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1120 citation(s) found for "Xu, Dong".

920 ETS-1 regulates the activation of human CD8 T-Cells in response to immune checkpoint inhibitors
Hirdler, Jacob, Mao, Zhiming , Lucien-Matteoni, Fabrice, Hirdler, Jacob B. , Correia, Cristina , Dong, Haidong

Regular and Young Investigator Award Abstracts | October 31, 2023 | Volume: No volume available | Issue: No issue available | Pages: A1023-A1023

10.1136/jitc-2023-sitc2023.0920 Get It

540 A novel antibody that induces PD-L1 degradation results in enhanced tumor responses in a humanized PD-L1 breast carcinoma mouse model compared to Atezolizumab
Liu, Xin , Harrington, Sue, Lucien-Matteoni, Fabrice, Hsu, Michelle A. , Barham, Whitney , Harrington, Sue, Dong, Haidong

Regular and Young Investigator Award Abstracts | October 31, 2023 | Volume: No volume available | Issue: No issue available | Pages: A614-A614

10.1136/jitc-2023-sitc2023.0540 Get It

539 Depletion of soluble PD-L1 with engineered NaNot® nanoparticles promotes antitumor immunity
Hirdler, Jacob, Lavoie, Roxane R. , Orme, Jacob J. , Hawthorne, Lou, Ruegg, Curtis , Dodgson, J, Lucien-Matteoni, Fabrice, Hsu, Michelle A. , Hirdler, Jacob B. , Pavelko, Kevin D. , Liu, Xin , Hawthorne, Lou, Park, Sean S. , Dong, Haidong

Regular and Young Investigator Award Abstracts | October 31, 2023 | Volume: No volume available | Issue: No issue available | Pages: A613-A613

10.1136/jitc-2023-sitc2023.0539 Get It

477 A novel antibody targeting human monocyte-intrinsic PD-L1 promotes immune stimulatory functions of monocytes for antitumor immunity
Li, Ying , Hirdler, Jacob, Lucien-Matteoni, Fabrice, Hsu, Michelle A. , Liu, Xin , Hirdler, Jacob B. , Dong, Haidong

Regular and Young Investigator Award Abstracts | October 31, 2023 | Volume: No volume available | Issue: No issue available | Pages: A536-A536

10.1136/jitc-2023-sitc2023.0477 Get It

28 Toward an automated microfluidic platform for monitoring immune response to immunotherapy
Zhang, Yuqian , Lucien-Matteoni, Fabrice, Liu, Yuguang , Kim, Yohan , Dong, Haidong

Regular and Young Investigator Award Abstracts | October 31, 2023 | Volume: No volume available | Issue: No issue available | Pages: A30-A31

10.1136/jitc-2023-sitc2023.0028 Get It

Effect of residual platelets in frozen-thawed plasma on results of dilute Russell’s viper venom time assay for lupus anticoagulant testing
Strande, Brenda J Nelson, Leger, Rachel, Stuart, Melissa S, Tange, Julie I, Navitska, Serena D, Heikal, Nahla, Ashrani, Aneel A. , Chen, Dong , Seheult, Jansen N. , Pruthi, Rajiv K. , Leger, Rachel R, Chen, Dong , Seheult, Jansen N , Sridharan, Meera

American Journal of Clinical Pathology | October 25, 2023 | Volume: 161 | Issue: 3 | Pages: 212-215

10.1093/ajcp/aqad138 | PMID 37878771 Get It

Abstract Objectives To determine the impact of residual platelets on dilute Russell’s viper venom time (DRVVT) assay in frozen-thawed plasma submitted for lupus anticoagulant (LAC) testing. Methods We measured platelet counts in frozen-thawed samples submitted for LAC testing and evaluated the association between platelet count and the DRVVT screening time and ratios. We also spiked platelets into a LAC-positive sample to observe the effect on the DRVVT. Results Progressive increase in platelet count resulted in a statistically significant shortening of the DRVVT assay results on plasma after 1 freeze-thaw cycle. A similar effect was noted on the LAC-positive sample. Conclusions Residual platelets in plasma samples result in shortening of DRVVT assay after 1 freeze-thaw cycle. This may result in a false-negative LAC test result.
An APRI+ALBI-Based Multivariable Model as a Preoperative Predictor for Posthepatectomy Liver Failure
Santol, Jonas , Gregory, Lindsey A., Baumgartner, Ruth , Birgin, Emrullah , Gloor, Severin , Braunwarth, Eva , Ammann, M. , Starlinger, Johannes , Ammon, Daphni , Ninkovic, Marijana , Kern, Anna , Rumpf, Benedikt , Ortmayr, Gregor , Herrmann, Yannic, Huber, Felix Xaver, Weninger, Jeremias, Smoot, Rory L. , Truty, Mark J. , Kendrick, Michael L. , Nagorney, David M. , Rahbari, Nuh N. , Hoffmann, Katrin , Hackl, Hubert , Maier, Eva , Smoot, Rory L , Hackl, Hubert , Santol, Jonas , Ammann, Markus , Kim, Sarang , Murtha-Lemekhova, Anastasia , Pereyra, David , Kern, Anna E., Dong, Yawen , Thiels, Cornelius A. , Warner, Susanne G. , Cleary, Sean P. , Beldi, Guido , Gilg, Stefan , Assinger, Alice , Gruenberger, Thomas , Starlinger, Patrick

Annals of Surgery | October 20, 2023 | Volume: 281 | Issue: 5 | Pages: 861-871

10.1097/sla.0000000000006127 | PMID 37860868 Get It

Objective and Background: Clinically significant posthepatectomy liver failure (PHLF B+C) remains the main cause of mortality after major hepatic resection. This study aimed to establish an aspartate aminotransferase to platelet ratio combined with an albumin-bilirubin grade (APRI+ALBI), based multivariable model (MVM) to predict PHLF and compare its performance to indocyanine green clearance (ICG-R15 or ICG-PDR) and albumin-ICG evaluation (ALICE). Methods: A total of 12,056 patients from the National Surgical Quality Improvement Program database were used to generate a MVM to predict PHLF B+C. The model was determined using stepwise backwards elimination. The performance of the model was tested using receiver operating characteristic curve analysis and validated in an international cohort of 2525 patients. In 620 patients, the APRI+ALBI MVM, trained in the National Surgical Quality Improvement Program cohort, was compared with the MVM’s based on other liver function tests (ICG clearance, ALICE) by comparing the areas under the curve (AUC). Results: A MVM including APRI+ALBI, age, sex, tumor type, and extent of resection was found to predict PHLF B+C with an AUC of 0.77, with comparable performance in the validation cohort (AUC: 0.74). In direct comparison with other MVM’s based on more expensive and time-consuming liver function tests (ICG clearance, ALICE), the APRI+ALBI MVM demonstrated equal predictive potential for PHLF B+C. A smartphone application for the calculation of the APRI+ALBI MVM was designed. Conclusion: Risk assessment through the APRI+ALBI MVM for PHLF B+C increases preoperative predictive accuracy and represents a universally available and cost-effective risk assessment before hepatectomy, facilitated by a freely available smartphone app.
Laying the Groundwork for a Fulfilling Career in Pediatric Infectious Diseases: The Transition From Fellowship to Faculty
Kushner, Lauren E. , Ristagno, Elizabeth H. , Dong, Sara W , Konold, Victoria , Fatemi, Yasaman , Stillwell, Terri, Wohrley, Julie, Sattler, Matthew M , Kalu, Ibukunoluwa C. , Boguniewicz, Juri , Boguniewicz, Juri

Journal of the Pediatric Infectious Diseases Society | October 10, 2023 | Volume: 12 | Issue: 12 | Pages: 627-633

10.1093/jpids/piad079 | PMID 37815429 Get It

Abstract There are limited resources for guidance on the transition from fellowship into a new faculty role in pediatric infectious diseases. This review aims to address this gap and provides a framework for a successful transition that is composed of four essential pillars—(1) stepping into your role, (2) finding your niche, (3) building your network, and (4) self-care—all of which are supported by strong mentorship/sponsorship and continual realignment with one’s personal mission statement. In addition to providing general principles and guidance, this review also outlines specific steps that a junior faculty member can take to expand their influence and build a successful, fulfilling career in pediatric infectious diseases.
An international multi-institution real-world study of the optimal surveillance frequency for stage II/III gastric cancer: the more, the better?
Lü, Jun, Lin, Jia, Xu, Binbin , Xue, Zhen , Zheng, Hua‐Long , Lin, Guosheng, Huang, Jiao-bao, Shen, Li-li, Zheng, Chao‐Hui , Li, Ping , Cao, Long‐Long, Ma, Yu‐Bin , Truty, Mark J. , Huang, Chang-Ming, Wu, Dong , Lin, Jia, Huang, Jiao-bao, Shen, Li-li, Xie, Jian‐Wei , Wang, Jia-Bin , Lin, Jian‐Xian , Chen, Qi‐Yue , Huang, Chang-Ming

International Journal of Surgery | October 6, 2023 | Volume: 109 | Issue: 12 | Pages: 4101-4112

10.1097/js9.0000000000000731 | PMID 37800589 Get It

Background: Due to lacking evidence on surveillance for gastric cancer (GC), this study aimed to determine the optimal postsurgical surveillance strategy for pathological stage (pStage) II/III GC patients and compare its cost-effectiveness with traditional surveillance strategies. Methods: Prospectively collected data from stage II/III GC patients (n=1661) who underwent upfront surgery at a large-volume tertiary cancer center in China (FJMUUH cohort) between January 2010 and October 2015. For external validation, two independent cohorts were included, which were composed of 380 stage II/III GC patients at an tertiary cancer center in U.S.A (Mayo cohort) between July 1991 and July 2012 and 270 stage II/III GC patients at another tertiary cancer center in China (QUAH cohort) between May 2010 and October 2014. Random forest models were used to predict dynamic recurrence hazards and to construct individual surveillance strategies for stage II/III GC. Cost-effectiveness was assessed by the Markov model. Results: The median follow-up period of the FJMUUH, the Mayo, and QUAH cohorts were 55, 158, and 70 months, respectively. In the FJMUUH cohort, the 5-year recurrence risk was higher in pStage III compared with pStage II GC patients (P<0.001). Our novel individual surveillance strategy achieved optimal cost-effectiveness for pStage II GC patients (ICER =$490/QALY). The most intensive NCCN surveillance guideline was more cost-effective (ICER =$983/QALY) for pStage III GC patients. The external validations confirmed our results. Conclusion: For patients with pStage II GC, individualized risk-based surveillance outperformed the JGCTG and NCCN surveillance guidelines. However, the NCCN surveillance guideline may be more suitable for patients with pStage III GC. Even though our results are limited by the retrospective study design, the authors believe that our findings should be considered when recommending postoperative surveillance for stage II/III GC with upfront surgery in the absence of a randomized clinical trial.