News
Research roundup: AI models independently interpret mammograms, and more

Femtech World explores the latest research and science developments in the world of women’s health.
AI models independently interpret mammograms
AI models have shown excellent performance for detecting breast cancers on mammography images.
The algorithms, submitted for a 2023 AI Challenge hosted by the Radiological Society of North America (RSNA), demonstrated increased screening sensitivity while maintaining low recall rates, according to a new study.
The goal of the Challenge was to source AI models that improve the automation of cancer detection in screening mammograms, helping radiologists work more efficiently, improving the quality and safety of patient care, and potentially reducing costs and unnecessary medical procedures.
A research team evaluated 1,537 working algorithms submitted to the Challenge, testing them on a set of 10,830 single-breast exams – completely separate from the training dataset – that were confirmed by pathology results as positive or negative for cancer.
The algorithms yielded median rates of 98.7 per cent specificity for confirming no cancer was present on mammography images, 27.6 per cent sensitivity for positively identifying cancer, and a recall rate, the percentage of the cases that AI judged positive, of 1.7 per cenr.
When the researchers combined the top three and top 10 performing algorithms, it boosted sensitivity to 60.7 per cent and 67.8 per cent, respectively.
According to the researchers, creating an ensemble of the 10 best-performing algorithms produced performance that is close to that of an average screening radiologist in Europe or Australia.
Individual algorithms showed significant differences in performance depending on factors such as the type of cancer, the manufacturer of the imaging equipment and the clinical site where the images were acquired.
Overall, the algorithms had greater sensitivity for detecting invasive cancers than for noninvasive cancers.
Since many of the participants’ AI models are open source, the results of the Challenge may contribute to the further improvement of both experimental and commercial AI tools for mammography, with the goal of improving breast cancer outcomes worldwide.
The research team plans to conduct follow-up studies to benchmark the performance of the top Challenge algorithms against commercially available products using a larger and more diverse dataset.
Cracking the cold case of endometriosis with big data
Records from millions of patients at UC health centers found correlations between endometriosis, one of the most common diseases in women, and a bounty of other diseases.
Scientists at UCSF have found that endometriosis often occurs alongside conditions like cancer, Crohn’s disease, and migraine.
The research could improve how endometriosis is diagnosed and, ultimately, how it is treated; and it paints the sharpest portrait yet of a condition that is as mysterious as it is prevalent.
The study used computational methods developed at UCSF to analyse anonymised patient records collected at the University of California’s six health centers.
Using algorithms developed for the task, researchers hunted for connections linking endometriosis with the rest of each patient’s health history.
Endometriosis patients were compared with patients who did not have it, and categorised the patients with endo into groups based on shared health histories.
The findings from the UCSF data were mapped against the rest of the UC’s health data to see if they held up across California.
The team say they found over 600 correlations between endometriosis and other conditions, ranging from infertility, autoimmune disease, and acid-reflux, to cancers, asthma, and eye-related diseases.
Some patients had migraines, bolstering previous studies suggesting that migraine drugs might help treat endometriosis.
The study supports the growing understanding of endometriosis as a “multi-system” disorder – a disease arising from dysfunction throughout the body.
Respiratory viruses can wake up breast cancer cells in lungs
Researchers have found the first direct evidence that common respiratory infections, including Covid-19 and influenza, can awaken dormant breast cancer cells that have spread to the lungs, setting the stage for new metastatic tumours.
The findings, obtained in mice, were supported by research showing increases in death and in metastatic lung disease among cancer survivors infected with SARS-CoV-2, the virus that causes Covid-19.
“Our findings indicate that individuals with a history of cancer may benefit from taking precautions against respiratory viruses, such as vaccination when available, and discussing any concerns with their healthcare providers,” said Julio Aguirre-Ghiso, a co-leader of the study and director of MECCC’s Cancer Dormancy Institute.
Prior to the study, some evidence suggested that inflammatory processes can awaken disseminated cancer cells (DCCs) – cells that have broken away from a primary tumor and spread to distant organs, often lying dormant for extended periods.
“During the COVID-19 pandemic, anecdotal reports suggested a possible increase in cancer death rates, bolstering the idea that severe inflammation might contribute to arousing dormant DCCs,” said Dr. Aguirre-Ghiso, who also serves as leader of MECCC’s Tumor Microenvironment and Metastasis Research Programme.
Researchers tested this hypothesis using Dr. Aguirre-Ghiso’s laboratory’s unique mouse models of metastatic breast cancer, which include dormant DCCs in the lungs and therefore closely resemble a key feature of the disease in humans.
The researchers exposed mice to SARS-CoV-2 or influenza virus. In both cases, the respiratory infections triggered the awakening of dormant DCCs in the lungs, leading to a massive expansion of metastatic cells within days of infection and the appearance of metastatic lesions within two weeks.
Molecular analyses revealed that the awakening of dormant DCCs is driven by interleukin-6 (IL-6), a protein that immune cells release in response to infections or injuries.
The Covid-19 pandemic offered a unique opportunity to investigate the effect of respiratory virus infections, in this case from the SARS-CoV-2 virus, on cancer progression.
The research team analysed two large databases and found support for their hypothesis that respiratory infections in cancer patients in remission are linked to cancer metastasis.
The UK Biobank is a general population cohort in which some of the more than 500,000 participants were diagnosed with cancer and other diseases prior to the Covid-19 pandemic.
Researchers from Utrecht University and Imperial College London investigated whether a Covid-19 infection increased the risk of cancer-related mortality among participants with cancer.
They focused on cancer survivors who had been diagnosed at least five years before the pandemic, ensuring they were likely in remission.
Among them, 487 individuals tested positive for COVID-19 and these were compared to 4,350 matched controls who tested negative.
After excluding those cancer patients who died from Covid-19, the researchers found that cancer patients who tested positive for Covid-19 faced an almost doubling of risk of dying from cancer compared to those patients with cancer who had tested negative.
From the second population study, the U.S. Flatiron Health database, researchers drew data pertaining to female breast cancer patients seen at 280 U.S. cancer clinics.
They compared the incidence of metastases to the lung among Covid-19-negative patients and Covid-19-positive patients (36,216 and 532 patients respectively).
During the follow-up period of approximately 52 months, those patients who came down with Covid-19 were almost 50 per cent more likely to experience metastatic progression to the lungs compared with patients with breast cancer without a diagnosis of Covid-19.
“Our findings suggest that cancer survivors may be at increased risk of metastatic relapse after common respiratory viral infections,” said Dr. Vermeulen.
Losing weight before IVF may increase chance of pregnancy
A systematic review and meta-analysis of randomised controlled trials (RCTs) has assessed whether weight loss interventions before in vitro fertilization (IVF) improved reproductive outcomes.
The review found that weight loss interventions before IVF could increase the chances of pregnancy, especially in unassisted conception, although the effect on live births was unclear.
The findings are published in Annals of Internal Medicine.
Researchers from the University of Oxford reviewed 12 RCTs comprising 1,921 patients conducted between 1980 through 27 of May 2025.
Inclusion criteria included studies conducted on women at least 18 years old with a BMI of 27 kg/m2 or greater who were seeking IVF with or without intracytoplasmic sperm injection treatment for infertility.
Outcomes of interest were the number of participants achieving pregnancy without IVF (unassisted pregnancy), with IVF (treatment-induced pregnancy), overall (unassisted plus treatment-induced) and those delivering a live infant.
The researchers found that participants were typically women in their early 30s with a median baseline BMI of 33.6 kg/m2.
Weight loss interventions studied included low-energy diets, an exercise program accompanied by healthy eating advice, and pharmacotherapy accompanied by diet and physical activity advice.
Overall, weight loss interventions before IVF were associated with greater unassisted pregnancy rates. Evidence was inconclusive on the effect of weight loss interventions on treatment-induced pregnancies.
Evidence on the association between weight loss interventions before IVF and live births was uncertain, although there was moderate certainty of no association with pregnancy loss.
The findings suggest that weight loss interventions before IVF increase total pregnancies, mainly through an increase in unassisted pregnancy rates.
However, further high-quality clinical trials testing different weight loss interventions, particularly those known to achieve greatest weight losses, such as low-energy total diet replacement programmes, are needed.
Diagnosis
Researchers teach AI to spot cancer risk by squeezing individual breast cells
Diagnosis
Experimental drug drowns triple-negative breast cancer cells in toxic fats

An experimental drug slowed triple-negative breast cancer in mice by flooding tumour cells with toxic fats.
Triple-negative breast cancer lacks three common drug targets, making it one of the hardest-to-treat and most aggressive forms of the disease.
The compound, known as DH20931, appears to push cancer cells past their limits by triggering a surge in ceramides, fat-like molecules that place the cells under intense stress until they self-destruct.
In lab experiments, the drug also made standard chemotherapy more effective. When combined with doxorubicin, researchers were able to reduce the dose needed to kill cancer cells by about fivefold.
The drug targets an enzyme known as CerS2 to sharply increase production of these lipids and stress cancer cells. Healthy cells, by contrast, showed lower sensitivity to the drug in lab tests.
While the early results are promising, further preclinical and clinical trials would still be needed to determine the safety and effectiveness of DH20931 in humans.
Satya Narayan, a professor in the University of Florida’s College of Medicine, led the study with an international group of collaborators.
The researchers published their results on human-derived tumours on 21 April and presented their findings on combination therapy at the annual meeting of the American Association for Cancer Research in San Diego.
Narayan likened the drug’s effects to a home’s electrical system handling a power surge.
While healthy cells act like a properly grounded and installed circuit, cancer cells are more like a jumble of mismatched wires and faulty fuses. DH20931 overwhelms cells not with electricity, but with fats.
He said: “When that surge goes into the cancer cells, they cannot handle the amount of power they are getting. The fuses burn out, the cell can’t handle the surge and it dies.”
The compound was developed at the University of Florida in the lab of Sukwong Hong.
Hong, now a professor at the Gwangju Institute of Science and Technology in South Korea, created DH20931 as one of many drug candidates tested for efficacy in Narayan’s lab.
In the study, researchers implanted human triple-negative breast cancer tumours into mice and treated them with DH20931.
The drug significantly slowed tumour growth without causing noticeable weight loss or signs of toxicity in the animals. In separate lab experiments, it also showed activity against other breast cancer subtypes.
In addition to increasing lipid levels, DH20931 triggers a second stress signal by flooding cells with calcium.
Together, these effects disrupt the mitochondria, the structures that produce a cell’s energy, ultimately leading to cell death.
Narayan said: “It does not just follow one pathway but it goes through multiple pathways. It’s a two-hit hypothesis.
“These pathways are common in all breast cancer types and other solid tumours, so we think this drug can be useful not only in triple-negative breast cancer but potentially other cancers as well.”
Entrepreneur
Future Fertility raises Series A financing to scale AI tools redefining fertility care worldwide

Future Fertility Inc. has announced the closing of a US$4.1 million Series A financing round.
The round was led by M Ventures (the corporate venture capital arm of Merck KGaA, Darmstadt, Germany) and Whitecap Venture Partners, with participation from new investors Sandpiper Ventures, Gaingels, and Jolt VC.
The financing will accelerate Future Fertility’s commercial expansion into Asia-Pacific and support its entry into the United States, including planned FDA 510(k) clearance for additional products as part of a broader U.S. market entry strategy.
Proceeds will also advance the development of a broader AI platform, from egg assessment through to embryo transfer, designed to support clinicians, embryologists, and patients across the full IVF journey.
M Ventures and Whitecap have supported Future Fertility’s mission to translate AI innovation into meaningful clinical outcomes since the company’s earliest stages.
Oliver Hardick, investment director, M Ventures, said: “Future Fertility is addressing a critical unmet need in reproductive medicine with a differentiated AI platform grounded in clinical data and real-world workflow integration.
“We are excited to continue supporting the company and team because we believe its technology has the potential to improve decision-making for clinicians, bring greater clarity to patients, and help advance a more personalised standard of care in fertility treatment.”
Future Fertility’s AI platform addresses a long-standing gap in fertility care: historically, there has been no objective, clinically validated method for assessing egg quality (Gardner et al., 2025), despite it being one of the most important drivers of reproductive success.
The company’s suite of deep learning tools includes VIOLET™, MAGENTA™, and ROSE™, purpose-built for egg freezing, IVF, and egg donation respectively.
The tools are based on AI models trained and validated on more than 650,000 oocyte images and are deployed in over 300 clinics across 35 countries.
Rhiannon Davies, founding and managing partner, Sandpiper Ventures, said: “The best outcomes in fertility care globally come from better data and smarter tools. Future Fertility understands that, and they’ve built a platform that delivers on it.
“Sandpiper is proud to back a team turning rigorous science into real results for patients and clinicians alike.”
Partnerships with the world’s leading fertility networks – including IVI RMA and Eugin Group across Latin America and Europe, FertGroup Medicina Reproductiva in Brazil, and most recently announced Kato Ladies Clinic in Japan – reflect growing demand for objective, AI-powered oocyte assessment in fertility care. In the United States, ROSE™ is newly available under an FDA 513(g) determination.
Research shows that approximately 50 per cent of IVF patients do not understand their likelihood of success, and many discontinue treatment prematurely, even though cumulative success rates improve significantly with multiple cycles (McMahon et al., 2024).
By delivering earlier clarity on egg quality, Future Fertility’s tools support more informed conversations between clinicians and patients, helping set realistic expectations and guide decisions about next steps.
Future Fertility’s growing evidence base spans seven peer-reviewed publications in Human Reproduction, Reproductive BioMedicine Online, Fertility & Sterility, and Nature’s Scientific Reports, and more than 70 scientific abstracts accepted and presented with partner clinics at conferences worldwide.
Christine Prada, CEO, Future Fertility, said: “Fertility treatment is one of the most emotionally and physically demanding experiences a person can go through.
“Every patient deserves objective data, not just a best guess, to support better decisions at critical moments in their care.
“This funding means we can bring that clarity to more patients, in more countries, at a moment when it matters most.”
Find out more about Future Fertility at futurefertility.com
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