Wendy Hsiao
University of Southern California
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Publication
Featured researches published by Wendy Hsiao.
Pharmaceuticals | 2015
Thomas G. Frazier; Kevin Fox; Judy Smith; Christine Laronga; Anita P. McSwain; Devchand Paul; Michael Schultz; Joseph Stilwill; Christine B. Teal; Tracey Weisberg; Judith Vacchino; Amy P. Sing; Dasha Cherepanov; Wendy Hsiao; Eunice Chang; Michael S. Broder
To assess clinical utility of the 21-gene assay (Oncotype DX® Recurrence Score®), we determined whether women with HER2(−)/ER+ pN1mi breast cancer with low (<18) Recurrence Scores results are given adjuvant chemotherapy in a lower proportion than those with high scores (≥31). This was a multicenter chart review of ≥18 year old women with pN1mi breast cancer, HER2(−)/ER+ tumors, ductal/lobular/mixed histology, with the assay ordered on or after 1 January 2007. One hundred and eighty one patients had a mean age of 60.7 years; 82.9% had ECOG performance status 0; 33.7% had hypertension, 22.7% had osteoporosis, 18.8% had osteoarthritis, and 8.8% had type-2 diabetes. Mean Recurrence Score was 17.8 (range: 0–50). 48.6% had a mastectomy; 55.8% had a lumpectomy. 19.8% of low-risk group patients were recommended chemotherapy vs. 57.9% in the intermediate-risk group and 100% in the high-risk group (p < 0.001). A total of 80.2% of the low-risk group were recommended endocrine therapy alone, while 77.8% of the high-risk group were recommended both endocrine and chemotherapy (p < 0.001). The Oncotype DX Recurrence Score result provides actionable information that can be incorporated into treatment planning for women with HER2(−)/ER+ pN1mi breast cancer. The Recurrence Score result has clinical utility in treatment planning for HER2(−)/ER+ pN1mi breast cancer patients.
Dermatologic Therapy | 2015
Jack J. Tian; Wendy Hsiao; Scott Worswick
In this case study, we present a safe and novel treatment for a patient with soft tissue hand disability caused by severe and chronic lupus and cutis laxa (CL). This patient was a woman in her 50s with a 20‐year history of systemic lupus erythematous (SLE) and multiple sclerosis who developed hand disability because of the drastic loss of firmness in her soft tissue, extending from the dermis down to the ligaments. The likely cause was CL with SLE synovitis, exacerbated by corticosteroid tapering. Fractional photothermolysis (FP) LASER (Fraxel DUAL 1550/1927; Solta Medical) therapy profoundly alleviated her joint locking in addition to improving the firmness of the overlying skin to reverse her hand disability. This case illustrates a novel approach to CL hand treatment and the profound impact the treatment had on the patients disabled hand. FP therapy is quick and safe, and its medical application to skin and joints should be further explored.
Journal of Medical Economics | 2014
Tanya Gk Bentley; Brock Schroeder; Catherine A. Schnabel; Mark G. Erlander; Wendy Hsiao; Jesse D. Ortendahl; Michael S. Broder
Abstract Objectives: To estimate the clinical and economic trade-offs involved in using a molecular assay (92-gene assay, CancerTYPE ID) to aid in identifying the primary site of difficult-to-diagnose metastatic cancers and to explore whether the 92-gene assay can be used to standardize the diagnostic process and costs for clinicians, patients, and payers. Methods: Four decision-analytic models were developed to project the lifetime clinical and economic impact of incorporating the 92-gene assay compared with standard care alone. For each model, total and incremental costs, life-years, quality-adjusted life-years (QALYs), incremental cost–effectiveness ratios (ICERs), and the proportion of patients treated correctly versus incorrectly were projected from the payer perspective. Model inputs were based on published literature, analyses of SEER (Surveillance Epidemiology and End Results) data, publicly available data, and interviews with clinical experts. Results: In all four models, the 92-gene assay increased the proportion of patients treated correctly, decreased the proportion of patients treated with empiric therapy, and increased quality-adjusted survival. In the primary model, the ICER was
Archive | 2013
Michael S. Broder; Wendy Hsiao
50,273/QALY; thus, the 92-gene assay is therefore cost effective when considering a societal willingness-to-pay threshold of
Journal of Surgical Oncology | 2015
Michael Alvarado; Dennis L. Carter; J. Michael Guenther; James Hagans; Rachel Y. Lei; Charles E. Leonard; Jennifer Manders; Amy P. Sing; Michael S. Broder; Dasha Cherepanov; Eunice Chang; Marianne Eagan; Wendy Hsiao; Michael Schultz
100,000/QALY. These findings were robust across sensitivity analyses. Conclusions: Use of the 92-gene assay for diagnosing metastatic tumors of uncertain origin is associated with reduced misdiagnoses, increased survival, and improved quality of life. Incorporating the assay into current practice is a cost-effective approach to standardizing diagnostic methods while improving patient care. Limitations of this analysis are the lack of data availability and resulting modeling simplifications, although sensitivity analyses showed these to not be key drivers of results.
Thrombosis Research | 2016
Thomas Delate; Wendy Hsiao; Benjamin Kim; Daniel M. Witt; Melissa R. Meyer; Alan S. Go; Margaret C. Fang
In the US, bilateral salpingo-oophorectomy (BSO) at the time of hysterectomy for benign disease is commonly done to prevent the subsequent development of ovarian cancer. Almost all BSOs (87%) are done at time of hysterectomy [1]. Oophorectomy rates appear to have peaked recently, with 55% of hysterectomies accompanied by the procedure in 1999 compared to 39-45% in more recent years [2, 3, 4]. Recent data show age remains the strongest predictor of elective BSO, with 40% of women 40-44 years old, 78% of women 50-54 years old, and 68% of women 55 years or older having had BSO at hysterectomy [5].
Journal of Clinical Oncology | 2017
Tanya Gk Bentley; Brock Schroeder; Catherine A. Schnabel; Jesse D. Ortendahl; Wendy Hsiao; Mark G. Erlander; Michael S. Broder
Journal of Clinical Oncology | 2017
Michael S. Broder; Irina Yermilov; Clifford Y. Ko; Melinda Maggard Gibbons; Eunice Chang; Tanya Gk Bentley; Dasha Cherepanov; Wendy Hsiao; Emmett B. Keeler
Journal of Clinical Oncology | 2016
Golnaz Vahdani; Ah-Reum Jeong; Zunera Ghaznavi; Wendy Hsiao; Mojtaba Akhtari
Clinical Lymphoma, Myeloma & Leukemia | 2015
Zunera Ghaznavi; Golnaz Vahdani; Wendy Hsiao; Mojtaba Akhtari