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Showing posts with label Statins. Show all posts
Showing posts with label Statins. Show all posts

Tuesday, 6 May 2025

Commonly prescribed drug could boost cancer survival rate - Statins

One of UK’s most prescribed drugs could reduce death rate of common blood cancer

Researchers discovered that patients who took a statin had a 61 per cent reduced risk of dying from their cancer

Rebecca Whittaker
Wednesday 23 April 2025 14:06 BST
1 min read   The Independent

Statin use has been linked to a lower risk of dying from blood cancer (PA)
Medicine stock
© PA Archive


  • A study has found that statin use is linked to a significantly reduced risk of death in patients with chronic lymphocytic leukaemia (CLL) and small lymphocytic lymphoma (SLL).
  • Researchers analysed data from 1,467 patients across four international trials and found that those taking statins had a 61 per cent lower risk of dying from their cancer.
  • The study also showed a 38 per cent reduction in all-cause mortality and a 26 per cent reduced risk of disease progression in statin users.
  • While the study highlights a strong association, further research is needed to determine if statins directly improve cancer outcomes.
  • Future research will involve laboratory studies to understand how statins affect cancer biology and clinical trials to assess the direct impact of statin use on CLL and SLL patients.


One of the most prescribed drugs in the UK could reduce the risk of dying from blood cancer by more than 60 per cent, a study has revealed.

Statin, a cholesterol-lowering medication taken by more than 7 million people in the UK, lowers the risk of heart disease, which can lead to heart attacks or strokes.

But it’s also been suggested that it can reduce the death rates of several cancers, including chronic lymphocytic leukaemia (CLL) and small lymphocytic lymphoma (SLL), according to a study published today in the journal Blood Advances.

These are both types of slow-growing cancers. CLL starts in the blood-forming cells of the bone marrow and is a common form of leukaemia. SLL affects the same type of cells but starts in lymphoid tissues such as the spleen instead of in the blood-forming cells.

Researchers analysed data from 1,467 patents with CLL or SLL who participated in four international trials conducted between 2012 and 2019.

Each patient was either newly diagnosed, their blood cancer had come back or had not responded to prior treatment.

These trials saw patients randomly assigned ibrutinib, a targeted cancer drug, either alone or in combination with other anti-cancer drugs, or to a drug regimen that did not include ibrutinib.

A total of 424 patients (29 per cent) were taking a statin at the time they started treatment across the four clinical trials, which looked at how long patients lived after starting treatment. They were followed up after five years for overall survival and 22 months for progression-free survival.

Researchers discovered that patients who took a statin had a 61 per cent reduced risk of dying from their cancer, a 38 per cent reduction in death of any cause and a 26 per cent reduced risk of disease progression.

Researchers adjusted their analysis for variables including each patient’s diagnosis, age, sex, weight, disease severity, length of time since their diagnosis, number of co-existing illnesses, use of other medications for heart conditions or high blood pressure, and the specific anti-cancer treatment regimen received.

“Our results highlight a strong link between statin use and improved survival in this patient population,” said the study’s principal investigator, Ahmad Abuhelwa, PhD, an assistant professor of pharmacy practice and pharmacotherapeutics at the University of Sharjah in the United Arab Emirates.

He added: “These findings don’t allow us to say for certain that statins directly improve cancer outcomes.

“However, the fact that this association remained strong even after accounting for multiple factors makes it an important area for future research.”

As next steps, he recommended conducting laboratory studies to better understand how statins may influence cancer biology, as well as prospective clinical trials in which patients with CLL or SLL are randomly assigned to take a statin or not.

One of UK’s most prescribed drugs could reduce death rate of common blood cancer | The Independent

Thursday, 2 December 2021

Statin use affects prostate cancer screening results

 

Summary:
Prostate cancer screening results differ in men taking cholesterol-lowering statin drugs compared with non-users, a study finds. In statin users, screening did not increase the incidence of prostate cancer as it did in other men.
Date:
November 29, 2021
Source:
Tampere University

FULL STORY

Prostate cancer screening results differ in men taking cholesterol-lowering statin drugs compared with non-users, a study conducted at Tampere University in Finland finds. In statin users, screening did not increase the incidence of prostate cancer as it did in other men.

The study found the clearest difference in low-risk cancer, which is often overdiagnosed due to screening. The number of low-risk tumours found in screening was significantly lower in statin users. However, statin use caused no difference in the detection of high-risk cancers. In the screened group, prostate cancer mortality was slightly lower than in the unscreened group, both in men taking statins and other men.

"The study provides significant new information because statin use is very common and the effects of prostate cancer screening have not been previously evaluated in relation to statin use," says Professor Teemu Murtola from the Faculty of Medicine and Health Technology at Tampere University.

The study was published in the JAMA Oncology journal on 24 November 2021.

The findings may be explained by the fact that statin use improves the accuracy of prostate cancer screening. This means that screening detects dangerous types of cancer in these men as well as in others, but in statin users, there is less of the so-called overdiagnosis, which means the detection of low-risk prostate cancers that do not pose a health threat due to their very slow growth rate.

Another possible explanation could be that men who use statins are a select group who already actively use health services and have had PSA tests outside systematic screening. In those cases, the additional screening done in the study does not have such a great impact.

The study was based on data from the Finnish Prostate Cancer Screening Trial which started in 1996-1999. A total of about 80,000 men were included in the study, of whom just under 32,000 were screened with the PSA test every four years. The project was carried out jointly by Tampere University and the University of Helsinki and the Helsinki and Tampere University Hospitals.


Story Source:

Materials provided by Tampere UniversityNote: Content may be edited for style and length.


Journal Reference:

  1. Arla Vettenranta, Teemu J. Murtola, Jani Raitanen, Paavo Raittinen, Kirsi Talala, Kimmo Taari, Ulf-HÃ¥kan Stenman, Teuvo L. J. Tammela, Anssi Auvinen. Outcomes of Screening for Prostate Cancer Among Men Who Use StatinsJAMA Oncology, 2021; DOI: 10.1001/jamaoncol.2021.5672

Cite This Page:

Tampere University. "Statin use affects prostate cancer screening results." ScienceDaily. ScienceDaily, 29 November 2021. <www.sciencedaily.com/releases/2021/11/211129105542.htm>.




RELATED STORIES

Tuesday, 14 January 2020

STATINS JAB NHS hospitals to trial life-saving heart treatment that ‘works better than statins’

HOSPITALS are to trial a life-saving heart treatment said to work better than statins.

https://www.thesun.co.uk/news/10732307/nhs-heart-treatment-jab-statins/

Ministers revealed that 40,000 Brits will get the twice-a-year jab of Inclisiran, which halves cholesterol in two weeks with no side-effects.
 40,000 Brits will receive the twice-a-year jab which is said to work better than statins
1
40,000 Brits will receive the twice-a-year jab which is said to work better than statinsCredit: Getty - Contributor
Statins cut bad fats by a third — but a fifth of patients complain of muscle pain and ditch them.
Inclisiran works by switching off genes in the liver that stop the body breaking down cholesterol.
Health Secretary Matt Hancock said it could save 30,000 lives in a decade if 300,000 take it every year.
The £60million trial will be funded by drug firm Novartis. If a success, ­officials say the jab could be available on the NHS next year.
Professor Sir Nilesh Samani, of the British Heart Foundation, said it could be “rapidly adopted” to “maximise” lives saved.

https://www.thesun.co.uk/news/10732307/nhs-heart-treatment-jab-statins/

Wednesday, 25 September 2019

Dirt Cheap Drugs Outperform Trumpeted New Treatments - MUST READ

Doctors tend to push these expensive new entries instead of older, cheaper drugs that work just as well.


By Lee Euler / November 25, 2018
It costs over a billion dollars and takes more than a decade to bring a new cancer drug to the marketplace. Even then, it may be relevant to only a small patient population and extend life by just a few months – and that’s being optimistic. The hope for a few extra months assumes you can trust the cherry-picked test data the big drug companies use to gain FDA approval.
All the same, doctors tend to push these expensive new entries instead of older, cheaper drugs that work just as well.
Now, I know some readers have a fit if I even mention a drug in a favorable way. But many readers or their loved ones do opt for chemo, for a variety of reasons.
If they’re going to do that, they should at least try to avoid spending themselves into bankruptcy. A good place to start is to be skeptical of the latest cancer wonder drug.
Instead, consider drugs whose patents have expired, and drugs already prescribed for other health conditions but not licensed for the treatment of cancer. Many of these “off-label” medicines have great potential in cancer therapy.
Organization devoted to cheap but effective drugs
The Repurposing Drugs in Oncology (ReDo) Project is a US and European collaboration between two not-for-profit organizations that include doctors and scientists. They look for effective therapies that aren’t being explored because Big Pharma can’t profit from them.
ReDo has identified over 250 drugs prescribed for a wide range of conditions that have anti-cancer activity, yet are not used by conventional oncologists.
The most interesting ones have been in widespread use for many years, are low in toxicity, have an anti-cancer mechanism that makes sense, and strong evidence to support them.
In London’s famous Harley Street, the private Care Oncology Clinic (COC) is pioneering the use of four of these drugs. They are prescribed in addition to conventional treatments, which their patients usually receive under the National Health Service (NHS). Oncologists working within the NHS usually have no objections and are willing to share patients’ clinical records with COC.
Four off-label drugs of choice
The cost of the drugs is just £400 ($520) a year. The four drugs are metformin (diabetes control), atorvastatin (cholesterol lowering), doxycycline (antibiotic) and mebendazole (Vermox) (anti-parasitic).
Established in 2014, COC has now treated over 1,500 patients with a wide range of cancers from stage 1 to stage 4. Audited data on 95 of these cases has recently been analyzed. All were suffering with the most common and aggressive type of brain tumor (glioblastoma).
The results are very encouraging, with a substantial improvement in expected survival times. Under usual protocols – “standard of care” – people live an average of 14.8 months, but this almost doubled to 27.1 months in those taking the four drugs. The two-year survival rate rose from 28.7% to 55.8%. These results are far better than the new, much hyped, hugely expensive immunotherapy drugs.
It pays to target metabolism
COC focuses on the metabolic approach to treating cancer.
Tumors have unique metabolic characteristics that can be targeted while doing little or no harm to healthy cells. One factor unique to cancer cells is an increased uptake of nutrients such as glucose (blood sugar) and glutamine. As we’ve said many times, for many years, cancer cells are gluttons for sugar.
Healthy cells take up glucose too, of course, but cancer cells take up more and they use it in a different way. They convert glucose into energy using biochemical pathways that don’t require oxygen (The Warburg Effect).
Other aspects of metabolism are also altered in cancer cells because, besides their hunger for sugar, they need greatly increased amounts of protein, nucleic acids and lipids to support their high rate of growth.
Justin Stebbing, professor of cancer medicine and oncology at St George’s Hospital, London, is one of several top cancer specialists associated with COC.
He believes targeting metabolism can make a “big difference” to cancer treatments, saying, “it will be increasingly relevant as we think outside the box and understand cancer in different ways.”
The “right” theory of cancer is finally winning
COC focuses on the metabolic approach to treating cancer.
Cancer Defeated has been a longtime advocate of the metabolic theory of cancer, and we’re delighted to see more and more mainstream doctors jump on the bandwagon.
Dr. Padman Vamadevan, scientist and oncology consultant at COC, said, “When we started, not many oncologists were familiar with treating the metabolic features of cancer, so they were skeptical, but now patients report that their doctors are genuinely interested in this research as they see the apparent benefits.”
Pan Pantziarka, Program Director for Drug Repurposing and coordinator of the ReDo Project, explained that modern cancer drugs are aimed at very specific targets in cancer cells.
“But these older medicines are known as ‘dirty drugs’ because they have multiple targets, interfering with more than one protein or signaling pathway at a time. Used in combination they could be very effective.
“If these medicines were coming out today, some would be blockbuster cancer drugs.”
The four-drug cocktail
Metformin: Potentially this old diabetes drug has multiple metabolic mechanisms for inhibiting cancer development and growth. For instance, it reduces the release of sugar from the liver to lower blood sugar, and lowers circulating insulin levels to decrease insulin signaling in cancer cells. It activates an enzyme (AMPK) which decreases glucose uptake, protein synthesis, cell proliferation and cell cycle progression.
The relationship between diabetes and cancer has been recognized for over 100 years. A review of studies found that among diabetics taking metformin compared to non-users, incidence of total cancers was down by a third, colorectal cancer was lowered by 32%, there was a 33% reduced risk for lung cancer and the risk of death from all cancers was lowered by more than a third — 34%.
In September, researchers from Vanderbilt University, Nashville, found patients taking metformin had a substantially reduced rate of liver cancer compared to patients taking an alternative anti-diabetes drug.
Dr. Jonathan Stegall, who specializes in integrative oncology and heads The Center for Advanced Medicine in Atlanta, uses metformin in almost all his patients. He describes it as very safe, well tolerated and “one of the best tools in our toolbox.”
He explains that metformin disrupts a particular pathway called mechanistic target of rapamycin (mTOR) which cancer cells use to grow. Even better, it destroys the cancer cells that help kick off cancer development, growth, spread and recurrence- – cancer stem cells. Dr. Stegall describes this as “a huge deal.”
I agree with Dr. Stegall, in spades. Killing cancer stem cells is the holy grail of cancer treatment.
Statins: have anti-inflammatory properties, benefit the immune system, and block the enzyme HMG CoA Reductase in the liver to reduce cholesterol, which cancer cells use for energy. A recent study covering 197,048 women with breast cancer found statins cut the risk of death by 27%. I’m not a big fan of statins for cholesterol, but I’ll keep an open mind on their uses for cancer. It does seem they are an effective anti-inflammatory.
Doxycycline: obstructs mitochondrial function. A trial published in October found breast cancer patients taking this antibiotic had a sizable reduction in cancer stem cells, making cancer recurrence much less likely.
One of the study authors, professor Michael Lisanti from the University of Salford, England, said, “…to find a drug that is effective, readily-available and costs just 10 pence (13 cents) per patient per day is highly significant, particularly as around two-thirds of cancer deaths occur due to recurrence after initial treatment.”
His colleague, professor Federica Sotgia, explained how the drug works: “What we infer here is that the stem cells selectively over-express key mitochondrial-related proteins, which means that if we can inhibit mitochondrial function we can disrupt the stem cells.”
Mebendazole: helps to block glucose uptake and targets a protein that disrupts the energy supply to cancer cells. It also impedes microtubules which have important roles in cell division and intracellular transport. It’s also been shown to slow angiogenesis – the formation of blood vessels cancer cells need in order to spread.
Culture studies show mebendazole slowed lung cancer cell growth five-fold compared to controls and also inhibited breast, ovary, colon and bone cancers. Arrest of tumor growth and spread has also been demonstrated in mice. Last year a research team from New York suggested mebendazole should be used routinely to treat brain tumors.
Other drugs of interest
The antacid cimetidine (Tagamet), the anti-fungal itraconazole, the acne drug isotretinoin (Accutane), and the antidepressant clomipramine (Anafranil) all look promising candidates for drug repurposing. I’m not a fan of any of these for their original purposes (except maybe the anti-fungal), but cancer is a four alarm fire. If we can confirm these drugs will help, they may be worth a try.
Dr. Stegall also uses aspirin and propranolol.
He prescribes aspirin for his cancer patients because research showed a baby aspirin taken every day for five years reduced the risk of colon cancer by almost a quarter. Those already suffering cancer had a 20% reduced risk of death, and the cancer was less likely to spread.
Pretty good for a drug introduced in 1899 and costing mere pennies. And I bet even your hidebound conventional cancer doctor will let you take it.
Aspirin also hinders the hijacking of blood platelets that cancer cells need in order to grow; lowers the possibility of blood clots, which is at increased risk in cancer patients; and may also inhibit cancer through its anti-inflammatory effects.
As for propranolol, it’s a beta blocker prescribed for high blood pressure, but it also works on a receptor that lowers stress. Dr. Stegall says that because cancer patients are under a lot of stress “they really feel like a weight has been lifted off their shoulders once they’re on this medication.”
A COC success story
When 19-year-old Henry Searle was diagnosed with an inoperable brain tumor in 2015, he was given 14 months to live. After chemo and radiation, his mother Vicki asked the consultants whether natural therapies would help.
She describes their response:
“I was shocked and surprised at how negative the consultants were whenever I asked if diets or supplements could help his immune system…they just said there was no evidence for any of them and that he was getting the gold-standard treatment.”
Ignoring their advice, she put her son on an organic sugar-free diet and added supplements including zinc and selenium. Following this, blood tests showed his low functioning immune system improving week by week.
She then ignored objections from Henry’s oncologist and visited COC, where the doctors are receptive not only to unconventional uses of drugs but to natural therapies, too.
The COC treatment showed evidence it was working after only a month, with the tumor shrinking. Two years later Henry’s NHS consultant wrote to say there was “no evidence of active disease.”
The latest update, in March, 2018, finds him still taking COC’s drug cocktail and his condition remains stable.
Professor Justin Stebbing had this to say:
“As a profession, we can be cruel to cancer patients, giving them treatments that are horribly toxic, with minimal benefits. I find it very frustrating when my colleagues are dismissive of patients who want to try other things that are non-toxic and may extend their lives.”
Oncologists reluctant to prescribe
Although doctors are entitled to prescribe drugs “off label” if they believe they could be beneficial, in practice oncologists are reluctant to consider this option for several reasons.
Researchers have not conducted final stage cancer trials on them, and probably won’t because their patents have expired and no billion-dollar payday is likely. The drugs may also interfere with conventional treatment or have unforeseen side effects. There may also be consequences for the doctor personally or professionally, as Angus Dalgleish, another professor of oncology at St George’s, found out.
He prescribes repurposed drugs for his patients and liaises with their family doctors.
“I’ve had a lot of hassle for that,” he says. “There’s no room for freedom to do the best thing for your patients, just because someone hasn’t put up millions of pounds to do a big drugs trial.
“I call it creative compassion because it’s not in the rule book, but it’s what I would want for myself if I were in the same position. I wouldn’t want to just be told to go and see the palliative care person [essentially hospice].”

References:

  1. http://www.redo-project.org/
  2. http://careoncologyclinic.com/
  3. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0033411
  4. https://nyaspubs.onlinelibrary.wiley.com/doi/full/10.1111/j.1749-6632.2011.06285.x
  5. http://news.vumc.org/2018/09/14/diabetes-drug-may-prevent-cancer/
  6. https://www.ncbi.nlm.nih.gov/pubmed/28432513
  7. https://medicalxpress.com/news/2018-10-antibiotic-effective-breast-cancer-clinical.html
  8. https://www.ncbi.nlm.nih.gov/pubmed/28386621
https://www.cancerdefeated.com/dirt-cheap-dirty-drugs-outperform-trumpeted-new-treatments/

ALSO READ:  MUST READ - Could £400-per-year drug cocktail be the key to beating one of the most-deadly cancers? Henry was given 14 months to live now his cancer is stable thanks to his four everyday medicines