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Is it Time to Tap MicroStrategy ETFs Amid Bitcoin Surge?
Is it Time to Tap MicroStrategy ETFs Amid Bitcoin Surge?

Yahoo

time4 days ago

  • Business
  • Yahoo

Is it Time to Tap MicroStrategy ETFs Amid Bitcoin Surge?

With Bitcoin prices soaring to new highs, TD Cowen analyst Lance Vitanza has recently increased his price target for MicroStrategy shares to $680, up from the previous target of $590, as quoted on CNBC. Several companies have attempted to replicate MicroStrategy's (also known as Strategy) business model, but Vitanza emphasized that none can rival the company's cost of capital advantage. Strategy has uniquely leveraged a diverse array of securities to raise funds for acquiring Bitcoin, giving it a strategic edge in the market. MicroStrategy – the software and bitcoin-treasury company – said it now owns more than 600,000 bitcoins, valued in excess of $70 billion at current prices. It disclosed that it has resumed buying Bitcoin, as prices surged further into record territory. Bitcoin Momentum Fuels Optimism TD Cowen's bullish outlook is driven by expectations of continued Bitcoin price appreciation and MicroStrategy's aggressive pace of Bitcoin accumulation. On Monday, Bitcoin hit a new all-time high of $123,000, fueled by strong inflows into Bitcoin ETFs. Although it has since dipped slightly to $120,437.06, the overall trend remains upward. MicroStrategy Stock Performance MicroStrategy shares have rallied about 54% year to date, reflecting growing investor confidence in the company's crypto-centric strategy. Even before TD Cowen boosted its target price for MicroStrategy, the average price target for MicroStrategy was $534.77 (offered by 13 analysts). The forecasts ranged from a low of $175.00 to a high of $650.00. The average price target represented a 23.05% increase from the last closing price of $434.58, recorded on July 11, 2025. The stock, however, surged 3.1% on July 15, 2025. ETFs in Focus Against this backdrop, below, we have highlighted a few winning MicroStrategy-based exchange-traded funds (ETFs) that can be tapped now. T-Rex 2X Long MSTR Daily Target ETF MSTU The T-Rex 2X Long MSTR Daily Target ETF seeks daily investment results, before fees and expenses, of 200% of the daily performance of MSTR. The fund charges 105 bps in fees. Grayscale Bitcoin Adopters ETF BCOR The underlying Indxx Bitcoin Adopters Index consists of U.S. and non-U.S. equity securities of companies that have been adopting Bitcoin as an asset for corporate treasury management. The fund charges 59 bps in fees. MSTR stock takes 21.34% of the fund. First Trust SkyBridge Crypto Industry & Digital Economy ETF CRPT The First Trust SkyBridge Crypto Industry and Digital Economy ETF seeks to provide investors with capital appreciation. The fund charges 85 bps in fees. MSTR stock takes 20.49% of the fund. Bitwise Bitcoin Standard Corporations ETF OWNB The underlying Bitwise Bitcoin Standard Corporations Index provides exposure to the performance of corporations that have adopted the Bitcoin standard. Such corporations are those that hold Bitcoin as a corporate treasury asset. The fund charges 85 bps in fees. MSTR stock takes 19.19% of the fund. Want the latest recommendations from Zacks Investment Research? Today, you can download 7 Best Stocks for the Next 30 Days. Click to get this free report First Trust SkyBridge Crypto Industry and Digital Economy ETF (CRPT): ETF Research Reports This article originally published on Zacks Investment Research ( Zacks Investment Research

Experimental treatment borrowed from blood cancer shows promise for pediatric brain tumors
Experimental treatment borrowed from blood cancer shows promise for pediatric brain tumors

Yahoo

time19-03-2025

  • Health
  • Yahoo

Experimental treatment borrowed from blood cancer shows promise for pediatric brain tumors

Gavin Nielsen was 2 years old when he was diagnosed with a rare and aggressive brain cancer. The smiley toddler had diffuse intrinsic pontine glioma, or DIPG, a cancer that occurs in the part of the brain stem that controls vital functions including breathing, blood pressure and heart rate. Very few treatment options exist and the prognosis for children diagnosed with the disease is, on average, less than one year. 'When we have a child newly diagnosed with this disease, we walk into the room and tell the child's parents their child has a terminal disease and the only option is palliative radiation,' said Dr. Robbie Majzner, director of the pediatric and young adult cancer cell therapy program at Dana-Farber Cancer Institute and Boston Children's Hospital. Gavin's parents started him on radiation. For 30 days, he had to be sedated daily for the treatment. But they also started looking for clinical trials to enroll Gavin in. At the time, many of the trials for DIPG had a minimum age requirement of 3 years old, his parents, Nate and Ashlee, said. But Gavin did qualify for one trial, led by Dr. Nicholas Vitanza, a pediatric neuro-oncologist at the Seattle Children's Hospital Cancer and Blood Disorders Center. Vitanza is part of a growing group of researchers exploring whether an immunotherapy called CAR-T therapy, or chimeric antigen receptor T-cell therapy, could be effective for treating Gavin's type of brain cancer. The treatment programs a person's own T cells — immune cells that usually fight infection — to identify and attack proteins found on tumor cells. CAR-T has been used to treat certain blood cancers for two decades and got its first Food and Drug Administration approval in 2017. In recent years, doctors have been exploring the treatment in solid tumors, including those in the brain, where patients have few options. Gavin enrolled in Vitanza's trial before his third birthday, after he had already completed his radiation treatment. Doctors started by extracting T cells from Gavin's blood. Those cells were then modified in a lab to go after the tumor target, called B7-H3. About a month later, he started getting infusions of the T cells, delivered directly into his cerebrospinal fluid. Once reintroduced back into the body, the T cells replicate, creating a surge of cancer-fighting immune cells. The results of Vitanza's early-stage clinical trial were published in Nature Medicine in January. In addition to Gavin, 20 children and young adults with DIPG got CAR-T therapy every two to four weeks. The median survival was about 20 months — nearly double the expected prognosis. Three patients, however, are still alive 3 ½ to 4 ½ years after starting their treatment. Gavin is one of those patients. Now 6 years old, he's lived four times longer than doctors initially predicted. 'It's the biggest miracle that I could ever ask for, just to have time,' Ashlee said. Gavin is still getting CAR-T infusions every two to three weeks. Sometimes, for about 12 hours after the infusions, he has headaches, nausea and vomiting. Other times, he's ready to run around on the soccer field. Dr. Mark Souweidane, director of pediatric neurosurgery at Weill Cornell Medicine and NewYork-Presbyterian Hospital, who wasn't involved with the trial, said the results were encouraging, but added that it's not 'out of the realm of the norm' to have some patients survive longer. 'There are going to be outliers. You will get 5%-10% of kids who live beyond two years,' he said. Souweidane said more trials will need to confirm whether CAR-T therapy is, indeed, the reason Gavin and the two other patients in the trial are living much longer than expected. If so, doctors will need to understand whether the therapy could be this effective for everyone with the disease. 'I'm cautiously optimistic that this at least shows some efficacy we can build on in the future,' said Dr. Patrick Grogan, a neuro-oncologist at the Moffitt Cancer Center in Florida. 'Until there is a Phase 3 clinical trial with a control group that gets the current standard of care, or robust data from a Phase 2 trial, I tend to take results with a grain of salt.' While CAR-T therapy can be highly effective for certain blood cancers like leukemia and lymphoma, scientists are still in the beginning stages of understanding whether the treatment can be used for solid tumors, which make up the majority of cancers. 'This is entirely experimental,' Vitanza said. The reason CAR-T therapy works so well in certain blood cancers is because these cancers tend to be homogeneous, meaning their tumor cells are uniform. This gives the immune cells a clear target to latch onto. That's not the case for solid tumors, which tend to have many different cell types that often differ within individual tumors. The proteins found in abundance on solid-tumor cells also usually aren't unique to cancer cells, meaning modified CAR-T cells will also attack healthy cells that have the same target proteins. 'It's very difficult to find a target specifically on the surface of cancer but not on any tissue,' said Majzner. The goal, he said, is to find a target that's found in much higher numbers on cancer cells than on healthy cells. The nonuniform nature of solid tumors means it's also possible many cancer cells will go undetected by CAR-T cells. 'If you happen to go after a target that is only expressed in 50% of cells, you may have an effect against those 50% of cells but the rest are spared,' Grogan said. Treating anything in the brain presents additional challenges. The brain is surrounded by a difficult-to-penetrate barrier called the blood-brain barrier, which blocks toxins from entering. In their trial, Vitanza and his team opted to deliver the modified cells directly into the cerebrospinal fluid, in part to bypass the blood-brain barrier. This also ensured a high concentration of the modified T cells ended up in the cancerous part of the brain rather than in other parts of the body, possibly blunting the number of healthy cells the modified cells come into contact with. The goal of Phase 1 clinical trials like this is to show whether a therapy shows promise and appears to be safe. 'When you're dealing with experimental therapies, especially Phase 1 trials, they're designed to find what is a safe, tolerable dose. You obviously hope there's a benefit, but it is impossible to quote any benefit, because you're learning this in real time,' Vitanza said. Just one patient out of 21 in Vitanza's trial had a severe side effect, bleeding in the tumor. Several other early CAR-T trials for DIPG are happening at cancer centers across the U.S. While many questions remain, experts said they are cautiously optimistic the therapy could become a badly needed treatment for DIPG. Kids like Gavin are a crucial piece of the research. 'One thing I always think of is it's not just Gavin, it's those kids coming after him, that we've met along the way, that didn't get this chance,' his father, Nate, said. 'I think it's for those kids that we continue.' This article was originally published on

Experimental treatment borrowed from blood cancer shows promise for pediatric brain tumors
Experimental treatment borrowed from blood cancer shows promise for pediatric brain tumors

NBC News

time19-03-2025

  • Health
  • NBC News

Experimental treatment borrowed from blood cancer shows promise for pediatric brain tumors

Cancer In an early-stage clinical trial, the therapy nearly doubled the expected survival time of young patients. Still, experts caution that more research is needed. By Kaitlin Sullivan, Akshay Syal, M.D. and Patrick Martin Gavin Nielsen was 2 years old when he was diagnosed with a rare and aggressive brain cancer. The smiley toddler had diffuse intrinsic pontine glioma, or DIPG, a cancer that occurs in the part of the brain stem that controls vital functions including breathing, blood pressure and heart rate. Very few treatment options exist and the prognosis for children diagnosed with the disease is, on average, less than one year. 'When we have a child newly diagnosed with this disease, we walk into the room and tell the child's parents their child has a terminal disease and the only option is palliative radiation,' said Dr. Robbie Majzner, director of the pediatric and young adult cancer cell therapy program at Dana-Farber Cancer Institute and Boston Children's Hospital. Gavin's parents started him on radiation. For 30 days, he had to be sedated daily for the treatment. But they also started looking for clinical trials to enroll Gavin in. At the time, many of the trials for DIPG had a minimum age requirement of 3 years old, his parents, Nate and Ashlee, said. But Gavin did qualify for one trial, led by Dr. Nicholas Vitanza, a pediatric neuro-oncologist at the Seattle Children's Hospital Cancer and Blood Disorders Center. Vitanza is part of a growing group of researchers exploring whether an immunotherapy called CAR-T therapy, or chimeric antigen receptor T-cell therapy, could be effective for treating Gavin's type of brain cancer. The treatment programs a person's own T cells — immune cells that usually fight infection — to identify and attack proteins found on tumor cells. CAR-T has been used to treat certain blood cancers for two decades and got its first Food and Drug Administration approval in 2017. In recent years, doctors have been exploring the treatment in solid tumors, including those in the brain, where patients have few options. Gavin enrolled in Vitanza's trial before his third birthday, after he had already completed his radiation treatment. Doctors started by extracting T cells from Gavin's blood. Those cells were then modified in a lab to go after two tumor targets, b7 and h3. About a month later, he started getting infusions of the T cells, delivered directly into his cerebrospinal fluid. Once reintroduced back into the body, the T cells replicate, creating a surge of cancer-fighting immune cells. The results of Vitanza's early-stage clinical trial were published in Nature Medicine in January. In addition to Gavin, 20 children and young adults with DIPG got CAR-T therapy every two to four weeks. The median survival was about 20 months — nearly double the expected prognosis. Three patients, however, are still alive 3 ½ to 4 ½ years after starting their treatment. Gavin is one of those patients. Now 6 years old, he's lived four times longer than doctors initially predicted. 'It's the biggest miracle that I could ever ask for, just to have time,' Ashlee said. Gavin is still getting CAR-T infusions every two to three weeks. Sometimes, for about 12 hours after the infusions, he has headaches, nausea and vomiting. Other times, he's ready to run around on the soccer field. Dr. Mark Souweidane, director of pediatric neurosurgery at Weill Cornell Medicine and NewYork-Presbyterian Hospital, who wasn't involved with the trial, said the results were encouraging, but added that it's not 'out of the realm of the norm' to have some patients survive longer. 'There are going to be outliers. You will get 5%-10% of kids who live beyond two years,' he said. Souweidane said more trials will need to confirm whether CAR-T therapy is, indeed, the reason Gavin and the two other patients in the trial are living much longer than expected. If so, doctors will need to understand whether the therapy could be this effective for everyone with the disease. 'I'm cautiously optimistic that this at least shows some efficacy we can build on in the future,' said Dr. Patrick Grogan, a neuro-oncologist at the Moffitt Cancer Center in Florida. 'Until there is a Phase 3 clinical trial with a control group that gets the current standard of care, or robust data from a Phase 2 trial, I tend to take results with a grain of salt.' Brain tumors present unique hurdles While CAR-T therapy can be highly effective for certain blood cancers like leukemia and lymphoma, scientists are still in the beginning stages of understanding whether the treatment can be used for solid tumors, which make up the majority of cancers. 'This is entirely experimental,' Vitanza said. The reason CAR-T therapy works so well in certain blood cancers is because these cancers tend to be homogeneous, meaning their tumor cells are uniform. This gives the immune cells a clear target to latch onto. That's not the case for solid tumors, which tend to have many different cell types that often differ within individual tumors. The proteins found in abundance on solid-tumor cells also usually aren't unique to cancer cells, meaning modified CAR-T cells will also attack healthy cells that have the same target proteins. 'It's very difficult to find a target specifically on the surface of cancer but not on any tissue,' said Majzner. The goal, he said, is to find a target that's found in much higher numbers on cancer cells than on healthy cells. The nonuniform nature of solid tumors means it's also possible many cancer cells will go undetected by CAR-T cells. 'If you happen to go after a target that is only expressed in 50% of cells, you may have an effect against those 50% of cells but the rest are spared,' Grogan said. Treating anything in the brain presents additional challenges. The brain is surrounded by a difficult-to-penetrate barrier called the blood-brain barrier, which blocks toxins from entering. In their trial, Vitanza and his team opted to deliver the modified cells directly into the cerebrospinal fluid, in part to bypass the blood-brain barrier. This also ensured a high concentration of the modified T cells ended up in the cancerous part of the brain rather than in other parts of the body, possibly blunting the number of healthy cells the modified cells come into contact with. The goal of Phase 1 clinical trials like this is to show whether a therapy shows promise and appears to be safe. 'When you're dealing with experimental therapies, especially Phase 1 trials, they're designed to find what is a safe, tolerable dose. You obviously hope there's a benefit, but it is impossible to quote any benefit, because you're learning this in real time,' Vitanza said. Just one patient out of 21 in Vitanza's trial had a severe side effect, bleeding in the tumor. Several other early CAR-T trials for DIPG are happening at cancer centers across the U.S. While many questions remain, experts said they are cautiously optimistic the therapy could become a badly needed treatment for DIPG. Kids like Gavin are a crucial piece of the research. 'One thing I always think of is it's not just Gavin, it's those kids coming after him, that we've met along the way, that didn't get this chance,' his father, Nate, said. 'I think it's for those kids that we continue.' Kaitlin Sullivan Kaitlin Sullivan is a contributor for who has worked with NBC News Investigations. She reports on health, science and the environment and is a graduate of the Craig Newmark Graduate School of Journalism at City University of New York. Akshay Syal, M.D. Dr. Akshay Syal is a board-certified internal medicine physician at UCLA Health and instructor of medicine at the David Geffen School of Medicine at UCLA. He also is a member of the NBC News Health Unit, reporting for both NBC News Digital and on air for NBC News NOW and MSNBC. Patrick Martin Patrick Martin is a producer in the NBC News Health & Medical Unit.

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