Jacob Y. Shin
Rush University Medical Center
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Publication
Featured researches published by Jacob Y. Shin.
Journal of Neuro-oncology | 2017
Jacob Y. Shin; Ja Kyoung Yoon; Aidnag Z. Diaz
To determine the impact of insurance status and income for anaplastic astrocytoma (AA). Data were extracted from the National Cancer Data Base. Chi square test, Kaplan–Meier method, and Cox regression models were employed in SPSS 22.0 (Armonk, NY: IBM Corp.) for data analyses. 4325 patients with AA diagnosed from 2004 to 2013 were identified. 2781 (64.3%) had private insurance, 925 (21.4%) Medicare, 396 (9.2%) Medicaid, and 223 (5.2%) were uninsured. Those uninsured were more likely to be Black or Hispanic versus White or Asian (p < 0.001), have lower median income (p < 0.001), less educated (p < 0.001), and not receive adjuvant chemoradiation (p < 0.001). 1651 (38.2%) had income ≥
Journal of Clinical Neuroscience | 2017
Jacob Y. Shin; Ja Kyoung Yoon; Aidnag Z. Diaz
63,000, 1204 (27.8%)
Archives of Otolaryngology-head & Neck Surgery | 2017
Jacob Y. Shin; Ja Kyoung Yoon; Aaron K. Shin; Philip Blumenfeld; Miranda Mai; Aidnag Z. Diaz
48,000–
Journal of Clinical Neuroscience | 2017
Jacob Y. Shin; Ja Kyoung Yoon; Aidnag Z. Diaz
62,999, 889 (20.5%)
Journal of Neuro-oncology | 2016
Jacob Y. Shin; Aidnag Z. Diaz
38,000–
Lung | 2018
Jacob Y. Shin; Ja Kyoung Yoon; G. Marwaha
47,999, and 581 (13.4%) had income <
International Journal of Oral and Maxillofacial Surgery | 2018
Jacob Y. Shin; Ja Kyoung Yoon; Aaron K. Shin; Aidnag Z. Diaz
38,000. Those with lower income were more likely to be Black or Hispanic versus White or Asian (p < 0.001), uninsured (p < 0.001), reside in a rural area (p < 0.001), less educated (p < 0.001), and not receive adjuvant chemoradiation (p < 0.001). Those with private insurance had significantly higher overall survival (OS) than those uninsured, on Medicaid, or on Medicare (p < 0.001). Those with income ≥
Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2018
Jacob Y. Shin; Ja Kyoung Yoon; Aaron K. Shin; Aidnag Z. Diaz
63,000 had significantly higher OS than those with lower income (p < 0.001). On multivariate analysis, age, insurance status, income, and adjuvant therapy were independent prognostic factors for OS. Being uninsured and having income <
International Journal of Radiation Oncology Biology Physics | 2017
Jacob Y. Shin; G.A. Russo
38,000 were independent prognostic factors for worse OS in AA. Further investigations are warranted to help determine ways to ensure adequate medical care for those who may be socially disadvantaged so that outcome can be maximized for all patients regardless of socioeconomic status.
Clinical Lung Cancer | 2017
Jacob Y. Shin; Ja Kyoung Yoon; G. Marwaha
The objective of our study is to determine the influence of race on overall survival (OS) for anaplastic oligodendroglioma (AO). Data were extracted from the National Cancer Data Base (NCDB). Chi-square test, Kaplan-Meier method, and Cox regression models were employed in SPSS 22.0 (Armonk, NY: IBM Corp.) for data analyses. 1643 patients with AO were identified. 1386 (84.3%) were White, 83 (5.0%) Black, 133 (8.1%) Hispanic, and 41 (2.5%) were Asian. White and Black patients were significantly older than Hispanic and Asian patients (49.3% vs. 49.4% vs. 33.1% vs. 39.0%, p=0.003). Black patients were significantly less likely to be insured than White patients (12.8 vs. 7.2%, p<0.001) and significantly more likely to have lower income than other races (p<0.001). A trend towards higher comorbidity burden and lower rate of gross total resection was seen in Black patients. Black patients had significantly worse five-year OS compared to White, Hispanic, and Asian patients (40.3% vs. 52.3% vs. 67.8% vs. 67.7%, p=0.028). Of those who received adjuvant chemoRT, Black patients still had significantly worse OS compared to White patients (p=0.021). On multivariate analysis, Black race, older age at diagnosis, and not receiving adjuvant chemoradiotherapy were independent prognostic factors for worse OS in anaplastic oligodendroglioma. Future studies are warranted to help determine predictors for unfavorable molecular status, ways to optimize management of comorbidities, and interventions to help ensure adequate access to medical care for all patients to better care for those who may be at more risk for poorer outcome.