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Liver cancer cases are projected to double, but more than half could be preventable

Liver cancer cases are projected to double, but more than half could be preventable

NBC News7 days ago
At least 60% of liver cancers could be preventable, according to an analysis published Monday in The Lancet.
Liver cancer is the sixth most common cancer in the world, with around 870,000 cases in 2022. That's projected to increase to 1.52 million cases in 2050, the new report found, if no changes are made.
The leading cause of liver cancer is viral infections, including the hepatitis B and C viruses. Hepatitis B infections — which are preventable with a vaccine — accounted for 39% of liver cancers in 2022. That's expected to fall slightly, to 36.9%, by 2025. Hepatitis C accounted for 29.1% of liver cancers in 2022 and is also projected to fall, to 25.9%, by 2050.
The proportions of alcohol- and obesity-related liver cancers, however, are projected to rise in the next 25 years. Alcohol accounted for 18.8% of liver cancers in 2022, and that is expected to increase to 21.1% in 2050. The share of liver cancers caused by obesity-related disease is projected to increase from 8% to 10.8% by 2050 due to increasing rates of obesity, diabetes and high cholesterol and other metabolic risk factors.
Dr. Hashem El-Serag, one of the report's co-authors and chair of the department of medicine at the Baylor College of Medicine in Houston, said the public usually thinks of alcohol as the biggest risk factor for liver cancer.
'I think for most people, if you say cirrhosis, they immediately think of a relative, of someone who was a heavy drinker,' El-Serag said. 'I think the vast majority do not make the tie between MASLD, or fatty liver, and cirrhosis and liver cancer.'
MASLD, or metabolic dysfunction-associated steatotic liver disease, affects about 25% of adults in the U.S. It's caused by a buildup of fat in the liver. About 5% of U.S. adults have a more severe form, called metabolic dysfunction-associated steatohepatitis (MASH), which can lead to scarring, or cirrhosis, of the liver, significantly increasing the risk of cancer.
Excess alcohol consumption can also lead to cirrhosis.
Liver cancer is still relatively rare in the United States, representing 2.1% of all new cancer diagnoses in 2025. The report estimated that by 2040, U.S. rates of MASLD could more than double, affecting more than 55% of adults.
Detecting liver cancer risk factors
Earlier detection and effective treatment plans for MASLD can reduce the risk of obesity-related liver cancer, El-Serag said. The most common treatment is weight loss. GLP-1 weight loss drugs, which include Ozempic and Wegovy, are promising, he said. (A clinical trial published in April found that Wegovy treated MASH in about two-thirds of patients.)
However, people aren't screened for MASLD like they are for viral hepatitis, El-Serag said.
Dr. Arun Jesudian, a hepatologist and the director of liver quality and inpatient liver services at Weill Cornell Medicine and NewYork-Presbyterian, said patients are tested for MASLD and/or MASH if they have elevated liver enzymes in their blood.
Raising awareness about MASLD among both patients and doctors can lead to more effective testing and diagnosis, Jesudian said.
'I think then we need to make sure that providers who are interacting with these patients are looking at the liver disease component of metabolic syndrome,' he said, referring to patients with a cluster of conditions including high blood sugar, high blood pressure and excess weight. 'So checking liver enzymes, that they know how to assess for fibrosis, even based on these blood test scores.'
MASLD and MASH can often be asymptomatic, making self-detection more challenging.
'Right now, it's haphazard. Some people get tested. Others get suspected. Third, who knows?' El-Serag said.
Dr. Neehar Parikh, a hepatologist at the University of Michigan who specializes in liver cancer, said he is seeing more patients with MASLD as a driving factor for liver cancer.
Patients with MASLD can develop liver cancer without developing cirrhosis, making it even more challenging to detect those cases, Parikh said. Up to 40% of those with liver cancers linked to MASLD don't develop cirrhosis, according to the report.
Figuring out who those patients are is the 'million-dollar question,' he said. 'Those patients that develop MASLD that develop liver cancer, you know, how do you screen that population? We don't really know what to do.'
Still, Parikh said these types of cases are rare.
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Peptides: performance-boosting, anti-aging drugs or harmful snake oil?
Peptides: performance-boosting, anti-aging drugs or harmful snake oil?

UPI

time10 minutes ago

  • UPI

Peptides: performance-boosting, anti-aging drugs or harmful snake oil?

Today over 100 peptide medications are approved, including semaglutide – better known as Ozempic and Wegovy. Photo by Haberdoedas Photography/ Pexels For a growing number of middle-aged men, aging no longer means surrendering to sagging skin, sore joints or slowing metabolism. Instead, it's becoming a science experiment. The new frontier? Injectable peptides -- experimental compounds that promise rapid recovery, fat loss and muscle gains with the ease of a twice-daily to weekly jab. Once confined to elite labs and obscure bodybuilding forums, these amino acid chains are now flooding wellness spaces, social media feeds and online marketplaces. Although they are marketed as "next-generation biohacks" and "research chemicals, "many peptides are not approved for human use and lack basic clinical testing. Still, their popularity is growing -- fueled by testimonials, influencer hype and the seductive promise of turning back time. But beneath the surface of glossy marketing and fitness fantasies lies a far more sobering truth: many of these substances operate in a medical gray zone, with unknown long-term risks, questionable manufacturing standards and, in some cases, life-threatening side-effects. Peptides aren't entirely new to medicine. The first peptide drug -- insulin -- was isolated in 1921 and became commercially available in 1923. Today, more than 100 peptide medications are approved, including semaglutide -- better known as Ozempic and Wegovy. But the compounds now circulating in fitness communities represent a very different category. They're experimental substances that have shown promise in animal studies but have never undergone proper human trials. The 'Wolverine stack' One such compound, first discovered in human gastric juice, that is attracting lots of attention is BPC-157. Early animal studies suggest it may help repair damaged tissue throughout the body. Researchers tested it on mice, rats, rabbits and dogs without finding serious side-effects. The compound appears to support healing of the tendons, teeth and digestive organs, including the stomach, intestines, liver and pancreas. Scientists don't yet fully understand how BPC-157 works, but animal studies suggest it triggers several biological processes essential for healing. The compound appears to help cells move to damaged areas and encourages the growth of new blood vessels, bringing nutrients and oxygen to tissues in need of repair. Another compound gaining attention is TB500. It is a synthetic version of thymosin beta-4, a naturally occurring protein fragment that plays an important role in repairing and regenerating damaged cells and tissues. It also helps protect cells from further harm by reducing inflammation and defending against microbes. The combination of BPC-157 and TB500 has earned the nickname "the Wolverine stack," named after the Marvel superhero famous for his rapid healing. Then there's IGF-1 LR3, a modified version of a natural protein (IGF-1) linked to muscle growth. This synthetic compound was shown to increase muscle mass by 2.5 times in animal studies, though it has never been studied in humans. The limited human research that does exist for these compounds offers inconclusive results. For example, a study showed that over 90% of patients experienced reduced knee pain after BPC-157 injections. However, the study had no control group and several methodological issues, so the results should be viewed with caution. Hidden dangers Even though the early results seem exciting, these experimental compounds can be dangerous. Making them involves special chemicals called coupling agents, which can trigger serious allergic reactions, including anaphylaxis -- a life-threatening condition. The health consequences extend well beyond allergic reactions. Long-term injection of performance-enhancing substances can lead to heart failure that can occur rapidly with little warning, as documented in recent medical case studies of young bodybuilders. Injection-related injuries pose another significant threat. "Compartment syndrome" can develop at injection sites in leg muscles, causing numbness, blood clots and muscle spasms that result in permanent loss of function. In severe cases, skin and underlying tissue can suffer necrosis (tissue death), requiring antibiotics or surgery to treat. More alarming still are reports of users contracting HIV, hepatitis B and C, and serious eye infections from contaminated injections. These compounds don't just target muscles -- they affect the entire body in ways scientists are only beginning to understand. Some interfere with natural insulin production, while others activate biological pathways that healthy cells use for growth and repair. The concern is that these same pathways are exploited by cancer cells. The VEGF pathway, which promotes blood vessel growth, is active in about half of all human cancers, including melanoma and ovarian cancer. Laboratory studies suggest that thymosin beta-4 may play a role in helping colorectal and pancreatic cancers spread. While there's no direct evidence linking compounds like BPC-157 or TB500 to cancer, researchers emphasize that the long-term effects remain unknown because these substances have never undergone proper human trials. The World Anti-Doping Agency has banned these compounds, noting they lack approval from any health regulatory authority and are intended only as research tools. A growing problem Yet, their use appears to be spreading rapidly. A 2014 study found that 8.2% of gym members used performance-enhancing drugs. By 2024, a comprehensive review suggested the figure could be as high as 29%. Perhaps most concerning: only 38% of users recognized the health risks involved. These experimental compounds represent a dangerous gamble with long-term health. Unlike approved drugs, they haven't undergone the rigorous testing required to understand their safety profile in humans. While they may promise enhanced performance and healing, they deliver it at a cost that users may not fully understand until it's too late. The appeal is understandable -- who wouldn't want faster healing and better muscle tone? But the reality is these substances remain experimental for good reason. Until proper human trials are conducted, users are essentially volunteering as test subjects in an uncontrolled experiment with their own bodies. Adam Taylor is a professor of anatomy at Lancaster University. This article is republished from The Conversation under a Creative Commons license. Read the original article. The views and opinions in this commentary are solely those of the author.

Nearly 17 Million Young Americans Could Benefit From Ozempic-like Drugs
Nearly 17 Million Young Americans Could Benefit From Ozempic-like Drugs

Newsweek

time2 hours ago

  • Newsweek

Nearly 17 Million Young Americans Could Benefit From Ozempic-like Drugs

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. Nearly 17 million young Americans could be eligible for GLP-1RAs—a class of medications used to treat type 2 diabetes and obesity—including Ozempic and Wegovy. This is based on estimations from Yale School of Medicine researchers who have assessed how many adolescents and young adults in the US are eligible for the drugs and how many can realistically access them. Despite millions being eligible, one in five young adults who meet the criteria are uninsured and one-third denied having a routine place for healthcare. The researchers describe this as "a barrier to identifying, treating, and preventing cardio-kidney-metabolic diseases". The prevalence of type 2 diabetes and obesity continues to increase in youth across the country, hence the need for improved intervention. "Assuming that all individuals who were appropriate candidates for these medications could receive them after shared-decision making with their clinician, we could see substantial progress made in treating and preventing obesity-related diseases in US youth, such as dyslipidemia and hypertension," paper author Ashwin K. Chetty told Newsweek. This, he explained, "could lead to the prevention of severe complications of obesity into adulthood, such as strokes and heart attacks." Hand holding Ozempic-like injection pens on dark background. Hand holding Ozempic-like injection pens on dark said the GLP-1RA eligibility criteria they used covered indications for semaglutide (Ozempic, Rybelsus and Wegovy), liraglutide (Saxenda and Victoza), Bydureon BCise (exenatide), Trulicity (dulaglutide) and tirzepatide (Zepbound and Mounjaro). While some medications contain the same ingredient under a different brand name, the drugs are licensed in different ways. In the U.S., Ozempic, for example, is approved for use in people with type 2 diabetes, while Wegovy is approved for those with obesity or who are overweight and have related health problems. Wegovy and Ozempic mimic a hormone called glucagon-like peptide-1—hence 'GLP-1'—which targets areas of the brain that regulate appetite. "Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are approved to treat pediatric obesity and T2D, and a small but growing number of adolescents and young adults receive GLP-1RAs, which are largely covered through private insurance or Medicaid," the researchers wrote. "Insurance status, access to care and clinical profile of the broader population of youth eligible for GLP-1RAs are unclear but important for policy development. We characterized demographic, clinical, and socioeconomic characteristics of US adolescents and young adults eligible for any GLP-1RA." To inform the estimations, the cross-sectional study pooled publicly available data from the National Health and Nutrition Examination Survey (NHANES) January 2017–March 2020 and August 2021–August 2023. They included US adolescents aged 12–17 and young adults aged 18–25 who met U.S. Food and Drug Administration criteria for GLP-1RA treatment. Over-the-shoulder view of a person in bed checking a smartphone. Over-the-shoulder view of a person in bed checking a adolescents, GLP-1RA indications included type 2 diabetes or obesity defined either as BMI in the 95th percentile or higher for age and sex or body weight greater than 60kg and BMI corresponding to 30 for adults by international cutoffs. For young adults, GLP-1RA indications included type 2 diabetes, obesity (a BMI greater than 30) or a BMI of 27 or higher with a weight-related condition (dyslipidemia, hypertension, cardiovascular disease, or type 2 diabetes). The sample included 572 adolescents and 590 young adults eligible for GLP-1RA treatment, representing an estimated 5.8 million adolescents and 11.1 million young adults. Adolescents eligible for the drugs included 40.3 percent insured by Medicaid, 40.5 percent privately insured and 7.2 percent uninsured. Eligible young adults included 20.8 percent insured by Medicaid, 49 percent privately insured and 19.4 percent uninsured. While 92.2 percent of adolescents reported having a routine place for healthcare, 68.1 percent of young adults reported the same, according to the study. Among both groups, cardio-kidney-metabolic risk factors (dyslipidemia, impaired kidney function, hypertension and prediabetes) were prevalent. "Of note, some indications for young adults were fully encompassed by other indications and were not analyzed separately," said Chetty. For example, the indication of type 2 diabetes may include having also a cardiovascular disease. The analysis also did not include people aged 10–11 years with type 2 diabetes as there were too few participants in their sample in that age group with the condition. "While Medicare is not allowed to cover anti-obesity medications that are indicated only for obesity, Medicaid can cover anti-obesity medications, though only a fraction of state Medicaid programs do," said Chetty. The researchers say their findings indicate broad Medicaid coverage could increase access to GLP-1RAs for a large portion of U.S. youth who may benefit from them. "This could look like state-level formulary changes that include anti-obesity medications or federal policy changes that foster coverage for these therapies," said Chetty. "Beyond expanding insurance coverage, improving access also involves ensuring these individuals have access to general healthcare and clinician appointments, which we show in this study is a particularly significant concern for young adults." Why are we seeing rising rates of metabolic diseases in America's youth? Paper author and pediatric nephrologist Dr. James Nugent told Newsweek: "Changes in lifestyle behaviors and structural factors like increased screen time, decreased physical activity, poor sleep, and consumption of ultra-processed foods and sugar-sweetened beverages are important contributors to obesity in youth. "The COVID-19 pandemic has further accelerated the rise in obesity due to its effect on these lifestyle behaviors. Chronic stress, food insecurity, poverty, and adverse childhood experiences are also strongly associated with obesity in youth. Additionally, in utero exposure to maternal obesity and diabetes are risk factors for obesity and type 2 diabetes in childhood." The authors said study limitations include self-reported data subject to recall bias and potential misclassification of the type of diabetes. They also flagged GLP-1RAs should be considered alongside intensive health behavior and lifestyle treatment (and surgery where applicable). And while expanded insurance coverage may substantially increase access, uninsurance and lack of routine care are barriers to this therapy. How can we ensure young people receive holistic care too? "Improving access to comprehensive obesity treatment will involve ensuring that individuals receive access to healthcare with regular follow-ups and support to engage in health behavior and lifestyle treatment, such as specific programs tailored to providing intensive health behavior and lifestyle treatment," said Chetty. "As Dr. Mona Sharifi, a co-author of this paper, has shown, intensive health behavior and lifestyle treatment programs can be cost-effective but inadequate funding is the main barrier to implementing and sustaining these programs." What's next? "Given the size and clinical characteristics of the U.S. youth population eligible for GLP-1RAs, there should be greater discussion of how to improve access to GLP-1RAs and other anti-obesity interventions among this population." Do you have a tip on a health story that Newsweek should be covering? Do you have a question about GLP-1 drugs? Let us know via health@ Reference Chetty, A. K., Sharifi, M., & Nugent, J. T. (2025). Glucagon-like peptide-1 receptor agonist eligibility among US adolescents and young adults. JAMA Pediatrics.

GLP-1s: Life after FDA enforcement returns
GLP-1s: Life after FDA enforcement returns

Business Journals

time3 hours ago

  • Business Journals

GLP-1s: Life after FDA enforcement returns

Unless you've been living on another planet over the past few years, you have heard of and probably know several people that are taking glucagon-like peptide-1 drugs or GLP-1s. These revolutionary drugs, originally developed for type 2 diabetes, have become the pharmaceutical industry's most sought-after innovation thanks to their weight-loss benefits. Brand names include Ozempic® and Wegovy®, which are based on semaglutide and owned by Novo Nordisk, and Mounjaro® and Zepboud®, which are based on tirzepatide and owned by Eli Lilly. Their commercial trajectory is unparalleled with $52 billion in global sales in 2024, $64 billion predicted for 2025, and $130 billion per year expected by 2030. Humira, the best selling drug of all time won't come close to these as it has 'only' generated around $250 billion since 2003 and is expected to generate another $9-10 billion per year for the foreseeable future. However, the road to this commercial success has been one of the more interesting ones as it has brought up FDA, patent, national, and international issues. These issues began in March of 2022 for semaglutide GLP-1s and in December of 2022 for tirzepatide GLP-1s when the FDA listed each of them on the drug shortage list. Inclusion on the drug shortage list means that the FDA has determined that the demand for a specific drug exceeds its supply and that shortage has a significant impact on public health. During the time a drug is on the shortage list, the FDA does not generally institute any enforcement actions against compounders that are making copies. Once compounders were free to make compounded versions of GLP-1s, demand surged even higher as compounders began offering these drugs. Costs to consumers plummeted from $1000/month or more for the brand name drugs to $150/month or less for the compounded versions. Overnight, an entire cottage industry was born. However, this all came crashing to a halt when the FDA declared the shortage over, thereby ending its enforcement discretion. The FDA provided a phaseout period for the compounded drugs and their compounding facilities based the drug, semaglutide or tirzepatide, and the type of compounding pharmacy. The phaseout for all of the drugs and pharmacies ended on May 22, 2025. Thus, in order for compounders to continue offering these drugs, they must be presented with a valid patient-specific prescription to prepare the medications and the medications they compound must be tailored to that individual's specific needs that prevent them from taking the brand-name version. Novo Nordisk and Eli Lilly wasted no time notifying compounders that they must cease compounding these drugs. Eli Lilly filed suits against some of the larger compounding pharmacies, Empower Pharmacy and Strive Phramacy in April 2025. These suits were filed under the Lanham Act, based on the alleged illegal compounding of tirzepatide mixed with additives like vitamin B12 and glycine and thereby misleading customers into believing these products were FDA-approved. Compounders either continued to add or began adding these ingredients in order to fall under the exceptions for compounders based on the patient's specific needs. Novo Nordisk began working with Hims and Hers Health, Inc in April after the shortage for Wegovy® was declared over. This agreement was terminated in June 2025 when Novo Nordisk alleged that Hims and Hers was not complying with the law which prohibits mass sales of compounded drugs under the false guise of "personalization" and are disseminating deceptive marketing that put patient safety at risk. Novo Nordisk is also investigating additional compounders and telehealth providers for deceptive marketing based on this 'personalization' exception. With respect to the patent issues at play, Novo Nordisk has patents on semaglutide in the U.S. and most of the world that last until 2033 while Eli Lilly's tirzepatide U.S. and worldwide patents don't expire until 2036. However, generic versions of semaglutide are on the near term horizon. How you might ask? Well, Novo Nordisk failed to pay their patent maintenance fee in Canada in 2020. This means that the patent in Canada officially expired in 2020 but has been protected under Canadian laws governing data exclusivity which prevent generics from copying the drugs until January 4, 2026. Major generic-producing companies like Sandoz and Dr. Reddy's have already announced that they will be launching generic versions of semaglutide in 2026. The impact on consumers in Canada will be felt almost immediate. Additionally, consumers in the U.S. stand to benefit from the availability of generic semaglutide as the FDA generally turns a blind eye to individuals in the U.S. receiving their medications from Canada. Thus, the result of their failure to pay this maintenance fee will extend beyond Canada into semaglutide's largest commercial market. All in all, the market for GLP-1s has changed significantly since the FDA declared their shortages over. Most U.S. compounders have now ceased large-scale GLP 1 production. However, some continue to operate under state pharmacy boards or under legal protest, challenging the FDA's interpretation of "commercially available" in compounding laws. In a sense, they contend that the demand is still higher than Novo Nordisk and Eli Lilly can address. How this will play out legally remains to be seen. Sandberg Phoenix is a full-service law firm specializing in business, business litigation, health law, products liability, and intellectual property. Tracey joined Sandberg Phoenix as a shareholder in 2023, and is Practice Group Leader of the Intellectual Property practice group. With over 25 years of experience in intellectual property law, Tracey serves clients of all sizes across industries including biotechnology, agribusiness, food, health care and life sciences. He counsels clients on patent, trademark, and copyright acquisition, licensing, enforcement issues, due diligence, prosecution, litigation and other general business matters.

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