Cancer
HPV awareness could save thousands from cervical cancer in low-resource nations – report

A widespread lack of awareness of how a common virus is the primary cause of cervical cancer is leading to thousands of needless deaths every year, concludes a global report.
But embracing more advanced screening tools and the willingness of more women to self-collect health data could be pivotal in addressing the issue.
That is according to a study spanning 12 countries in Europe and Latin America commissioned by the pharmaceutical giant Roche.
Half of those polled had either limited or no awareness of the important role human papillomavirus (HPV) plays in cervical cancer.
HPV is a common virus transmitted through sexual contact and is the primary cause of cervical cancer, responsible for over 99 per cent of cases.
Every year, more than 600,000 women worldwide are diagnosed with cervical cancer and over 340,000 die, with nine in every ten of these women living in low-resource countries.
However, 93 per cent of cervical cancers could be prevented entirely through appropriate screening and HPV vaccination.
The research also demonstrates that with screening rates varying between regions, significant barriers continue to exist that are preventing women from seeking testing.
Respondents in all countries, including both developed and developing nations, reported that concerns about the testing procedure being painful were common – up to 63 per cent in some countries.
Also cited was a sense of discomfort about discussing their sexual history or sexuality with a healthcare provider – up to 57 per cent in some countries.
Joanna Sickler, vice-president, health policy and external affairs at Roche Diagnostics, said: “Thousands of women are needlessly dying from cervical cancer every year. This survey highlights some of the most important barriers to screening, as well as the opportunities we have to prevent disease and improve women’s health.
“With many women reporting being open to new screening tools like self-collection, it has never been more important that communities, health systems, governments and innovators come together to seize this opportunity, and provide the early detection and treatment needed to avoid so many preventable deaths.”
The World Health Organisation is focused on accelerating the elimination of cervical cancer globally, with its latest guidelines recommending HPV DNA testing as primary screening for all women.
Its strategy seeks to ensure that by 2030, 90 per cent of girls are fully vaccinated against HPV by age 15.
It also aims for 70 per cent of women to have been screened using a high-performance test by age 35, and again by age 45, with 90% of those eligible linked to treatment.
This, along with vaccination against HPV, could prevent more than 62 million deaths in the next 100 years.
More than 50 per cent of new cervical cancers occur in women who have never been screened, or have not been screened in the previous five years of their lives.
Many factors can contribute to individuals not participating in cervical cancer screening programs, such as access to healthcare, social and economic barriers, history of traumatic experience, cultural concerns and embarrassment.
The many barriers preventing women from seeking HPV screening could explain the widespread interest in self-testing revealed by the survey.
In European countries, where testing is more routinely available, 57 per cent of women were interested in the opportunity to collect their own samples for testing. This figure rose to 77 per cent in Latin American countries, where routine screening is less readily available because of a lack of infrastructure and available appointment means.
This discrepancy was also reflected in healthcare professional-reported results, which showed 72 per cent of healthcare professionals and government workers in Latin American countries agree their country needs a self-collection programme, compared to 48% in Europe.
Susana Wong, patient advocate and director of Lazo Rosado, Perú, is working to expand access to HPV testing in her country.
She said: “We know very well how to prevent and treat cervical cancer. Now, with HPV molecular tests and vaccination, there really is hope to eliminate this disease. This test gives you the opportunity to live and to live well with your family. It can help women to empower themselves as to their health.”
Men demonstrated even lower levels of awareness compared to women, particularly in Europe.
While 55 per cent to 76 per cent of men in Latin America reported some understanding of HPV, only 35 per cent to 51 per cent of men in Europe had any understanding of HPV at all.
The lower awareness among men highlights the need for educational initiatives to include men, given their potential role in the transmission and prevention of HPV, says the report.
“This survey highlights both the challenges ahead and the significant opportunities we have to advance HPV prevention,” Sickler said.
“By enhancing public education about HPV risks and reimagining how we deliver care, we can drive higher screening rates and make meaningful progress in combating cervical cancer.”
Fighting cervical cancer
Screening for HPV can help identify women who are at risk of developing cervical cancer, so that the disease can be treated early before invasive cancer has a chance to develop.
In poorer countries, women are often diagnosed with cervical cancer at a more advanced stage, where the opportunity for a cure is low.
Last mont, Roche joined the Global HPV Consortium which aims to advance cervical cancer prevention efforts and raise the prominence of early screening and timely detection using high-performance HPV-DNA tests.
Conducted in Q1 2024, the HPV Health Understanding Survey involved 8,703 men and women across 12 countries.
It also measured perceptions among 2,585 healthcare professionals (HCPs) and government professionals of HPV testing availability in their own market.
Wellness
Cancer patient receives ‘landmark’ treatment in world-first

A woman with advanced ovarian cancer has become the first patient globally to receive an experimental off-the-shelf cell therapy.
Tracy Tomlinson, 58, was given the experimental drug ZI-MA4-1 at the Christie NHS Foundation Trust in Manchester.
The treatment forms part of a clinical trial evaluating its use against several cancer types, including ovarian, lung, head and neck cancers and sarcomas.
The Christie is leading the trial, with a second site at the Royal Marsden in London. It involves patients with advanced cancers who may have few other treatment options.
Tomlinson, from Chadderton in Greater Manchester, has undergone surgery and multiple rounds of chemotherapy since she was diagnosed in 2020.
She said: “They’ve got rid of the cancer twice but then it came back about two and a half years ago, and we’ve never seemed to get rid of it since then.
“The chemotherapy has shrunk it but when treatment stops, it has come back.
“It is a lot to live with and there’s been ups and downs – there’s been elation, there’s been disappointment, and bits in between.
“But I try very, very hard to remain very positive. Every day that I wake up is a positive. You’ve got to have hope.”
ZI-MA4-1 combines two approaches to cancer treatment.
It uses natural killer cells, known as NK cells, which are specialist immune cells that identify and destroy abnormal cells.
T-cell receptors on the donor cells are also engineered to recognise and target tumours producing a protein called Mage-A4.
Mage-A4 is found in several types of cancer and is considered by experts to be a potential target for attacking abnormal cells.
Unlike personalised treatments, ZI-MA4-1 is designed as an off-the-shelf therapy using immune cells from donors.
The treatment is manufactured in advance rather than being made separately for each patient, with hundreds of doses potentially produced from one manufacturing batch.
Experts believe this approach could make advanced cell therapies available to more patients, more quickly and at a lower cost.
Tomlinson was diagnosed with ovarian cancer that had spread shortly before Christmas 2020 and began treatment immediately.
By summer 2021, scans showed no evidence of disease, but the cancer returned around a year later.
Despite further treatment and 48 chemotherapy infusions, the cancer continued to return.
The former Civil Service manager was diagnosed with stage 3C ovarian cancer, meaning cancer growths had spread into the peritoneum, the tissue lining the abdominal cavity.
She currently has a tumour between her liver and kidney, as well as smaller tumours elsewhere.
She said: “They’ve got rid of the cancer twice but then it came back about two and a half years ago, and we’ve never seemed to get rid of it since then.
“The chemotherapy has shrunk it but when treatment stops, it has come back.
“It is a lot to live with and there’s been ups and downs – there’s been elation, there’s been disappointment, and bits in between.
“But I try very, very hard to remain very positive. Every day that I wake up is a positive. You’ve got to have hope.”
Tomlinson said she had been target-driven during her working life and had set herself high standards.
“But you can’t control cancer,” she said. “What I can control is how I look at it, how I deal with it, and trying to eat healthily and taking the positives in everything.
“And I’ve learned to appreciate the smallest of things that we take for granted – and the people around you and what they mean to you.
“Also, the beauty of outside and the trees and the colour of the trees and the birds singing.
“We just go from A to B, don’t we? Busy, busy, busy. But we never slow down and take in the wonder of what’s around us.
“I often think, ‘I’m still here’, and that’s helped me think, ‘Why can’t I still be here in 10 years?’, ‘Why can’t I still be here in 15 years?’
“And I believe taking all the treatments offered to me is helping me kick that can a bit further down the road.
“I don’t want to go anywhere. I’ve still got a lot of things I want to do and things I want to achieve.”
Tomlinson said her husband Paul, whom she married in 2022, is her “rock”. She is also close to her son Harry, 28.
Last year, she was referred to the Christie’s early-phase clinical trials team for extensive screening and learned she was eligible for the Zima-101 clinical trial.
She said: “I decided almost straight away that I was going to go for it.
“Then afterwards you think, ‘Am I doing the right thing?’, because it is a little bit scary being the first person in the world to have the treatment.”
She has received three infusions of the therapy, with the option of a fourth depending on her scan results.
She said: “If it benefits me, absolutely fantastic. But if it benefits other people in the future, that’s important too.
“I don’t want to have gone through everything I’ve gone through for nothing. I want to feel like I have made a difference.”
Professor Fiona Thistlethwaite, consultant medical oncologist at the Christie, said: “While this is an early-stage study primarily focused on safety, it represents an exciting step forward in efforts to develop new treatment options for people like Tracy with advanced solid tumours.
“We hope the knowledge gained will help shape future cancer treatments and ultimately improve outcomes for patients.”
Dr Jon Lim, consultant medical oncologist in advanced immunotherapy and cell therapy at the Christie, told PA: “What’s very exciting about this is that these are essentially not kind of antibody-based, but living cells.
“These are live immune cells that are infused in hundreds of millions back to the patient, and the idea of this is that it is a little bit more targeted.
“The reason this is very interesting is because this is the first of its kind globally in this approach, where it’s taking donor immune cells, manipulating or engineering them, and putting them into the recipient.
“Tracy is essentially getting somebody else’s immune cells that have been engineered to ‘see’ her cancer.
“We’re very excited. This is a novel approach in the cell therapy space. We are also really showcasing what we can do in the UK.”
Namir Hassan, chief executive of Norwegian company Zelluna, which makes ZI-MA4-1, described Tomlinson’s first dose as a “landmark moment”.
He said: “It represents the moment when years of research moved beyond the laboratory and into the clinic, offering a new potential treatment option for patients facing advanced cancers with limited alternatives.”
Only around 15 per cent of women survive ovarian cancer for five years or more after diagnosis.
Dr Diana Hernandez, director of immune and advanced therapies at Anthony Nolan, said: “NK cells have huge potential as off-the-shelf therapies, and this trial takes us one step closer to a wider application of engineered NK cells in the targeted treatment of cancers.”
Insight
Johnson & Johnson offers to pay US$5.5bn to settle talc cancer lawsuits

Johnson & Johnson has offered an estimated US$5.5bn settlement covering about 76,000 claims that its talc products caused ovarian cancer.
The proposed agreement could end a contentious legal dispute over the company’s baby powder and other talc-based products that has lasted around a decade.
Johnson & Johnson said the settlement covers claims consolidated in a federal court in New Jersey and related cases in state court.
The claims represent nearly all the remaining talc cases against the US multinational, according to the company.
Johnson & Johnson has previously settled most claims alleging that its talc contained asbestos and caused mesothelioma.
Mesothelioma is a rare cancer affecting the lining of organs, most commonly the lungs, and is usually linked to asbestos exposure.
Law firms representing claimants confirmed the proposed deal, describing it as a good resolution after around 10 years of litigation.
The agreement must be accepted by 95 per cent of ovarian cancer claimants in state or federal court before it becomes final.
Erik Haas, vice-president of litigation at Johnson & Johnson, said the claims were “meritless” and that the company was willing to settle to bring the litigation to a close.
“While we are confident the company would have ultimately prevailed with further litigation, as it has in the vast majority of cases tried to date, this resolution allows the company to put this matter behind it and remain focused on its mission to develop medicines and devices that save lives,” Haas said.
The company expects to pay US$3bn in 2027, with further payments due in 2028.
The deal could be worth more, depending on how many people take part in the settlement.
Chris Seeger, a lawyer representing around 2,500 clients with talc claims who helped negotiate the agreement, said Johnson & Johnson could ultimately pay US$7bn or more.
The settlement assigns specific values to qualifying ovarian cancer claims but does not cap the company’s total payout.
“We got a fair settlement, and our clients are going to be happy with it,” Seeger said.
Johnson & Johnson reached the agreement after a series of court victories, including wins in individual trials and successful efforts to disqualify claimants’ lawyers from the litigation.
The company also secured court rulings against experts used by claimants to support their cases.
A federal judge last week questioned whether individual claimants could prove that talc had specifically caused their ovarian cancer.
Johnson & Johnson has consistently denied that its talc products caused cancer, maintaining that the products were safe and did not contain asbestos.
The company stopped selling talc-based baby powder in the US in 2020 and switched to a cornstarch-based product.
Litigation resumed in March 2025 after being paused for more than three years while Johnson & Johnson pursued a bankruptcy strategy known as the “Texas two step”.
The company filed three bankruptcies through a shell-company subsidiary in an attempt to settle the cases. Each bankruptcy was dismissed.
Before the bankruptcy attempts, Johnson & Johnson had a mixed record in talc trials.
These included a multibillion-dollar verdict for 22 women who said baby powder caused their ovarian cancer, alongside trials won by Johnson & Johnson and other verdicts later reduced on appeal.
Unlike the proposed bankruptcy settlements, the latest agreement applies only to existing claims and does not cover future lawsuits.
Seeger said excluding future claims made more money available for current claimants than the bankruptcy proposal and would allow all claims to be paid within 18 months rather than over more than a decade.
Wellness
Welsh Government urged to invest in breast cancer services

The Welsh Government has been urged to invest in breast cancer services after figures showed continuing delays in diagnosis and treatment.
Breast Cancer Now said the target for 75 per cent of patients to be seen within 62 days of initial referral has been met only three times since the Suspected Cancer Pathway was introduced in 2020.
The latest figures, published on July 23, showed that 172 patients, or 60 per cent, were seen within 62 days of being initially referred.
The charity said performance varied widely between health boards.
Melanie Sturtevant, associate director of policy, evidence and influencing at Breast Cancer Now, said: “We have a bold vision that by 2050, everyone diagnosed with breast cancer, lives and lives well, but to see this become reality in Wales we need real action and ambition from the new government for quicker and earlier diagnosis of breast cancer to save and improve lives.
“We’re ready to work with the new government to ensure people in Wales are diagnosed quicker and start treatment faster through reduced waiting times, and earlier with improved breast screening uptake through a breast screening awareness campaign, and provision of more convenient, flexible access to breast screening services.”
Breast Cancer Now called on the Welsh Government to invest in improving waiting times and warned of what it described as “complacency” in Wales.
It said health boards need greater support to identify and address the underlying causes of delays and measure performance at key stages of the cancer pathway.
The charity also urged the new government to prioritise earlier diagnosis by improving participation in NHS breast screening.
It called for Wales to meet the minimum screening uptake standard of 70 per cent and aim for the achievable standard of 80 per cent.
The charity said the NHS breast screening uptake target has been missed in Wales for the past seven years.
Breast cancer is the most common cancer among women in Wales, with 2,800 people diagnosed each year.
The number is projected to rise by 23 per cent to 3,449 cases by 2035.
Breast Cancer Now said urgent action was therefore needed from the new Welsh Government to make early diagnosis a priority.
In response, the Welsh Government said: “We recognise that performance against cancer waiting times is not where we want it to be which is why, as a new Government, we are taking decisive action on cancer by developing a 10-year National Cancer Strategy to transform the way the health service prevents, diagnoses, and treats the disease.
“The strategy will set out an ambitious vision for cancer care in Wales. This will include emphasis on earlier diagnosis of cancer, including breast cancer.
“Optimal pathways of care for all types of cancer will be developed in partnership with patients and clinical experts to ensure that modern, evidence-based care is available wherever a person lives in Wales.
“In the meantime, NHS Performance and Improvement is working with health boards in Wales to improve cancer waiting time performance.”
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