Digital Pathology Podcast

Digital Pathology Podcast

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Digital Pathology Podcast episodes

  • 244: Why AI Still Hasn't Revolutionized Drug Discovery (Yet) | Thibault Geoui, PhD

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    If AI is already being used across the drug development pipeline, why hasn’t its impact matched the investment?

    AI can help researchers review scientific literature, predict protein structures, prioritize molecules, assess toxicity, support clinical trials, and monitor adverse events. But access to better tools doesn’t automatically create better drugs.

    In this episode, I speak with Thibault Geoui, Science CDO and host of the Tech & Drugs Podcast, about where AI is making a practical difference in drug discovery and development—and where the results remain limited. 

    We map AI across the full drug development funnel, from basic research and target identification to preclinical testing, clinical trials, regulatory documentation, commercialization, and pharmacovigilance.

    We also discuss why digital-native tech-bio companies may be better positioned to benefit from AI than traditional pharmaceutical organizations. The difference isn’t simply the model. It’s how data, people, laboratory experiments, and AI tools are connected inside the workflow.

    For digital pathology professionals, the conversation becomes especially relevant when we examine AI-powered biomarker development, the role of pathology in pharmaceutical research, and the Roche–PathAI case discussed in the episode.

    And, of course, we talk about the problem every AI user eventually faces: an answer can look polished, specific, and completely convincing—and still be wrong.

    Episode Highlights

    00:00 — When convincing AI output creates more work
    Why AI can accelerate information generation while increasing the time required for review and verification.

    02:15 — From structural biology to science and technology leadership
    Thibault shares his background in X-ray crystallography, structural biology, scientific data, and digital product development.

    15:36 — Understanding the drug discovery and development funnel
    How thousands of potential compounds are narrowed down through discovery, preclinical research, clinical trials, and approval.

    20:00 — AI for scientific literature review
    How alerts, filtering, summarization, and information extraction can help researchers manage a rapidly growing scientific literature base.

    22:32 — AlphaFold and protein structure prediction
    What faster access to predicted protein structures changes for researchers—and why structural prediction alone doesn’t solve drug discovery.

    24:13 — Searching an enormous chemical space
    How AI can help design and prioritize potential molecules for synthesis and experimental testing.

    25:50 — Predicting efficacy and toxicity
    Where AI supports preclinical research, why the models remain imperfect, and why experimental validation still matters.

    29:38 — Has AI changed drug development outcomes yet?
    A practical discussion about drug approval rates, AI investment, uneven returns, and the difference between deploying a tool and integrating it into a process.

    34:33 — Why traditional pharma struggles to scale AI
    Siloed data, legacy systems, organizational complexity, and the need to build reusable data workflows.

    37:57 — The “lab in the loop” model
    How tech-bio companies connect AI predictions with wet-lab experiments and feed the new data back into their models.

    44:37 — Can tech-bio companies shorten development timelines?
    How digital-native organizations are changing parts of the discovery and preclinical process.

    58:00 — AI, pharma, and digital pathology
    What the Roche–PathAI case discussed in the episode may indicate about the role of pathology data, biomarker discovery, and pharmaceutical workflows.

    01:06:17 — AI errors in regulated environments
    Why responsibility remains with the person or company submitting AI-assisted work, regardless of which tool produced it.

    01:17:37 — The growing cost of AI tools
    Subscriptions, token limits, model selection, AI orchestrators, and the need to use expensive tools more intentionally.

    01:27:50 — What successful AI adoption requires
    Starting with focused pilots, training scientists and technologists together, and treating implementation as organizational change.

    01:30:26 — The AI quirks that still frustrate users
    Hallucinated information, ignored writing instructions, stylistic habits, and poor awareness of time and context.

    The episode’s timestamped themes and examples are documented in the supplied summary. The broader discussion covers AI from literature mining and molecular design through clinical development and post-market monitoring. 

    Resources Mentioned

    •  Thibault Geoui’s LinkedIn profile 
    • Tech & Drugs Podcast
    • MIT NANDA study on generative AI implementation and return on investment 
    • Insilico Medicine as an example of a digital-native tech-bio company 

    AI is already changing how scientific work gets done. The bigger question is whether organizations can redesign their workflows, train their teams, and maintain the human oversight needed to use it well.

    Listen to the full episode for a practical look at AI in drug discovery, drug development, and digital pathology.

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    1 hr 36 min
  • 243: How to Teach AI to Healthcare Professionals | Podcast with Candice Chu

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    What does AI literacy actually look like for pathologists, researchers, and future clinicians? And how do you teach it in a way that is practical, not abstract?

    In this episode, I talk with Candice Chu, DVM, PhD about something I think a lot of people in digital pathology and computational pathology are feeling right now: AI is moving fast, but education is still catching up.

    Candice is a clinical pathologist, veterinarian, and educator building AI-focused teaching and research at Texas A&M. We worked together before on digital pathology and image analysis projects, so this conversation felt especially grounded. We talk about her AI literacy curriculum framework for veterinary education, why she decided to build it, and what it takes to teach AI in a way that is useful, ethical, and realistic.

    This episode is about understanding what AI tools are good for, where they can waste your time, and why hands-on experience matters. Candice explains why she sees AI as a set of tools, not a belief system. Try them. Learn them. Keep what improves your workflow. Drop what does not.

    We also talk about the difference between putting educational content online and building formal institutional teaching. That matters because social media can move quickly, but curriculum changes, research, and professional organizations shape longer-term adoption. Candice shares how her course started as a low-stakes elective, then grew into a more structured framework that combines education with publishable research.

    A big part of this conversation is the curriculum itself. We go through what students actually learn: AI fundamentals without heavy math, machine learning and image analysis, large language models, prompt engineering, chatbot building, ethics, literature research, and final projects where students evaluate real tools and workflows. I liked that the course does not stop at theory. It asks students to use tools, question them, and explain where they help and where they do not.

    We also get into something that matters far beyond veterinary medicine: professional responsibility. If AI is involved in a workflow, the clinician is still responsible. That includes fabricated citations, bad outputs, weak prompts, and the temptation to trust tools too quickly. Candice makes a strong case that AI education needs ethics, legal context, and interdisciplinary teaching built in from the start.

    If you are trying to think more clearly about AI in pathology, education, workflow design, or professional training, this episode gives you a concrete example of what responsible AI literacy can look like.


    Episode Highlights

    00:00 – Why AI tools are just tools, and why trying them matters even if you later decide not to keep using them

    00:33 – Who Candice Chu is and why her work on AI literacy in veterinary medicine is worth paying attention to

    02:33 – Why going back to Texas A&M changed the scale of Candice’s AI research and teaching

    07:53 – How the AI course was designed as a low-stakes elective first, and why that helped student engagement

    11:16 – Where veterinary AI education stands now, and what professional organizations like ACVP are doing

    13:08 – Why AI adoption in veterinary medicine is still slow, and what skepticism usually sounds like in practice

    15:19 – Real examples of how Candice uses LLMs and computer vision in pathology, medical records, and research

    19:58 – What is actually inside the 15-week AI literacy curriculum, from fundamentals to final projects

    24:16 – Why ethics and legal responsibility are not optional in AI education

    31:35 – Why no-code tools and vibe coding are entering the curriculum already

    38:50 – The AI tools Candice is testing in her own workflow, including Claude, Codex, and Perplexity


    Resources mentioned

    • Candice Chu’s AI literacy curriculum framework paper in Frontiers in Veterinary Science
    • Candice’s earlier work on ChatGPT in veterinary medicine
    • Texas A&M and the institutional setting where Candice is building AI research and teaching
    • Mr. Don Riddick and the AVMA AI working group, mentioned in the ethics and legal context
    • Claude, Codex, and Perplexity as AI tools Candice is actively testing
    • Digital Pathology 101, mentioned in the conversation as a teaching resource
    • Candice’s online educational work on Instagram.

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    43 min
  • 242: Foundation Models in Pathology: Strong on Paper, Ready for Labs?

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    Are pathology foundation models actually ready for labs, or are they still stronger on paper than in practice?

    In this episode of DigiPath Digest #49, I unpack a timely review on pathology foundation models and ask the question that matters most to me: not just what these models can do, but what has to be true before they are genuinely useful in real pathology workflows.

    I walk through how pathology AI moved from narrow, task-specific models into the era of transformer-based foundation models. That shift matters because pathology is no longer only about looking at H&E in isolation. Today, pathologists are expected to integrate morphology, immunohistochemistry, molecular assays, genomics, and clinical context. That growing complexity is one reason foundation models are getting so much attention.

    In this discussion, I explain how transformers entered pathology, why image patches are treated like tokens, and how shared embeddings can support classification, regression, segmentation, and multimodal retrieval. I also go through the major pathology foundation models mentioned in the paper, including Virchow/Virchow2, Mayo Clinic Atlas, UNI, CONCH, H-Optimus, GigaPath, and TITAN, and why scale alone is not the full story.

    A big part of this episode is about the gap between benchmark performance and clinical readiness. I talk about the persistent limitations in training data diversity, the overuse of TCGA, and why public benchmarks can still miss what real pathology practice looks like. I also cover where foundation models still struggle, especially in cytopathology, hematopathology, and underrepresented disease areas, along with the real-world problems of artifacts, domain shift, concept drift, infrastructure burden, regulatory complexity, and workflow disruption.

    For me, one of the most important themes is this: AI in pathology should augment, not replace, pathologists. The future is not about handing diagnosis to a model. It is about building tools that support pathologists better, fit real workflows, and can be validated in ways that deserve trust.

    I also spend time on what comes next: explainable AI, counterfactual explanations, conversational interfaces, retrieval-augmented systems, multimodal fusion, and the need for deployment-centric validation rather than paper-only excitement.

    If you are trying to understand where pathology foundation models really stand today, this episode will help you separate the promise from the practical barriers.

    Episode Highlights

    00:01 – Why I chose this paper, what is changing at Digital Pathology Place, and why foundation models are worth paying attention to now.

    02:15 – The core questions: what pathology foundation models are, where they are, and how difficult they are to apply in pathology.

    04:50 – Why pathology is becoming more cognitively demanding, and how multimodal complexity is driving interest in scalable AI.

    07:02 – From narrow AI to transformers: how pathology moved beyond single-task CNN models.

    10:16 – How transformers work in pathology: image patches as tokens, self-attention, embeddings, and downstream tasks.

    14:16 – Why multimodality matters, and what kinds of data foundation models may eventually integrate.

    15:27 – Timeline of key model developments, from “Attention Is All You Need” to gigapixel-scale pathology foundation models.

    17:13 – The leading models and what scale really looks like: Virchow, Mayo Clinic Atlas, UNI, CONCH, H-Optimus, and GigaPath.

    19:51 – Why dataset diversity matters more than sheer volume, and why TCGA is not enough.

    23:17 – Where foundation models still struggle: cytopathology, hematopathology, rare disease, artifacts, scanner shifts, and pen marks.

    28:06 – Explainability, counterfactual explanations, and why trust in pathology AI needs more than attention maps.

    30:17 – The real deployment hurdles: regulation, infrastructure, workflow fit, and economics.

    36:32 – Why AI should augment pathologists, not replace them, and which tedious tasks pathologists would gladly hand over.

    38:36 – Retrieval-augmented and conversational AI in pathology: where interactive systems may actually help.

    40:51 – Vision-language models and multimodal fusion with histology, radiology, genomics, and clinical notes.

    42:16 – The path forward: deployment-centric design, prospective multi-site validation, and human-AI collaboration.

    44:08 – Closing thoughts on AI literacy, community learning, and what needs to happen next.

    Resources Mentioned

    • Main paper discussed:
      Pathology Foundation Models: Evolution, Current Landscape, Challenges and Opportunities from a Technical and Clinical Perspective
      https://doi.org/10.3390/bioengineering13050577
    • Review article / journal landing page:
      https://doi.org/10.3390/bioengineering13050577
    • Benchmarks mentioned:
      • PathoBench — discussed in the review paper; use the review link here for context until you want to swap in a canonical project page:
        https://doi.org/10.3390/bioengineering13050577
      • PathBench — public benchmark paper:
        https://arxiv.org/abs/2505.20202
      • MEDFAIR — benchmark paper:
        https://arxiv.org/abs/2210.01725
      • MEDFAIR code repository:
        https://github.com/ys-zong/MEDFAIR
    • Models mentioned:
      • Model overview in the review (Virchow/Virchow2, UNI, CONCH, H-Optimus, GigaPath, TITAN, Mayo Clinic Atlas):
        https://doi.org/10.3390/bioengineering13050577
      • Virchow:
        https://arxiv.org/abs/2309.07778
      • UNI:
        https://arxiv.org/abs/2308.15474
      • CONCH:
        https://arxiv.org/abs/2307.12914
      • Mayo Clinic Atlas:
        https://arxiv.org/abs/2501.05409
      • TITAN:
        https://arxiv.org/abs/2411.19666
    • Dataset mentioned:
      The Cancer Genome Atlas (TCGA)
      https://portal.gdc.cancer.gov/
    • Book mentioned:
      Digital Pathology 101: All You Need to Know to Start and Continue Your Digital Pathology Journey
      https://digitalpathologyplace.com/
    • Platform:
      Digital Pathology Place
      https://digitalpathologyplace.com/

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    43 min
  • 241: AI-Powered Companion Diagnostics: The Future of Precision Medicine | Podcast with Doug Bowman, VP Precision Medicine at Indica Labs, Inc.

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    How far can pathologists take visual biomarker scoring before human vision becomes the bottleneck?

    In this episode, I talk with Doug Bowman. PhD, VP Precision Medicine at Indica Labs, about what happens when companion diagnostics move from traditional visual scoring into the era of AI-powered image analysis. Doug comes from a biomedical and electrical engineering background, with experience in microscopy, digital image analysis, pharma workflows, and now precision medicine at Indica Labs. That combination makes him a great person to talk to about how image analysis actually fits into real companion diagnostic development.

    We start with a very practical question: what is a companion diagnostic, and why is it becoming so important in precision medicine? Doug explains that companion diagnostics are developed alongside therapeutics to help identify which patients are most likely to benefit from a specific treatment, especially in more complex therapies like antibody-drug conjugates (ADCs). We use HER2 as an example, and from there we get into the real challenge: once a biomarker cutoff matters clinically, visual estimation around that cutoff becomes much harder than many people want to admit.

    That is where this conversation gets especially useful for pathologists and digital pathology trailblazers. We talk about the limits of human vision, why low or ultra-low biomarker expression is difficult to score consistently, and how AI helps at multiple levels of the workflow: slide QC, tissue classification, cell segmentation, membrane and cytoplasmic measurement, and spatial analysis. Doug makes the case that AI is not only a convenience here. In some cases, it is the only realistic way to capture the kind of quantitative information modern therapies need.

    We also get into one of the more interesting examples from the episode: the Trop2 story, where a ratio of cytoplasmic to membrane expression appears to predict therapeutic efficacy better than looking at one compartment alone. That kind of compartment-level quantitation is exactly where computational pathology becomes more than a digital version of what the eye already does. It starts uncovering measurements and signatures the eye cannot reliably extract on its own.

    Another important part of the discussion is workflow and regulation. Doug walks through how AI-powered companion diagnostics are developed from preclinical work, to human feasibility studies, to RUO or clinical trial assays, and eventually toward analytical and clinical validation with regulatory engagement happening early. We also talk about the Indica Labs and Leica Biosystems partnership, and why end-to-end capability matters when you are trying to build something clinically deployable rather than just analytically interesting.

    What I liked about this conversation is that it stayed grounded. We did not talk about AI as magic. We talked about image analysis as a method, companion diagnostics as a workflow, and precision medicine as something that only works when the measurement is good enough to support real decisions.


    Episode Highlights

    00:00 – Why AI matters in slide QC, tissue classification, and cell-level analysis before you even get to the biomarker score.

    00:54 – Doug Bowman’s background in biomedical engineering, microscopy, and digital image analysis.

    05:16 – What a companion diagnostic actually is, and why it is critical for targeted therapies and ADCs.

    07:34 – Why visual biomarker scoring becomes unreliable around critical cutoffs, especially in low-expression cases.

    10:09 – How AI expands the workflow: slide QC, tissue classification, and precise cell segmentation.

    13:07 – Why pathologists remain central in AI workflows through validation, markup review, and model refinement.

    16:31 – The Trop2 example: when cytoplasmic-to-membrane ratio tells you more than one compartment alone.

    20:23 – The Indica Labs + Leica Biosystems partnership and why end-to-end workflow matters in companion diagnostics.

    22:53 – What the development journey looks like from early algorithm work to RUO, validation, and regulatory interaction.

    26:51 – Multiplexing, spatial analysis, and why more clinical value often comes with more deployment complexity.

    33:29 – Why image analysis literacy matters, and how shared language between pathologists and scientists becomes essential.

    40:13 – Where to learn more about Indica Labs and who to contact for collaboration.


    Resources mentioned

    • Indica Labs 
    • Indica Labs contact – [email protected]
    • HALO software / HALO AI diagnostic image analysis – discussed in the context of companion diagnostic deployment and pharma services.
    • Leica Biosystems GT450DX – referenced as an FDA-cleared slide scanner in the Indica-Leica partnership.
    • Digital Pathology Association – mentioned as part of the broader educational ecosystem for digital pathology and image analysis.
    • Digital Pathology Place / Digital Pathology Podcast – the platform hosting this conversation and related education around digital pathology and AI.

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    42 min
  • 240: Can AI Copilots Keep Up with Pathologists?

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    Can AI copilots really keep up with pathologists when the cases are new, the workflow is messy, and the benchmark is actually protected from leakage?

    In this episode of DigiPath Digest #48, I focus on one paper: DALPHIN: Benchmarking Digital Pathology AI Copilots Against Pathologists on an Open Multicentric Dataset. I chose this paper because I think the field needs more of this kind of work. Less hype. More evaluation. Less “look what AI can do.” More “how do we test it in a way that actually means something?” 

    In this session, I look at what makes DALPHIN important for pathologists, lab leaders, and digital pathology trailblazers trying to make sense of pathology AI right now. The paper benchmarks three models against human pathologists: two general-purpose models, Gemini 2.5 Pro and GPT-5, and one pathology-specific model, PathChat+. The dataset includes 1,236 images from 300 cases, covering 130 diagnoses, 14 pathology subspecialties, and cases from six countries. Human performance is benchmarked with 31 pathologists from 10 countries. 

    What I like about this paper is that it does not stop at top-line performance. It deals with the benchmarking problem itself. The authors built a sequestered, indirectly accessible ground truth so the evaluation data could not simply be scraped into model training. That matters because without that protection, benchmarking can become an illusion of genius rather than a real test of generalization. 

    The results are interesting and more nuanced than a simple win-or-lose story. PathChat+ reached expert-level performance in four of six tasks, Gemini in two of six, and GPT in one of six. That tells us something important already: pathology-specific training matters. But it also does not mean pathology is solved. In organ recognition, expert pathologists still outperformed all the models. In rare cancers, none of the models reached expert-level performance. And in ambiguous cases, the models still struggled with something human pathologists do all the time: expressing uncertainty. 

    I also spend time on one of the most practical parts of the paper: model behavior. Gemini tended to overcall. GPT tended to undercall. PathChat was more balanced. That matters in practice. A pathologist using a copilot needs to know the tool’s calibration bias before they can safely interpret what it is telling them. I also talk about anchoring bias in conversational interfaces, where early hallucinations can propagate through later answers if memory is not reset between questions. That is not just a technical curiosity. That is a workflow and safety issue. 

    Why should you listen? Because this episode is really about a bigger question: What kind of evidence should pathologists demand before AI copilots enter real workflows? If you want to understand validation, data leakage, rare-case performance, uncertainty, and why these tools should still be treated as co-pilots rather than autopilots, this is a useful paper to know. 

    Episode Highlights

    01:20 – Why I chose the DALPHIN preprint and why benchmarking matters right now. 

    05:38 – What is in the DALPHIN dataset: 300 cases, 130 diagnoses, 14 subspecialties, 6 countries. 

    07:57 – Top-line performance: PathChat+ reaches expert-level performance in 4 of 6 tasks. 

    09:41 – The benchmarking trap of data leakage and why DALPHIN’s sequestered ground truth matters. 

    12:19 – Why real pathology diagnosis is not text-only and why macro + micro context matters. 

    15:26 – Tissue recognition, neoplasm detection, ambiguity, and conversational memory: how the testing was structured. 

    21:29 – The diagnostic personalities of the models: overcalling, undercalling, and balanced behavior. 

    24:36 – Rare cancers: where AI copilots still fall short of expert human performance. 

    28:00 – Why binary outputs are not enough when pathology often lives in uncertainty. 

    31:37 – Anchoring bias and conversational memory: how early hallucinations can keep propagating. 

    37:11 – Why these tools should be treated as co-pilots, not autopilots. 

    40:29 – Resources for beginners: Digital Pathology 101 and continued AI literacy. 

    Resources mentioned

    • DALPHIN preprint: arXiv:2605.03544v1 
    • DALPHIN evaluation platform: dalphin.grand-challenge.org 
    • PathChat+ pathology-specific AI model discussed in the benchmark. 
    • Digital Pathology 101 free eBook by Dr. Aleksandra Zuraw. 
    • Educational streams on tissue recognition and computer vision literacy mentioned in the session.

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    34 min
  • 239: The Four Steps Pathology AI Demos Quietly Skip and Why They Matter

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    What happens when a pathology AI model misses the tissue before it even begins—and can better segmentation, education, and virtual staining close the gaps?

    In DigiPath Digest #47, I review four recent studies that expose both the promise and the weak points of AI-assisted digital pathology. We start with a step that sounds simple: detecting tissue on a whole slide image. Yet when that first step fails, the downstream algorithm may miss cancer entirely.

    From there, I look at a practical resource designed to improve communication between pathologists and computational scientists, a self-refining Segment Anything Model that reduces the burden of pixel-perfect nuclear annotations, and a virtual HER2 immunohistochemistry method generated from H&E images.

    The common lesson? Digital pathology AI is only as reliable as the workflow underneath it. Tissue processing, scanning, segmentation, annotation, model design, and clinical interpretation all matter. Every step needs validation.

    Discussion highlights

    00:00 – Welcome to DigiPath Digest #47 and an overview of the four papers

    02:31 – Why tissue detection is the foundation of pathology AI workflows

    05:01 – A large prostate pathology study using 33,823 whole slide images for tissue detection and 70,000 images for downstream Gleason grading

    06:28 – Classical thresholding missed tissue completely on 118 slides, compared with 24 slides using U-Net++ tissue detection

    07:51 – How artifacts and uneven slide color can disrupt classical detection methods

    09:59 – AI-based tissue detection reduced total failures by 79% but didn’t eliminate them

    10:39 – Why validating only the final algorithm output can hide upstream sources of error

    12:05 – Tissue detection choice produced clinically significant differences in final Gleason grade in 3.5% of malignant slides

    13:33 – The communication gap between pathology and computer science—and why it still slows progress

    15:29 – “Decoding Digital Histopathology” as an accessible guide for computational researchers entering pathology

    18:03 – Digital Pathology 101, my free companion resource for anyone starting or continuing a digital pathology journey

    20:18 – From collected tissue to glass slide, whole slide image, interpretation, and computational analysis

    25:08 – The role of TCGA and the growth of digital pathology datasets across clinical, veterinary, preclinical, and research settings

    27:14 – Why pixel-level nuclear annotation remains a bottleneck for deep learning

    30:39 – Replacing detailed nuclear outlines with simple point prompts

    31:23 – How the self-refining SAM framework uses sparse labels, contrastive learning, and a correction loop

    33:25 – Do we really need to keep annotating the same structures for every new model?

    37:49 – Generating virtual HER2 IHC from H&E with a score-aware, non-contrastive multitask model

    39:53 – Study results: 83.01% accuracy for virtual IHC alone and 97.85% accuracy when H&E and virtual IHC were combined

    40:56 – Where virtual IHC may fit as a complementary or triage tool—and why confirmatory testing still matters

    44:06 – My perspective on trust, interpretation, and the difference between predicting IHC and predicting molecular alterations

    46:17 – Final thoughts and an invitation to continue the discussion

    Resources mentioned

    • “Impact of Tissue Detection on Diagnostic Artificial Intelligence Algorithms in Prostate Digital Pathology” – Scientific Reports
    • “Decoding Digital Histopathology: The Building Blocks for Computational Researchers” – PLOS Digital Health
    • “Self-Refining Segment Anything Model for Nuclear Segmentation: A Contrastive Learning Approach to Label-Efficient Pathological Imaging” – Diagnostics
    • “HER2 Score-Aware Virtual Immunohistochemistry via Non-Contrastive Multitask Translation” – Diagnostics
    • Digital Pathology 101: All You Need to Know to Start and Continue Your Digital Pathology Journey
    • European Society of Digital and Integrative Pathology
    • The Cancer Genome Atlas (TCGA)

    If you work in pathology, computational science, image analysis, or AI development, this episode is a useful reminder to look beyond the headline performance metric. The errors that matter may begin much earlier in the workflow.

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    48 min
  • 238: How Do We Know AI Is Ready for Pathology

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    Do you really need a scanner, whole slide images, and AI infrastructure before you can start in digital pathology?

    In this episode, I argue that you do not.

    I’m Dr. Aleksandra Zuraw, veterinary pathologist and digital pathology educator, and this talk is about a belief I hear all the time: I don’t have the tools yet, so there is no point learning digital pathology. I used to think that too. When I was training in Berlin, there was one Leica 6-slide scanner, and it felt like digital pathology was only for a small group of chosen people. That experience made the field feel distant, exclusive, and not really available to beginners. 

    What changed for me was not a new scanner. It was a small project.

    I needed a more consistent way to quantify a senescence marker in archived skin samples, so I used a microscope camera, captured images, opened them in Microsoft Paint, and manually marked cells with colored dots. It was scrappy. Very low tech. But it was also digital, consistent, and verifiable. That project became my first real step into digital pathology and helped me get my first job in the field, where I worked between pathologists and image analysis scientists on biomarker quantification and patient stratification problems. 

    That is the core point of this episode: knowledge unlocks technology.

    Scanners matter. AI tools matter. But the deeper bottleneck is whether enough people understand how to use these tools, ask good questions, and connect pathology expertise with digital workflows. That is why this episode is really about readiness. Not readiness of the hardware. Readiness of the people.

    I also talk about Dr. Taladzer from Pakistan, whose story makes this point even more clearly. At the time, Pakistan had around 220 million people, about 500 pathologists, and zero scanners. She still started learning digital pathology during COVID using a microscope and camera, joined the Digital Pathology Association, taught herself from papers and online resources, and kept going even after multiple AI vendors rejected her because she did not have whole slide images. Eventually, she found a DIY image analysis platform, learned to annotate and train models on static images, completed projects quickly, and went on to publish more than 10 digital pathology papers without ever using WSI.

    Why should you listen?

    Because this episode is for pathologists and lab leaders who are interested in digital pathology but still feel stuck at the beginning. It is for people waiting for permission, perfect infrastructure, or a formal roadmap. And it is for trailblazers who came back from a meeting or conference energized, but need a practical way to turn that energy into action before it fades.

    I also address an important AI question near the end: How do we know an AI model is good enough for pathology? I talk about why models are only as good as the pathologist annotations used to train them, why concordance between pathologists matters, how orthogonal labels like IHC can improve model quality, and why pathologists still need to stay in the loop as these systems develop and get deployed.

    If you are trying to figure out where to start, this episode gives you a practical answer: start where you are. Start with what you have. Start learning now.

    Episode Highlights

    00:00 – Why the real barrier to digital pathology is usually not the hardware
    00:33 – What it feels like to be at the beginning of the digital pathology journey
    02:50 – My first practical digital pathology project using a microscope camera and Microsoft Paint
    05:37 – How that low-tech project led to my first digital pathology job
    08:52 – Why knowledge, not infrastructure, is the real unlock
    09:57 – Dr. Taladzer’s story: starting digital pathology in Pakistan with zero scanners
    12:03 – What happened after repeated vendor rejection and why persistence mattered
    14:39 – The “forgetting loop” vs the “commitment loop” after conferences
    16:48 – Practical next steps: book, PubMed alerts, journal clubs, webinars, vendor resources
    18:52 – Why I believe digital pathology is the gateway to faster diagnosis
    20:00 – How to think about whether an AI model is really ready for pathology

    Resources Mentioned

    • Digital Pathology 101 – free book recommended as a starting point for learning digital pathology. 
    • Digital Pathology Association – mentioned as a learning resource and professional community. 
    • PubMed alerts for AI and digital pathology. 
    • Journal clubs – mentioned as one way to keep learning consistently. 
    • Webinars and vendor resources – suggested as practical ways to keep building knowledge. 
    • A4A – the DIY image analysis platform that supported Dr. Taladzer’s early work with static image annotation and model training. 

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    21 min
  • 237: Why Pathology Vendor's Don't Speak the Same Language?

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    Why are pathology vendors still speaking different image languages when radiology solved that problem decades ago?

    In this episode of DigiPath Digest #46, I talk through four papers that all point to a bigger issue in digital pathology: we are not only dealing with better algorithms. We are dealing with interoperability, workflow design, explainability, and whether the field is actually ready to use these tools well.

    I start with DICOM in digital pathology, because I think this is still one of the most important infrastructure questions in the field. Digital pathology has clear value for consultation, image analysis, archival, and workflow, but vendor-specific whole slide image formats still create silos. In the episode, I explain why DICOM matters, why adoption is still low, how the multi-resolution pyramid works, and why this is really about enterprise imaging and future-proofing, not just file conversion. 

    Then I move into kidney transplant rejection, where the paper makes a strong case for multimodal precision diagnostics. Creatinine is late. Antibody testing can miss important biology. Biopsies can miss the area that matters. So the opportunity is not to replace pathology, but to combine biomarkers, biopsy, and machine learning in a way that is more useful than any one signal alone. I also talk about explainability here, because if a model gives a risk score, we need to know what contributed to it. 

    The third paper focuses on perineural invasion in solid tumors, and I liked this one a lot because it shows how AI can help standardize something that is clinically important but still inconsistently detected and reported. Perineural invasion is not just a passive pathway of spread. The biology is more active than that, and the quantification can go far beyond a simple yes-or-no answer. This is a good example of where digital pathology can do something humans cannot realistically do by eye at scale. 

    The last paper is on gastric cancer immunohistochemistry biomarkers and advanced quantification, including HER2, PD-L1, mismatch repair, and CLDN18.2. This section is really about complexity. We are now asking pathologists to visually score biology that is getting harder and harder to summarize consistently, especially when markers, spatial context, and multiplexing all start to matter at once. I make the case that computational pathology is becoming necessary here, not because pathologists are failing, but because the biology is outgrowing purely visual workflows. 

    What ties these four papers together is simple: digital pathology is not only about remote reading anymore. It is about interoperability, quantification, explainable AI, and making pathology more precise in places where the old workflow is reaching its limit. If you are a pathologist, lab leader, or digital pathology trailblazer trying to figure out what actually matters right now, this episode will help you connect the dots.

    Episode Highlights

     07:41 – Why DICOM still matters if we want digital pathology systems to work together.
    14:39 – Current adoption of SVS, MRXS, and DICOM, and why DICOM is still lagging.
    16:44 – How the DICOM whole slide image pyramid works and why it matters for workflow.
    24:29 – Why kidney transplant rejection is still difficult to diagnose with any single marker.
    29:18 – Why perineural invasion is clinically important and still inconsistently reported.
    34:44 – How AI can quantify tumor-nerve relationships more consistently than visual review alone.
    46:39 – Why gastric cancer biomarker scoring is getting too complex for purely visual workflows.
    54:55 – Multiplexing, spatial biology, and why explainable AI matters in biomarker interpretation.
    01:04:01 – What is really blocking digital pathology adoption: cost, workflow, regulation, or mindset? 

    Resources mentioned

    • DICOM / digital pathology interoperability paper
      https://pubmed.ncbi.nlm.nih.gov/42093730/
    • Kidney transplant rejection, biomarkers, and artificial intelligence
      https://pubmed.ncbi.nlm.nih.gov/42073482/
    • Perineural invasion in solid tumors with AI and machine learning applications
      https://pubmed.ncbi.nlm.nih.gov/42100436/
    • Gastric cancer IHC biomarkers, advanced detection methods, and perspectives
      https://pubmed.ncbi.nlm.nih.gov/42075555/
    • Digital Pathology Place
      https://digitalpathologyplace.com
    • Digital Pathology 101
      Free PDF book mentioned at the end of the episode through Digital Pathology Place.

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    34 min
  • 236: What Happens When a Patient Sees Their Cancer for the First Time | Podcast with Michele Mitchell

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    What if the most frightening part of a pathology report is not the word cancer, but the silence that follows?

    In this episode of the Digital Pathology Podcast, Dr. Aleksandra Zuraw talks with Michele Mitchell—breast cancer survivor, caregiver, national patient advocate, and longtime volunteer across Michigan Medicine, ASCP, the Digital Pathology Association, and MyPathologyReport.ca—about what happened when she saw her own cancer slide years after treatment. That moment changed how she understood her disease, her risk, and her role as a patient advocate.

    This is not just a patient story. It is a digital pathology implementation story.

    The episode looks at how digital pathology removes practical barriers to sharing slides, why pathology clinics matter, and what becomes possible when pathologists move from being hidden in the background to becoming direct contributors to patient understanding. Michelle and Dr. Aleks talk through the communication gap around pathology reports, the emotional cost of delayed explanation, and the real-world workflow of pathology clinic visits built to help patients review their slides with the pathologist who made the diagnosis.

    They also discuss what the 21st Century Cures Act changed for patients, why immediate access to reports without interpretation can still create fear, and how pathology clinics can bridge the gap between raw data and real understanding. The conversation gets practical too: how patients can request a pathology clinic visit, what virtual pathology consults can look like, how billing and workflow concerns are already being addressed, and why the infrastructure question is smaller than many people assume.

    If you work in digital pathology, pathology informatics, patient communication, or implementation, this episode is a reminder that visibility is not extra. It is part of the value proposition. And for pathologists who worry this is too far outside the traditional role, the episode offers a grounded counterpoint: the workflows, templates, billing structures, and virtual options already exist.

    Highlights

    • 00:00 – Why pathology needs to become more patient-centered
      Michele frames the core problem clearly: what often scares patients is not only cancer, but the silence around the diagnosis. 
    • 00:34 – How digital pathology changes the patient experience
      Digital slides make it possible for patients to see their diagnosis, compare normal and abnormal tissue, and ask better questions. 
    • 11:13 – What happened when Michele saw her cancer for the first time
      More than a decade after treatment, seeing her own slide changed how she understood her grade, her risk, and her daily health decisions. 
    • 16:19 – Why visual pathology can change adherence and lifestyle
      Michele explains how the image-based explanation became a practical turning point, not just an emotional one. 
    • 20:43 – The case for direct pathologist-patient communication
      The episode reviews why this can improve clarity, treatment understanding, clinic efficiency, and even professional satisfaction for pathologists. 
    • 38:40 – What a pathology clinic actually looks like
      From preparation and consent to slide review, plain language, empathy, and follow-up, the workflow is much more concrete than many people assume. 
    • 45:35 – ASCP’s certification workshop for pathology clinics
      Michele describes the national effort to make pathology clinics reproducible, scalable, and easier to implement. 
    • 49:32 – What the 21st Century Cures Act changed
      Patients now get near real-time access to reports, but that access still needs interpretation, context, and support. 
    • 01:03:23 – Pushback, logistics, and why the barriers are not where people think
      Time, reimbursement, scheduling, and virtual setup are addressed directly with examples already in practice. 
    • 01:16:57 – The future: patient-friendly reports, AI, and pathology as part of the care team
      The episode closes on a practical vision: not hype, but tools and workflows that already exist and can be connected now. 

    Resources mentioned

    • Digital Pathology Place – website and educational platform referenced by Dr. Aleks as the home for her work and resources. 
    • Digital Pathology 101 – Dr. Aleks’s book, referenced in the broader discussion of patient and pathologist education. 
    • Michigan Medicine breast pathology clinic – launched in 2023 as a patient-facing breast pathology clinic model. 
    • ASCP pathology clinic certification workshop – national workshop co-developed to help institutions build pathology clinics. 
    • 21st Century Cures Act – legal framework behind near real-time patient access to pathology reports and related health data. 
    • MyPathologyReport.ca – patient-friendly pathology education resource reviewed with patient advocate involvement. 
    • American Cancer Society Reach to Recovery – support resource mentioned for breast cancer patients. 
    • Scanslated – patient-friendly report interface discussed as part of a future-facing model for pathology communication. 
    • Virtual pathology consults/telehealth setup – discussed as a scalable way to lower implementation friction.

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    1 hr 14 min
  • 235: From Cytology to Omics: Where Pathology AI Gets Harder

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    DigiPath Digest #45 asks a practical question: can AI in pathology move from correlation to real clinical use? In this episode, I review four papers that push on that question from different angles: computational pathology moving toward morphology-driven molecular inference, the current state of digital cytopathology and AI, multi-omics and precision oncology in hepatocellular carcinoma, and AI literacy in veterinary education. What ties them together is not model performance alone. It is the harder question of validation, workflow fit, quantitative use, ethics, and human oversight.

    In the first paper, I talk about computational pathology as more than pattern recognition. The focus is on morphology-driven molecular inference, digital biomarkers, and why spatial omics matters as biological ground truth. I also discuss why continuous quantitative scoring is more useful than forcing biology into rough scoring buckets. 

    The second paper focuses on digital cytopathology. Cytology was early for FDA-cleared AI in cervical screening, but non-gynecologic cytology is still much harder to digitize because of specimen variability and workflow complexity. I also cover telecytology, rapid onsite evaluation, automation, and quality control. 

    The third paper looks at hepatocellular carcinoma and AI-driven precision oncology. This part is about using AI and machine learning to integrate genomics, transcriptomics, proteomics, metabolomics, radiomics, and pathology to support biomarker discovery, tumor microenvironment analysis, and treatment stratification. 

    The fourth paper may be the most broadly useful. It proposes an AI literacy curriculum for veterinary education that covers AI fundamentals, machine learning evaluation, LLMs, ethics, liability, and academic integrity. I think that matters far beyond veterinary medicine, because if clinicians are expected to use AI tools responsibly, AI literacy cannot stay optional. 

    Highlights
    00:01 Welcome and overview of the four papers
    03:02 Computational pathology and morphology-driven molecular inference
    11:01 Digital cytopathology, telecytology, and QC
    20:47 AI/ML in hepatocellular carcinoma precision oncology
    31:04 AI literacy in veterinary education
    47:42 Final takeaways and Digital Pathology 101 update 

    Resources

    1. Computational Pathology as a Mechanistic Discipline: From Morphology to Molecular Data
      https://pubmed.ncbi.nlm.nih.gov/42052846/

    2. Advances in Digital Cytopathology and Artificial Intelligence Applications
      https://pubmed.ncbi.nlm.nih.gov/42046894/

    3. Navigating the Labyrinth of Hepatocellular Carcinoma: Leveraging AI/ML for Precision Oncology
      https://pubmed.ncbi.nlm.nih.gov/42065059/

    4. Curriculum Framework for Artificial Intelligence Literacy in Veterinary Education
      Front Vet Sci. 2026;13:1801756 

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    34 min

About Digital Pathology Podcast

From the publisher's feed

Aleksandra Zuraw from Digital Pathology Place discusses digital pathology from the basic concepts to the newest developments, including image analysis and artificial intelligence. She reviews…

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