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Dive into the research topics where Robert S. Svatek is active.

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Featured researches published by Robert S. Svatek.


Cancer and Metastasis Reviews | 2009

Role of epithelial-to-mesenchymal transition (EMT) in drug sensitivity and metastasis in bladder cancer

David J. McConkey; Woonyoung Choi; Lauren Marquis; Frances Martin; Michael Williams; Jay B. Shah; Robert S. Svatek; Aditi Das; Liana Adam; Ashish M. Kamat; Arlene O. Siefker-Radtke; Colin P. Dinney

Epithelial-to-mesenchymal transition (EMT) is a process that plays essential roles in development and wound healing that is characterized by loss of homotypic adhesion and cell polarity and increased invasion and migration. At the molecular level, EMT is characterized by loss of E-cadherin and increased expression of several transcriptional repressors of E-cadherin expression (Zeb-1, Zeb-2, Twist, Snail, and Slug). Early work established that loss of E-cadherin and increased expression of MMP-9 was associated with a poor clinical outcome in patients with urothelial tumors, suggesting that EMT might also be associated with bladder cancer progression and metastasis. More recently, we have used global gene expression profiling to characterize the molecular heterogeneity in human urothelial cancer cell lines (n = 20) and primary patient tumors, and unsupervised clustering analyses revealed that the cells naturally segregate into two discrete “epithelial” and “mesenchymal” subsets, the latter consisting entirely of muscle-invasive tumors. Importantly, sensitivity to inhibitors of the epidermal growth factor receptor (EGFR) or type-3 fibroblast growth factor receptor (FGFR3) was confined to the “epithelial” subset, and sensitivity to EGFR inhibitors could be reestablished by micro-RNA-mediated molecular reversal of EMT. The results suggest that EMT coordinately regulates drug resistance and muscle invasion/metastasis in urothelial cancer and is a dominant feature of overall cancer biology.


The Journal of Urology | 2013

Perioperative Outcomes and Oncologic Efficacy from a Pilot Prospective Randomized Clinical Trial of Open Versus Robotic Assisted Radical Cystectomy

Dipen J. Parekh; Jamie C. Messer; John Fitzgerald; Barbara Ercole; Robert S. Svatek

PURPOSE Robotic assisted laparoscopic radical cystectomy for bladder cancer has been reported with potential for improvement in perioperative morbidity compared to the open approach. However, most studies are retrospective with significant selection bias. MATERIALS AND METHODS A pilot prospective randomized trial evaluating perioperative outcomes and oncologic efficacy of open vs robotic assisted laparoscopic radical cystectomy for consecutive patients was performed from July 2009 to June 2011. RESULTS To date 47 patients have been randomized with data available on 40 patients for analysis. Each group was similar with regard to age, gender, race, body mass index and comorbidities, as well as previous surgeries, operative time, postoperative complications and final pathological stage. We observed no significant differences between oncologic outcomes of positive margins (5% each, p = 0.50) or number of lymph nodes removed for open radical cystectomy (23, IQR 15-28) vs robotic assisted laparoscopic radical cystectomy (11, IQR 8.75-21.5) groups (p = 0.135). The robotic assisted laparoscopic radical cystectomy group (400 ml, IQR 300-762.5) was noted to have decreased estimated blood loss compared to the open radical cystectomy group (800 ml, IQR 400-1,100) and trended toward a decreased rate of excessive length of stay (greater than 5 days) (65% vs 90%, p = 0.11) compared to the open radical cystectomy group. The robotic group also trended toward fewer transfusions (40% vs 50%, p = 0.26). CONCLUSIONS Our study validates the concept of randomizing patients with bladder cancer undergoing radical cystectomy to an open or robotic approach. Our results suggest no significant differences in surrogates of oncologic efficacy. Robotic assisted laparoscopic radical cystectomy demonstrates potential benefits of decreased estimated blood loss and decreased hospital stay compared to open radical cystectomy. Our results need to be validated in a larger multicenter prospective randomized clinical trial.


The Journal of Urology | 2009

Soft Tissue Surgical Margin Status is a Powerful Predictor of Outcomes After Radical Cystectomy: A Multicenter Study of More Than 4,400 Patients

Giacomo Novara; Robert S. Svatek; Pierre I. Karakiewicz; Eila C. Skinner; Vincenzo Ficarra; Yves Fradet; Yair Lotan; Hendrik Isbarn; Umberto Capitanio; Patrick J. Bastian; Wassim Kassouf; Hans Martin Fritsche; Jonathan I. Izawa; Derya Tilki; Colin P. Dinney; Seth P. Lerner; Mark P. Schoenberg; Bjoern G. Volkmer; Arthur I. Sagalowsky; Shahrokh F. Shariat

PURPOSE We evaluated the association of soft tissue surgical margins with characteristics and outcomes of patients treated with radical cystectomy for urothelial carcinoma of the bladder. MATERIALS AND METHODS We retrospectively collected the data of 4,410 patients treated with radical cystectomy and pelvic lymphadenectomy without neoadjuvant chemotherapy at 12 academic centers in the United States, Canada and Europe. A positive soft tissue surgical margin was defined as presence of tumor at inked areas of soft tissue on the radical cystectomy specimen. RESULTS Positive soft tissue surgical margins were identified in 278 patients (6.3%). On univariate analysis positive soft tissue surgical margin was significantly associated with advanced pT stage, higher tumor grade, lymphovascular invasion and lymph node metastasis (p <0.001). Actuarial 5-year recurrence-free and cancer specific survival probabilities were 62.8% +/- 0.8% and 69% +/- 0.8% for patients without soft tissue surgical margins vs 21.6% +/- 3.1% and 26.4% +/- 3.3% for those with positive soft tissue surgical margins (p <0.001). On multivariable analyses adjusting for the effect of standard clinicopathological features and adjuvant chemotherapy positive soft tissue surgical margin was an independent predictor of disease recurrence and cancer specific mortality (HR 1.52 and HR 1.51, p <0.001, respectively). Soft tissue surgical margin retained independent predictive value in subgroups with advanced disease such as pT3Nany, pT4Nany or Npositive. CONCLUSIONS Positive soft tissue surgical margin is a strong predictor of recurrence and eventual death from urothelial carcinoma of the bladder. Soft tissue surgical margin status should always be reported in the pathological reports after radical cystectomy. Due to uniformly poor outcomes patients with positive soft tissue surgical margins should be considered for studies on adjuvant local and/or systemic therapy.


BJUI | 2007

Intermediate comparison of partial nephrectomy and radiofrequency ablation for clinical T1a renal tumours

Joshua M. Stern; Robert S. Svatek; Sangtae Park; Michael P. Hermann; Yair Lotan; Arthur I. Sagalowsky; Jeffrey A. Cadeddu

To compare the intermediate‐term outcomes of patients with clinical T1a renal tumours who were treated with nephron‐sparing surgery by partial nephrectomy (PN), the preferred approach for small (cT1a) renal tumours, or radiofrequency ablation (RFA), recently offered to selected patients as an alternative, less morbid technique.


European Urology | 2013

ICUD-EAU international consultation on bladder cancer 2012: Screening, diagnosis, and molecular markers

Ashish M. Kamat; Paul K. Hegarty; Jason R. Gee; Peter E. Clark; Robert S. Svatek; Nicholas J. Hegarty; Shahrokh F. Shariat; Evanguelos Xylinas; Bernd J. Schmitz-Dräger; Yair Lotan; Lawrence C. Jenkins; Michael J. Droller; Bas W.G. van Rhijn; Pierre I. Karakiewicz

CONTEXT AND OBJECTIVE To present a summary of the 2nd International Consultation on Bladder Cancer recommendations on the screening, diagnosis, and markers of bladder cancer using an evidence-based strategy. EVIDENCE ACQUISITION A detailed Medline analysis was performed for original articles addressing bladder cancer with regard to screening, diagnosis, markers, and pathology. Proceedings from the last 5 yr of major conferences were also searched. EVIDENCE SYNTHESIS The major findings are presented in an evidence-based fashion. Large retrospective and prospective data were analyzed. CONCLUSIONS Cystoscopy alone is the most cost-effective method to detect recurrence of bladder cancer. White-light cystoscopy is the gold standard for evaluation of the lower urinary tract; however, technology like fluorescence-aided cystoscopy and narrow-band imaging can aid in improving evaluations. Urine cytology is useful for the diagnosis of high-grade tumor recurrence. Molecular medicine holds the promise that clinical outcomes will be improved by directing therapy toward the mechanisms and targets associated with the growth of an individual patients tumor. The challenge remains to optimize measurement of these targets, evaluate the impact of such targets for therapeutic drug development, and translate molecular markers into the improved clinical management of bladder cancer patients. Physicians and researchers eventually will have a robust set of molecular markers to guide prevention, diagnosis, and treatment decisions for bladder cancer.


BJUI | 2010

International validation of the prognostic value of lymphovascular invasion in patients treated with radical cystectomy.

Shahrokh F. Shariat; Robert S. Svatek; Derya Tilki; Eila C. Skinner; Pierre I. Karakiewicz; Umberto Capitanio; Patrick J. Bastian; Bjoern G. Volkmer; Wassim Kassouf; Giacomo Novara; Hans Martin Fritsche; Jonathan I. Izawa; Vincenzo Ficarra; Seth P. Lerner; Arthur I. Sagalowsky; Mark P. Schoenberg; Ashish M. Kamat; Colin P. Dinney; Yair Lotan; M. Marberger; Yves Fradet

Study Type – Prognosis (retrospective cohort)
Level of Evidence 2b


European Urology | 2014

Alvimopan Accelerates Gastrointestinal Recovery After Radical Cystectomy: A Multicenter Randomized Placebo-Controlled Trial

Cheryl T. Lee; Sam S. Chang; Ashish M. Kamat; Gilad E. Amiel; Timothy L. Beard; Amr Fergany; R. Jeffrey Karnes; Andrea Kurz; Venu Menon; Wade J. Sexton; Joel W. Slaton; Robert S. Svatek; Shandra Wilson; Lee Techner; Richard Bihrle; Gary D. Steinberg; Michael O. Koch

BACKGROUND Radical cystectomy (RC) for bladder cancer is frequently associated with delayed gastrointestinal (GI) recovery that prolongs hospital length of stay (LOS). OBJECTIVE To assess the efficacy of alvimopan to accelerate GI recovery after RC. DESIGN, SETTING, AND PARTICIPANTS We conducted a randomized double-blind placebo-controlled trial in patients undergoing RC and receiving postoperative intravenous patient-controlled opioid analgesics. INTERVENTION Oral alvimopan 12 mg (maximum: 15 inpatient doses) versus placebo. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS The two-component primary end point was time to upper (first tolerance of solid food) and lower (first bowel movement) GI recovery (GI-2). Time to discharge order written, postoperative LOS, postoperative ileus (POI)-related morbidity, opioid consumption, and adverse events (AEs) were evaluated. An independent adjudication of cardiovascular AEs was performed. RESULTS AND LIMITATIONS Patients were randomized to alvimopan (n=143) or placebo (n=137); 277 patients were included in the modified intention-to-treat population. The alvimopan cohort experienced quicker GI-2 recovery (5.5 vs 6.8 d; hazard ratio: 1.8; p<0.0001), shorter mean LOS (7.4 vs 10.1 d; p=0.0051), and fewer episodes of POI-related morbidity (8.4% vs 29.1%; p<0.001). The incidence of opioid consumption and AEs or serious AEs (SAEs) was comparable except for POI, which was lower in the alvimopan group (AEs: 7% vs 26%; SAEs: 5% vs 20%, respectively). Cardiovascular AEs occurred in 8.4% (alvimopan) and 15.3% (placebo) of patients (p=0.09). Generalizability may be limited due to the exclusion of epidural analgesia and the inclusion of mostly high-volume centers utilizing open laparotomy. CONCLUSIONS Alvimopan is a useful addition to a standardized care pathway in patients undergoing RC by accelerating GI recovery and shortening LOS, with a safety profile similar to placebo. PATIENT SUMMARY This study examined the effects of alvimopan on bowel recovery in patients undergoing radical cystectomy for bladder cancer. Patients receiving alvimopan experienced quicker bowel recovery and had a shorter hospital stay compared with those who received placebo, with comparable safety. TRIAL REGISTRATION ClinicalTrials.gov identifier NCT00708201.


Cancer | 2006

Should we screen for bladder cancer in a high-risk population? : A cost per life-year saved analysis

Yair Lotan; Robert S. Svatek; Arthur I. Sagalowsky

The U.S. Food and Drug Administration recently approved screening high‐risk patients for bladder cancer using urine‐based markers. The cost and life‐years saved associated with bladder cancer screening were evaluated.


Clinical Cancer Research | 2010

The Effectiveness of Off-Protocol Adjuvant Chemotherapy for Patients with Urothelial Carcinoma of the Urinary Bladder

Robert S. Svatek; Shahrokh F. Shariat; Robert E. Lasky; Eila C. Skinner; Giacomo Novara; Seth P. Lerner; Yves Fradet; Patrick J. Bastian; Wassim Kassouf; Pierre I. Karakiewicz; Hans Martin Fritsche; Stefan Müller; Jonathan I. Izawa; Vincenzo Ficarra; Arthur I. Sagalowsky; Mark P. Schoenberg; Arlene O. Siefker-Radtke; Randall E. Millikan; Colin P. Dinney

Purpose: The role of adjuvant chemotherapy for patients with high-risk urothelial carcinoma of the bladder (UCB) is not well defined. Here we address the value of adjuvant chemotherapy in patients undergoing radical cystectomy for UCB in an off-protocol routine clinical setting. Experimental Design: We collected and analyzed data from 11 centers contributing retrospective cohorts of patients with UCB treated with radical cystectomy without neoadjuvant chemotherapy. Patients were grouped into quintiles based on their risk of disease progression using estimates from a fitted multivariable Cox proportional hazards model. The association of adjuvant chemotherapy with survival was explored across separate quintiles. Results: The cohort consisted of 3,947 patients, 932 (23.6%) of whom received adjuvant chemotherapy. Adjuvant chemotherapy was independently associated with improved survival (hazard ratio, 0.83; 95% confidence interval, 0.72-0.97%, P = 0.017). However, the effect of adjuvant chemotherapy was significantly modified by the individuals risk of disease progression such that an increasing benefit from adjuvant chemotherapy was seen across higher-risk subgroups (P < 0.001). There was a significant improvement in survival between the treated and nontreated patients in the highest-risk quintile (hazard ratio, 0.75; 95% confidence interval, 0.62-0.90; P = 0.002). This group was characterized by an estimated 32.8% 5-year probability of cancer-specific survival, with 86.6% of patients having both advanced pathologic stage (≥T3) and nodal involvement. Conclusion: Adjuvant chemotherapy is associated with a significant improvement in survival for patients treated in an off-protocol clinical setting. Selective administration in patients at the highest risk for disease progression, such as those with advanced pathologic stage and nodal involvement, may optimize the therapeutic benefit of adjuvant chemotherapy. Clin Cancer Res; 16(17); 4461–7. ©2010 AACR.


BJUI | 2011

Discrepancy between clinical and pathological stage: External validation of the impact on prognosis in an international radical cystectomy cohort

Robert S. Svatek; Shahrokh F. Shariat; Giacomo Novara; Eila C. Skinner; Yves Fradet; Patrick J. Bastian; Ashish M. Kamat; Wassim Kassouf; Pierre I. Karakiewicz; Hans Martin Fritsche; Jonathan I. Izawa; Derya Tilki; Vincenzo Ficarra; Bjoern G. Volkmer; Hendrik Isbarn; Colin P. Dinney

Study Type – Prognosis (case series) Level of Evidence 4

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Yair Lotan

University of California

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Shahrokh F. Shariat

Medical University of Vienna

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Colin P. Dinney

University of Texas MD Anderson Cancer Center

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Ashish M. Kamat

University of Texas MD Anderson Cancer Center

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Arthur I. Sagalowsky

University of Texas at Austin

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Seth P. Lerner

Baylor College of Medicine

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