
Blood cancer survival odds could be ‘doubled' as bone marrow test trial is a success
Patients with a rare and aggressive type of blood cancer could soon have their chances of survival doubled as a groundbreaking trial to detect the disease earlier concludes.
Scientists working on the trial developed a highly sensitive test that that spots traces of disease in the bone marrow of patients to identify of acute myeloid leukaemia (AML).
The 10-minute procedure – which involves an injection in the hip bone every three months – was able to identify signs of AML returning in patients before it showed in blood tests.
This gives medics a 'window of opportunity' to treat people while they are still well, researchers said.
Experts hope the test could become routine care for patients with acute myeloid leukaemia (AML) in the UK and beyond.
AML is a cancer which causes the bone marrow to produce a large number of abnormal blood cells and around 3,100 people are diagnosed in the UK each year.
The risk of developing the disease increases with age and it is most common in people over 75.
After treatment, patients are usually seen every few weeks for blood tests.
Professor Nigel Russell, honorary consultant at Guy's and St Thomas' NHS Foundation Trust and chief investigator on the trial, said: 'There's a significant risk for these patients that the leukaemia is going to come back again, and that's normally detected by a deterioration in the blood tests.
'Sometimes it can happen very quickly, and sometimes it can happen over a period of weeks.
'So normally, the patient comes along, has a blood test done, the blood test is okay, they're sent off again. That's the procedure that's been the case for many years.
'But the trial included these extra tests in the bone marrow every three months to detect if there's any evidence of what we call residual leukaemia; it's such a low level that the blood tests are normal, but the disease can still be present at very low levels in the bone marrow.'
The bone marrow test takes around 10 minutes and is performed under local anaesthetic, with a hollow needle inserted into the patient's hip bone to take the sample.
'It detects the the RNA present in the leukaemia cells, but not present in normal cells,' Prof Russell added.
For the study, led by King's College London and published in The Lancet Haematology, patients were screened for mutations in the NPM1 and FLT3 genes, which are common in younger people with AML.
The trial involved 637 people who were in remission from AML who, over three years, either received standard monitoring or standard monitoring with additional bone marrow tests every three months.
Prof Russell said: 'It was about one third of patients that really benefited from this approach that had a doubling of their survival, which was a massive improvement in outcome for these patients.
'And really, it's quite a simple extra procedure to have done. Since the results of the trial have become available, this sort of technology is now part of what we call the standard of care.
'The important thing is that it gives you a window of opportunity to treat the patient before they become unwell.
'Because if the patient relapses, they can become quite unwell very quickly, and their blood counts are very abnormal.
'They have to come into hospital, and they have to have further treatment of chemotherapy, and then possibly go on to a bone marrow transplant.
'The advantage of detecting it early is the patients can have these treatments when they're still well. Even potentially as an outpatient, because their blood tests are normal.
'They don't need to come into hospital as an emergency and they're starting with a fresh start, really, rather than being ill again.'
Jane Leahy, 51, from Wimbledon, is one of the patients who took part in the trial.
She was diagnosed with AML in December 2014, at the age of 41, and after chemotherapy went into remission the following April.
The mother-of-two had her bone marrow tested as part of the trial, which picked up abnormalities a few months later.
After restarting treatment, the bone marrow test results also showed the chemotherapy was not working, with a stem cell transplant her only chance of going into remission again.
'Without testing, I wouldn't have gone on to have my transplant, because my blood showed I was still in remission,' Mrs Leahy told PA.
Nine years after her bone marrow transplant – which was donated by her sister – Mrs Leahy is still in remission.
She added: 'It's pretty scary, really, when I think about potentially what could have happened. And there were so many things throughout my my treatment journey, it felt like the stars were aligning.
'I feel incredibly lucky.'
Mrs Leahy said bone marrow testing gives doctors 'more time', adding: 'The time is always critical, because it's so acute and so aggressive.
'And a lot of people die from AML before they get to treatment, because it's just diagnosed so late.
'So it just gives more time, more opportunities to try different treatment approaches and pick it up earlier, before it becomes too late to do anything about.'
Dr Richard Dillon, a clinical senior lecturer in cancer genetics from King's College London, said: 'Acute myeloid leukaemia is the most aggressive form of blood cancer, so knowing early that a patient's cancer is going to relapse is crucial for planning their treatment.
'We hope that these tests become part of routine care for this type of cancer across the UK and worldwide, and ultimately improve long-term survival rates for patients.'
Laura Challinor, from the Blood Cancer UK charity, which part-funded the study, said the findings 'could help shift the dial in a positive direction'.
She added: 'As this involves a bone marrow test every three months, we must also continue to push ahead with research into kinder therapies for the 280,000 people with blood cancer in the UK.'
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Daily Record
a day ago
- Daily Record
Scots woman 'saved by handprint bruise' after devastating cancer diagnosis
Nichola Smith, 44, began her battle with cancer at just 12-years-old. A Scots woman diagnosed with blood cancer three times has told how a handprint bruise "saved her life". Nichola Smith, 44, from Glasgow, fell unwell at the age of 12, suffering fatigue, high temperatures and bouts of diarrhoea. After playing with her brother and cousins, she noticed a strange bruise on her hand. Speaking to our sister title, Glasgow Live, said: 'I remember one of them had grabbed me and it left a bruise on my arm in the shape of a handprint.' She went to the GP with her mum, where she was diagnosed with a viral illness. After being sent home, Nichola collapsed and was rushed to hospital. Just hours later, the then-schoolgirl was diagnosed with Acute Myeloid Leukaemia (AML). Nichola said: 'Mum watched a lot of medical programmes and as soon as I was taken to hospital she said she had a feeling it was leukaemia. She knew that the extreme bruises were a symptom. I went into complete panic mode. I thought I was going to die.' Treatment began immediately for Nichola, and after several blood transfusions and five rounds of chemotherapy, she returned home to begin the road to recovery. But the following year, received the devastating news that her AML was back. She then underwent a bone marrow transplant to put her in remission. Thankfully, the treatment was successful and she was finally able to resume normal teenage life. She went on to attend regular testing to monitor the potential after-effects of the harsh treatment she had received. It was during one of these appointments in 2006 that a routine mammogram revealed she had pre-cancerous cells in both her breasts - a common side effect of the leukaemia treatment she had received. Nichola was 26 at the time. She said: 'It was another trauma to get through. They said I would need a double mastectomy. I had three major operations and a lot of recovery time. I still get checked every year for any breast cancer cells.' Just when Nichola thought she was finally in the clear, bad news struck again in January 2022, when she contracted COVID-19 and found she struggled to recover. Tests revealed she had myelodysplasia, a blood cancer that could eventually lead, once more, to AML. For the fourth time, Nichola's world was rocked by cancer. Nichola said: 'I was devastated. I kept saying to myself 'Here we go again' and 'why me'. I have had so much bad luck in my life with my health and I couldn't believe I was going to have to fight again.' Nichola was placed on the 'watch and wait' list, then started on blood transfusions. In August 2023, she received the news that her blood cancer had progressed and she once again needed chemotherapy, as well as radiotherapy and a stem cell transplant. With significant progress in cancer research since Nichola's first stem cell transplant in 1996, her brother, Andrew, was now able to donate stem cells with only a 50% match. Thankfully, the transplant was successful. Nichola is sharing her story in support of the #SPOTLeukaemia campaign. which aims to raise awareness about the signs and symptoms of the disease. The most common symptoms of leukaemia are: Extreme tiredness (fatigue) Bruising Unusual bleeding Repeated infections Colin Dyer, CEO at Leukaemia Care said: 'Nichola's story is a powerful reminder of why we all need to know the signs and symptoms of leukaemia. The reality is that leukaemia can develop quickly and be life-threatening, yet the early symptoms like fatigue, bruising or repeated infections are often mistaken for less serious illnesses. 'That's why our #SpotLeukaemia campaign is so important. We want everyone to be aware of the signs, because recognising something as seemingly simple as a handprint-shaped bruise can, quite literally, save a life.'


Scottish Sun
2 days ago
- Scottish Sun
Michael Mosley's family pay tribute after ‘hardest year of lives' on first anniversary of his death
The family have set up a research project to honour his memory ONGOING GRIEF Michael Mosley's family pay tribute after 'hardest year of lives' on first anniversary of his death Click to share on X/Twitter (Opens in new window) Click to share on Facebook (Opens in new window) THE family of TV doctor Michael Mosley have described the past year as 'the hardest of our lives' in a tribute on the first anniversary of his death. Michael, who died aged 67 while on holiday with his wife Clare on the Greek island of Symi last June, was known for popularising diets and fronting science programmes. Sign up for Scottish Sun newsletter Sign up 2 Michael Mosley died aged 67 while on holiday in Greece Credit: Getty His wife wrote on Instagram: 'It's hard to believe that a year has passed since we lost Michael. 'Not a day goes by without thinking of him — his warmth, his laughter, his endless curiosity about the world, and his deep love for our family. 'This past year has been the hardest of our lives.' Last month, the family set up a research project to honour his memory and help improve the nation's metabolic health. A clinical research fellowship will be established with King's College London and the Chronic Disease Research Foundation. The family added: 'We are trying to carry on the work Michael was so passionate about. "To live with purpose and joy, as he would have wanted us to.' In December, a coroner ruled that Michael's death on Symi was most likely due to 'heatstroke (accidental) or a non-identified pathological cause'. Michael Mosley's son Dr Jack makes This Morning debut 10 months after TV star's tragic death


BBC News
2 days ago
- BBC News
Michael Mosley's family say year since his death has been 'hardest of our lives'
The family of late TV doctor Michael Mosley have described the past year as "the hardest of our lives" in a message on the first anniversary of his died at the age of 67 after going missing while on holiday on the Greek island of Symi last was known for his TV and radio shows and books about health and diet."It's hard to believe that a year has passed since we lost Michael," his widow Clare wrote on Instagram. "Not a day goes by without thinking of him - his warmth, his laughter, his endless curiosity about the world, and his deep love for our family." The message added: "This past year has been the hardest of our lives. Navigating the loss of someone so central to our hearts and our home has changed everything."We have missed him in the big moments and the small ones. But we have also felt incredibly supported."It went on to note how the "outpouring of love, stories and memories from so many of you" online had "meant more than we can ever say"."We have taken real comfort in knowing just how many lives Michael touched - not only through his work, but through his kindness, humour, and deep desire to help people live well for longer." 'Carry on the work' Last month, his family announced a new Michael Mosley Memorial Research Fund, which will help to appoint a dedicated research scientist to help improve the metabolic health of the nation.A clinical research fellowship will be established to honour his memory in partnership with King's College London and the Chronic Disease Research family statement continued: "We are trying, as a family to look forward. To carry on the work Michael was so passionate about. To live with purpose and joy, as he would have wanted us to."Mosley was known for hosting BBC Radio 4's Just One Thing as well as TV series like Trust Me, I'm A Doctor, The Truth about Exercise, and Lose a Stone in 21 their one-year anniversary message, Mrs Mosley and her family thanked "everyone who has reached out, shared their grief, and carried us with their compassion."They noted: "Your messages, letters and acts of remembrance have helped us through the darkest days." The presenter went missing after going for a walk on Symi, and his disappearance sparked a high-profile search effort by emergency services. His body was found after four December, a coroner said his the cause of his death was "indeterminate" but "most likely attributable either to heatstroke (accidental) or non-identified pathological cause". Hall of Fame As well as hosting TV and radio shows, Mosley wrote a column for the Daily Mail, and published books about intermittent fasting diets, including through the 5:2 diet and The Fast 800 Dr Jack Mosley, who researched drugs including Ozempic with his father, has also written a book about weight loss and BBC honoured his father in July 2024 with a dedicated day of programming, when presenters and audiences where encouraged to do "just one thing" to improve their widow accepted the Hall of Fame award at the British Podcast Awards on her late husband's behalf in September 2024.