Radiomics model–based algorithm for preoperative prediction of pancreatic ductal adenocarcinoma grade
Objective To develop diagnostic radiomic model–based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction. Methods Ninety-one patients with histologically confirmed PDAC and preoperative CT were divided into subgroups based on tumor grade. Two histology-blinded radiologists indepen...
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| Published in | European radiology Vol. 33; no. 2; pp. 1152 - 1161 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.02.2023
Springer Nature B.V |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1432-1084 0938-7994 1432-1084 |
| DOI | 10.1007/s00330-022-09046-1 |
Cover
| Abstract | Objective
To develop diagnostic radiomic model–based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction.
Methods
Ninety-one patients with histologically confirmed PDAC and preoperative CT were divided into subgroups based on tumor grade. Two histology-blinded radiologists independently segmented lesions for quantitative texture analysis in all contrast enhancement phases. The ratio of densities of PDAC and unchanged pancreatic tissue, and relative tumor enhancement (RTE) in arterial, portal venous, and delayed phases of the examination were calculated. Principal component analysis was used for multivariate predictor analysis. The selection of predictors in the binary logistic model was carried out in 2 stages: (1) using one-factor logistic models (selection criterion was
p
< 0.1); (2) using regularization (LASSO regression after standardization of variables). Predictors were included in proportional odds models without interactions.
Results
There were significant differences in 4, 16, and 8 texture features out of 62 for the arterial, portal venous, and delayed phases of the study, respectively (
p
< 0.1). After selection, the final diagnostic model included such radiomics features as DISCRETIZED HU standard, DISCRETIZED HUQ3, GLCM Correlation, GLZLM LZLGE for the portal venous phase of the contrast enhancement, and CONVENTIONAL_HUQ3 for the delayed phase of CT study. On its basis, a diagnostic model was built, showing AUC for grade ≥ 2 of 0.75 and AUC for grade 3 of 0.66.
Conclusion
Radiomics features vary in PDAC of different grades and increase the accuracy of CT in preoperative diagnosis. We have developed a diagnostic model, including texture features, which can be used to predict the grade of PDAC.
Key Points
•
A diagnostic algorithm based on CT texture features for preoperative PDAC grade prediction was developed.
•
The assumption that the scanning protocol can influence the results of texture analysis was confirmed and assessed.
•
Our results show that tumor differentiation grade can be assessed with sufficient diagnostic accuracy using CT texture analysis presented in this study. |
|---|---|
| AbstractList | To develop diagnostic radiomic model-based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction.OBJECTIVETo develop diagnostic radiomic model-based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction.Ninety-one patients with histologically confirmed PDAC and preoperative CT were divided into subgroups based on tumor grade. Two histology-blinded radiologists independently segmented lesions for quantitative texture analysis in all contrast enhancement phases. The ratio of densities of PDAC and unchanged pancreatic tissue, and relative tumor enhancement (RTE) in arterial, portal venous, and delayed phases of the examination were calculated. Principal component analysis was used for multivariate predictor analysis. The selection of predictors in the binary logistic model was carried out in 2 stages: (1) using one-factor logistic models (selection criterion was p < 0.1); (2) using regularization (LASSO regression after standardization of variables). Predictors were included in proportional odds models without interactions.METHODSNinety-one patients with histologically confirmed PDAC and preoperative CT were divided into subgroups based on tumor grade. Two histology-blinded radiologists independently segmented lesions for quantitative texture analysis in all contrast enhancement phases. The ratio of densities of PDAC and unchanged pancreatic tissue, and relative tumor enhancement (RTE) in arterial, portal venous, and delayed phases of the examination were calculated. Principal component analysis was used for multivariate predictor analysis. The selection of predictors in the binary logistic model was carried out in 2 stages: (1) using one-factor logistic models (selection criterion was p < 0.1); (2) using regularization (LASSO regression after standardization of variables). Predictors were included in proportional odds models without interactions.There were significant differences in 4, 16, and 8 texture features out of 62 for the arterial, portal venous, and delayed phases of the study, respectively (p < 0.1). After selection, the final diagnostic model included such radiomics features as DISCRETIZED HU standard, DISCRETIZED HUQ3, GLCM Correlation, GLZLM LZLGE for the portal venous phase of the contrast enhancement, and CONVENTIONAL_HUQ3 for the delayed phase of CT study. On its basis, a diagnostic model was built, showing AUC for grade ≥ 2 of 0.75 and AUC for grade 3 of 0.66.RESULTSThere were significant differences in 4, 16, and 8 texture features out of 62 for the arterial, portal venous, and delayed phases of the study, respectively (p < 0.1). After selection, the final diagnostic model included such radiomics features as DISCRETIZED HU standard, DISCRETIZED HUQ3, GLCM Correlation, GLZLM LZLGE for the portal venous phase of the contrast enhancement, and CONVENTIONAL_HUQ3 for the delayed phase of CT study. On its basis, a diagnostic model was built, showing AUC for grade ≥ 2 of 0.75 and AUC for grade 3 of 0.66.Radiomics features vary in PDAC of different grades and increase the accuracy of CT in preoperative diagnosis. We have developed a diagnostic model, including texture features, which can be used to predict the grade of PDAC.CONCLUSIONRadiomics features vary in PDAC of different grades and increase the accuracy of CT in preoperative diagnosis. We have developed a diagnostic model, including texture features, which can be used to predict the grade of PDAC.• A diagnostic algorithm based on CT texture features for preoperative PDAC grade prediction was developed. • The assumption that the scanning protocol can influence the results of texture analysis was confirmed and assessed. • Our results show that tumor differentiation grade can be assessed with sufficient diagnostic accuracy using CT texture analysis presented in this study.KEY POINTS• A diagnostic algorithm based on CT texture features for preoperative PDAC grade prediction was developed. • The assumption that the scanning protocol can influence the results of texture analysis was confirmed and assessed. • Our results show that tumor differentiation grade can be assessed with sufficient diagnostic accuracy using CT texture analysis presented in this study. To develop diagnostic radiomic model-based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction. Ninety-one patients with histologically confirmed PDAC and preoperative CT were divided into subgroups based on tumor grade. Two histology-blinded radiologists independently segmented lesions for quantitative texture analysis in all contrast enhancement phases. The ratio of densities of PDAC and unchanged pancreatic tissue, and relative tumor enhancement (RTE) in arterial, portal venous, and delayed phases of the examination were calculated. Principal component analysis was used for multivariate predictor analysis. The selection of predictors in the binary logistic model was carried out in 2 stages: (1) using one-factor logistic models (selection criterion was p < 0.1); (2) using regularization (LASSO regression after standardization of variables). Predictors were included in proportional odds models without interactions. There were significant differences in 4, 16, and 8 texture features out of 62 for the arterial, portal venous, and delayed phases of the study, respectively (p < 0.1). After selection, the final diagnostic model included such radiomics features as DISCRETIZED HU standard, DISCRETIZED HUQ3, GLCM Correlation, GLZLM LZLGE for the portal venous phase of the contrast enhancement, and CONVENTIONAL_HUQ3 for the delayed phase of CT study. On its basis, a diagnostic model was built, showing AUC for grade ≥ 2 of 0.75 and AUC for grade 3 of 0.66. Radiomics features vary in PDAC of different grades and increase the accuracy of CT in preoperative diagnosis. We have developed a diagnostic model, including texture features, which can be used to predict the grade of PDAC. • A diagnostic algorithm based on CT texture features for preoperative PDAC grade prediction was developed. • The assumption that the scanning protocol can influence the results of texture analysis was confirmed and assessed. • Our results show that tumor differentiation grade can be assessed with sufficient diagnostic accuracy using CT texture analysis presented in this study. ObjectiveTo develop diagnostic radiomic model–based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction.MethodsNinety-one patients with histologically confirmed PDAC and preoperative CT were divided into subgroups based on tumor grade. Two histology-blinded radiologists independently segmented lesions for quantitative texture analysis in all contrast enhancement phases. The ratio of densities of PDAC and unchanged pancreatic tissue, and relative tumor enhancement (RTE) in arterial, portal venous, and delayed phases of the examination were calculated. Principal component analysis was used for multivariate predictor analysis. The selection of predictors in the binary logistic model was carried out in 2 stages: (1) using one-factor logistic models (selection criterion was p < 0.1); (2) using regularization (LASSO regression after standardization of variables). Predictors were included in proportional odds models without interactions.ResultsThere were significant differences in 4, 16, and 8 texture features out of 62 for the arterial, portal venous, and delayed phases of the study, respectively (p < 0.1). After selection, the final diagnostic model included such radiomics features as DISCRETIZED HU standard, DISCRETIZED HUQ3, GLCM Correlation, GLZLM LZLGE for the portal venous phase of the contrast enhancement, and CONVENTIONAL_HUQ3 for the delayed phase of CT study. On its basis, a diagnostic model was built, showing AUC for grade ≥ 2 of 0.75 and AUC for grade 3 of 0.66.ConclusionRadiomics features vary in PDAC of different grades and increase the accuracy of CT in preoperative diagnosis. We have developed a diagnostic model, including texture features, which can be used to predict the grade of PDAC.Key Points• A diagnostic algorithm based on CT texture features for preoperative PDAC grade prediction was developed.• The assumption that the scanning protocol can influence the results of texture analysis was confirmed and assessed.• Our results show that tumor differentiation grade can be assessed with sufficient diagnostic accuracy using CT texture analysis presented in this study. Objective To develop diagnostic radiomic model–based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction. Methods Ninety-one patients with histologically confirmed PDAC and preoperative CT were divided into subgroups based on tumor grade. Two histology-blinded radiologists independently segmented lesions for quantitative texture analysis in all contrast enhancement phases. The ratio of densities of PDAC and unchanged pancreatic tissue, and relative tumor enhancement (RTE) in arterial, portal venous, and delayed phases of the examination were calculated. Principal component analysis was used for multivariate predictor analysis. The selection of predictors in the binary logistic model was carried out in 2 stages: (1) using one-factor logistic models (selection criterion was p < 0.1); (2) using regularization (LASSO regression after standardization of variables). Predictors were included in proportional odds models without interactions. Results There were significant differences in 4, 16, and 8 texture features out of 62 for the arterial, portal venous, and delayed phases of the study, respectively ( p < 0.1). After selection, the final diagnostic model included such radiomics features as DISCRETIZED HU standard, DISCRETIZED HUQ3, GLCM Correlation, GLZLM LZLGE for the portal venous phase of the contrast enhancement, and CONVENTIONAL_HUQ3 for the delayed phase of CT study. On its basis, a diagnostic model was built, showing AUC for grade ≥ 2 of 0.75 and AUC for grade 3 of 0.66. Conclusion Radiomics features vary in PDAC of different grades and increase the accuracy of CT in preoperative diagnosis. We have developed a diagnostic model, including texture features, which can be used to predict the grade of PDAC. Key Points • A diagnostic algorithm based on CT texture features for preoperative PDAC grade prediction was developed. • The assumption that the scanning protocol can influence the results of texture analysis was confirmed and assessed. • Our results show that tumor differentiation grade can be assessed with sufficient diagnostic accuracy using CT texture analysis presented in this study. |
| Author | Revishvili, Amiran Sh Karmazanovsky, Grigory G. Mikhaylyuk, Kseniya A. Kondratyev, Evvgeny V. Gruzdev, Ivan S. Sinelnikov, Mikhail Y. Tikhonova, Valeriya S. |
| Author_xml | – sequence: 1 givenname: Valeriya S. surname: Tikhonova fullname: Tikhonova, Valeriya S. organization: A.V. Vishnevsky National Medical Research Centre of Surgery – sequence: 2 givenname: Grigory G. surname: Karmazanovsky fullname: Karmazanovsky, Grigory G. organization: A.V. Vishnevsky National Medical Research Centre of Surgery, Pirogov Russian National Research Medical University – sequence: 3 givenname: Evvgeny V. surname: Kondratyev fullname: Kondratyev, Evvgeny V. organization: A.V. Vishnevsky National Medical Research Centre of Surgery – sequence: 4 givenname: Ivan S. surname: Gruzdev fullname: Gruzdev, Ivan S. organization: A.V. Vishnevsky National Medical Research Centre of Surgery – sequence: 5 givenname: Kseniya A. surname: Mikhaylyuk fullname: Mikhaylyuk, Kseniya A. organization: A.V. Vishnevsky National Medical Research Centre of Surgery – sequence: 6 givenname: Mikhail Y. orcidid: 0000-0002-0862-6011 surname: Sinelnikov fullname: Sinelnikov, Mikhail Y. email: Mikhail.y.sinelnikov@gmail.com organization: Research Institute of Human Morphology, Sechenov University – sequence: 7 givenname: Amiran Sh surname: Revishvili fullname: Revishvili, Amiran Sh organization: A.V. Vishnevsky National Medical Research Centre of Surgery |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35986774$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_20517_ais_2023_18 crossref_primary_10_24835_1607_0763_1483 crossref_primary_10_3390_cancers17061036 crossref_primary_10_1007_s10278_024_01325_1 crossref_primary_10_1016_j_ejrad_2024_111327 crossref_primary_10_3390_diagnostics14070712 crossref_primary_10_1016_j_yacr_2024_04_003 crossref_primary_10_1186_s13550_023_00985_4 crossref_primary_10_1007_s00330_023_09728_4 crossref_primary_10_3390_biomedicines11061687 crossref_primary_10_1007_s00330_023_09653_6 |
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| Keywords | CT Texture analysis Pancreas Pancreatic ductal adenocarcinoma Radiomics |
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Radiology 206(2):373–378 GerlingerMRowanAJHorswellSMathMLarkinJEndesfelderDGronroosEMartinezPMatthewsNStewartATarpeyPVarelaIPhillimoreBBegumSMcDonaldNQButlerAJonesDRaineKLatimerCSantosCRNohadaniMEklundACSpencer-DeneBClarkGPickeringLStampGGoreMSzallasiZDownwardJFutrealPASwantonCIntratumor heterogeneity and branched evolution revealed by multiregion sequencingN Engl J Med20123668838921:CAS:528:DC%2BC38XktFOgtbw%3D10.1056/NEJMoa1113205 EilaghiABaigSZhangYCT texture features are associated with overall survival in pancreatic ductal adenocarcinoma - a quantitative analysisBMC Med Imaging.20171711710.1186/s12880-017-0209-5 Nioche C, Orlhac F, Boughdad S et al (2018) LifEx: a freeware for radiomic feature calculation in multimodality imaging to accelerate advances in the characterization of tumor heterogeneity. Cancer Res 78(16):4786–4789. Available at: https://pubmed.ncbi.nlm.nih.gov/29959149/. 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Accessed 2 Oct 2020 Chang N, Cui L, Luo Y, Chang Z, Yu B, Liu Z (2020) Development and multicenter validation of a CT-based radiomics signature for discriminating histological grades of pancreatic ductal adenocarcinoma //Quantitative imaging in medicine and surgery. – 2020. – Т. 10. – №. 3. – С. 692 Kulkarni A, Carrion-Martinez I, Jiang NN et al (2020) Hypovascular pancreas head adenocarcinoma: CT texture analysis for assessment of resection margin status and high-risk features. Eur Radiol 30(5):2853–2860. Available at: https://pubmed.ncbi.nlm.nih.gov/31953662/. Accessed 5 Oct 2020 HarrellFERegression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition2015Cham Heidelberg New YorkSpringer81010.1007/978-3-319-19425-7 LiuLXuHXHeMWangWWangWQWuCTWeiRQLiangYGaoHLLiuCXuJLongJNiQXShaoCHWangJYuXJA novel scoring system predicts postsurgical survival and adjuvant chemotherapeutic benefits in patients with pancreatic adenocarcinoma: implications for AJCC-TNM stagingSurgery20181631280129410.1016/j.surg.2018.01.017 HarrellFERegression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition2015Cham Heidelberg New YorkSpringer11011110.1007/978-3-319-19425-7 Machicado JD, Koay EJ, Krishna SG (2020) Radiomics for the diagnosis and differentiation of pancreatic cystic lesions. Diagnostics 10(7):505. Available at: https://www.mdpi.com/2075-4418/10/7/505. Accessed 2 Oct 2020 SteyerbergEWClinical prediction models: a practical approach to development, validation, and updating. 2nd ed. 2019 editionPlace of publication not identified2019Springer220221251-254 9046_CR15 FE Harrell (9046_CR26) 2015 9046_CR14 9046_CR17 9046_CR19 9046_CR18 FE Harrell (9046_CR28) 2015 9046_CR30 9046_CR11 9046_CR10 A Eilaghi (9046_CR16) 2017; 17 9046_CR13 9046_CR12 9046_CR3 WH Fang (9046_CR20) 2020; 20 EW Steyerberg (9046_CR24) 2019 9046_CR2 9046_CR1 L Liu (9046_CR5) 2018; 163 A Nurmi (9046_CR6) 2018; 57 M Gerlinger (9046_CR8) 2012; 366 FE Harrell (9046_CR27) 2015 9046_CR29 MA Eloubeidi (9046_CR7) 2006; 63 9046_CR9 9046_CR22 9046_CR21 9046_CR23 G James (9046_CR25) 2013 SH Han (9046_CR4) 2017; 40 |
| References_xml | – reference: Machicado JD, Koay EJ, Krishna SG (2020) Radiomics for the diagnosis and differentiation of pancreatic cystic lesions. Diagnostics 10(7):505. Available at: https://www.mdpi.com/2075-4418/10/7/505. Accessed 2 Oct 2020 – reference: Cassinotto C, Chong J, Zogopoulos G et al (2017) Resectable pancreatic adenocarcinoma: role of CT quantitative imaging biomarkers for predicting pathology and patient outcomes. Eur J Radiol 90:152–158. Available at: https://pubmed.ncbi.nlm.nih.gov/28583627/. Accessed 2 Oct 2020 – reference: Tamm EP, Bhosale PR, Lee JH (2007) Pancreatic ductal adenocarcinoma: ultrasound, computed tomography, and magnetic resonance imaging features. Semin Ultrasound CT MRI 28(5):330–338 – reference: Nioche C, Orlhac F, Boughdad S et al (2018) LifEx: a freeware for radiomic feature calculation in multimodality imaging to accelerate advances in the characterization of tumor heterogeneity. Cancer Res 78(16):4786–4789. Available at: https://pubmed.ncbi.nlm.nih.gov/29959149/. Accessed 2 Oct 2020 – reference: Kulkarni A, Carrion-Martinez I, Jiang NN et al (2020) Hypovascular pancreas head adenocarcinoma: CT texture analysis for assessment of resection margin status and high-risk features. Eur Radiol 30(5):2853–2860. Available at: https://pubmed.ncbi.nlm.nih.gov/31953662/. Accessed 5 Oct 2020 – reference: Goyen M (2014) Radiogenomic imaging-linking diagnostic imaging and molecular diagnostics. World J Radiol 6(8):519. Available at: /pmc/articles/PMC4147432/?report=abstract. Accessed 2 Oct 2020 – reference: HarrellFERegression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition2015Cham Heidelberg New YorkSpringer11011110.1007/978-3-319-19425-7 – reference: Treadwell JR, Zafar HM, Mitchell MD, Tipton K, Teitelbaum U, Jue J (2016) Imaging tests for the diagnosis and staging of pancreatic adenocarcinoma: a meta-analysis. Pancreas 45(6):789–795. Available at: https://pubmed.ncbi.nlm.nih.gov/26745859/. Accessed 2 Oct 2020 – reference: JamesGWittenDHastieTTibshiraniRAn introduction to statistical learning: with applications in R. 1st ed. 2013, Corr. 7th printing 2017 edition2013New YorkSpringer21922710.1007/978-1-4614-7138-7 – reference: HanSHHeoJSChoiSHActual long-term outcome of T1 and T2 pancreatic ductal adenocarcinoma after surgical resectionInt J Surg.201740687210.1016/j.ijsu.2017.02.007 – reference: Kakar S, Shi C, Adsay N, Volkan et al (2017) Protocol for the examination of specimens from patients with carcinoma of the pancreas with guidance from the CAP Cancer and CAP Pathology Electronic Reporting Committees. Available at: www.cap.org/cancerprotocols. Accessed 2 Oct 2020 – reference: LiuLXuHXHeMWangWWangWQWuCTWeiRQLiangYGaoHLLiuCXuJLongJNiQXShaoCHWangJYuXJA novel scoring system predicts postsurgical survival and adjuvant chemotherapeutic benefits in patients with pancreatic adenocarcinoma: implications for AJCC-TNM stagingSurgery20181631280129410.1016/j.surg.2018.01.017 – reference: Stark AP, Sacks GD, Rochefort MM et al (2016) Long-term survival in patients with pancreatic ductal adenocarcinoma. Surgery 159:1520–1527. https://doi.org/10.1016/j.surg.2015.12.024 – reference: Diehl SJ, Lehmann KJ, Sadick M, Lachmann R, Georgi M (1998) Pancreatic cancer: value of dual-phase helical CT in assessing resectability. Radiology 206(2):373–378 – reference: EilaghiABaigSZhangYCT texture features are associated with overall survival in pancreatic ductal adenocarcinoma - a quantitative analysisBMC Med Imaging.20171711710.1186/s12880-017-0209-5 – reference: Nagtegaal ID, Odze RD, Klimstra D, et al (2020) The 2019 WHO classification of tumours of the digestive system. Histopathology 76(2):182–188. Available at: https://pubmed.ncbi.nlm.nih.gov/31433515/. Accessed 2 Oct 2020 – reference: HarrellFERegression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition2015Cham Heidelberg New YorkSpringer81010.1007/978-3-319-19425-7 – reference: FangWHLiXDZhuHResectable pancreatic ductal adenocarcinoma: association between preoperative CT texture features and metastatic nodal involvementCancer Imaging.202020111010.1186/s40644-020-0296-3 – reference: HarrellFERegression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition2015Cham Heidelberg New YorkSpringer20921210.1007/978-3-319-19425-7 – reference: Chang N, Cui L, Luo Y, Chang Z, Yu B, Liu Z (2020) Development and multicenter validation of a CT-based radiomics signature for discriminating histological grades of pancreatic ductal adenocarcinoma //Quantitative imaging in medicine and surgery. – 2020. – Т. 10. – №. 3. – С. 692 – reference: NurmiAMustonenHParviainenHPeltolaKHaglundCSeppanenHNeoadjuvant therapy offers longer survival than upfront surgery for poorly differentiated and higher stage pancreatic cancerActa Oncol.20185767998061:CAS:528:DC%2BC2sXhvF2gtL3F10.1080/0284186X.2017.1415458 – reference: Yun G, Kim YH, Lee YJ, Kim B, Hwang JH, Choi DJ (2018) Tumor heterogeneity of pancreas head cancer assessed by CT texture analysis: association with survival outcomes after curative resection. Sci Rep 8(1):1–10. Available at: www.nature.com/scientificreports. Accessed 2 Oct 2020 – reference: Golan T, Sella T, Margalit O et al (2017) Short- and long-term survival in metastatic pancreatic adenocarcinoma, 1993-2013. J Natl Compr Canc Netw 15:1022–1027. https://doi.org/10.6004/jnccn.2017.0138 – reference: Sandrasegaran K, Lin Y, Asare-Sawiri, Taiyini T, Tann M (2019) CT texture analysis of pancreatic cancer. Eur Radiol 29(3):1067–1073. Available at: http://link.springer.com/10.1007/s00330-018-5662-1. Accessed 2 Oct 2020 – reference: SteyerbergEWClinical prediction models: a practical approach to development, validation, and updating. 2nd ed. 2019 editionPlace of publication not identified2019Springer220221251-254 – reference: Vincent A, Herman J, Schulick R, Hruban RH, Goggins M (2011) Pancreatic cancer. Lancet 378:607–620. Available at: https://pubmed.ncbi.nlm.nih.gov/21620466/. Accessed 2 Oct 2020 – reference: GerlingerMRowanAJHorswellSMathMLarkinJEndesfelderDGronroosEMartinezPMatthewsNStewartATarpeyPVarelaIPhillimoreBBegumSMcDonaldNQButlerAJonesDRaineKLatimerCSantosCRNohadaniMEklundACSpencer-DeneBClarkGPickeringLStampGGoreMSzallasiZDownwardJFutrealPASwantonCIntratumor heterogeneity and branched evolution revealed by multiregion sequencingN Engl J Med20123668838921:CAS:528:DC%2BC38XktFOgtbw%3D10.1056/NEJMoa1113205 – reference: Parekh V, Jacobs MA (2016) Radiomics: a new application from established techniques. Expert Rev Precis Med Drug Dev 1(2):207–226. Available at: https://pubmed.ncbi.nlm.nih.gov/28042608/. Accessed 2 Oct 2020 – reference: Yamashita R, Perrin T, Chakraborty J et al (2020) cRadiomic feature reproducibility in contrast-enhanced CT of the pancreas is affected by variabilities in scan parameters and manual segmentation. Eur Radiol 30(1):195–205. Available at: https://pubmed.ncbi.nlm.nih.gov/31392481/. Accessed 2 Oct 2020 – reference: EloubeidiMATamhaneAVaradarajuluSWilcoxCMFrequency of major complications after EUS-guided FNA of solid pancreatic masses: a prospective evaluationGastrointest Endosc20066362262910.1016/j.gie.2005.05.024 – ident: 9046_CR19 doi: 10.1038/s41598-018-25627-x – volume: 163 start-page: 1280 year: 2018 ident: 9046_CR5 publication-title: Surgery doi: 10.1016/j.surg.2018.01.017 – start-page: 209 volume-title: Regression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition year: 2015 ident: 9046_CR26 doi: 10.1007/978-3-319-19425-7 – ident: 9046_CR2 doi: 10.1016/j.surg.2015.12.024 – ident: 9046_CR21 doi: 10.1158/0008-5472.CAN-18-0125 – ident: 9046_CR11 doi: 10.3390/diagnostics10070505 – ident: 9046_CR14 doi: 10.1053/j.sult.2007.06.001 – volume: 366 start-page: 883 year: 2012 ident: 9046_CR8 publication-title: N Engl J Med doi: 10.1056/NEJMoa1113205 – ident: 9046_CR10 doi: 10.4329/wjr.v6.i8.519 – ident: 9046_CR9 doi: 10.1097/MPA.0000000000000524 – volume: 20 start-page: 1 issue: 1 year: 2020 ident: 9046_CR20 publication-title: Cancer Imaging. doi: 10.1186/s40644-020-0296-3 – volume: 17 start-page: 1 issue: 1 year: 2017 ident: 9046_CR16 publication-title: BMC Med Imaging. doi: 10.1186/s12880-017-0209-5 – ident: 9046_CR13 doi: 10.1148/radiology.206.2.9457188 – start-page: 8 volume-title: Regression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition year: 2015 ident: 9046_CR28 doi: 10.1007/978-3-319-19425-7 – ident: 9046_CR1 doi: 10.1016/S0140-6736(10)62307-0 – ident: 9046_CR15 doi: 10.1007/s00330-019-06381-8 – start-page: 219 volume-title: An introduction to statistical learning: with applications in R. 1st ed. 2013, Corr. 7th printing 2017 edition year: 2013 ident: 9046_CR25 doi: 10.1007/978-1-4614-7138-7 – ident: 9046_CR30 doi: 10.21037/qims.2020.02.21 – ident: 9046_CR17 doi: 10.1007/s00330-018-5662-1 – volume: 63 start-page: 622 year: 2006 ident: 9046_CR7 publication-title: Gastrointest Endosc doi: 10.1016/j.gie.2005.05.024 – volume: 57 start-page: 799 issue: 6 year: 2018 ident: 9046_CR6 publication-title: Acta Oncol. doi: 10.1080/0284186X.2017.1415458 – ident: 9046_CR29 doi: 10.1016/j.ejrad.2017.02.033 – start-page: 220 volume-title: Place of publication not identified year: 2019 ident: 9046_CR24 – volume: 40 start-page: 68 year: 2017 ident: 9046_CR4 publication-title: Int J Surg. doi: 10.1016/j.ijsu.2017.02.007 – ident: 9046_CR12 doi: 10.1080/23808993.2016.1164013 – ident: 9046_CR3 doi: 10.6004/jnccn.2017.0138 – start-page: 110 volume-title: Regression modeling strategies: with applications to linear models, logistic and ordinal regression, and survival analysis. 2nd ed. 2015 edition year: 2015 ident: 9046_CR27 doi: 10.1007/978-3-319-19425-7 – ident: 9046_CR18 doi: 10.1007/s00330-019-06583-0 – ident: 9046_CR22 doi: 10.1111/his.13975 – ident: 9046_CR23 |
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| Snippet | Objective
To develop diagnostic radiomic model–based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction.
Methods
Ninety-one patients with... To develop diagnostic radiomic model-based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction. Ninety-one patients with histologically... ObjectiveTo develop diagnostic radiomic model–based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction.MethodsNinety-one patients with... To develop diagnostic radiomic model-based algorithm for pancreatic ductal adenocarcinoma (PDAC) grade prediction.OBJECTIVETo develop diagnostic radiomic... |
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| SubjectTerms | Accuracy Adenocarcinoma Algorithms Carcinoma, Pancreatic Ductal - diagnostic imaging Carcinoma, Pancreatic Ductal - pathology Carcinoma, Pancreatic Ductal - surgery Computed tomography Diagnostic Radiology Diagnostic systems Discretization Histology Humans Imaging Internal Medicine Interventional Radiology Medicine Medicine & Public Health Neuroradiology Oncology Pancreas Pancreatic cancer Pancreatic Neoplasms Pancreatic Neoplasms - diagnostic imaging Pancreatic Neoplasms - pathology Pancreatic Neoplasms - surgery Phases Predictions Principal components analysis Radiology Radiomics Regularization Retrospective Studies Standardization Subgroups Texture Tomography, X-Ray Computed - methods Tumors Ultrasound |
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| Title | Radiomics model–based algorithm for preoperative prediction of pancreatic ductal adenocarcinoma grade |
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