Existing tools for post-radical prostatectomy (RP) prostate cancer biochemical recurrence (BCR) prognosis rely on human pathologist-derived parameters such as tumor grade, with the resulting inter-reviewer variability. Genomic companion diagnostic tests such as Decipher tend to be tissue destructive, expensive, and not routinely available in most centers. We present a tissue non-destructive method for automated BCR prognosis, termed "Histotyping", that employs computational image analysis of morphologic patterns of prostate tissue from a single, routinely acquired hematoxylin and eosin slide. Patients from two institutions (n = 214) were used to train Histotyping for identifying high-risk patients based on six features of glandular morphology extracted from RP specimens. Histotyping was validated for post-RP BCR prognosis on a separate set of n = 675 patients from five institutions and compared against Decipher on n = 167 patients. Histotyping was prognostic of BCR in the validation set (p < 0.001, univariable hazard ratio [HR] = 2.83, 95% confidence interval [CI]: 2.03–3.93, concordance index [c-index] = 0.68, median years-to-BCR: 1.7). Histotyping was also prognostic in clinically stratified subsets, such as patients with Gleason grade group 3 (HR = 4.09) and negative surgical margins (HR = 3.26). Histotyping was prognostic independent of grade group, margin status, pathological stage, and preoperative prostate-specific antigen (PSA) (multivariable p < 0.001, HR = 2.09, 95% CI: 1.40–3.10, n = 648). The combination of Histotyping, grade group, and preoperative PSA outperformed Decipher (c-index = 0.75 vs. 0.70, n = 167). These results suggest that a prognostic classifier for prostate cancer based on digital images could serve as an alternative or complement to molecular-based companion diagnostic tests.
Tumor morphology is associated with cancer aggressiveness in prostate cancer (PCa). Gleason grading, used by pathologists to score the loss of glandular structure and organization in tissue1, is strongly correlated with patient outcome2. While Gleason grading is done by pathologists and is therefore subjective3, computerized image analysis of tissue can quantitatively define tumor morphology. Quantitative histomorphometric (QH) approaches implicitly capture attributes of tumor grade through features of glandular and nuclear shape4, arrangement5, or disorder6, as well as tissue texture7. Characteristics of aggressive PCa, such as poorly formed lumens, can be captured by combinations of these features. Studies have shown an association between QH features and patient outcome6,7,8,9,10. However multi-site evaluation has been a challenge for QH approaches, in part due to pre-analytic variation between sites in specimen preparation, staining, and scanning.
Radical prostatectomy (RP), the surgical removal of the prostate, remains the most common curative therapy for PCa11. Following RP, some patients will experience biochemical recurrence (BCR), defined by consecutive serum prostate-specific antigen (PSA) test results >0.2 ng/mL. BCR is a surrogate endpoint for prostate cancer and is associated with a hazard ratio (HR) of 4.3212 for disease-specific death. In the STAMPEDE trial, adjuvant therapy reduced metastasis and disease-specific death13, though adjuvant therapy is not appropriate for all patients due to the low overall mortality rate of PCa14. Estimates of a patient’s risk of BCR post-surgery could help identify those patients who might benefit from adjuvant therapy while avoiding unnecessary treatment of low-risk patients. Nomograms, the current gold standard for BCR prognosis, produce a probability of BCR based on clinical variables15 but do not provide perfect risk stratification16, motivating the development of new assays. In addition to nomograms, prognostic molecular companion diagnostics exist17,18,19, but these are tissue destructive, preventing analysis of the entire tumor or retesting of the same sample, and expensive.
In this study, we present a QH method for BCR prognosis using automated analysis of an H&E slide from the dominant tumor nodule. A total of 242 features were extracted from slides of n = 889 patients. From the n = 214 of these patients used for training, 51 features that were stable across staining and scanner variation were used to construct an elastic-net penalized Cox regression model. The Cox model selected six features associated with high-risk disease and used the weighted sum of these features to estimate the BCR risk for each patient. This model, termed Histotyping, was then validated on n = 675 patients. Histotyping was compared to the Decipher genomic classifier in n = 167 patient subset. Decipher consists of 22 RNA-expression-based genomic markers that are involved in prostate cancer pathogenesis and have been validated for prognosis of metastasis18 and BCR20,21.
Robustness of Histotyping to site-specific effects
The results of UMAP embedding of the validation set are shown in Fig. 1. While the images from each site tended to segregate in the image-metric embedding, no site formed a distinct cluster in the Histotyping feature space. This suggests that the pathology images varied considerably in brightness, staining, and contrast across the sites, however, the Histotyping features were not adversely affected by variations in staining or scanning across the different laboratories.
Robustness of Histotyping to annotation perturbations
The concordance-index (c-index) of Histotyping remained nearly constant as boundary layers were removed from the annotations (Fig. 2), though 6% of patients had a different risk category when removing a single boundary layer, rising to 11% at three boundary layers. This suggests that Histotyping’s overall performance was relatively consistent across changes in the manually selected region of interest. However, additional study is needed on automated slide and tumor region selection, as well as approaches for aggregating Histotyping feature measurements across multiple cancer foci.
The prognostic power of histotyping
Histotyping was significantly prognostic of BCR in the training (p < 0.001, HR = 2.64, 95% confidence interval [CI]: 1.56–4.44, c-index = 0.63) and validation (p < 0.001, HR = 2.83, 95% CI: 2.03–3.93, c-index = 0.68) sets. The features selected by the Cox regression model on the training set are shown in Table 1 and consist of five measures of lumen shape and one feature of lumen arrangement. Histotyping results in each site of the validation cohort are shown in Fig. 3. While there was a separation between Histotyping low-risk and high-risk patients in all five sites, this separation was not significant in the UTurku and MS cohorts, a result potentially influenced by the small number of patients in these sets, with just 48 and 22 patients, respectively.
As shown in Fig. 4, Histotyping was prognostic in patients with (a) Gleason grade group 3 (HR = 4.09) and (b) negative surgical margins (HR = 3.26). In total, 15 clinically stratified groups were tested (low and high age, preoperative PSA, tumor stage, positive and negative surgical margins, patient Caucasian-American and African-American race, and each Gleason grade group). Bonferroni correction for multiple hypothesis testing yielded a corrected significance threshold of 0.05/15 = 0.0033. The Gleason grade group 3 and negative surgical margin subcohorts had p-values below this threshold, as did all other cohorts with the exception of some Gleason grade groups. Results in every subcohort are available in the supplementary information. Histotyping was prognostic independent of common clinical markers both as a continuous score (p = 0.002, HR = 1.17, 95% CI: 1.06–1.28) and as a categorical low/high-risk grouping (p < 0.001, HR = 2.09, 95% CI: 1.40–3.10), shown in Table 2.
For the n = 167 patients who had Decipher score information, to compare Decipher to Histotyping categorically, Decipher low-risk and intermediate-risk patients were grouped together as these groups did not have significantly different BCR-free survival (p = 0.14). Histotyping (p = 0.005, HR = 2.60, 95% CI: 1.41-4.81, c-index = 0.68, 95% CI: 0.59–0.74) performed slightly worse than Decipher (p < 0.001, HR=2.73, 95% CI: 1.38-5.41, c-index = 0.70, 95% CI: 0.61–0.78), as shown in Fig. 5. Histotyping+ surpassed Histotyping alone and Decipher (p < 0.001, HR = 3.77, 95% CI: 2.04–6.96, c-index = 0.75, 95% CI: 0.69–0.81) using five covariates selected by the model: Histotyping score, pre-operative PSA, and pathological Gleason grade groups 3, 4, and 5 (relative to 1). Though the 95% CIs of Histotyping+ and Decipher overlapped, Histotyping+ had the higher c-index in 81% of bootstrap iterations and the narrower 95% CI. In addition, Histotyping+ had a significantly higher c-index than Decipher in the bootstrap iterations (p < 0.001). In the validation set overall, Histotyping+ (c-index = 0.74) also outperformed a model using only pre-operative PSA and Gleason grade group (c-index = 0.72), as well as Gleason grade group (c-index = 0.69) and pre-operative PSA (c-index = 0.69) individually.
Figure 1d shows an overlay of the corresponding Gleason grade group for each patient in the validation set within the UMAP embedding of the Histotyping features. As may be observed, higher Gleason grade group patients were more likely to be Histotyping high-risk. However, the concordance between Gleason grade groups and Histotyping-determined low- and high-risk patients appears to be weak to moderate at best (Pearson correlation coefficient = 0.37), in turn suggesting that Histotyping is capturing morphologic attributes at least partially complementary to Gleason grade.
Accurate post-surgery prostate cancer (PCa) biochemical recurrence (BCR) prognosis has substantial implications for patient care and healthcare utilization. While the STAMPEDE trial13 has demonstrated that adjuvant therapy can improve patient survival after radical prostatectomy (RP), not every patient will benefit from further treatment. It is possible that the use of a companion diagnostic to direct adjuvant therapy only to high-risk patients would have resulted in a larger benefit in the STAMPEDE trial22. However, there is a shortage of accurate prognostic tools for the post-RP setting. Based on current adjuvant therapy guidelines, the number needed to treat to prevent one death related to PCa is 1023. Existing BCR prognosis tools, nomograms, are driven by Gleason grading, which is limited by the power of human perception and has only moderate inter-reviewer agreement3. Accordingly, there has been an increasing awareness of the need for an objective and accurate BCR prognosis tool.
Genomic assays, such as the Decipher genomic test, have been validated for post-RP metastasis16 and BCR20,21 prognosis, but consume the tested tissue. While most RP specimens have an abundance of tissue, this requirement prohibits performing multiple tests on the same sample. In small tumors, the tumor tissue could be exhausted by repeated testing. In addition, molecular testing protocols are expensive and sophisticated, reducing their availability. These limitations make it infeasible to perform genomic testing on all the cancerous tissue in an RP specimen.
Recently, quantitative histomorphometric (QH) approaches have been proposed as a complement to molecular assays. While some work has linked QH features to PCa disease-free survival24, much of the literature has focused on automated Gleason grading and cancer detection25,26,27,28,29,30. In this work, we presented a QH-based assay, termed Histotyping, for post-RP PCa risk assessment. Histotyping uses an H&E slide and handcrafted features of gland morphology. Deep learning, in which a model maps images directly to labels with no other guidance, has been used in a range of digital pathology applications, including PCa grading28,29,30, microsatellite instability prediction31, and mutation prediction32. While deep learning approaches have produced promising results, their black-box nature means that model decisions are not always readily explainable or related to known pathological features. Histotyping leverages deep learning for lumen segmentation, from which handcrafted features are extracted. Since each feature in Histotyping is human interpretable, it is possible to scrutinize the model’s decisions and verify that Histotyping is properly quantifying tumor morphology.
Histotyping was prognostic of post-RP BCR-free survival in the validation cohort independent of common clinical markers, both as a continuous score and categorical low/high-risk division. This evaluation mirrors the design used to validate the Decipher genomic test16. Histotyping’s hazard ratio (HR) of 2.83 was similar to gold-standard nomograms (HR = 1.09–2.74)33. Histotyping+, incorporating Histotyping, Gleason grade group, and preoperative prostate-specific antigen level, had a higher concordance index than Histotyping alone and Decipher. The difference in performance between Histotyping+ and Decipher was significant, though the overlapping 95% confidence intervals of these models suggest that further study with a larger cohort may be necessary to increase confidence with regard to the degree of prognostic performance improvement. Histotyping added value in two cohorts which would be low-risk or intermediate-risk by current methods: patients with Gleason grade group 3 and those with negative surgical margins. This suggests Histotyping is able to identify patients at risk of BCR who would not be likely to be recommended for additional therapy under current schemes. Histotyping may be especially suitable for identifying high-risk patients with lower-risk clinical markers due to the lower hazard associated with additional adjuvant therapy versus de-intensifying therapy for clinically high-risk patients.
Of the six features selected for Histotyping, all but one were gland lumen shape descriptors. These findings suggest that, in addition to the overall appearance of the glands, the variation in lumen shape and architecture across a tumor is related to PCa aggressiveness. Specifically, a greater proportion of disk-shaped lumen within a tumor was associated with elevated BCR risk, and that the mixing of these disk-shaped lumens with elongated elliptical or crescent-shaped lumens further increased risk. The other features indicate that higher variation in gland density across the tumor carried a higher risk of BCR. The biological rationale for these features is further described in the supplementary material. These features were found to be stable across sites, despite the images being clearly affected by site-specific factors and batch effects.
These findings are consistent with other studies which have found that lumen shape, disorder, and texture features are useful for cancer detection25,34, grading25,26,27, and BCR prognosis6,24. However, previous work in this area has used a lower proportion of shape features, potentially because these studies did not consider inter-site feature instability. It is possible that studies using unstable features would have worse results on independent validation sets, as was found in Leo et al.27.
The performance of Histotyping suggests that morphology alone, from a single lesion on a single slide, has prognostic power comparable to gold-standard methods. The finding that gland lumen shape and architecture is correlated with BCR risk is not surprising, as the Gleason scoring method is based on similar features analyzed by a human pathologist2. In contrast to existing companion diagnostics, Histotyping requires only a routinely acquired diagnostic H&E slide, a whole-slide scanner, and a typical desktop computer.
A limitation to this study was that metastasis outcome was not available for these patients. While Decipher has been validated for BCR prognosis20,21, it was calibrated for metastasis18. A further limitation of Histotyping, shared by all existing PCa companion diagnostics, is that it has not been validated for treatment response prediction. Future work may include comparing Decipher and Histotyping in metastasis prognosis and in biopsy specimens where tissue for pathological and molecular analysis is more limited.
In addition, Histotyping relies on a pathologist for the selection of a slide and tumor region containing the most aggressive cancer, though this could be automated in future work and the results of the annotation modification experiment suggest that Histotyping is relatively robust to inter-reader disagreement in tumor boundary delineation. Directly testing the effect of inter-reviewer variation in slide and lesion selection and attempting to automate this process could be an avenue for future work. A single diagnostic slide was used here due to the prohibitive expense of locating and scanning all patient slides. While Histotyping examines only a sample of the overall tumor, far more tissue is interrogated than in molecular tests performed on tissue cores, which also rely on manual identification.
Though the multi-site validation included a variety of scanners, the effect of different scanners was not explicitly examined beyond the feature stability filtering used to mitigate such effects, a method shown to be effective in previous work27,35,36. In a related point, one-third of the training set (70 of 214 patients) was composed of patients from the University of Pennsylvania (UPenn). While these patients were collected separately and scanned on a different scanner compared to the UPenn patients in the validation set, there was some institutional overlap between the training and validation sets, and the Decipher validation set was made up almost entirely of UPenn patients. While it was possible for this to result in an over-optimistic estimate of model performance, this concern is somewhat mitigated by Histotyping performing better on the NewYork Presbyterian Hospital/Weill Cornell Medical Center (HR = 4.22) and The Cancer Genome Atlas (HR = 10.50) cohorts than on the UPenn cohort (HR = 2.34). Finally, Histotyping was not significantly prognostic in some subsets, such as the University of Turku cohort and in Gleason grade groups other than 3, though it achieved a hazard ratio >1 and p < 0.10 in grade groups 1, 2, and 4.
In this work, we have demonstrated an automated method that can stratify patients by BCR risk using a single H&E slide with performance similar to that of the Decipher molecular companion diagnostic.
This study used n = 889 patients (Table 3) from six sources: University of Pennsylvania (UPenn), University Hospitals Cleveland Medical Center (UH), NewYork-Presbyterian Hospital/Weill Cornell Medical Center (WCM), University of Turku (UTurku), The Cancer Genome Atlas (TCGA)37, and the Icahn School of Medicine at Mount Sinai (MS). Patients were digitized on a variety of whole-slide scanners (Supplementary Table 1). TCGA patients with discrepancies in outcome information were excluded37. A training set was selected to include patients from multiple institutions totaling approximately a quarter of the dataset and contained n = 70 UPenn patients and n = 144 UH patients. The validation set consisted of the remaining n = 675 patients from five sites (UPenn, WCM, UTurku, TCGA, MS), with no training set patients included in the validation set. UPenn patients were split between training and validation sets based on the scanner used. This division is shown visually in Fig. 6. Data collection was approved by institutional review boards at each institution and conducted in accordance with U.S. Common Rule guidelines. Specimen Gleason grades were assigned by a genitourinary specialist pathologist for all patients, with the potential exception of TCGA patients, where particulars of the grading pathologist were not available. The requirement for written consent from patients was waived due to the retrospective nature of the study.
Inclusion criteria were a successfully digitized diagnostic slide, post-RP PSA test results for at least 30 days post-surgery, and no neo-adjuvant or adjuvant therapy. Patients were labeled BCR at the date of second PSA serum tests >0.2 ng/mL or censored at the date of the last available PSA test.
A subset of the validation set consisting of 145 UPenn and 22 MS patients had Decipher genomic classifier18 results available and were used to compare Histotyping to Decipher. These UPenn patients constituted a consecutive cohort operated on by a single surgeon.
The highest grade (for UTurku patients) or diagnostic (for all other sources) slide of each patient was digitized in a whole-slide scanner. Slide and tumor nodule used were determined by a genitourinary pathologist. A single representative cancerous region with at least 10 glands, selected to include the highest grade cancer on the slide, was annotated on each digital image. This mirrors the manual selection of a representative tissue block for molecular companion diagnostic tests38. One pathologist (X.F.) annotated the images from UTurku, a second pathologist (R.E.) annotated all other images. Training set images also had a representative non-cancerous region annotated for the feature stability filtering step of model training.
The Histotyping design workflow is shown in Fig. 7. Lumen were first segmented to enable feature extraction. This segmentation was performed by a UNet-inspired39 deep learning model. Images were resized to 1 micron-per-pixel (×10 magnification) resolution for this step. The model was trained on 41 1000 × 1000 pixel regions cropped from 37 training slides annotated for a total of 4927 gland lumens. On the four regions held out for testing, the model yielded a per-pixel true positive rate of 0.94, a true negative rate of 0.97, and an F1 score of 0.90. Segmentation was performed on all 889 images, and results were visually examined, with segmentations found to be sufficiently accurate for feature extraction.
A total of 242 features were extracted from the annotated tumor region on each slide, of which a subset of six was used in Histotyping. 216 features were descriptors of morphology and architecture extracted from lumen segmentation. 26 Haralick texture features were extracted from the tumor region, disregarding the segmentations. These features were selected based on their performance in PCa grading27 and BCR prognosis6.
All 242 features were subjected to filtering for stability across sites using the method of Leo et al.34 on the training set. Features that passed stability filtering were used to train a Cox regression model via 10-fold elastic-net regularization (α = 0.5)40. In this process, the set of features and their weights in the model were optimized by minimizing a penalty term consisting of both the model error in the training set and the sum of feature weights. This approach performs feature selection, by forcing the weights of some features to zero, and model fitting, by selecting the weights associated with the lowest error on the training set. Features were normalized using the training set to have a mean of 0 and standard deviation of 1 so that HRs would be comparable across features. The final model, containing six features, was then applied to all slides to obtain a risk score for each patient. A threshold was learned on the training set to stratify patients as low-risk or high-risk. The supplemental material includes details of the segmentation procedure, model framework, and extracted features.
Evaluating reproducibility of Histotyping
UMAP embedding41 was performed on the validation set to assess the inter-site variation between images prior to Histotyping analysis and to verify that Histotyping features were resilient to batch effects across multiple sites. Such sources of pre-analytic variation can arise from differences in specimen preparation and scanning between laboratories, are correlated with the site, and have been shown to degrade the performance of digital pathology analysis algorithms34,42,43. UMAP was used to reduce the feature space to two dimensions for evaluating the clustering between slides from different laboratories. If distinct clusters emerged in the UMAP space and those clusters corresponded to slides from a specific site, that would reflect the presence of site-specific attributes or batch effects. On the other hand, if the images from all sites were more homogeneously distributed in the UMAP space, it would suggest that the original set of features was resilient to the batch effects.
The UMAP embedding was performed on both the (1) original set of images and then (2) the set of Histotyping features from the same set of images. This was done to test the hypothesis that, though the input images exhibited site-specific effects and would cluster in the UMAP space, the features extracted for Histotyping were stable across sites. A digital pathology analysis tool, HistoQC42, was used to extract 29 quantitative metrics describing the brightness, contrast, color distribution, and stain intensities from the validation set images. A full list of metrics is available in the supplemental material. The embedding was repeated on the same set of images, but this time on the six features comprising Histotyping.
Simulating the effect of inter-reviewer variability in tumor annotation on Histotyping
To test the robustness of Histotyping to simulated inter-reviewer variation in tumor annotation, Histotyping analysis was rerun on each validation set image by iteratively perturbing and eroding the original tumor annotation. Since reader disagreement on the cancerous region was most likely to occur at the edges of the tumor, where cancerous glands begin to mix with non-cancerous ones, the outer layer of glands was removed from each annotation and the resulting Histotyping score was recalculated. This process was repeated 10 times on every validation set annotation, at which point a layer 10 glands thick had been removed from the original annotation (see Fig. 2). This simulated the effect of variation in pathologist annotation of tumor extent. The c-index of Histotyping and fraction of patients whose Histotyping risk category changed at each boundary layer removal was measured. If Histotyping was highly sensitive to the precise extent and annotation of the cancerous region, a large number of patients changing risk categories and steep drop-off in c-index would be observed.
Histotyping performance evaluation
The performance of Histotyping was evaluated in the validation set using the separation in BCR-free survival time between the low-risk and high-risk groups by logrank p-value, hazard ratio, and Harrell’s c-index. Model independence was evaluated in a Cox proportional hazards model with Histotyping risk score, Gleason grade group, margin positivity, pathological tumor stage, and preoperative PSA. Clinically stratified cohorts were analyzed separately to determine if Histotyping added value. Two such cohorts (Gleason grade group 3, margin negative) are discussed here, with further results in the supplemental material.
Comparison of Histotyping and decipher
Histotyping was compared to Decipher for BCR prognosis in the 167 patients of the validation set who had Decipher score information. Decipher scores were calculated based on the predefined 22-marker Decipher classifier18. The Decipher score is a score between 0 and 1, with lower scores indicating a lower risk of metastasis. Decipher categorizes patients as high-risk (Decipher score >0.60), intermediate-risk (0.45–0.60), or low-risk (<0.45).
In addition, a second elastic-net Cox model was constructed on the training set using the continuous Histotyping score, preoperative PSA level, and Gleason grade group to create the Histotyping+ model. These covariates were chosen as they were available in n = 148 training set patients, more than for any other set of covariates. Histotyping+ was compared to Decipher by c-index in the n = 167 patients of the Decipher validation set in absolute terms and in 1000 iterations of bootstrapping. The 95% CI of c-index was computed from these bootstrap iterations and a two-tailed t-test was used to test for a significant difference in the distributions. For low/high-risk stratification, a new decision threshold was chosen using the training set in the same process as for Histotyping.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The data generated and analyzed during this study are described in the following data record: https://doi.org/10.6084/m9.figshare.1422627844. The following files are openly available as part of this data record: the Histotyping scores of each patient in the training set (n = 214) in the file “training_set_HT_scores.xlsx”; the Histotyping scores of each validation set patients during successive boundary layer removals in the file “boundary_layer_data.xlsx’; image metrics, Histotyping scores, Histotyping+ scores, and UMAP components for each patient in the validation set in the file “HT_UMAP_supporting_data.xlsx”; ground truth masks and segmentation results on lumen segmentation model validation set images in the folder “gland_segmentations.zip”. The patient clinical data are contained in the Excel spreadsheet “patient_clinical_info.xlsx”. These data are not publicly available for the following reason: material transfer agreements from source hospitals do not allow public sharing of patient information. However, the data can be made available upon reasonable request to the corresponding author.
This study made use of publicly available code41,45,46, with in-house developed feature extraction code available at https://github.com/pjl54/matlab-feature-extraction.
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Research reported in this publication was supported by the National Cancer Institute under award numbers 1U24CA199374-01, R01CA249992-01A1 R01CA202752-01A1 R01CA208236-01A1 R01CA216579-01A1 R01CA220581-01A1 1U01CA239055-01 1U01CA248226-01 1U54CA254566-01 National Heart, Lung and Blood Institute 1R01HL15127701A1, National Institute for Biomedical Imaging and Bioengineering 1R43EB028736-01, National Center for Research Resources 1 C06 RR12463-01, VA Merit Review Award IBX004121A from the United States Department of Veterans Affairs Biomedical Laboratory Research and Development Service, the Office of the Assistant Secretary of Defense for Health Affairs, through the Breast Cancer Research Program (W81XWH-19-1-0668), the Prostate Cancer Research Program (W81XWH-15-1-0558, W81XWH-20-1-0851), the Lung Cancer Research Program (W81XWH-18-1-0440, W81XWH-20-1-0595), the Peer Reviewed Cancer Research Program (W81XWH-18-1-0404), the Kidney Precision Medicine Project Glue Grant, the Ohio Third Frontier Technology Validation Fund, the Department of Defense Prostate Cancer Disparity Award (W81XWH-19-1-0720), the Clinical and Translational Science Collaborative of Cleveland (UL1TR0002548) from the National Center for Advancing Translational Sciences (NCATS) component of the National Institutes of Health and NIH roadmap for Medical Research, The Wallace H. Coulter Foundation Program in the Department of Biomedical Engineering at Case Western Reserve University, the National Science Foundation Graduate Research Fellowship Program (CON501692), the Sigrid Jusélius Fellowship, and the Finnish Cancer Foundation. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health, the U.S. Department of Veterans Affairs, the Department of Defense, the National Science Foundation, or the United States Government.
A.J. has reported a consulting or advisory role with Merck. M.F. has reported consulting fees from Philips Digital Pathology. A.M. has reported being an equity holder in Elucid Bioimaging and in Inspirata Inc. In addition, he has served as a scientific advisory board member for Inspirata Inc, AstraZeneca, Bristol Meyers-Squibb, and Merck. Currently, he serves on the advisory board of Aiforia Inc. He also has sponsored research agreements with Philips, AstraZeneca, Boehringer-Ingelheim, and Bristol Meyers-Squibb. His technology has been licensed to Elucid Bioimaging. He is also involved in an NIH U24 grant with PathCore Inc, and 3 different R01 grants with Inspirata Inc. The remaining authors declare no competing interests.
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Leo, P., Janowczyk, A., Elliott, R. et al. Computer extracted gland features from H&E predicts prostate cancer recurrence comparably to a genomic companion diagnostic test: a large multi-site study. npj Precis. Onc. 5, 35 (2021). https://doi.org/10.1038/s41698-021-00174-3