Abstract
Objectives
To perform a systematic review of design and reporting of imaging studies applying convolutional neural network models for radiological cancer diagnosis.
Methods
A comprehensive search of PUBMED, EMBASE, MEDLINE and SCOPUS was performed for published studies applying convolutional neural network models to radiological cancer diagnosis from January 1, 2016, to August 1, 2020. Two independent reviewers measured compliance with the Checklist for Artificial Intelligence in Medical Imaging (CLAIM). Compliance was defined as the proportion of applicable CLAIM items satisfied.
Results
One hundred eighty-six of 655 screened studies were included. Many studies did not meet the criteria for current design and reporting guidelines. Twenty-seven percent of studies documented eligibility criteria for their data (50/186, 95% CI 21–34%), 31% reported demographics for their study population (58/186, 95% CI 25–39%) and 49% of studies assessed model performance on test data partitions (91/186, 95% CI 42–57%). Median CLAIM compliance was 0.40 (IQR 0.33–0.49). Compliance correlated positively with publication year (ρ = 0.15, p = .04) and journal H-index (ρ = 0.27, p < .001). Clinical journals demonstrated higher mean compliance than technical journals (0.44 vs. 0.37, p < .001).
Conclusions
Our findings highlight opportunities for improved design and reporting of convolutional neural network research for radiological cancer diagnosis.
Key Points
• Imaging studies applying convolutional neural networks (CNNs) for cancer diagnosis frequently omit key clinical information including eligibility criteria and population demographics.
• Fewer than half of imaging studies assessed model performance on explicitly unobserved test data partitions.
• Design and reporting standards have improved in CNN research for radiological cancer diagnosis, though many opportunities remain for further progress.
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Avoid common mistakes on your manuscript.
Introduction
Recent years have seen an increase in the volume of artificial intelligence (AI) research in the field of cancer imaging, prompting calls for appropriately rigorous design and appraisal standards [1,2,3,4,5,6]. Evaluation of AI research requires a skillset which is distinct from those of classical medical statistics and epidemiology. The problems of high dimensionality, overfitting and model generalisation are central challenges in AI modelling [7,8,9,10]. These phenomena potentially compromise the generalisation of AI models to the reality of clinical practice [11]. However, the reliability of these models may be estimated and maximised through rigorous experimental design and reporting [1, 12].
EQUATOR was founded to improve the quality of scientific research through standardisation of reporting guidelines [13, 14]. Established EQUATOR guidelines such as STARD [15], STROBE [16] and CONSORT [17] were not designed specifically to address the challenges of AI research. AI-focused guidelines have recently been developed including CLAIM [18], SPIRIT-AI [19], MI-CLAIM [20] and, prospectively, STARD-AI [21]. These are welcome measures as AI remains at an early phase of clinical implementation for diagnostic tasks. Although each set of reporting standards addresses a specific task, a high degree of overlap exists between these guidelines, reflecting the fundamental importance of many of the criteria.
CLAIM aims to promote clear, transparent and reproducible scientific communication about the application of AI to medical imaging and provides a framework to assure high-quality scientific reporting. Current conformity to these standards has not been formally quantified to date. Consequently, a need exists for a contemporary evaluation of design and reporting standards in the domain of cancer imaging AI research.
Following ImageNet 2012 [22], convolutional neural network (CNN) models have been adapted to various biomedical tasks. The approach is now the industry standard in AI applications for diagnostic radiology [23, 24]. In this study, we aim to quantify explicit satisfaction of the CLAIM criteria in recent studies applying CNNs to cancer imaging. We examine the adequacy of data and ground truth collection, model evaluation, result reporting, model interpretation, benchmarking and transparency in the field. We identify key areas for improvement in the design and reporting of CNN research in the field of diagnostic cancer imaging.
Materials and methods
Inclusion criteria
-
1.
The article evaluates a CNN model for radiological cancer diagnosis in humans.
-
2.
The model receives a radiological image as its sole input.
-
3.
The article was published in a peer-reviewed journal between January 1, 2016, and August 1, 2020.
-
4.
The article is published in the English language.
Exclusion criteria
-
1.
The model addresses a non-diagnostic task such as pre-processing, segmentation or genotyping.
-
2.
The model receives non-radiological images such as histopathology, dermoscopy, endoscopy or retinoscopy.
-
3.
The article presents experiments on animal or synthetic data.
-
4.
The article primarily addresses economic aspects of model implementation.
-
5.
The article is published in a low-impact journal.
-
6.
The article is unavailable in full-text format.
Search
PubMed, EMBASE, MEDLINE and SCOPUS databases were searched systematically for original articles from January 1, 2016, to August 14, 2020, for articles meeting our inclusion and exclusion criteria. Search queries for each database are included in the supplementary material. The search was performed on August 14, 2020. No other sources were used to identify articles. Screening and decisions regarding inclusion based on the full text were performed independently by 2 reviewers (R.O.S., A.S., clinical fellows with 3 years and 1 year of experience of AI research, respectively) and disagreements resolved by consensus. A senior reviewer (V.G.) was available to provide a final decision on unresolved disagreements. Duplicated articles were removed. Articles were not screened with the QUADAS tool [25], as it shares several items with the CLAIM guideline. Exclusion of QUADAS-incompliant articles would have biased subsequent estimations of CLAIM compliance.
Data extraction
Data items were defined to measure compliance with CLAIM proposal and previously published proposals [1, 18]. Complex items with multiple conditions were subdivided as appropriate. Data items are listed in Table 1. First author, journal, publication year, modality and body system were also extracted. Studies which served to validate existing models were exempt from all items pertaining to model development. Studies not employing model ensembling were exempt from item 27.
Articles were read and annotated by R.O.S. and A.S., and disagreements were resolved by consensus. Articles were read in random order, using a fixed sequence generated in R [26]. Journal H-index was extracted from the Scimago journal rankings database [27]. Journals were categorised as either “clinical” or “technical” according to the journal name—names containing any term related to computer science, artificial intelligence or machine learning were assigned the “technical” category. The remaining journals were assigned the “clinical” category.
Data analysis
Statistical analysis was conducted using R version 3.5.3 [26] and RStudio version 1.1.463 [28]. For each item, the proportion of compliant studies was measured, excluding those with applicable exemptions. For items with ≥ 3 response categories, proportions were also measured for each category. Ninety-five percent confidence intervals (95% CI) were estimated around binary proportions using the method of Clopper and Pearson [29] and around multinomial proportions using the method of Sison and Glaz [30, 31]. Following adherence assessment recommendations [32], an overall CLAIM compliance score was defined per article by the proportion of applicable items satisfied. Items and subitems were weighted equally.
Temporal change in CLAIM compliance was evaluated by two-sided test of Spearman rank correlation between CLAIM score and year of publication. Association between journal impact factor and compliance was evaluated with a two-sided test of Spearman rank correlation between journal H-index and CLAIM score. The difference in mean CLAIM compliance between clinical and technical journals was evaluated with a two-sided t test. All code and data required to support the findings of this research are available from the corresponding author upon request. As a methodological review assessing study reporting, this study was not eligible for registration with the PROSPERO database.
Results
Search
Six hundred fifty-five articles were identified in the primary database search, of which 267 were duplicates. One hundred twenty articles were excluded during title screen, and 82 articles were excluded during abstract screening. One hundred eighty-six articles were included in the final analysis. A flow diagram for the literature search process is provided in Fig. 1. The dataset included articles from 106 journals. Fifty-four clinical journals and 44 technical journals were included. Assigned journal categories are provided in Supplementary Table 1. The distributions of article publication year, body system and modality for are provided in Fig. 2.
Title, abstract and introduction
Compliance for items 1–13 is shown in Fig. 3. Ninety-one percent of studies identified their model as a convolutional neural network (170/186, 95% CI 86–95%) and 70% presented a structured abstract (131/186, 95% CI 63–77%). Ninety-eight percent included scientific and clinical background (183/186, 95% CI 95–100%). Although 92% of studies stated objectives (171/186, 95% CI 87–95%), only 4% included explicit hypotheses (8/186, 95% CI 2–8%).
Study design
Thirty-three percent of studies documented a retrospective or prospective timeframe (62/186, 95% CI 27–41%). Of these, 87% were retrospective (54/62, 95% CI 81–95%), 10% were prospective (6/62, 95% CI 3–18%) and 3% used both retrospective and prospective data (2/62, 95% CI 0–11%). Twenty-five percent of studies specified a goal (47/186, 95% CI 19–32%).
Data
Ninety-four percent of studies documented their data sources (174/186, 95% CI 89–97%). Of these, 45% used publicly available datasets only (79/174, 95% CI 38–53%), 49% used local data only (85/174, 95% CI 41–57%) and 6% combined public datasets with locally collected data (10/174, 95% CI 0–14%). Seventy-two percent of studies documented the centres from which the data was sourced (134/185, 95% CI 65–79%). Of these, 50% used data from multiple centres (67/135, 95% CI 41–58%). Fifty-one percent of studies detailed the imaging equipment used (94/186, 95% CI 43–58%). Of these, 53% employed equipment from multiple vendors (50/94, 95% CI 43–64%). Image acquisition parameters were documented in 37% of studies (69/186, 95% CI 30–44%). Amongst studies which collected local data, 83% documented institutional review board approval (79/95, 95% CI 74–90%) and 26% documented participant consent (25/95, 95% CI 18–36%). In studies of publicly available data, 9% documented institutional review board approval (7/79, 95% CI 4–17%) and 8% documented participant consent (6/79, 95% CI 3–16%). Twenty-seven percent of studies documented eligibility criteria for their data (50/186, 95% CI 21–34%).
Pre-processing was documented in 69% of studies (128/186, 95% CI 62–75%), though only 53% provided a reproducible methodology (98/186, 95% CI 46–60%). Data subsetting was applied in 42% of studies (78/186, 95% CI 35–49%), of which 95% included methods (74/78, 95% CI 87–99%). As per our inclusion criteria, all studies employed convolutional neural network models, which define predictor features autonomously. We also required an outcome in the domain of radiological cancer diagnosis. Therefore, relevant data elements were defined in 100% of included studies (186/186, 95% CI 98–100%). Nineteen percent of studies performing local data collection documented data anonymisation (18/95, 95% CI 12–28%), though only 3% detailed the methodology (3/95, 95% CI 0–11%). Eighty-four percent of studies performing local data collection documented data anonymisation, institutional review board approval or both (80/95, 95% CI 75–91%). Three percent of studies of publicly available data documented data anonymisation (3/91, 95% CI 1–9%), and none detailed the methodology. Missing data procedures were documented in 17% of studies (31/186, 95% CI 12–23%). Case exclusion was the only strategy employed to manage missing data in these studies (31/31, 95% CI 89–100%).
Ground truth
Compliance for items 14–27 is shown in Fig. 4. Twenty-five percent of studies defined the reference standard or used a Common Data Element such as the American College of Radiology Reporting and Data Systems (46/186, 95% CI 19–32%). Three percent of studies provided rationale for the reference standard (5/186, 95% CI 1–6%). However, 50% employed definitive clinical standards such as histopathology, case follow-up or definitive imaging modalities (93/186, 95% CI 43–57%). Of these, 77% used histopathology (72/93, 95% CI 70–86%), 15% used histopathology in combination with follow-up imaging (14/93, 95% CI 8–23%) and 2% used histopathology in combination with definitive imaging (2/93, 95% CI 0–10%). Four percent used follow-up only (14/93, 95% CI 8–23%), and 1% used definitive imaging only (1/93, 95% CI 0–9%).
Forty percent of studies documented image annotation by a radiologist with relevant subspecialist expertise (75/186, 95% CI 33–48%). A further 32% documented annotation by a radiologist with unspecified expertise (60/186, 95% CI 25–40%) and 4% used other clinicians (8/186, 95% CI 0–12%). Of the studies which utilised histopathological ground truth, 8% specified annotation by a pathologist with relevant subspecialist experience (7/88, 95% CI 3–16%). Twelve percent of studies documented the software tools used for image annotation (22/186, 95% CI 8–17%). Eighteen percent of studies provided inter-rater or intra-rater variability statistics (34/186, 95% CI 13–25%), and 27% provided their aggregation strategy (50/186, 95% CI 21–34%), though only 16% provided both (30/186, 95% CI 11–22%).
Data partitions
Eighty-seven percent of studies reported the number of images modelled (161/186, 95% CI 81–91%), though only 1% provided a power calculation (1/186, 95% CI 0–3%). Seventy-two percent specified the number of study participants in their dataset (133/186, 95% CI 64–78%). Of these, a median of 367 participants were included (IQR 172–1000). Seven studies served only to validate existing models and were exempted from criteria pertaining to model development and data partitioning. Seventy-six percent of modelling studies defined data partitions and their proportions (136/179, 95% CI 69–82%), though 32% specified the level of partition disjunction (58/179, 95% CI 26–40%).
Model
Sixty-six percent of modelling studies provided a detailed model description (119/179, 95% CI 59–73%) and 20% of modelling studies provided access to source code (35/179, 95% CI 14–26%). Sixty-eight percent documented the development software (122/179, 95% CI 61–75%), though only 41% included the software version (74/179, 95% CI 34–49%). Sixty-eight percent of modelling studies reported model initialisation parameters (122/179, 95% CI 61–75%). Of these, 52% employed transfer learning (93/179, 95% CI 44–59%) and 3% compared transfer learning with random initialisation (4/124, 95% CI 1–8%).
Training
Sixty-five percent of modelling studies reported data augmentation (117/179, 95% CI 58–72%), though only 54% documented reproducible methodology (96/179, 95% CI 46–61%). Sixty-one percent of modelling studies documented the optimisation algorithm (109/179, 95% CI 53–68%), 61% documented learning rate (110/179, 95% CI 54–69%), 44% documented loss function (78/179, 95% CI 36–51%) and 52% documented batch size (93/179, 95% CI 44–59%). Model selection strategies were documented in 69% of modelling studies (123/179, 95% CI 61–75%). Of 30 studies which employed model ensembling, 93% reported their aggregation methodology (28/30, 95% CI 78–99%).
Evaluation
Compliance with CLAIM items 28–42 is shown in Fig. 5. Fifty-five percent of studies defined performance metrics (103/186, 95% CI 48–63%) and 36% provided some rationale for these (67/186, 95% CI 29–43%). Statistical significance of results was reported with methodology in 61% of studies (114/186, 95% CI 54–68%) and without methodology in 97% (181/186, 95% CI 94–99%). Twelve percent of studies evaluated model robustness (22/186, 95% CI 8–17%). Although 25% of studies attempted some interpretation of the model (47/186, 95% CI 19–32%), only 9% provided validated methodology for their procedure (17/186, 95% CI 5–14%).
Forty-nine percent of studies assessed model performance on test data which was explicitly disjunct from training and validation data (91/186, 95% CI 42–57%). Forty-five percent of studies mentioned only two data partitions (83/186, 95% CI 38–53%); their reported results may have represented validation rather than test performance. A further 6% failed to document any data partitions (12/186, 95% CI 0–14%); their reported results may have represented training performance. Forty-one percent of studies benchmarked models against other computational methods (77/186, 95% CI 34–49%). Seventeen percent of studies benchmarked their model against radiologists with relevant subspecialist expertise (31/186, 95% CI 11–23%). Five percent of studies benchmarked their model against radiologists without specifying expertise (9/186, 95% CI 0–11%) and 1% employed other clinicians (1/186, 95% CI 0–7%).
Results
Case flow diagrams were provided in 8% of studies (14/186, 95% CI 4–12%). Thirty-one percent of studies reported demographic and clinical characteristics of their population (58/186, 95% CI 25–38%). However, only 10% described separate distributions for each data partition (18/186, 95% CI 6–15%). Fifteen percent of studies reported performance metrics on test data from another institution (28/186, 95% CI 8–23%). Thirty-four percent used test data from the same institution (63/186, 95% CI 27–41%). Diagnostic accuracy was reported with confidence intervals in 40% of studies (75/186, 95% CI 33–48%). Twenty-four percent of studies discussed misclassified examples (44/186, 95% CI 18–30%).
Discussion
Forty-six percent of studies discussed limitations (85/186, 95% CI 38–53%) and 37% clinical implications of their findings (69/186, 95% CI 30–44%).
Other information
Study registration numbers were provided in 7% of studies (13/186, 95% CI 3.8–11.7%), and study protocols in 1% (2/186, 95% CI 0.1–3.8%). Funding was documented in 65% of studies (121/186, 95% CI 57.7–71.9%) though only 3% included the role of the funding institution (6/186, 95% CI 0.0–10.9%). A further 6% of studies stated that they did not receive funding (12/186, 95% CI 0.0–14.1%). Compliance for items 1–42 is provided in Supplementary Table 3.
Overall CLAIM compliance
Median CLAIM compliance was 0.40 (IQR 0.33–0.49). Compliance correlated positively with publication year (ρ = 0.15, p = .04) and journal H-index (ρ = 0.27, p < .001). Clinical journals demonstrated higher mean compliance than technical journals (0.44 vs. 0.37, p < .001). Compliance distribution is visualised with respect to publication year, journal H-index and journal category in Fig. 6.
Discussion
Radiological AI is undergoing a development phase, reflected in growing annual publication volume and recognition by clinical researchers [33,34,35,36,37]. To safely harness the potential of new methodologies, clinicians have called for realistic, reproducible and ethical research practices [1, 38,39,40,41,42,43,44]. The CLAIM guidance sets stringent standards for research in this domain, amalgamating the technical requirements of the statistical learning field [9, 45] with the practicalities of clinical research [1, 2, 15, 46]. We observed improvements in documentation standards improved over time, a finding concurrent with previous reviews of AI research [43, 45]. Compliance was highest in impactful clinical journals, demonstrating the value of design and reporting practices at peer review.
A key opportunity for improvement is model testing, addressed by items 20, 21, 32 and 35. Documentation should specify three disjoint data partitions for CNN modelling (which may be resampled with cross-validation or bootstrapping). Training data is used for model learning, validation data for model selection and test data to assess performance of a finalised model [47, 48]. Half of studies documented two or less partitions—in these cases, results may have represented validation or even training performance. Where data partitions were not disjoint on per-patient basis, data leakage may have occurred despite partitioned model testing. These scenarios bias generalisability metrics optimistically. Some multi-centre studies partitioned data at the patient level rather than the institutional level, missing an opportunity to evaluate inter-institution generalisability.
Evidently, CLAIM has also introduced requirements which depart from current norms. Few studies satisfied item 12, which requires the documentation of data anonymisation methods, an issue which has developed with image recognition capabilities [41, 49, 50]. This requirement may have previously been relaxed for studies of publicly available data or those which documented institutional review board approval, as either case suggests previous certification of data governance procedures. The spirit of the CLAIM guidance is obviation of such assumptions with clear documentation, promoting a culture of research transparency. In many such cases, the burden of improved compliance is minimal, mandating only the documentation of additional information.
Our findings concur with previous reviews of design and reporting standards in both clinical and general-purpose AI research. A review of studies benchmarking AI against radiologists identified deficient documentation of data availability, source code, eligibility and study setting [38]. Reviews of TRIPOD adherence in multivariate diagnostic modelling found deficient model assessment and data description [12, 51, 52]. Reviews of reproducibility in AI research have reported insufficient documentation of data availability, source code, protocols and study registration [43, 45, 53]. Many commentators have advocated for transparency in clinical AI research [19, 38, 40, 42, 43, 53, 54].
We note several limitations to this systematic review. First, as scope was limited to studies published in English, findings were susceptible to language bias. Second, although reporting standards were directly measurable, items relating to study design were only measurable if reported. Consequently, design compliance may have been underestimated in poorly reported studies. This is a general limitation of reviews in this field. Third, articles were read sequentially and therefore readers were potentially susceptible to anchoring bias. The effect of anchoring on the trend and subgroup analyses was minimised by randomisation of the reading order.
Conclusions
Design and reporting standards have improved in CNN research for radiological cancer diagnosis, though many opportunities remain for further progress. The CLAIM guidance sets a high standard for this developing field, consolidating clinical and technical research requirements to enhance the quality of evidence. Our data supports the need for integration of CLAIM guidance into the design and reporting of CNN studies for radiological cancer diagnosis.
Abbreviations
- AI:
-
Artificial intelligence
- CLAIM:
-
Checklist for AI in Medical Imaging
- CNN:
-
Convolutional neural network
- CONSORT:
-
Consolidated Standards of Reporting Trials
- EQUATOR:
-
Enhancing the Quality and Transparency Of health Research
- IQR:
-
Interquartile range
- MI-CLAIM:
-
Minimum Information about Clinical Artificial Intelligence Modelling
- PRISMA:
-
Preferred Reporting Items for Systematic reviews and Meta-Analyses
- QUADAS:
-
Quality Assessment Tool for Diagnostic Accuracy Studies
- SPIRIT-AI:
-
Standard Protocol Items: Recommendations for Interventional Trials-Artificial Intelligence extension
- STARD:
-
Standards for Reporting of Diagnostic Accuracy Studies
- STARD-AI:
-
Standards for Reporting of Diagnostic Accuracy Studies - Artificial Intelligence extension
- STROBE:
-
Reporting of Observational studies in Epidemiology
References
Bluemke DA, Moy L, Bredella MA et al (2019) Assessing radiology research on artificial intelligence: a brief guide for authors, reviewers, and readers-from the Radiology Editorial Board. Radiology:192515. https://doi.org/10.1148/radiol.2019192515
Bi WL, Hosny A, Schabath MB et al (2019) Artificial intelligence in cancer imaging: clinical challenges and applications. CA Cancer J Clin 69:127–157. https://doi.org/10.3322/caac.21552
Mendelson EB (2019) Artificial intelligence in breast imaging: potentials and limitations. AJR Am J Roentgenol 212:293–299
Gilbert FJ, Smye SW, Schönlieb CB (2020) Artificial intelligence in clinical imaging: a health system approach. Clin Radiol 75:3–6
O’Regan DP (2020) Putting machine learning into motion: applications in cardiovascular imaging. Clin Radiol 75:33–37
Liu X, Faes L, Kale AU et al (2019) A comparison of deep learning performance against health-care professionals in detecting diseases from medical imaging: a systematic review and meta-analysis. Lancet Digit Health 1:e271–e297. https://doi.org/10.1016/S2589-7500(19)30123-2
Lecun Y, Bengio Y, Hinton G (2015) Deep learning. Nature 521:436–444
Erickson BJ, Korfiatis P, Kline TL et al (2018) Deep learning in radiology: does one size fit all? J Am Coll Radiol 15:521–526. https://doi.org/10.1016/j.jacr.2017.12.027
Cawley GC, Talbot NLC (2010) On over-fitting in model selection and subsequent selection bias in performance evaluation. J Mach Learn Res 11:2079–2107
Yasaka K, Akai H, Kunimatsu A et al (2018) Deep learning with convolutional neural network in radiology. Jpn J Radiol 36:257–272
Kelly CJ, Karthikesalingam A, Suleyman M et al (2019) Key challenges for delivering clinical impact with artificial intelligence. BMC Med 17:195. https://doi.org/10.1186/s12916-019-1426-2
Yusuf M, Atal I, Li J et al (2020) Reporting quality of studies using machine learning models for medical diagnosis: a systematic review. BMJ Open 10:e034568. https://doi.org/10.1136/bmjopen-2019-034568
Simera I, Altman DG, Moher D et al (2008) Guidelines for reporting health research: the EQUATOR network’s survey of guideline authors. PLoS Med 5:0869–0874. https://doi.org/10.1371/journal.pmed.0050139
Pandis N, Fedorowicz Z (2011) The international EQUATOR network: enhancing the quality and transparency of health care research. J Appl Oral Sci:19. https://doi.org/10.1590/S1678-77572011000500001
Bossuyt PM, Reitsma JB, Bruns DE et al (2015) STARD 2015: an updated list of essential items for reporting diagnostic accuracy studies1. Radiology 277:826–832. https://doi.org/10.1148/radiol.2015151516
Vandenbroucke JP, Von Elm E, Altman DG et al (2007) Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration. PLoS Med 4:1628–1654. https://doi.org/10.1371/journal.pmed.0040297
Schulz KF, Altman DG, Moher D (2010) CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. BMJ 340:698–702. https://doi.org/10.1136/bmj.c332
Mongan J, Moy L, Kahn CE (2020) Checklist for Artificial Intelligence in Medical Imaging (CLAIM): a guide for authors and reviewers. Radiol Artif Intell 2:e200029. https://doi.org/10.1148/ryai.2020200029
Rivera SC, Liu X, Chan A-W et al (2020) Consensus statement Guidelines for clinical trial protocols for interventions involving artificial intelligence: the SPIRIT-AI extension The SPIRIT-AI and CONSORT-AI Working Group*, SPIRIT-AI and CONSORT-AI Steering Group and SPIRIT-AI and CONSORT-AI Cons. Nat Med 26:1351–1363. https://doi.org/10.1038/s41591-020-1037-7
Norgeot B, Quer G, Beaulieu-jones BK et al (2020) Minimum information about clinical artificial intelligence modeling: the MI-CLAIM checklist. Nat Med 26. https://doi.org/10.1038/s41591-020-1042-x
Sounderajah V, Ashrafian H, Aggarwal R et al (2020) Developing specific reporting guidelines for diagnostic accuracy studies assessing AI interventions: The STARD-AI Steering Group. Nat Med 26:807–808. https://doi.org/10.1038/s41591-020-0941-1
Hinton GE, Srivastava N, Krizhevsky A, Sutskever I, Salakhutdinov RR (2012) Improving neural networks by preventing co-adaptation of feature detectors. arXiv:12070580v1
Soffer S, Ben-Cohen A, Shimon O et al (2019) Convolutional neural networks for radiologic images: a radiologist’s guide. Radiology 290:590–606
Litjens G, Kooi T, Bejnordi BE et al (2017) A survey on deep learning in medical image analysis. Med Image Anal 42:60–88
Whiting P, Rutjes AWS, Reitsma JB et al (2003) The development of QUADAS: a tool for the quality assessment of studies of diagnostic accuracy included in systematic reviews. BMC Med Res Methodol 3:1–13
Team R Development Core (2019) A language and environment for statistical computing. R Found Stat Comput 2. https://www.R-project.org
SCImago (n.d.). SJR — SCImago Journal & Country Rank [Portal]. Retrieved from http://www.scimagojr.com/. Accessed 14 Dec 2020
RStudio Team (2020) RStudio: integrated development for R. Version 1.1.463. http://www.rstudio.com/
Clopper CJ, Pearson ES (1934) The use of confidence or fiducial limits illustrated in the case of the binomial. Biometrika 26:404. https://doi.org/10.2307/2331986
Sison CP, Glaz J (1995) Simultaneous confidence intervals and sample size determination for multinomial proportions. J Am Stat Assoc 90:366–369. https://doi.org/10.1080/01621459.1995.10476521
Signorell A et al. (2020) DescTools: Tools for Descriptive Statistics. R package version 0.99.37. https://cloud.rproject.org/web/packages/DescTools/citation.html
Heus P, Damen JAAG, Pajouheshnia R et al (2019) Uniformity in measuring adherence to reporting guidelines: the example of TRIPOD for assessing completeness of reporting of prediction model studies. BMJ Open 9. https://doi.org/10.1136/bmjopen-2018-025611
Recht MP, Dewey M, Dreyer K et al (2020) Integrating artificial intelligence into the clinical practice of radiology: challenges and recommendations. Eur Radiol:1–9. https://doi.org/10.1007/s00330-020-06672-5
Hosny A, Parmar C, Quackenbush J et al (2018) Artificial intelligence in radiology. Nat Rev Cancer 18:500–510. https://doi.org/10.1038/s41568-018-0016-5
Killock D (2020) AI outperforms radiologists in mammographic screening. Nat Rev Clin Oncol 17:134. https://doi.org/10.1038/s41571-020-0329-7
Bluemke DA (2018) Radiology in 2018: are you working with AI or being replaced by AI? Radiology 287:365–366
Davenport T, Kalakota R (2019) The potential for artificial intelligence in healthcare. Future Healthc J 6:94–98. https://doi.org/10.7861/futurehosp.6-2-94
Nagendran M, Chen Y, Lovejoy CA et al (2020) Artificial intelligence versus clinicians: systematic review of design, reporting standards, and claims of deep learning studies in medical imaging. BMJ 368:m689. https://doi.org/10.1136/bmj.m689
Kitamura FC, Pan I, Kline TL (2020) Reproducible artificial intelligence research requires open communication of complete source code. Radiol Artif Intell 2:e200060. https://doi.org/10.1148/ryai.2020200060
Geis JR, Brady AP, Wu CC et al (2019) Ethics of artificial intelligence in radiology: summary of the joint European and North American multisociety statement. J Am Coll Radiol 16:1516–1521. https://doi.org/10.1016/j.jacr.2019.07.028
Jaremko JL, Azar M, Bromwich R et al (2019) Canadian Association of Radiologists white paper on ethical and legal issues related to artificial intelligence in radiology. Can Assoc Radiol J 70:107–118. https://doi.org/10.1016/j.carj.2019.03.001
Haibe-Kains B, Adam GA, Hosny A et al (2020) Transparency and reproducibility in artificial intelligence. Nature 586:E14–E16. https://doi.org/10.1038/s41586-020-2766-y
Wallach JD, Boyack KW, Ioannidis JPA (2018) Reproducible research practices, transparency, and open access data in the biomedical literature, 2015–2017. PLoS Biol 16. https://doi.org/10.1371/journal.pbio.2006930
Vollmer S, Mateen BA, Bohner G et al (2020) Machine learning and artificial intelligence research for patient benefit: 20 critical questions on transparency, replicability, ethics, and effectiveness. BMJ 368. https://doi.org/10.1136/bmj.l6927
Gundersen OE, Kjensmo S (2018) State of the art: reproducibility in artificial intelligence. 32nd AAAI Conf Artif Intell AAAI 2018 1644–1651
Lambin P, Leijenaar RTH, Deist TM et al (2017) Radiomics: the bridge between medical imaging and personalized medicine. Nat Rev Clin Oncol 14:749–762
Ripley BD (2014) Pattern recognition and neural networks. Pattern Recognit Neural Netw:1–403. https://doi.org/10.1017/CBO9780511812651
Russell S, Norvig P (2010) Artificial intelligence: a modern approach, 3rd edn. Prentice Hall
Moore SM, Maffitt DR, Smith KE et al (2015) De-identification of medical images with retention of scientific research value. Radiographics 35:727–735. https://doi.org/10.1148/rg.2015140244
Schwarz CG, Kremers WK, Therneau TM et al (2019) Identification of anonymous MRI research participants with face-recognition software. N Engl J Med 381:1684–1686. https://doi.org/10.1056/nejmc1908881
Heus P, Damen JAAG, Pajouheshnia R et al (2018) Poor reporting of multivariable prediction model studies: towards a targeted implementation strategy of the TRIPOD statement. BMC Med:16. https://doi.org/10.1186/s12916-018-1099-2
Wynants L, Van Calster B, Collins GS et al (2020) Prediction models for diagnosis and prognosis of covid-19: systematic review and critical appraisal. BMJ 369. https://doi.org/10.1136/bmj.m1328
Wright BD, Vo N, Nolan J et al (2020) An analysis of key indicators of reproducibility in radiology. Insights Imaging 11. https://doi.org/10.1186/s13244-020-00870-x
Luo W, Phung D, Tran T et al (2016) Guidelines for developing and reporting machine learning predictive models in biomedical research: a multidisciplinary view. J Med Internet Res 18:e323. https://doi.org/10.2196/jmir.5870
Funding
The authors acknowledge financial support from the UK Research & Innovation London Medical Imaging and Artificial Intelligence Centre and Wellcome Trust EPSRC Centre for Medical Engineering at King’s College London (WT203148/Z/16/Z).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Guarantor
The scientific guarantor of this publication is Vicky Goh (Vicky.goh@kcl.ac.uk).
Conflict of interest
The authors of this manuscript declare no relationships with any companies whose products or services may be related to the subject matter of the article.
Statistics and biometry
No complex statistical methods were necessary for this paper.
Informed consent
Written informed consent was not required for this study because this was a systematic review using published studies in the literature but not analysing specific human subjects.
Ethical approval
Institutional review board approval was not required because this was a systematic review using published studies in the literature but not analysing specific human subjects.
Methodology
• Retrospective
• Multicentre study
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
ESM 1
(DOCX 89 kb)
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
O’Shea, R.J., Sharkey, A.R., Cook, G.J.R. et al. Systematic review of research design and reporting of imaging studies applying convolutional neural networks for radiological cancer diagnosis. Eur Radiol 31, 7969–7983 (2021). https://doi.org/10.1007/s00330-021-07881-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00330-021-07881-2