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1.
Dig Dis Sci ; 65(6): 1669-1678, 2020 06.
Article in English | MEDLINE | ID: mdl-31643036

ABSTRACT

BACKGROUND: Racial/ethnic disparities in prognosis have been reported in patients with hepatocellular carcinoma (HCC); however, few studies have evaluated racial/ethnic disparities in the context of insurance status. AIMS: Characterize racial/ethnic and insurance status in early tumor detection, receipt of curative therapy and overall survival in a multicenter diverse cohort of HCC patients from the USA. STUDY: We included patients with HCC diagnosed between June 2012 and May 2013 at four centers in the USA. Generalized linear mixed effects models were used to compare early tumor detection (defined using Milan Criteria) and curative treatment receipt (liver transplantation, surgical resection, or local ablation) as a function of patient race/ethnicity and insurance status. A multivariable frailty survival model was used to compare risk of death between patient groups. RESULTS: Of 379 HCC patients (52.8% non-Hispanic White, 19.5% Hispanic White, 19.8% Black), 46.4% and 48.0% were found at an early stage and underwent curative therapy, respectively, and median overall survival of the cohort was 25.7 months. Early detection of HCC was associated with gastroenterology subspecialty care and receipt of HCC surveillance but not race/ethnicity or insurance status in adjusted models. However, commercial insurance was significantly associated with higher odds of curative treatment receipt, which in turn was the strongest correlate for overall survival. After adjusting for health system and insurance status, race/ethnicity was not associated with curative treatment receipt or overall survival. CONCLUSIONS: Insurance status and access to gastroenterology subspecialty care may be important drivers of racial/ethnic disparities in prognosis among HCC patients.


Subject(s)
Carcinoma, Hepatocellular/therapy , Healthcare Disparities/ethnology , Insurance, Health , Liver Neoplasms/therapy , Racial Groups , Carcinoma, Hepatocellular/economics , Carcinoma, Hepatocellular/epidemiology , Carcinoma, Hepatocellular/ethnology , Cohort Studies , Female , Humans , Liver Neoplasms/economics , Liver Neoplasms/epidemiology , Liver Neoplasms/ethnology , Male , Middle Aged , Retrospective Studies , United States/epidemiology
2.
Int J Radiat Oncol Biol Phys ; 100(1): 122-130, 2018 01 01.
Article in English | MEDLINE | ID: mdl-29066120

ABSTRACT

PURPOSE: To conduct a large single-institution comparison of transarterial chemoembolization (TACE) and stereotactic body radiation therapy (SBRT) outcomes in similar groups of patients with hepatocellular carcinoma (HCC). METHODS AND MATERIALS: From 2006 to 2014, 209 patients with 1 to 2 tumors underwent TACE (n=84) to 114 tumors or image guided SBRT (n=125) to 173 tumors. Propensity score analysis with inverse probability of treatment weighting was used to compare outcomes between treatments while adjusting for imbalances in treatment assignment. Local control (LC), toxicity, and overall survival (OS) were retrospectively analyzed. RESULTS: The TACE and SBRT groups were similar with respect to the number of tumors treated per patient, underlying liver disease, and baseline liver function. Patients treated with SBRT were older (65 vs 61 years, P=.01), had smaller tumors (2.3 vs 2.9 cm, P<.001), and less frequently underwent liver transplantation (8% vs 18%, P=.01). The 1- and 2-year LC favored SBRT: 97% and 91%, respectively, for SBRT and 47% and 23% for TACE (hazard ratio 66.5, P<.001). For patients treated with TACE, higher alpha-fetoprotein (hazard ratio 1.11 per doubling, P=.008) and segmental portal vein thrombosis (hazard ratio 9.9, P<.001) were associated with worse LC. Predictors associated with LC after SBRT were not identified. Grade 3+ toxicity occurred after 13% and 8% of TACE and SBRT treatments, respectively (P=.05). There was no difference in OS between patients treated with TACE or SBRT. CONCLUSIONS: Stereotactic body radiation therapy is a safe alternative to TACE for 1 to 2 tumors and provides better LC, with no observed difference in OS. Prospective comparative trials of TACE and SBRT are warranted.


Subject(s)
Carcinoma, Hepatocellular/drug therapy , Carcinoma, Hepatocellular/surgery , Chemoembolization, Therapeutic , Liver Neoplasms/drug therapy , Liver Neoplasms/surgery , Radiosurgery , Radiotherapy, Image-Guided/methods , Adult , Aged , Carcinoma, Hepatocellular/blood , Carcinoma, Hepatocellular/pathology , Chemoembolization, Therapeutic/adverse effects , Chemoembolization, Therapeutic/mortality , Female , Humans , Liver Neoplasms/blood , Liver Neoplasms/pathology , Liver Transplantation/statistics & numerical data , Male , Middle Aged , Portal Vein , Propensity Score , Radiosurgery/adverse effects , Radiosurgery/mortality , Retrospective Studies , Treatment Outcome , Tumor Burden , Venous Thrombosis/etiology , alpha-Fetoproteins/analysis
4.
J Nutr ; 132(6 Suppl 2): 1604S-6S, 2002 06.
Article in English | MEDLINE | ID: mdl-12042469

ABSTRACT

In vitro and in vivo studies of human tissues have demonstrated telomeric attrition with age and have linked this attrition to cellular senescence and aging. Telomere studies in canine subjects have not thus far consistently uncovered the same pattern of telomere attrition that would be expected because of the end replication problem. In this report we describe the investigation of telomere lengths in a broad age range of dogs from three different breeds: the Labrador Retriever, Miniature Schnauzer and Beagle. Peripheral blood mononuclear cell-derived DNA samples were subjected to terminal restriction fragment (TRF) analysis and demonstrated a range of mean TRFs from 9.7 to 22.3 kbp. Telomeric attrition tended to be associated with increasing donor age (P = 0.06). Interbreed differences in mean TRF values were also noted (P = 0.006). These results warrant further investigation of possible interbreed differences, given that shorter telomeres may contribute to differing life expectancy between breeds.


Subject(s)
Aging/genetics , Dogs/genetics , Telomere/genetics , Animals , Monocytes/physiology , Restriction Mapping , Species Specificity
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