Alice Yu

Dr. Alice Yu

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 August 2022 in Cancers
Verified
Journal Article
Open access
PDF file
Nagi KumarNagi Kumar
Nagi Kumar
SHStephanie Hogue
Stephanie Hogue
JPJulio Pow-Sang
Julio Pow-Sang
MPMichael Poch
Michael Poch
BMBrandon J. Manley
Brandon J. Manley
DBDoratha A. Byrd
Doratha A. Byrd
Accumulating evidence supports green tea catechins (GTCs) in chemoprevention for prostate cancer (PCa), a leading cause of cancer morbidity and mortality among men. GTCs include (−)-epigallocatechin-3-gallate, which may modulate the molecular pathways implicated in prostate carcinogenesis. Prior studies of GTCs suggested that they are bioavailable, safe, and effective for modulating clinical and biological markers implicated in prostate carcinogenesis. GTCs may be of particular benefit to those with low-grade PCas typically managed with careful monitoring via active surveillance (AS). Though AS is recommended, it has limitations including potential under-grading, variations in eligibility, and anxiety reported by men while on AS. Secondary chemoprevention of low-grade PCas using GTCs may help address these limitations. When administrated orally, the gut microbiome enzymatically transforms GTC structure, altering its bioavailability, bioactivity, and toxicity. In addition to xenobiotic metabolism, the gut microbiome has multiple other physiological effects potentially involved in PCa progression, including regulating inflammation, hormones, and other known/unknown pathways. Therefore, it is important to consider not only the independent roles of GTCs and the gut microbiome in the context of PCa chemoprevention, but how gut microbes may relate to individual responses to GTCs, which, in turn, can enhance clinical decision-making.

8 June 2024 in Cancers
Verified
Journal Article
Open access
PDF file
AGArvin K. George
Arvin K. George
RMRanko Miocinovic
Ranko Miocinovic
APAmit R. Patel
Amit R. Patel
DLDerek J. Lomas
Derek J. Lomas
ACAndres F. Correa
Andres F. Correa
JCJonathan Coleman
Jonathan Coleman
The PRESERVE study (NCT04972097) aims to evaluate the safety and effectiveness of the NanoKnife System to ablate prostate tissue in patients with intermediate-risk prostate cancer (PCa). The NanoKnife uses irreversible electroporation (IRE) to deliver high-voltage electrical pulses to change the permeability of cell membranes, leading to cell death. A total of 121 subjects with organ-confined PCa ≤ T2c, prostate-specific antigens (PSAs) ≤ 15 ng/mL, and a Gleason score of 3 + 4 or 4 + 3 underwent focal ablation of the index lesion. The primary endpoints included negative in-field biopsy and adverse event incidence, type, and severity through 12 months. At the time of analysis, the trial had completed accrual with preliminary follow-up available. Demographics, disease characteristics, procedural details, PSA responses, and adverse events (AEs) are presented. The median (IQR) age at screening was 67.0 (61.0–72.0) years and Gleason distribution 3 + 4 (80.2%) and 4 + 3 (19.8%). At 6 months, all patients with available data (n = 74) experienced a median (IQR) percent reduction in PSA of 67.6% (52.3–82.2%). Only ten subjects (8.3%) experienced a Grade 3 adverse event; five were procedure-related. No Grade ≥ 4 AEs were reported. This study supports prior findings that IRE prostate ablation with the NanoKnife System can be performed safely. Final results are required to fully assess oncological, functional, and safety outcomes.

1 April 2022 in Urologic Oncology: Seminars and Original Investigations
Verified
Journal Article
Closed access
AYAlice Yu
Alice Yu
YWYe Wang
Ye Wang
MMMatthew Mossanen
Matthew Mossanen
MPMark Preston
Mark Preston
FCFilipe Lf Carvalho
Filipe Lf Carvalho
SCSteven L. Chang
Steven L. Chang

27 February 2025 in Cancers
Verified
Journal Article
Open access
PDF file
KAKapil K Avasthi
Kapil K Avasthi
JCJung W. Choi
Jung W. Choi
TGTetiana Glushko
Tetiana Glushko
BMBrandon J. Manley
Brandon J. Manley
AYAlice Yu
Alice Yu
YBYoganand Balagurunathan
Yoganand Balagurunathan
Background/Objectives: Prostate cancer (PCa) is the most diagnosed cancer in men worldwide. Early diagnosis of the disease provides better treatment options for these patients. Recent studies have demonstrated that plasma-based extracellular vesicle microRNAs (miRNAs) are functionally linked to cancer progression, metastasis, and aggressiveness. The use of magnetic resonance imaging (MRI) as the standard of care provides an overall assessment of prostate disease. Quantitative metrics (radiomics) from the MRI provide a better evaluation of the tumor and have been shown to improve disease detection. Methods: We conducted a study on prostate cancer patients, analyzing baseline blood plasma and MRI data. Exosomes were isolated from blood plasma samples to quantify miRNAs, while MRI scans provided detailed tumor morphology. Radiomics features from MRI and miRNA expression data were integrated to develop predictive models, which were evaluated using ROC curve analysis, highlighting the multivariable model’s effectiveness. Results: Our findings indicate that the univariate feature-based model with the highest Youden’s index achieved average areas under the receiver operating characteristic (ROC) curve of 0.76, 0.82, and 0.84 for miRNA, MR-T2W, and MR-ADC features, respectively, in identifying clinically aggressive (Gleason grade) disease. The multivariable feature-based model yielded an average area under the curve (AUC) of 0.88 and 0.95 using combinations of miRNA markers with imaging features in MR-ADC and MR-T2W, respectively. Conclusions: Our study demonstrates that combining miRNA markers with MRI-based radiomics improves the identification of clinically aggressive prostate cancer.

8 October 2021 in Urologic Oncology: Seminars and Original Investigations
Verified
Journal Article
Open access
AAAhmet Murat Aydin
Ahmet Murat Aydin
RRRichard R. Reich
Richard R. Reich
BCBiwei Cao
Biwei Cao
SCSalim K. Cheriyan
Salim K. Cheriyan
AHAli Hajiran
Ali Hajiran
SGScott M. Gilbert
Scott M. Gilbert
To assess predictors, indicators and medical necessity of readmissions after neoadjuvant chemotherapy (NAC) and radical cystectomy in order to identify opportunities for reducing readmission rates. Records for patients treated with cisplatin-based NAC followed by radical cystectomy between 2007 and 2017 were reviewed for 90-day complications and readmission. Readmissions were classified as necessary vs. discretionary based on independent clinician review. The association between postoperative complications and necessary or discretionary readmission were examined with adjusted regression models. Among a total of 250 patients, 76 patients (30.4%) were readmitted within 90 days of surgery (19 discretionary and 57 necessary). Age, insurance coverage, and comorbidity were similar between readmitted and non-readmitted patients. Readmission was more likely after neobladder than ileal conduit (39% vs. 23%, p=0.02). Major (grade ≥ 3) complications within 90-day of surgery including index admission and post-discharge period were significantly more common among re-admitted patients compared to patients who were not readmitted (40% in necessary, 21% in discretionary, 3% in none, p<0.001). Median length of stay on readmission was twice as long in necessary cases compared to discretionary cases (5 vs. 2.5 days, p<0.001). Gastrointestinal and infectious complications were associated with discretionary readmission in adjusted analyses, while infectious, renal/genitourinary and thromboembolic complications were associated with necessary readmission. Twenty-five percent of readmissions were categorized as discretionary and were driven primarily by low-grade gastrointestinal complications, marginal oral intake and failure to thrive, suggesting that better coordinated post-discharge supportive care could help avoid a substantial proportion of readmissions.

18 January 2025 in BJU International
Verified
Journal Article
Closed access
AYAlice Yu
Alice Yu
PHPatrick J. Hensley
Patrick J. Hensley
HHHeather L. Huelster
Heather L. Huelster
AMAustin Martin
Austin Martin
APAaron Potrezke
Aaron Potrezke
PSPhilippe E. Spiess
Philippe E. Spiess