Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Timothy Bui is active.

Publication


Featured researches published by Timothy Bui.


JAMA Dermatology | 2015

Concurrent Vismodegib and Radiotherapy for Recurrent, Advanced Basal Cell Carcinoma

Erqi L. Pollom; Timothy Bui; Anne Lynn S. Chang; A. Dimitrios Colevas; Wendy Hara

IMPORTANCE Vismodegib is a targeted agent recently approved for treating patients who develop recurrent or locally advanced basal cell carcinoma (BCC), and will inevitably be integrated into existing therapy for advanced BCC as it becomes increasingly used. Improved understanding of how vismodegib interacts with other treatment modalities, including radiotherapy, would help optimize multidisciplinary therapy and clinical outcomes. OBSERVATIONS We report 2 cases of recurrent, advanced BCC treated from April 1, 2012, through October 31, 2014, with concurrent radiotherapy and vismodegib. Concurrent treatment appeared to be well tolerated and efficacious, with both patients having no evidence of progressive disease at last follow-up. CONCLUSIONS AND RELEVANCE We found that the combination of vismodegib and radiotherapy is feasible for patients with recurrent or locally advanced BCC and that combined use of currently available therapies for advanced BCC warrants further prospective study.


Oral Oncology | 2015

A prospective study of electronic quality of life assessment using tablet devices during and after treatment of head and neck cancers.

Erqi L. Pollom; Ellen Wang; Timothy Bui; Grant Ognibene; Rie von Eyben; Vasu Divi; John B. Sunwoo; Michael Kaplan; A. Dimitri Colevas; Quynh-Thu Le; Wendy Hara

OBJECTIVES Electronic data collection is increasingly used for quality of life (QOL) assessments in the field of oncology. It is important to assess the feasibility of these new data capture technologies. MATERIALS AND METHODS Patients at our institution who were 18 years or older with a pathological diagnosis of head and neck cancer were prospectively enrolled. Each patient completed two questionnaires [EORTC-QLQ-C30 and EORTC-QLQ-H&N35] administered on a touch-screen tablet device (iPad) at initial consult, during treatment, at the completion of treatment and at each subsequent follow up visit for one year after treatment. RESULTS A total of 50 patients were included in this study. Although all patients completed the surveys at the initial consult, 86% of initially enrolled patients completed surveys at the end of radiation treatment, and 48% of initially enrolled patients completed surveys by the fourth follow-up visit. Average time to complete the survey for all patients over all time points was 9.8 min (standard deviation 6.1). Age as a continuous variable was significantly associated with time for survey completion (p<0.001), with older age associated with longer survey completion times. CONCLUSION QOL assessment using tablet devices in head and neck cancer patients is feasible, but may be more challenging in elderly patients. Patients ⩾70 years old may benefit from more assistance with electronic forms and should be allotted more time for completing tablet-based QOL surveys.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2016

Prognostic value of midtreatment FDG-PET in oropharyngeal cancer.

Erqi L. Pollom; Jie Song; Benjamin Y. Durkee; Sonya Aggarwal; Timothy Bui; Rie von Eyben; Ruijiang Li; David M. Brizel; Billy W. Loo; Quynh-Thu Le; Wendy Hara

Prognostic metabolic imaging indices are needed for risk stratification for patients with locally advanced oropharyngeal cancer.


Medical Physics | 2015

TU-AB-BRA-10: Prognostic Value of Intra-Radiation Treatment FDG-PET and CT Imaging Features in Locally Advanced Head and Neck Cancer

Jie Song; Yi Cui; Erqi L. Pollom; Ben Y. Durkee; Sonya Aggarwal; Timothy Bui; Quynh-Thu Le; Billy W. Loo; Wendy Hara; Ruijiang Li

Purpose: To predict response to radiation treatment using computational FDG-PET and CT images in locally advanced head and neck cancer (HNC). Methods: 68 patients with State III-IVB HNC treated with chemoradiation were included in this retrospective study. For each patient, we analyzed primary tumor and lymph nodes on PET and CT scans acquired both prior to and during radiation treatment, which led to 8 combinations of image datasets. From each image set, we extracted high-throughput, radiomic features of the following types: statistical, morphological, textural, histogram, and wavelet, resulting in a total of 437 features. We then performed unsupervised redundancy removal and stability test on these features. To avoid over-fitting, we trained a logistic regression model with simultaneous feature selection based on least absolute shrinkage and selection operator (LASSO). To objectively evaluate the prediction ability, we performed 5-fold cross validation (CV) with 50 random repeats of stratified bootstrapping. Feature selection and model training was solely conducted on the training set and independently validated on the holdout test set. Receiver operating characteristic (ROC) curve of the pooled Result and the area under the ROC curve (AUC) was calculated as figure of merit. Results: For predicting local-regional recurrence, our model built on pre-treatment PET of lymph nodes achieved the best performance (AUC=0.762) on 5-fold CV, which compared favorably with node volume and SUVmax (AUC=0.704 and 0.449, p<0.001). Wavelet coefficients turned out to be the most predictive features. Prediction of distant recurrence showed a similar trend, in which pre-treatment PET features of lymph nodes had the highest AUC of 0.705. Conclusion: The radiomics approach identified novel imaging features that are predictive to radiation treatment response. If prospectively validated in larger cohorts, they could aid in risk-adaptive treatment of HNC.


BMC Cancer | 2015

γ-Glutamyl transferase 7 is a novel regulator of glioblastoma growth

Timothy Bui; Ryan T. Nitta; Suzana Assad Kahn; Seyed-Mostafa Razavi; Maya Agarwal; Parvir Aujla; Sharareh Gholamin; Lawrence Recht; Gordon Li

BackgroundGlioblastoma (GBM) is the most malignant primary brain tumor in adults, with a median survival time of one and a half years. Traditional treatments, including radiation, chemotherapy, and surgery, are not curative, making it imperative to find more effective treatments for this lethal disease. γ-Glutamyl transferase (GGT) is a family of enzymes that was shown to control crucial redox-sensitive functions and to regulate the balance between proliferation and apoptosis. GGT7 is a novel GGT family member that is highly expressed in brain and was previously shown to have decreased expression in gliomas. Since other members of the GGT family were found to be altered in a variety of cancers, we hypothesized that GGT7 could regulate GBM growth and formation.MethodsTo determine if GGT7 is involved in GBM tumorigenesis, we modulated GGT7 expression in two GBM cell lines (U87-MG and U138) and monitored changes in tumorigenicity in vitro and in vivo.ResultsWe demonstrated for the first time that GBM patients with low GGT7 expression had a worse prognosis and that 87% (7/8) of primary GBM tissue samples showed a 2-fold decrease in GGT7 expression compared to normal brain samples. Exogenous expression of GGT7 resulted in a 2- to 3-fold reduction in proliferation and anchorage-independent growth under minimal growth conditions (1% serum). Decreasing GGT7 expression using either short interfering RNA or short hairpin RNA consistently increased proliferation 1.5- to 2-fold. In addition, intracranial injections of U87-MG cells with reduced GGT7 expression increased tumor growth in mice approximately 2-fold, and decreased mouse survival. To elucidate the mechanism by which GGT7 regulates GBM growth, we analyzed reactive oxygen species (ROS) levels in GBM cells with modulated GGT7 expression. We found that enhanced GGT7 expression reduced ROS levels by 11-33%.ConclusionOur study demonstrates that GGT7 is a novel player in GBM growth and that GGT7 can play a critical role in tumorigenesis by regulating anti-oxidative damage. Loss of GGT7 may increase the cellular ROS levels, inducing GBM occurrence and growth. Our findings suggest that GGT7 can be a promising biomarker and a potential therapeutic target for GBM.


Journal of Spine & Neurosurgery | 2014

Non-Surgical Treatment for Racemic Neurocysticercosis with Compression of the OpticNerve

Mario Moreno; Timothy Bui; Maya Agarwal; Ryan T. Nitta; Y Joyce Liao; Gordon Li

Non-Surgical Treatment for Racemic Neurocysticercosis with Compression of the Optic Nerve There are very few reports in the literature to guide treatment for patients with racemic neurocysticercosis with direct compression of the optic nerves leading to vision loss. Although the current approach to a patient with sudden neurologic decline with a large mass lesion is surgical decompression, we present a case of a patient who improved with antiparasitics and steroids alone. A 32-year-old Hispanic male presented with a several-month history of headache and new onset left eye vision loss.


Journal of Clinical Oncology | 2017

Low pre-operative absolute monocyte count to predict overall survival benefit for oral cavity squamous cell carcinoma.

Timothy Bui; J.L. Shah; Michael Kaplan; A. Dimitrios Colevas; Quynh-Thu Le; Wendy Hara


Journal of Clinical Oncology | 2017

Prognostic value of mid-treatment total lesion glycolysis in p16+ oropharyngeal cancer.

Erqi L. Pollom; Jie Song; Ben Y. Durkee; Sonya Aggarwal; Timothy Bui; Ruijiang Li; Quynh-Thu Le; Billy W. Loo; Wendy Hara


International Journal of Radiation Oncology Biology Physics | 2016

Pattern of Perineural Invasion Is an Important Prognostic Factor for Oral Cavity Cancer

Jeremy P. Harris; J.L. Shah; Kurt B. Schaberg; J.J. Chen; Timothy Bui; Michael Kaplan; Quynh-Thu Le; Christina S. Kong; Wendy Hara


International Journal of Radiation Oncology Biology Physics | 2016

A Pilot Study of Electronic Quality of Life Assessments Using Tablet Devices During and After Treatment of Head and Neck Cancers

E. Wang; Erqi L. Pollom; Timothy Bui; Grant Ognibene; R. von Eyben; Vasu Divi; John B. Sunwoo; Michael Kaplan; A.D. Colevas; Quynh-Thu Le; Wendy Hara

Collaboration


Dive into the Timothy Bui's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge