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Highlights in Cancer Research: April 2026

April 28, 2026
Highlights in Cancer Research: November 2022

The EACR’s ‘Highlights in Cancer Research’ is a regular summary of the most interesting and impactful recent papers in cancer research, curated by the Board of the European Association for Cancer Research (EACR).

The list below appears in no particular order, and the summary information has been provided by the authors unless otherwise indicated.

Use the dropdown menu or ‘Previous’ and ‘Next’ buttons to navigate the list.


3. A large-scale retrospective study in metastatic breast cancer patients using circulating tumour DNA and machine learning to predict treatment outcome and progression-free survival

  • 1. The local microenvironment suppresses the synergy between irradiation and anti-PD1 therapy in breast-to-brain metastasis
  • 2. Understanding and reversing mammary tumor-driven reprogramming of myelopoiesis to reduce metastatic spread
  • 3. A large-scale retrospective study in metastatic breast cancer patients using circulating tumour DNA and machine learning to predict treatment outcome and progression-free survival
  • 4. Humoral determinants of checkpoint immunotherapy
  • 5. AKR1B10 dictates c-Myc stability to suppress colorectal cancer metastasis via PP2A nitration
  • 6. NNMT inhibition in cancer-associated fibroblasts restores antitumour immunity
  • 7. Paneth-like transition drives resistance to dual targeting of KRAS and EGFR in colorectal cancer
  • 8. Respiratory viral infections awaken metastatic breast cancer cells in lungs
  • 9. DNA fragmentation factor B suppresses interferon to enable cancer persister cell regrowth
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Beddowes, E.J. et al. Molecular Oncology. 19: 3518-3534. (2025).
doi: 10.1002/1878-0261.70015.

Summary of the findings

Monitoring circulating tumour DNA (ctDNA) in blood offers a practical, non-invasive way to track cancer in real time. In this real-world study, we evaluated whether repeated ctDNA measurements could predict treatment response in patients with metastatic breast cancer.

We analysed 1,013 serial blood samples from 149 patients treated in routine clinical practice, using a rapid and low-cost sequencing method to estimate the proportion of tumour DNA in the bloodstream. We identified a 7% tumour DNA threshold that stratified patients by risk of disease progression, consistent across breast cancer subtypes and treatments, and outperforming standard blood tests and targeted sequencing.

Using longitudinal ctDNA data, we developed a Bayesian machine learning model to predict treatment response with good accuracy. This approach enables dynamic, patient-specific risk assessment over time.

These findings show that real-world ctDNA monitoring, combined with machine learning, can provide early and clinically meaningful insight into treatment effectiveness. This strategy has the potential to support more timely, data-driven treatment decisions and improve patient outcomes, and warrants prospective evaluation in large-scale clinical trials.

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Integration of longitudinal data from patients with metastatic breast cancer, incorporating both static and dynamic biomarkers, to develop a Bayesian learning model capable of predicting treatment response.

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Future impact

Real-world longitudinal ctDNA monitoring could significantly change how metastatic breast cancer is managed. By providing an early, non-invasive indication of treatment response, clinicians could identify ineffective therapies weeks to months before conventional imaging. This would enable faster treatment changes, reducing unnecessary toxicity and avoiding prolonged exposure to ineffective drugs. The use of low-cost, scalable sequencing also makes this approach feasible for routine clinical practice. If validated prospectively, ctDNA-guided decision-making could support more personalised, dynamic treatment strategies, improve patient outcomes, and optimise healthcare resources by aligning therapy more closely with tumour biology in real time.
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Read more in Molecular Oncology
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3. A large-scale retrospective study in metastatic breast cancer patients using circulating tumour DNA and machine learning to predict treatment outcome and progression-free survival

  • 1. The local microenvironment suppresses the synergy between irradiation and anti-PD1 therapy in breast-to-brain metastasis
  • 2. Understanding and reversing mammary tumor-driven reprogramming of myelopoiesis to reduce metastatic spread
  • 3. A large-scale retrospective study in metastatic breast cancer patients using circulating tumour DNA and machine learning to predict treatment outcome and progression-free survival
  • 4. Humoral determinants of checkpoint immunotherapy
  • 5. AKR1B10 dictates c-Myc stability to suppress colorectal cancer metastasis via PP2A nitration
  • 6. NNMT inhibition in cancer-associated fibroblasts restores antitumour immunity
  • 7. Paneth-like transition drives resistance to dual targeting of KRAS and EGFR in colorectal cancer
  • 8. Respiratory viral infections awaken metastatic breast cancer cells in lungs
  • 9. DNA fragmentation factor B suppresses interferon to enable cancer persister cell regrowth
Previous
Next
Tags: EACR Top Ten Cancer Research PublicationsHighlights in Cancer Research

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