Simon Ching-Shun Kao
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Simon Ching-Shun Kao has a total of 342 co-authors. Here are the top co-authors by number of shared publications:
- Yutaka Sato
Department of Radiology, University of Iowa Hospitals and Clinics, Iowa City, USA
25 shared publications Douglas S. Hawkins
University of Washington, Seattle, WA
7 shared publications- Kevin S. Berbaum
Univ. of Iowa (United States)
7 shared publications - Mary Beth McCarville
Department of Radiology, St Jude Children's Research Hospital, Memphis, TN
7 shared publications - Sheri L. Spunt
Department of Pediatrics Stanford University School of Medicine Stanford California USA
6 shared publications - Aaron R. Weiss
Department of Pediatrics, MaineHealth Maine Medical Center, Portland, ME, USA
5 shared publications
Latest Publications
- Open Access
- 6 July 2026
- Published by Springer Nature in Pediatric Radiology
- Vol. 56 (11) , 2564-2572
Widely available, general-purpose generative AI applications for radiology education: determining the teaching quality of synthetic pediatric neuroradiology images
Background: Artificial intelligence (AI) is increasingly incorporated into medical education. Widely available, general-purpose generative AI applications are increasingly capable of producing high-fidelity synthetic medical images, which may have potential educational uses. Objective: To assess the ability of widely available, general-purpose generative AI applications to produce synthetic pediatric neuroradiology images of teaching quality. Materials and methods: Ten significant diagnostic errors in pediatric neuroradiologic emergencies were identified and divided into 22 individual clinical scenarios. Two widely available, general-purpose generative AI applications, GPT-5 (OpenAI, San Francisco, CA) and Gemini 3 Pro with the Nano Banana Pro image-generation engine (Google, Mountain View, CA), were prompted to generate five separate images for each scenario, yielding a total of 220 images. Eight fellowship-trained pediatric radiologists independently assessed each image for teaching quality. Ratings were recorded and analyzed. Differences between applications were evaluated using Fisher’s exact test. Results: Overall, 8.6% of generated images (19/220) were deemed suitable for teaching by more than half of the pediatric radiologists. GPT-5 produced a higher proportion of acceptable images meeting this >50% criterion compared to Gemini 3 Pro (12.7% [14/110] vs. 4.5% [5/110]; P =0.031). Conclusion: At present, widely available, general-purpose generative AI applications should not be used to produce synthetic radiological images for educational purposes. Inaccuracies and inconsistencies limit reliability and may actively impair learning.
- 6 July 2026
- Published by Springer Nature in Pediatric Radiology
- Vol. 56 (11) , 2564-2572
Open AccessWidely available, general-purpose generative AI applications for radiology education: determining the teaching quality of synthetic pediatric neuroradiology images
Background: Artificial intelligence (AI) is increasingly incorporated into medical education. Widely available, general-purpose generative AI applications are increasingly capable of producing high-fidelity synthetic medical images, which may have potential educational uses. Objective: To assess the ability of widely available, general-purpose generative AI applications to produce synthetic pediatric neuroradiology images of teaching quality. Materials and methods: Ten significant diagnostic errors in pediatric neuroradiologic emergencies were identified and divided into 22 individual clinical scenarios. Two widely available, general-purpose generative AI applications, GPT-5 (OpenAI, San Francisco, CA) and Gemini 3 Pro with the Nano Banana Pro image-generation engine (Google, Mountain View, CA), were prompted to generate five separate images for each scenario, yielding a total of 220 images. Eight fellowship-trained pediatric radiologists independently assessed each image for teaching quality. Ratings were recorded and analyzed. Differences between applications were evaluated using Fisher’s exact test. Results: Overall, 8.6% of generated images (19/220) were deemed suitable for teaching by more than half of the pediatric radiologists. GPT-5 produced a higher proportion of acceptable images meeting this >50% criterion compared to Gemini 3 Pro (12.7% [14/110] vs. 4.5% [5/110]; P =0.031). Conclusion: At present, widely available, general-purpose generative AI applications should not be used to produce synthetic radiological images for educational purposes. Inaccuracies and inconsistencies limit reliability and may actively impair learning.
- 1 November 2023
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 41 (31) , 4842-4848
Outcomes After Preoperative Chemoradiation With or Without Pazopanib in Non-Rhabdomyosarcoma Soft Tissue Sarcoma: A Report From Children's Oncology Group and NRG Oncology
Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported. ARST1321 was a phase II study designed to compare the near complete pathologic response rate after preoperative chemoradiation with/without pazopanib in children and adults with intermediate-/high-risk chemotherapy-sensitive body wall/extremity non-Rhabdomyosarcoma Soft Tissue Sarcoma (ClinicalTrials.gov identifier: NCT02180867 ). Enrollment was stopped early following a predetermined interim analysis that found the rate of near complete pathologic response to be significantly greater with the addition of pazopanib. As a planned secondary aim of the study, the outcome data for this cohort were analyzed. Eight-five eligible patients were randomly assigned to receive (regimen A) or not receive (regimen B) pazopanib in combination with ifosfamide and doxorubicin + preoperative radiotherapy followed by primary resection at week 13 and then further chemotherapy at week 25. As of December 31, 2021, at a median survivor follow-up of 3.3 years (range, 0.1-5.8 years), the 3-year event-free survival for all patients in the intent-to-treat analysis was 52.5% (95% CI, 34.8 to 70.2) for regimen A and 50.6% (95% CI, 32 to 69.2) for regimen B ( P = .8677, log-rank test); the 3-year overall survival was 75.7% (95% CI, 59.7 to 91.7) for regimen A and 65.4% (95% CI, 48.1 to 82.7) for regimen B ( P = .1919, log-rank test). Although the rate of near complete pathologic response was significantly greater with the addition of pazopanib, outcomes were not statistically significantly different between the two regimens.
- 1 November 2023
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 41 (31) , 4842-4848
Outcomes After Preoperative Chemoradiation With or Without Pazopanib in Non-Rhabdomyosarcoma Soft Tissue Sarcoma: A Report From Children's Oncology Group and NRG Oncology
Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported. ARST1321 was a phase II study designed to compare the near complete pathologic response rate after preoperative chemoradiation with/without pazopanib in children and adults with intermediate-/high-risk chemotherapy-sensitive body wall/extremity non-Rhabdomyosarcoma Soft Tissue Sarcoma (ClinicalTrials.gov identifier: NCT02180867 ). Enrollment was stopped early following a predetermined interim analysis that found the rate of near complete pathologic response to be significantly greater with the addition of pazopanib. As a planned secondary aim of the study, the outcome data for this cohort were analyzed. Eight-five eligible patients were randomly assigned to receive (regimen A) or not receive (regimen B) pazopanib in combination with ifosfamide and doxorubicin + preoperative radiotherapy followed by primary resection at week 13 and then further chemotherapy at week 25. As of December 31, 2021, at a median survivor follow-up of 3.3 years (range, 0.1-5.8 years), the 3-year event-free survival for all patients in the intent-to-treat analysis was 52.5% (95% CI, 34.8 to 70.2) for regimen A and 50.6% (95% CI, 32 to 69.2) for regimen B ( P = .8677, log-rank test); the 3-year overall survival was 75.7% (95% CI, 59.7 to 91.7) for regimen A and 65.4% (95% CI, 48.1 to 82.7) for regimen B ( P = .1919, log-rank test). Although the rate of near complete pathologic response was significantly greater with the addition of pazopanib, outcomes were not statistically significantly different between the two regimens.
- 25 July 2023
- Published by Elsevier in European Journal of Radiology
- Vol. 166, 111012
INternational Soft Tissue saRcoma ConsorTium (INSTRuCT) consensus statement: Imaging recommendations for the management of rhabdomyosarcoma
- 25 July 2023
- Published by Elsevier in European Journal of Radiology
- Vol. 166, 111012
INternational Soft Tissue saRcoma ConsorTium (INSTRuCT) consensus statement: Imaging recommendations for the management of rhabdomyosarcoma
- 8 December 2022
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 70 (S4) , e29966
Imaging of pediatric extragonadal pelvic soft tissue tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper
The most common pediatric extragonadal pelvic cancers include germ cell tumors, sacrococcygeal teratomas, and rhabdomyosarcomas (arising from the urinary bladder, prostate, paratesticular tissues, vagina, uterus, and perineum). This paper describes the radiological and nuclear medicine features of these entities and provides consensus‐based recommendations for the assessment at diagnosis, during, and after treatment.
- 8 December 2022
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 70 (S4) , e29966
Imaging of pediatric extragonadal pelvic soft tissue tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee White Paper
The most common pediatric extragonadal pelvic cancers include germ cell tumors, sacrococcygeal teratomas, and rhabdomyosarcomas (arising from the urinary bladder, prostate, paratesticular tissues, vagina, uterus, and perineum). This paper describes the radiological and nuclear medicine features of these entities and provides consensus‐based recommendations for the assessment at diagnosis, during, and after treatment.
- 1 August 2022
- Published by American Roentgen Ray Society in American Journal of Roentgenology
- Vol. 219 (2) , 314
Editorial Comment: Imaging of Pediatric Chronic Pancreatitis Requires Standardized Interpretation Criteria
This Editorial Comment discusses the following AJR article: Interobserver Agreement for CT and MRI Findings of Chronic Pancreatitis in Children: A Multicenter Ancillary Study Under the INSPPIRE Consortium.
- 1 August 2022
- Published by American Roentgen Ray Society in American Journal of Roentgenology
- Vol. 219 (2) , 314
Editorial Comment: Imaging of Pediatric Chronic Pancreatitis Requires Standardized Interpretation Criteria
This Editorial Comment discusses the following AJR article: Interobserver Agreement for CT and MRI Findings of Chronic Pancreatitis in Children: A Multicenter Ancillary Study Under the INSPPIRE Consortium.
- Top Cited Papers
- 20 July 2020
- Published by Elsevier in The Lancet Oncology
- Vol. 21 (8) , 1110-1122
Pathological response in children and adults with large unresected intermediate-grade or high-grade soft tissue sarcoma receiving preoperative chemoradiotherapy with or without pazopanib (ARST1321): a multicentre, randomised, open-label, phase 2 trial
- 20 July 2020
- Published by Elsevier in The Lancet Oncology
- Vol. 21 (8) , 1110-1122
Top Cited PapersPathological response in children and adults with large unresected intermediate-grade or high-grade soft tissue sarcoma receiving preoperative chemoradiotherapy with or without pazopanib (ARST1321): a multicentre, randomised, open-label, phase 2 trial
- 1 July 2020
- Published by Elsevier in Pancreatology
- Vol. 20 (5) , 1019-1020
Progression from acute to chronic pancreatitis associated with CFTR and SPINK1 mutations
- 1 July 2020
- Published by Elsevier in Pancreatology
- Vol. 20 (5) , 1019-1020
Progression from acute to chronic pancreatitis associated with CFTR and SPINK1 mutations
- Top Cited Papers
- 1 January 2020
- Published by Elsevier in The Lancet Oncology
- Vol. 21 (1) , 145-161
A risk-based treatment strategy for non-rhabdomyosarcoma soft-tissue sarcomas in patients younger than 30 years (ARST0332): a Children's Oncology Group prospective study
- 1 January 2020
- Published by Elsevier in The Lancet Oncology
- Vol. 21 (1) , 145-161
Top Cited PapersA risk-based treatment strategy for non-rhabdomyosarcoma soft-tissue sarcomas in patients younger than 30 years (ARST0332): a Children's Oncology Group prospective study