Florian Schroeck

Dr. Florian Schroeck

orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

View All Publications
1 October 2008 in European Urology
Verified
Journal Article
Closed access
FSFlorian Schroeck
Florian Schroeck
TKTracey L. Krupski
Tracey L. Krupski
LSLeon Sun
Leon Sun
DADavid M. Albala
David M. Albala
MPMarva M. Price
Marva M. Price
JMJudd W. Moul
Judd W. Moul

26 June 2013 in JAMA
Verified
Journal Article
Open access
PDF file
BJBruce L. Jacobs
Bruce L. Jacobs
YZYun Zhang
Yun Zhang
FSFlorian Schroeck
Florian Schroeck
TSTed A. Skolarus
Ted A. Skolarus
JWJohn T. Wei
John T. Wei
BHBrent K. Hollenbeck
Brent K. Hollenbeck
Prostate cancer is a common and expensive disease in the United States.1,2 In part because of the untoward morbidity of traditional radiation and surgical therapies, advances in the treatment of localized disease have evolved over the last decade. Chief among these are the development of intensity-modulated radiotherapy (IMRT) and robotic prostatectomy. Although the evidence underlying these technologies is mixed,3,4 both are generally perceived as being more targeted and less toxic than prior therapies. During a period of increasing population-based rates of prostate cancer treatment,5,6 both of these advanced treatment technologies have disseminated rapidly.

1 November 2017 in European Urology
Verified
Journal Article
Closed access
FSFlorian Schroeck
Florian Schroeck
BJBruce L. Jacobs
Bruce L. Jacobs
SBSam B. Bhayani
Sam B. Bhayani
PNPaul L. Nguyen
Paul L. Nguyen
DPDavid Penson
David Penson
JHJim Hu
Jim Hu

1 April 2008 in Urology
Verified
Journal Article
Closed access
FSFlorian Schroeck
Florian Schroeck
CSChiquita A. Palha de Sousa
Chiquita A. Palha de Sousa
RKRoss A. Kalman
Ross A. Kalman
MKMaitri S. Kalia
Maitri S. Kalia
SPSean A. Pierre
Sean A. Pierre
DADavid M. Albala
David M. Albala

1 October 2017 in Urology
Verified
Journal Article
Closed access
KKKevin Koo
Kevin Koo
LZLisa Zubkoff
Lisa Zubkoff
BSBrenda E. Sirovich
Brenda E. Sirovich
PGPhilip P. Goodney
Philip P. Goodney
DRDouglas J. Robertson
Douglas J. Robertson
FSFlorian Schroeck
Florian Schroeck

28 April 2009 in Cancer
Verified
Journal Article
Open access
PDF file
TPThomas J. Polascik
Thomas J. Polascik
JMJanice M. Mayes
Janice M. Mayes
FSFlorian Schroeck
Florian Schroeck
LSLeon Sun
Leon Sun
JMJohn F. Madden
John F. Madden
VMVladimir Mouraviev
Vladimir Mouraviev
BACKGROUND: The application of focal therapy for low‐risk prostate cancer (PCa) depended on appropriate patient selection. No definitive criteria existed to characterize patients who may potentially benefit from an organ‐sparing approach. We evaluated pretreatment clinical parameters that may predict unilateral PCa amenable to hemigland thermoablation.METHODS: In total, 538 patients with complete data from the Duke Prostate Center (DPC) Outcomes database with low‐ to low‐intermediate–risk PCa (prostate‐specific antigen<10 ng/mL, biopsy Gleason score ≤7, and clinical stage T1c‐T2b) treated with radical prostatectomy (RP) were included in the dataset. Patients underwent diagnostic prostate biopsy (PBx) at Duke or community hospitals from 1996 to 2006. Clinical and biopsy parameters were assessed as to the ability to predict PCa unilaterality verified by RP pathology.RESULTS: The strongest predictor of pathologic unilaterality was PBx unilaterality. The sensitivity and specificity for biopsy unilaterality to predict pathologic unilaterality was 88.4% and 34%, with a positive predictive value of 28% and a negative predictive value of 91%. PBx unilaterality (odds ratio [OR] = 3.88; 95% confidence interval [CI], 2.14‐7.05; P < .0005) and negative family history of PCa (OR = 1.83; 95% CI, 1.09‐3.05; P = .21) was associated with a higher probability of unilateral disease by multivariate regression.CONCLUSIONS: Two pretreatment clinical variables were significantly predictive of unilateral PCa: negative family history of PCa and PBx unilaterality. These variables may be used to select men with low‐ to low‐moderate–risk PCa for hemiablation. Further work is necessary to decrease the false‐negative and false‐positive rates associated with PBx to improve predictability for PCa laterality. Cancer 2009. © 2009 American Cancer Society.