Brian Lee Egleston

Dr. Brian Lee Egleston

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Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

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

Representative Publications

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26 January 2006 in New England Journal of Medicine
Verified
Journal Article
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EMEllen J. MacKenzie
Ellen J. MacKenzie
FRFrederick P. Rivara
Frederick P. Rivara
GJGregory J. Jurkovich
Gregory J. Jurkovich
ANAvery B. Nathens
Avery B. Nathens
KFKatherine P. Frey
Katherine P. Frey
DSDaniel O. Scharfstein
Daniel O. Scharfstein
Hospitals have difficulty justifying the expense of maintaining trauma centers without strong evidence of their effectiveness. To address this gap, we examined differences in mortality between level 1 trauma centers and hospitals without a trauma center (non–trauma centers).

1 September 2015 in Medical Care
Verified
Journal Article
Closed access
SASteven R. Austin
Steven R. Austin
YWYu-Ning Wong
Yu-Ning Wong
RURobert G. Uzzo
Robert G. Uzzo
JBJ. Robert Beck
J. Robert Beck
BEBrian Lee Egleston
Brian Lee Egleston
Background: Comorbidity adjustment is an important component of health services research and clinical prognosis. When adjusting for comorbidities in statistical models, researchers can include comorbidities individually or through the use of summary measures such as the Charlson Comorbidity Index or Elixhauser score. We examined the conditions under which individual versus summary measures are most appropriate. Methods: We provide an analytic proof of the utility of comorbidity summary measures when used in place of individual comorbidities. We compared the use of the Charlson and Elixhauser scores versus individual comorbidities in prognostic models using a SEER-Medicare data example. We examined the ability of summary comorbidity measures to adjust for confounding using simulations. Results: We devised a mathematical proof that found that the comorbidity summary measures are appropriate prognostic or adjustment mechanisms in survival analyses. Once one knows the comorbidity score, no other information about the comorbidity variables used to create the score is generally needed. Our data example and simulations largely confirmed this finding. Conclusions: Summary comorbidity measures, such as the Charlson Comorbidity Index and Elixhauser scores, are commonly used for clinical prognosis and comorbidity adjustment. We have provided a theoretical justification that validates the use of such scores under many conditions. Our simulations generally confirm the utility of the summary comorbidity measures as substitutes for use of the individual comorbidity variables in health services research. One caveat is that a summary measure may only be as good as the variables used to create it.

9 November 2016 in Annals of Oncology
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Journal Article
Open access
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NZN. G. Zaorsky
N. G. Zaorsky
TCT. M. Churilla
T. M. Churilla
BEBrian Lee Egleston
Brian Lee Egleston
SFS. G. Fisher
S. G. Fisher
JRJ. A. Ridge
J. A. Ridge
JMJoshua E Meyer
Joshua E Meyer
The purpose of our study was to characterize the causes of death among cancer patients as a function of objectives: (i) calendar year, (ii) patient age, and (iii) time after diagnosis. US death certificate data in Surveillance, Epidemiology, and End Results Stat 8.2.1 were used to categorize cancer patient death as being due to index-cancer, nonindex-cancer, and noncancer cause from 1973 to 2012. In addition, data were characterized with standardized mortality ratios (SMRs), which provide the relative risk of death compared with all persons. The greatest relative decrease in index-cancer death (generally from > 60% to < 30%) was among those with cancers of the testis, kidney, bladder, endometrium, breast, cervix, prostate, ovary, anus, colorectum, melanoma, and lymphoma. Index-cancer deaths were stable (typically >40%) among patients with cancers of the liver, pancreas, esophagus, and lung, and brain. Noncancer causes of death were highest in patients with cancers of the colorectum, bladder, kidney, endometrium, breast, prostate, testis; >40% of deaths from heart disease. The highest SMRs were from nonbacterial infections, particularly among 1,000 for lymphomas, P < 0.001). The highest SMRs were typically within the first year after cancer diagnosis (SMRs 10–10,000, P < 0.001). Prostate cancer patients had increasing SMRs from Alzheimer's disease, as did testicular patients from suicide. The risk of death from index- and nonindex-cancers varies widely among primary sites. Risk of noncancer deaths now surpasses that of cancer deaths, particularly for young patients in the year after diagnosis.

1 March 2016 in JAMA Oncology
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Journal Article
Closed access
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RBRichard J. Bleicher
Richard J. Bleicher
KRKaren Ruth
Karen Ruth
ESElin R. Sigurdson
Elin R. Sigurdson
JBJ. Robert Beck
J. Robert Beck
EREric Ross
Eric Ross
BEBrian Lee Egleston
Brian Lee Egleston
Delays in the treatment of breast cancer have been feared for decades, as even William Halsted proclaimed in 1907 that “we no longer need the proof…[that] the slightest delay is dangerous…in the early stage of breast cancer.”1 There is little doubt that waiting for treatment causes anxiety, but the published medical literature has not provided a consistent answer as to whether any specific preoperative time to surgery (TTS) is associated with an effect on overall or disease-specific survival.

1 October 2009 in Journal of Clinical Oncology
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Journal Article
Closed access
KSKaryn B. Stitzenberg
Karyn B. Stitzenberg
ESElin R. Sigurdson
Elin R. Sigurdson
BEBrian Lee Egleston
Brian Lee Egleston
RSRussell B. Starkey
Russell B. Starkey
NMNeal J. Meropol
Neal J. Meropol
Purpose: The volume-outcomes relationship has led many to advocate centralization of cancer procedures at high volume hospitals (HVH). We hypothesized that in response cancer surgery has become increasingly centralized and that this centralization has resulted in increased travel burden for patients. Patients and Methods: Using 1996 to 2006 discharge data from NY, NJ, PA, all patients ≥ 18 years old treated with extirpative surgery for colorectal, esophageal, or pancreatic cancer were examined. Patients and hospitals were geocoded. Annual hospital procedure volume for each tumor site was examined, and multiple quantile and logistic regressions were used to compare changes in centralization and distance traveled. Results: Five thousand two hundred seventy-three esophageal, 13,472 pancreatic, 202,879 colon, and 51,262 rectal procedures were included. A shift to HVH occurred to varying degrees for all tumor types. The odds of surgery at a low volume hospital decreased for esophagus, pancreas and colon: per year odds ratios (ORs) were 0.87 (95% CI, 0.85 to 0.90), 0.85 (95% CI, 0.84 to 0.87), and 0.97 (95% CI, 0.97 to 0.98). Median travel distance increased for all sites: esophagus 72%, pancreas 40%, colon 17%, and rectum 28% (P < .0001). Travel distance was proportional to procedure volume (P < .0001). The majority of the increase in distance was attributable to centralization. Conclusion: There has been extensive centralization of complex cancer surgery over the past decade. While this process should result in population-level improvements in cancer outcomes, centralization is increasing patient travel. For some subsets of the population, increasing travel requirements may pose a significant barrier to access to quality cancer care.

1 April 2008 in Journal of Urology
Verified
Journal Article
Closed access
DKDavid A. Kunkle
David A. Kunkle
BEBrian Lee Egleston
Brian Lee Egleston
RURobert G. Uzzo
Robert G. Uzzo
The incidence of renal cell carcinoma is increasing due to the incidental detection of small renal masses. Resection, predominantly by nephron sparing surgery, remains the standard of care due to its durable oncological outcomes. Active surveillance and ablative technologies have emerged as alternatives to surgery in select patients. We performed a meta-analysis of published data evaluating nephron sparing surgery, cryoablation, radio frequency ablation and observation for small renal masses to define the current data. A MEDLINE search was performed for clinically localized sporadic renal masses. Patient age, tumor size, duration of followup, available pathological data and oncological outcomes were evaluated. A total of 99 studies representing 6,471 lesions were analyzed. Significant differences in mean patient age (p <0.001), tumor size (p <0.001) and followup duration (p <0.001) were detected among treatment modalities. The incidence of unknown/indeterminate pathological findings was significantly different among cryoablation, radio frequency ablation and observation (p = 0.003), and a significant difference in the rates of malignancy among lesions with known pathological results was detected (p = 0.001). Compared to nephron sparing surgery significantly increased local progression rates were calculated for cryoablation (RR = 7.45) and radio frequency ablation (RR = 18.23). However, no statistical differences were detected in the incidence of metastatic progression regardless of whether lesions were excised, ablated or observed. Nephron sparing surgery, ablation and surveillance are viable strategies for small renal masses based on short-term and intermediate term oncological outcomes. However, a significant selection bias exists in the application of these techniques. While long-term data have demonstrated durable outcomes for nephron sparing surgery, extended oncological efficacy is lacking for ablation and surveillance strategies. The extent to which treatment alters the natural history of small renal masses is not yet established.