randomized patients to receive radiation in metastatic patients vs observation. These trials showed that radiation delayed the PSA progression that occurs among this patient population, and radiation by itself, delays the progression. According to Tang, other trials have also shown that radiation therapy can combine synergistically with hormone therapy. In earlier trials, upfront hormonal therapy for metastatic disease has also resulted in benefits in overall survival when compared with delaying hormone therapy. Advertisement Then, the EXTEND trial (NCT03599765) recently evaluated patients with oligometastatic prostate cancer and showed there to be improvements in progression-free survival (PFS) and eugonadal PFS when given the combination of metastasis-directed therapy with intermittent hormone therapy. However, Tang notes that questions still remain regarding how experts think about oligometastatic prostate cancer, the way it is defined, and how it is treated. Transcription: 0:10 | I think the biggest unmet need is how we think about oligometastatic prostate cancer. In my opinion, there are 2 ways that you can change therapy with high level evidence. One is to do a randomized control compared with standard of care and number 2 is staging changes. With PSMA PETS and with improved imaging overall, maybe we need to better define, biologically, what oligometastatic prostate cancer is. If that’s true, then maybe we should treat them like metastatic prostate cancers to understand these processes a little bit better and find the optimum treatment recommendations for these patients. REFERENCE: Tang C, Sherry AD, Haymaker C, et al. Addition of metastasis-directed therapy to intermittent hormone therapy for oligometastatic prostate cancer (EXTEND): A multicenter, randomized phase II trial. J Radiat Oncol. 2022;114(5):P1059-1060. doi:10.1016/j.ijrobp.2022.09.006
In Tanzania, researchers are unlocking the mysteries of a mold (fungus) that infects patients who have already contracted the bacterial disease tuberculosis. According to World Health Organization statistics, tuberculosis is the leading cause of death globally from infectious disease, with over a quarter of TB deaths occurring in Africa. Fungal lung disease, particularly chronic pulmonary aspergillosis is significantly under-diagnosed, under-treated and a common cause of death in Africa: a 2022 study found the Aspergillosis mold develops in the lesions caused by TB, worsening them and resulting in a deteriorating clinical situation. Dr Martha F. Mushi, a lecturer consultant medical mycologist, at the Catholic University of Health and Allied Sciences (CUHAS) and Bugando Medical Centre in Mwanza, Tanzania, explaines that her research explores the prevalence, risk factors, and clinical outcomes of CPA among patients with smear-negative (lower bacterial load) TB, contributing to improved patient care in vulnerable populations. “The fact that approximately 45% of clinically diagnosed pulmonary TB cases have negative-smear or PCR test results highlighted the need of this project,” she says, adding that while CPA is documented as the major cause of smear negative TB, the mortality rate of untreated CPA is estimated at 75% to 80% over five years. “Africa’s capacity to diagnose lung fungal infection is still very low,” she says, “This calls for the global attention in increasing awareness of fungal infection among clinicians and training of technical staff (radiology and clinical laboratory) on the WHO essential diagnostic tests, to attain the sustainable development goals.” Mushi explained that the project is a result of collaboration with Prof David Denning, the founder and retired executive director of Global Action Fund for Fungal Infections (GAFFI), which partially funds and supports the project. Dr Martha Mushi reading gram stain results all in in microbiology laboratory of CUHAS with taken on … [+] 30th June 2023 Martha Mushi Importance of Mycology Mushi grew up in in Kilimanjaro region Northeastern part of Tanzania. “As a university student I was very much inspired by my microbiology professor, who interested me in this field that explores the intricate world of microorganisms,” she says, adding that the neglect of mycology as a whole result in limited research funding, making it challenging to generate evidence-based data for teaching and to foster interest among junior researchers. “Despite these obstacles, mycology plays a crucial role in understanding and addressing fungal infections, which have significant impacts on public health,” she says. According to Mushi, addressing public health issues requires more than just medical interventions. “Scientists from the Global South understand the local healthcare systems, traditional healing practices, community dynamics, and social determinants of health,” she says, “This understanding enables them to design interventions that are sensitive to cultural beliefs and practices, promote community engagement, and enhance the likelihood of successful implementation. Mushi explains that scientists from the Global South can shed light on ethical dilemmas specific to their contexts and ensure that research is conducted in a way that respects the dignity, autonomy, and rights of individuals and communities. “This not only enhances the relevance and applicability of the solutions but also promotes a sense of ownership and empowerment among the communities affected by the global challenges,” she says. Mwanza, Tanzania. getty Phage Approach Another researcher from the region interested in tuberculosis is 20-year old Rutendo Kahari. Kahari, from Zimbabwe, is already on a path to use viruses that infect bacteria to fight some of sub-Saharan Africa’s deadliest infectious diseases. The budding biomedical researcher interested in bacteriophages (viruses that whose hosts are bacteria) and genetic engineering as potential tools for fighting TB and other infectious diseases. Recent studies have focused on phage-based treatments as a solution to treating multidrug-resistant tuberculosis. After hearing a podcast on bacteriophages, Kahari delved into how phages could potentially combat the spread of antibiotic-resistant bacteria. “I was intrigued by the idea of using viruses to control populations of pathogenic bacteria,” she says.
The final analysis included data from the ILUMIEN IV trial, OCTOBER trial and several previously completed studies comparing intravascular imaging-guided PCI and angiography-guided PCI. Adding up all of the included trials, researchers were left to compare 7,038 patients treated with intravascular imaging-guided PCI, including 3,120 who underwent IVUS-guided PCI, 2,826 who underwent OCT-guided PCI and another 1,029 who were randomized to undergo IVUS- or OCT-guided PCI. These patients were compared with 5,390 treated with angiography-guided PCI, and each participant was followed for a period of 6 months to five years. The primary endpoint of the meta-analysis was target lesion failure, which the authors defined as a composite of cardiac death, target vessel myocardial infarction (MI) or target lesion revascularization. Overall, intravascular imaging-guided PCI helped reduce that composite endpoint by 31%. It also was linked to significant reductions in cardiac death, target vessel MI, target lesion revascularization and stent thrombosis. “The results of this network meta-analysis emphasize the importance of physicians using intravascular imaging with either OCT or IVUS to optimize stent outcomes and improve the long-term prognosis of their patients,” Gregg Stone, MD, a cardiologist and professor of cardiology with Icahn School of Medicine at Mount Sinai in New York, said in a statement. Additional ESC Congress 2023 coverage is available here, here and here.
ORLANDO, Fla. — OneBlood is issuing an urgent call for blood donations before Tropical Storm Idalia makes landfall in Florida. Officials said there is a need for all blood types, but there is an increased need for types O negative and O positive as well as platelets. ▶ WATCH CHANNEL 9 EYEWITNESS NEWS “Hurricanes and tropical systems often disrupt blood collections for several days,” said Susan Forbes, OneBlood’s senior vice president of corporate communications and public relations. “The most critical time for blood donations is prior to any storm or hurricane in order to sustain the blood supply during and immediately after the event.” Read: All blood donors regardless of gender, sexual orientation now screened the same way OneBlood encourages all eligible donors to make blood donation part of their storm preparations and visit a donor center or Big Red Bus as soon as possible. For a list of OneBlood locations, click here. New FDA regulations make it easier for LGBTQ+ members to donate blood, 7 years after Pulse tragedy New FDA regulations make it easier for LGBTQ+ members to donate blood, 7 years after Pulse tragedy (Jeff Levkulich, WFTV.com/WFTV) Click here to download our free news, weather and smart TV apps. And click here to stream Channel 9 Eyewitness News live. ©2023 Cox Media Group
NEW YORK – Researchers from Quest Diagnostics and collaborators have found that changes in levels of the cardiovascular risk marker free myeloperoxidase (MPO) appear correlated with an individual’s overall mortality risk. The finding, described in a study published last month in PLOS One, indicate that longitudinal measurement of MPO could help physicians assess patients’ mortality risk and response to interventions. It also suggests that MPO could prove useful outside the cardio-metabolic context in which it has most commonly been used, including potentially for identifying patients at elevated risk of conditions like cancer and Alzheimer’s disease, said Marc Penn, senior advisor and medical director of Quest’s cardio metabolic endocrine franchise and first author on the study. MPO is an enzyme released by white blood cells in response to infection and inflammation. It was originally used primarily to help assess patients presenting with symptoms indicative of a potential heart attack but in whom heart injury markers like troponin were negative. This application stemmed from the realization that in such cases, patients were often suffering not from a heart condition, but from a vascular problem, Penn said. “We were looking at heart markers to determine if someone had a vascular problem,” he said, noting that this prompted the question of, “Could we develop a vascular marker for vascular events?” Today, MPO is most commonly used in the ambulatory setting to help assess the likelihood of cardiovascular events in high risk individuals, Penn said, noting that the marker provides information on cardiometabolic health not captured by traditional measures. He cited the example of a patient with LDL cholesterol levels just above optimal and a hemoglobin A1c at the high end of normal. “The patient doesn’t really want to go on a statin, but they measure MPO and it is elevated and maybe then the physician is more adamant about that patient lowering their lipids, lowering weight, [improving] diet and exercise,” he said. While MPO’s value as a marker of cardiovascular risk has been established through a number of studies, researchers had not previously shown that longitudinal changes in MPO levels reflected a change in a person’s risk of cardiovascular events. “The most important finding in this study is that we’ve shown for the first time that if you lower MPO, you lower risk, and if you let MPO go up, you raise risk,” Penn said. To establish that relationship, the researchers collected demographic and lab data (MPO, LDL cholesterol, hemoglobin A1c, and ApoB lipoprotein) from a cohort of 3,658 patients seen between 2011 and 2015 by doctors in the national primary care network MDVIP. They analyzed both the correlation between an individual’s baseline MPO level and their risk of adverse events including myocardial infarction, stroke, coronary revascularization, and all-cause death and the correlation between changes in MPO level and risk of adverse events. Running counter to prior studies, the authors found that at baseline the “risk of cardiovascular death did not differ significantly between patients with high and low MPO” once they had adjusted for age, sex, and other cardiovascular risk factors. Penn said that this was due to the fact that incidences of cardiovascular death was small in the relatively healthy population looked at in the study. The researchers did find, however, that patients with high MPO levels were at elevated risk for death due to non-cardiovascular conditions and had higher levels of all-cause mortality. Additionally, as Penn noted, the study found that decreasing MPO levels were linked to mortality reduction, with, the authors wrote, “a 100 pmol/L decrease in MPO correlated with a 5 percent reduction in mortality over five years.” That finding could allow physicians to better assess whether or not particular interventions are mitigating a patient’s mortality risk, Penn said. “It’s a reflection of vascular health,” he said. For instance, “we’ve known for years that there is a link between gum disease and heart disease. In people with periodontal abscesses, gingivitis, things of that nature, MPOs are very high. Sending someone to the dentist and having their mouth cleaned up actually lowers MPO. Getting on top of inflammatory bowel disease, rheumatoid arthritis, things that are known to be associated with heart disease… MPO reflects that.” “The real goal of this study was, we have a population where we lowered MPO. Does that have an impact on health and outcomes?” he said. “And I think this study shows that it does.” The fact that baseline MPO levels and longitudinal changes in levels were corelated with non-cardiovascular health and death from non-cardiovascular conditions suggests the marker could prove useful in other patient populations. For instance, Penn said that elevated MPO in a patient with no signs of elevated cardiovascular risk could lead doctors to more closely examine them for other potential causes, like cancer or Alzheimer’s disease. He suggested that liquid biopsy-based cancer detection is one area that could benefit from such an approach, given the relatively low sensitivity of such tests. Patients with high MPO but no apparent cardiovascular condition might, for instance, be prioritized for more intensive cancer testing or additional follow-up. Penn said he and his colleagues have not begun any studies exploring the usefulness of MPO in this context but that they are “thinking about looking at patients who have MPO [test results] who go on to get a liquid biopsy to see if higher MPO patients are more likely to have a true positive liquid biopsy.” He noted that the MDVIP network offers its patients liquid biopsies for cancer detection and that he and his collaborators are in discussions with the network about possibly using their patient data to look at correlations between MPO levels and liquid biopsy results. MPO tests cost $50.86 under the current Centers for Medicare and Medicaid Services Clinical Laboratory Fee Schedule and is widely available. Penn said the primary challenge in testing MPO levels is with sample collection and the requirement that samples be spun down within 10 to 20 minutes after collection. “Otherwise, the white blood cells sit in the
Summary: Researchers found a live eight-centimeter Ophidascaris robertsi roundworm in the brain of a 64-year-old Australian woman. The parasitic roundworm, typically found in carpet pythons, was successfully extracted following brain surgery. The patient likely contracted the parasite from touching or consuming a type of native grass, Warrigal greens, contaminated with the python’s fecal matter. This alarming case raises concerns about the increasing risk of zoonotic diseases as human and animal habitats continue to overlap. Key Facts: This is the first-ever human case of Ophidascaris robertsi roundworm, which is common to carpet pythons. The roundworm was found in the woman’s brain, a first for any mammalian species. The patient likely contracted the parasite from Warrigal greens beside a lake where the python had shed the parasite through its feces. Source: Australian National University The world’s first case of a new parasitic infection in humans has been discovered by researchers at The Australian National University (ANU) and the Canberra Hospital after they detected a live eight-centimetre roundworm from a carpet python in the brain of a 64- year-old Australian woman. The Ophidascaris robertsi roundworm was pulled from the patient after brain surgery – still alive and wriggling. It is suspected larvae, or juveniles, were also present in other organs in the woman’s body, including the lungs and liver. “This is the first-ever human case of Ophidascaris to be described in the world,” leading ANU and Canberra Hospital infectious disease expert and co-author of the study Associate Professor Sanjaya Senanayake said. “To our knowledge, this is also the first case to involve the brain of any mammalian species, human or otherwise. “Normally the larvae from the roundworm are found in small mammals and marsupials, which are eaten by the python, allowing the life cycle to complete itself in the snake.” Ophidascaris robertsi roundworms are common to carpet pythons. It typically lives in a python’s oesophagus and stomach, and sheds its eggs in the host’s faeces. Humans infected with Ophidascaris robertsi larvae would be considered accidental hosts. Roundworms are incredibly resilient and able to thrive in a wide range of environments. In humans, they can cause stomach pain, vomiting, diarrhoea, appetite and weight loss, fever and tiredness. The researchers say the woman, from southeastern New South Wales in Australia, likely caught the roundworm after collecting a type of native grass, Warrigal greens, beside a lake near where she lived in which the python had shed the parasite via its faeces. The patient used the Warrigal greens for cooking and was probably infected with the parasite directly from touching the native grass or after eating the greens. Canberra Hospital’s Director of Clinical Microbiology and Associate Professor at the ANU Medical School, Karina Kennedy, said her symptoms first started in January 2021. “She initially developed abdominal pain and diarrhoea, followed by fever, cough and shortness of breath. In retrospect, these symptoms were likely due to migration of roundworm larvae from the bowel and into other organs, such as the liver and the lungs. Respiratory samples and a lung biopsy were performed; however, no parasites were identified in these specimens,” she said. “At that time, trying to identify the microscopic larvae, which had never previously been identified as causing human infection, was a bit like trying to find a needle in a haystack. “In 2022, she began experiencing subtle changes in memory and thought processing and underwent a brain MRI scan which demonstrated an atypical lesion within the right frontal lobe of the brain.” The patient was first admitted to a local hospital in late January 2021 after suffering three weeks of abdominal pain and diarrhoea, followed by a constant dry cough, fever and night sweats. By 2022, the patient was experiencing forgetfulness and depression, prompting an MRI scan. A neurosurgeon at Canberra Hospital explored the abnormality and it was then that the unexpected eight-centimetre roundworm was found. Its identity was later confirmed through parasitology experts, initially through its appearance and then through molecular studies. Associate Professor Senanayake said the world-first case highlighted the danger of diseases and infections passing from animals to humans, especially as we start to live more closely together and our habitats overlap more and more. “There have been about 30 new infections in the world in the last 30 years. Of the emerging infections globally, about 75 per cent are zoonotic, meaning there has been transmission from the animal world to the human world. This includes coronaviruses,” he said. “This Ophidascaris infection does not transmit between people, so it won’t cause a pandemic like SARS, COVID-19 or Ebola. However, the snake and parasite are found in other parts of the world, so it is likely that other cases will be recognised in coming years in other countries.” Associate Professor Karina Kennedy said the important message from this case is about general food safety, particularly when gardening or foraging for food where there may be other wildlife in close proximity. “People who garden or forage for food should wash their hands after gardening and touching foraged products. Any food used for salads or cooking should also be thoroughly washed, and kitchen surfaces and cutting boards, wiped downed and cleaned after use,” she said. The patient continues to be monitored by the team of infectious disease and brain specialists. “It is never easy or desirable to be the first patient in the world for anything. I can’t state enough our admiration for this woman who has shown patience and courage through this process,” Associate Professor Senanayake said. The researchers’ findings have been described in the journal Emerging Infectious Diseases. The research team included scientists and infectious diseases, immunology and neurosurgical doctors from ANU, Canberra Health Services, CSIRO, the University of Melbourne and the University of SydneyThe world’s first case of a new parasitic infection in humans has been discovered by researchers at The Australian National University (ANU) and the Canberra Hospital after they detected a live eight-centimetre roundworm from a carpet python in the brain of a 64- year-old Australian woman. The Ophidascaris
So, laughter really is the best medicine. A mere chuckle is enough to expand cardiac tissue and increase the flow of oxygen throughout the body, thus exercising a weakened heart, according to a new study. Scientists in Brazil set out to prove that “laughter therapy” can improve cardiovascular health and ease symptoms of heart disease. “Our study found that laughter therapy increased the functional capacity of the cardiovascular system,” said lead author professor Marco Saffi, of the Hospital de Clínicas de Porto Alegre in Brazil, via the Guardian. “Laughter therapy could be implemented in institutions and health systems like the NHS [National Health System of the UK] for patients at risk of heart problems.” The research was presented at the annual meeting of the European Society of Cardiology in Amsterdam, the world’s largest heart conference. Scientists in Brazil wanted to see if “laughter therapy” could improve cardiovascular health and ease symptoms of heart disease.Getty Images/iStockphoto Researchers looked at 26 adults, at an average age of 64 who had previously been diagnosed with coronary artery disease. Every week for three months, half of the group viewed comedy programs while the other half watched serious documentaries about topics such as the Amazon rainforest or politics. Results showed that the group who watched comedies had a 10% advancement in the amount of oxygen the heart could pump into the body as well as an improvement in their arteries’ ability to expand. Blood testing also detected notable reductions in inflammatory biomarkers, which can indicate if people are at risk for heart attack or stroke and show how much plaque is built up in blood vessels. “When patients with coronary artery disease arrive at hospital, they have a lot of inflammatory biomarkers,” Saffi said. “Inflammation is a huge part of the process of atherosclerosis when plaque builds up in the arteries.” It’s believed that laughter has this effect because it releases endorphins, which are needed to maintain healthy blood pressure and reduce strain on the heart by keeping stress hormones low. “This study found that laughter therapy is a good intervention that could help reduce that inflammation and decrease the risk of heart attack and stroke,” Saffi said. He suggested that laughter therapy could eventually reduce reliance on medications. Saffi noted that these results don’t have to be a result of TV programs alone — it can also come from live comedy shows or fun evenings with friends and family. “People should try do do things that make them laugh at least twice a week,” Saffi said. “Laughing helps people feel happier overall, and we know when people are happier they are better at adhering to medication.”
A new COVID-19 variant may be more likely to cause breakthrough infection, according to the Centers for Disease Control and Prevention (CDC). The CDC released a risk assessment Wednesday, breaking down information regarding the new variant. “BA.2.86 may be more capable of causing infection in people who have previously had COVID-19 or who have received COVID-19 vaccines,” the assessment read. Meaning, it may be more likely to cause breakthrough infections than previous strains of the virus. The CDC also broke down where the variant has been spotted, how severe an illness it may cause, and whether current treatments are effective against it. Here’s what experts currently know about BA.2.86. Getty Images / AzmanL Nicknamed “Pirola,” BA.2.86 was first identified on July 24, 2023. The World Health Organization recently added the new variant to its list of “currently circulating variants under monitoring,” noting that the strain has a “large number of mutations identified.” So far, nine cases of BA.2.86 have been detected—three in Denmark, two in South Africa, two in the U.S., one in the U.K., and one in Israel. One of the cases in the U.S. was a person in Michigan, with the Michigan Health Department noting in a statement on X (formerly known as Twitter) that the patient who contracted the strain is an older adult with “mild symptoms” who hasn’t been hospitalized. BA.2.86 is a subvariant of Omicron, which has been the dominant strain in the U.S. since late 2021, but “it has many, many more mutations than the mutations of each of the variants before,” Timothy Murphy, MD, senior associate dean for clinical and translational research at the University at Buffalo Jacobs School of Medicine and Biomedical Sciences, told Health. Specifically, BA.2.86 has more than 35 amino acid changes to its spike protein than the recently circulating XBB.1.5, which the fall COVID-19 booster was based on, Murphy said. The CDC pointed out that this change is “roughly of the same magnitude” as the switch between the Delta strain of COVID-19 and the initial Omicron variant, BA.1. It’s the spike protein mutations that make this variant likely to cause breakthrough infections. “The virus uses the spike protein to bind the disease to cells,” Murphy said. “That’s what the vaccines are directed against.” With so many mutations in the spike protein, there is a greater chance that the vaccine and having previously been infected with COVID-19 won’t offer as much protection against BA.2.86 as prior strains of the virus, William Schaffner, MD, an infectious disease specialist and professor at the Vanderbilt University School of Medicine, told Health. “Initially, officials thought that BA.2.86 was not all that much different but, now that they’ve noted there are many mutations, they’ve at least raised the question about whether there may be some immune evasion on the part of this strain,” Schaffner said. The CDC said it’s “too soon to know the real-world impacts on immunity” of BA.2.86. However, the agency noted that many people have immunity, either from previous infection, the vaccine, or both. “It is likely that these antibodies will continue to provide some protection against severe disease from this variant,” the CDC said. While testing for COVID-19 is highly encouraged, new variants can be tricky to accurately test for. “We have no lab data or experimental data whatsoever to say how this will impact immunity,” Murphy said. “It simply hasn’t been studied at this point, but likely will be soon.” Samples of the new strain aren’t broadly available for reliable lab testing at this point, but are expected to happen eventually. Meanwhile, existing treatments for older COVID-19 strains can most likely provide relief for patients who are infected with BA.2.86. According to the CDC, the mutation profile of BA.2.86 suggests that treatments like Paxlovid, Veklury, and Lagevrio will be effective against the variant. “The medications don’t target the spike protein—they go after different proteins in the virus and those do not appear to be any different,” Murphy said. Schaffner agreed. “The treatments for sure ought to work, but we’ll see whether over-the-counter tests continue to be able to detect this new variant as we go forward,” he said. Overall, it’s hard to say how different BA.2.86 is from other variants. The CDC stressed that there have just been nine cases, making it hard to know how infectious this variant is and how severe of an illness it may cause. “There’s really zero information here,” Murphy said. “With nine cases, it’s just not enough to know anything.”
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