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A Multinational, Multi-institutional Study Comparing Positive Surgical Margin Rates Among 22 393 Open, Laparoscopic, and Robot-assisted Radical Prostatectomy Patients

Identifieur interne : 000267 ( PascalFrancis/Corpus ); précédent : 000266; suivant : 000268

A Multinational, Multi-institutional Study Comparing Positive Surgical Margin Rates Among 22 393 Open, Laparoscopic, and Robot-assisted Radical Prostatectomy Patients

Auteurs : Prasanna Sooriakumaran ; Abhishek Srivastava ; Shahrokh F. Shariat ; Phillip D. Strieker ; Thomas Ahlering ; Christopher G. Eden ; Peter N. Wiklund ; Rafael Sanchez-Salas ; Alexandre Mottrie ; David Lee ; David E. Neal ; Reza Ghavamian ; Peter Nyirady ; Andreas Nilsson ; Stefan Carlsson ; Evanguelos Xylinas ; Wolfgang Loidl ; Christian Seitz ; Paul Schramek ; Claus Roehrborn ; Xavier Cathelineau ; Douglas Skarecky ; Greg Shaw ; Anne Warren ; Warick J. Delprado ; Anne-Marie Haynes ; Ewout Steyerberg ; Monique J. Roobol ; Ashutosh K. Tewari

Source :

RBID : Pascal:14-0223163

Descripteurs français

English descriptors

Abstract

Background: Positive surgical margins (PSMs) are a known risk factor for biochemical recurrence in patients with prostate cancer (PCa) and are potentially affected by surgical technique and volume. Objective: To investigate whether radical prostatectomy (RP) modality and volume affect PSM rates. Design, setting, and participants: Fourteen institutions in Europe, the United States, and Australia were invited to participate in this study, all of which retrospectively provided margins data on 9778 open RP, 4918 laparoscopic RP, and 7697 robotic RP patients operated on between January 2000 and October 2011. Outcome measurements and statistical analyses: The outcome measure was PSM rate. Multivariable logistic regression analyses and propensity score methods identified odds ratios for risk of a PSM for one modality compared with another, after adjustment for age, preoperative prostate-specific antigen, postoperative Gleason score, pathologic stage, and year of surgery. Classic adjustment using standard covariates was also implemented to compare PSM rates based on center volume for each minimally invasive surgical cohort. Results and limitations: Open RP patients had higher-risk PCa at time of surgery on average and were operated on earlier in the study time period on average, compared with minimally invasive cohorts. Crude margin rates were lowest for robotic RP (13.8%), intermediate for laparoscopic RP (16.3%), and highest for open RP (22.8%); significant differences persisted, although were ameliorated, after statistical adjustments. Lower-volume centers had increased risks of PSM compared with the highest-volume center for both laparoscopic RP and robotic RP. The study is limited by its nonrandomized nature; missing data across covariates, especially year of surgery in many of the open cohort cases; lack of standardized histologic processing and central pathology review; and lack of information regarding potential confounders such as patient comorbidity, nerve-sparing status, lymph node status, tumor volume, and individual surgeon caseload.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A02 01      @0 EUURAV
A03   1    @0 Eur. urol.
A05       @2 66
A06       @2 3
A08 01  1  ENG  @1 A Multinational, Multi-institutional Study Comparing Positive Surgical Margin Rates Among 22 393 Open, Laparoscopic, and Robot-assisted Radical Prostatectomy Patients
A11 01  1    @1 SOORIAKUMARAN (Prasanna)
A11 02  1    @1 SRIVASTAVA (Abhishek)
A11 03  1    @1 SHARIAT (Shahrokh F.)
A11 04  1    @1 STRIEKER (Phillip D.)
A11 05  1    @1 AHLERING (Thomas)
A11 06  1    @1 EDEN (Christopher G.)
A11 07  1    @1 WIKLUND (Peter N.)
A11 08  1    @1 SANCHEZ-SALAS (Rafael)
A11 09  1    @1 MOTTRIE (Alexandre)
A11 10  1    @1 LEE (David)
A11 11  1    @1 NEAL (David E.)
A11 12  1    @1 GHAVAMIAN (Reza)
A11 13  1    @1 NYIRADY (Peter)
A11 14  1    @1 NILSSON (Andreas)
A11 15  1    @1 CARLSSON (Stefan)
A11 16  1    @1 XYLINAS (Evanguelos)
A11 17  1    @1 LOIDL (Wolfgang)
A11 18  1    @1 SEITZ (Christian)
A11 19  1    @1 SCHRAMEK (Paul)
A11 20  1    @1 ROEHRBORN (Claus)
A11 21  1    @1 CATHELINEAU (Xavier)
A11 22  1    @1 SKARECKY (Douglas)
A11 23  1    @1 SHAW (Greg)
A11 24  1    @1 WARREN (Anne)
A11 25  1    @1 DELPRADO (Warick J.)
A11 26  1    @1 HAYNES (Anne-Marie)
A11 27  1    @1 STEYERBERG (Ewout)
A11 28  1    @1 ROOBOL (Monique J.)
A11 29  1    @1 TEWARI (Ashutosh K.)
A14 01      @1 Surgical Intervention Trials Unit, Nuffield Department of Surgical Sciences, University of Oxford @2 Oxford @3 GBR @Z 1 aut.
A14 02      @1 Department of Molecular Medicine and Surgery, Karolinska Institutet @2 Stockholm @3 SWE @Z 1 aut. @Z 7 aut. @Z 14 aut. @Z 15 aut.
A14 03      @1 Department of Urology, Montefiore Medical Center @2 New York, NY @3 USA @Z 2 aut. @Z 12 aut.
A14 04      @1 Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital @2 New York, NY @3 USA @Z 3 aut. @Z 16 aut. @Z 29 aut.
A14 05      @1 Department of Urology, Medical University of Vienna @2 Vienna @3 AUT @Z 3 aut. @Z 18 aut.
A14 06      @1 Prostate Cancer Centre, St. Vincent's Clinic @2 Sydney @3 AUS @Z 4 aut. @Z 25 aut. @Z 26 aut.
A14 07      @1 Department of Urology, University of California-Irvine School of Medicine @2 Irvine, CA @3 USA @Z 5 aut. @Z 22 aut.
A14 08      @1 Department of Urology, Royal Surrey County Hospital @2 Guildford @3 GBR @Z 6 aut.
A14 09      @1 Department of Urology, L'Institut Mutualiste Montsouris @2 Paris @3 FRA @Z 8 aut. @Z 21 aut.
A14 10      @1 Department of Urology, Onze-Lieve-Vrouwziekenhuis Hospital @2 Aalst @3 BEL @Z 9 aut.
A14 11      @1 Department of Urology, University of Pennsylvania @2 Philadelphia, PA @3 USA @Z 10 aut.
A14 12      @1 Department of Uro-oncology, University of Cambridge @2 Cambridge @3 GBR @Z 11 aut.
A14 13      @1 Uro-oncology Research Group, Cancer Research UK, Cambridge Research Institute @2 Cambridge @3 GBR @Z 11 aut. @Z 23 aut.
A14 14      @1 Department of Urology, Semmelweis University @2 Budapest @3 HUN @Z 13 aut.
A14 15      @1 Department of Urology, St. Vincent's Hospital @2 Linz @3 AUT @Z 17 aut.
A14 16      @1 Department of Urology, Saint John of God Hospital @2 Vienna @3 AUT @Z 19 aut.
A14 17      @1 Department of Urology, University of Texas Southwestern Medical Center @2 Dallas, TX @3 USA @Z 20 aut.
A14 18      @1 Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust @2 Cambridge @3 GBR @Z 24 aut.
A14 19      @1 Department of Public Health, Erasmus MC-University Medical Center Rotterdam @2 Rotterdam @3 NLD @Z 27 aut. @Z 28 aut.
A20       @1 450-456
A21       @1 2014
A23 01      @0 ENG
A43 01      @1 INIST @2 16847 @5 354000504835110130
A44       @0 0000 @1 © 2014 INIST-CNRS. All rights reserved.
A45       @0 27 ref.
A47 01  1    @0 14-0223163
A60       @1 P
A61       @0 A
A64 01  1    @0 European urology
A66 01      @0 GBR
C01 01    ENG  @0 Background: Positive surgical margins (PSMs) are a known risk factor for biochemical recurrence in patients with prostate cancer (PCa) and are potentially affected by surgical technique and volume. Objective: To investigate whether radical prostatectomy (RP) modality and volume affect PSM rates. Design, setting, and participants: Fourteen institutions in Europe, the United States, and Australia were invited to participate in this study, all of which retrospectively provided margins data on 9778 open RP, 4918 laparoscopic RP, and 7697 robotic RP patients operated on between January 2000 and October 2011. Outcome measurements and statistical analyses: The outcome measure was PSM rate. Multivariable logistic regression analyses and propensity score methods identified odds ratios for risk of a PSM for one modality compared with another, after adjustment for age, preoperative prostate-specific antigen, postoperative Gleason score, pathologic stage, and year of surgery. Classic adjustment using standard covariates was also implemented to compare PSM rates based on center volume for each minimally invasive surgical cohort. Results and limitations: Open RP patients had higher-risk PCa at time of surgery on average and were operated on earlier in the study time period on average, compared with minimally invasive cohorts. Crude margin rates were lowest for robotic RP (13.8%), intermediate for laparoscopic RP (16.3%), and highest for open RP (22.8%); significant differences persisted, although were ameliorated, after statistical adjustments. Lower-volume centers had increased risks of PSM compared with the highest-volume center for both laparoscopic RP and robotic RP. The study is limited by its nonrandomized nature; missing data across covariates, especially year of surgery in many of the open cohort cases; lack of standardized histologic processing and central pathology review; and lack of information regarding potential confounders such as patient comorbidity, nerve-sparing status, lymph node status, tumor volume, and individual surgeon caseload.
C02 01  X    @0 002B14
C03 01  X  FRE  @0 Marge chirurgicale @5 01
C03 01  X  ENG  @0 Surgical margin @5 01
C03 01  X  SPA  @0 Margen quirúrgica @5 01
C03 02  X  FRE  @0 Etude comparative @5 02
C03 02  X  ENG  @0 Comparative study @5 02
C03 02  X  SPA  @0 Estudio comparativo @5 02
C03 03  X  FRE  @0 Chirurgie endoscopique @5 03
C03 03  X  ENG  @0 Endoscopic surgery @5 03
C03 03  X  SPA  @0 Cirugía endoscópica @5 03
C03 04  X  FRE  @0 Taux @5 05
C03 04  X  ENG  @0 Rate @5 05
C03 04  X  SPA  @0 Tasa @5 05
C03 05  X  FRE  @0 Prostatectomie @5 06
C03 05  X  ENG  @0 Prostatectomy @5 06
C03 05  X  SPA  @0 Prostatectomía @5 06
C03 06  X  FRE  @0 Coeliochirurgie @5 08
C03 06  X  ENG  @0 Laparoscopic surgery @5 08
C03 06  X  SPA  @0 Cirugía laparoscopica @5 08
C03 07  X  FRE  @0 Robotique @5 09
C03 07  X  ENG  @0 Robotics @5 09
C03 07  X  SPA  @0 Robótica @5 09
C03 08  X  FRE  @0 Homme @5 11
C03 08  X  ENG  @0 Human @5 11
C03 08  X  SPA  @0 Hombre @5 11
C03 09  X  FRE  @0 Laparoscopie @5 12
C03 09  X  ENG  @0 Laparoscopy @5 12
C03 09  X  SPA  @0 Laparoscopia @5 12
C03 10  X  FRE  @0 Télémédecine @5 17
C03 10  X  ENG  @0 Telemedicine @5 17
C03 10  X  SPA  @0 Telemedicina @5 17
C03 11  X  FRE  @0 Néphrologie @5 18
C03 11  X  ENG  @0 Nephrology @5 18
C03 11  X  SPA  @0 Nefrología @5 18
C03 12  X  FRE  @0 Urologie @5 19
C03 12  X  ENG  @0 Urology @5 19
C03 12  X  SPA  @0 Urología @5 19
C03 13  X  FRE  @0 Traitement @5 25
C03 13  X  ENG  @0 Treatment @5 25
C03 13  X  SPA  @0 Tratamiento @5 25
C07 01  X  FRE  @0 Endoscopie @5 37
C07 01  X  ENG  @0 Endoscopy @5 37
C07 01  X  SPA  @0 Endoscopía @5 37
N21       @1 265
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 14-0223163 INIST
ET : A Multinational, Multi-institutional Study Comparing Positive Surgical Margin Rates Among 22 393 Open, Laparoscopic, and Robot-assisted Radical Prostatectomy Patients
AU : SOORIAKUMARAN (Prasanna); SRIVASTAVA (Abhishek); SHARIAT (Shahrokh F.); STRIEKER (Phillip D.); AHLERING (Thomas); EDEN (Christopher G.); WIKLUND (Peter N.); SANCHEZ-SALAS (Rafael); MOTTRIE (Alexandre); LEE (David); NEAL (David E.); GHAVAMIAN (Reza); NYIRADY (Peter); NILSSON (Andreas); CARLSSON (Stefan); XYLINAS (Evanguelos); LOIDL (Wolfgang); SEITZ (Christian); SCHRAMEK (Paul); ROEHRBORN (Claus); CATHELINEAU (Xavier); SKARECKY (Douglas); SHAW (Greg); WARREN (Anne); DELPRADO (Warick J.); HAYNES (Anne-Marie); STEYERBERG (Ewout); ROOBOL (Monique J.); TEWARI (Ashutosh K.)
AF : Surgical Intervention Trials Unit, Nuffield Department of Surgical Sciences, University of Oxford/Oxford/Royaume-Uni (1 aut.); Department of Molecular Medicine and Surgery, Karolinska Institutet/Stockholm/Suède (1 aut., 7 aut., 14 aut., 15 aut.); Department of Urology, Montefiore Medical Center/New York, NY/Etats-Unis (2 aut., 12 aut.); Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital/New York, NY/Etats-Unis (3 aut., 16 aut., 29 aut.); Department of Urology, Medical University of Vienna/Vienna/Autriche (3 aut., 18 aut.); Prostate Cancer Centre, St. Vincent's Clinic/Sydney/Australie (4 aut., 25 aut., 26 aut.); Department of Urology, University of California-Irvine School of Medicine/Irvine, CA/Etats-Unis (5 aut., 22 aut.); Department of Urology, Royal Surrey County Hospital/Guildford/Royaume-Uni (6 aut.); Department of Urology, L'Institut Mutualiste Montsouris/Paris/France (8 aut., 21 aut.); Department of Urology, Onze-Lieve-Vrouwziekenhuis Hospital/Aalst/Belgique (9 aut.); Department of Urology, University of Pennsylvania/Philadelphia, PA/Etats-Unis (10 aut.); Department of Uro-oncology, University of Cambridge/Cambridge/Royaume-Uni (11 aut.); Uro-oncology Research Group, Cancer Research UK, Cambridge Research Institute/Cambridge/Royaume-Uni (11 aut., 23 aut.); Department of Urology, Semmelweis University/Budapest/Hongrie (13 aut.); Department of Urology, St. Vincent's Hospital/Linz/Autriche (17 aut.); Department of Urology, Saint John of God Hospital/Vienna/Autriche (19 aut.); Department of Urology, University of Texas Southwestern Medical Center/Dallas, TX/Etats-Unis (20 aut.); Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust/Cambridge/Royaume-Uni (24 aut.); Department of Public Health, Erasmus MC-University Medical Center Rotterdam/Rotterdam/Pays-Bas (27 aut., 28 aut.)
DT : Publication en série; Niveau analytique
SO : European urology; ISSN 0302-2838; Coden EUURAV; Royaume-Uni; Da. 2014; Vol. 66; No. 3; Pp. 450-456; Bibl. 27 ref.
LA : Anglais
EA : Background: Positive surgical margins (PSMs) are a known risk factor for biochemical recurrence in patients with prostate cancer (PCa) and are potentially affected by surgical technique and volume. Objective: To investigate whether radical prostatectomy (RP) modality and volume affect PSM rates. Design, setting, and participants: Fourteen institutions in Europe, the United States, and Australia were invited to participate in this study, all of which retrospectively provided margins data on 9778 open RP, 4918 laparoscopic RP, and 7697 robotic RP patients operated on between January 2000 and October 2011. Outcome measurements and statistical analyses: The outcome measure was PSM rate. Multivariable logistic regression analyses and propensity score methods identified odds ratios for risk of a PSM for one modality compared with another, after adjustment for age, preoperative prostate-specific antigen, postoperative Gleason score, pathologic stage, and year of surgery. Classic adjustment using standard covariates was also implemented to compare PSM rates based on center volume for each minimally invasive surgical cohort. Results and limitations: Open RP patients had higher-risk PCa at time of surgery on average and were operated on earlier in the study time period on average, compared with minimally invasive cohorts. Crude margin rates were lowest for robotic RP (13.8%), intermediate for laparoscopic RP (16.3%), and highest for open RP (22.8%); significant differences persisted, although were ameliorated, after statistical adjustments. Lower-volume centers had increased risks of PSM compared with the highest-volume center for both laparoscopic RP and robotic RP. The study is limited by its nonrandomized nature; missing data across covariates, especially year of surgery in many of the open cohort cases; lack of standardized histologic processing and central pathology review; and lack of information regarding potential confounders such as patient comorbidity, nerve-sparing status, lymph node status, tumor volume, and individual surgeon caseload.
CC : 002B14
FD : Marge chirurgicale; Etude comparative; Chirurgie endoscopique; Taux; Prostatectomie; Coeliochirurgie; Robotique; Homme; Laparoscopie; Télémédecine; Néphrologie; Urologie; Traitement
FG : Endoscopie
ED : Surgical margin; Comparative study; Endoscopic surgery; Rate; Prostatectomy; Laparoscopic surgery; Robotics; Human; Laparoscopy; Telemedicine; Nephrology; Urology; Treatment
EG : Endoscopy
SD : Margen quirúrgica; Estudio comparativo; Cirugía endoscópica; Tasa; Prostatectomía; Cirugía laparoscopica; Robótica; Hombre; Laparoscopia; Telemedicina; Nefrología; Urología; Tratamiento
LO : INIST-16847.354000504835110130
ID : 14-0223163

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Pascal:14-0223163

Le document en format XML

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<name sortKey="Wiklund, Peter N" sort="Wiklund, Peter N" uniqKey="Wiklund P" first="Peter N." last="Wiklund">Peter N. Wiklund</name>
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<name sortKey="Lee, David" sort="Lee, David" uniqKey="Lee D" first="David" last="Lee">David Lee</name>
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<name sortKey="Neal, David E" sort="Neal, David E" uniqKey="Neal D" first="David E." last="Neal">David E. Neal</name>
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<name sortKey="Ghavamian, Reza" sort="Ghavamian, Reza" uniqKey="Ghavamian R" first="Reza" last="Ghavamian">Reza Ghavamian</name>
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<name sortKey="Nyirady, Peter" sort="Nyirady, Peter" uniqKey="Nyirady P" first="Peter" last="Nyirady">Peter Nyirady</name>
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<name sortKey="Nilsson, Andreas" sort="Nilsson, Andreas" uniqKey="Nilsson A" first="Andreas" last="Nilsson">Andreas Nilsson</name>
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<name sortKey="Carlsson, Stefan" sort="Carlsson, Stefan" uniqKey="Carlsson S" first="Stefan" last="Carlsson">Stefan Carlsson</name>
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<s1>Department of Molecular Medicine and Surgery, Karolinska Institutet</s1>
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<sZ>1 aut.</sZ>
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<sZ>14 aut.</sZ>
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<name sortKey="Xylinas, Evanguelos" sort="Xylinas, Evanguelos" uniqKey="Xylinas E" first="Evanguelos" last="Xylinas">Evanguelos Xylinas</name>
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<inist:fA14 i1="04">
<s1>Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital</s1>
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<s3>USA</s3>
<sZ>3 aut.</sZ>
<sZ>16 aut.</sZ>
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</inist:fA14>
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<name sortKey="Loidl, Wolfgang" sort="Loidl, Wolfgang" uniqKey="Loidl W" first="Wolfgang" last="Loidl">Wolfgang Loidl</name>
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<inist:fA14 i1="15">
<s1>Department of Urology, St. Vincent's Hospital</s1>
<s2>Linz</s2>
<s3>AUT</s3>
<sZ>17 aut.</sZ>
</inist:fA14>
</affiliation>
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<author>
<name sortKey="Seitz, Christian" sort="Seitz, Christian" uniqKey="Seitz C" first="Christian" last="Seitz">Christian Seitz</name>
<affiliation>
<inist:fA14 i1="05">
<s1>Department of Urology, Medical University of Vienna</s1>
<s2>Vienna</s2>
<s3>AUT</s3>
<sZ>3 aut.</sZ>
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</inist:fA14>
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<author>
<name sortKey="Schramek, Paul" sort="Schramek, Paul" uniqKey="Schramek P" first="Paul" last="Schramek">Paul Schramek</name>
<affiliation>
<inist:fA14 i1="16">
<s1>Department of Urology, Saint John of God Hospital</s1>
<s2>Vienna</s2>
<s3>AUT</s3>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Roehrborn, Claus" sort="Roehrborn, Claus" uniqKey="Roehrborn C" first="Claus" last="Roehrborn">Claus Roehrborn</name>
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<inist:fA14 i1="17">
<s1>Department of Urology, University of Texas Southwestern Medical Center</s1>
<s2>Dallas, TX</s2>
<s3>USA</s3>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Cathelineau, Xavier" sort="Cathelineau, Xavier" uniqKey="Cathelineau X" first="Xavier" last="Cathelineau">Xavier Cathelineau</name>
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<inist:fA14 i1="09">
<s1>Department of Urology, L'Institut Mutualiste Montsouris</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Skarecky, Douglas" sort="Skarecky, Douglas" uniqKey="Skarecky D" first="Douglas" last="Skarecky">Douglas Skarecky</name>
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<inist:fA14 i1="07">
<s1>Department of Urology, University of California-Irvine School of Medicine</s1>
<s2>Irvine, CA</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>22 aut.</sZ>
</inist:fA14>
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</author>
<author>
<name sortKey="Shaw, Greg" sort="Shaw, Greg" uniqKey="Shaw G" first="Greg" last="Shaw">Greg Shaw</name>
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<inist:fA14 i1="13">
<s1>Uro-oncology Research Group, Cancer Research UK, Cambridge Research Institute</s1>
<s2>Cambridge</s2>
<s3>GBR</s3>
<sZ>11 aut.</sZ>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Warren, Anne" sort="Warren, Anne" uniqKey="Warren A" first="Anne" last="Warren">Anne Warren</name>
<affiliation>
<inist:fA14 i1="18">
<s1>Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust</s1>
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<s3>GBR</s3>
<sZ>24 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Delprado, Warick J" sort="Delprado, Warick J" uniqKey="Delprado W" first="Warick J." last="Delprado">Warick J. Delprado</name>
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<inist:fA14 i1="06">
<s1>Prostate Cancer Centre, St. Vincent's Clinic</s1>
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<sZ>4 aut.</sZ>
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<sZ>26 aut.</sZ>
</inist:fA14>
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</author>
<author>
<name sortKey="Haynes, Anne Marie" sort="Haynes, Anne Marie" uniqKey="Haynes A" first="Anne-Marie" last="Haynes">Anne-Marie Haynes</name>
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<sZ>4 aut.</sZ>
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<sZ>26 aut.</sZ>
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</affiliation>
</author>
<author>
<name sortKey="Steyerberg, Ewout" sort="Steyerberg, Ewout" uniqKey="Steyerberg E" first="Ewout" last="Steyerberg">Ewout Steyerberg</name>
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<inist:fA14 i1="19">
<s1>Department of Public Health, Erasmus MC-University Medical Center Rotterdam</s1>
<s2>Rotterdam</s2>
<s3>NLD</s3>
<sZ>27 aut.</sZ>
<sZ>28 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Roobol, Monique J" sort="Roobol, Monique J" uniqKey="Roobol M" first="Monique J." last="Roobol">Monique J. Roobol</name>
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<inist:fA14 i1="19">
<s1>Department of Public Health, Erasmus MC-University Medical Center Rotterdam</s1>
<s2>Rotterdam</s2>
<s3>NLD</s3>
<sZ>27 aut.</sZ>
<sZ>28 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Tewari, Ashutosh K" sort="Tewari, Ashutosh K" uniqKey="Tewari A" first="Ashutosh K." last="Tewari">Ashutosh K. Tewari</name>
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<inist:fA14 i1="04">
<s1>Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>3 aut.</sZ>
<sZ>16 aut.</sZ>
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<title xml:lang="en" level="a">A Multinational, Multi-institutional Study Comparing Positive Surgical Margin Rates Among 22 393 Open, Laparoscopic, and Robot-assisted Radical Prostatectomy Patients</title>
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<name sortKey="Sooriakumaran, Prasanna" sort="Sooriakumaran, Prasanna" uniqKey="Sooriakumaran P" first="Prasanna" last="Sooriakumaran">Prasanna Sooriakumaran</name>
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<inist:fA14 i1="01">
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</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Molecular Medicine and Surgery, Karolinska Institutet</s1>
<s2>Stockholm</s2>
<s3>SWE</s3>
<sZ>1 aut.</sZ>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Srivastava, Abhishek" sort="Srivastava, Abhishek" uniqKey="Srivastava A" first="Abhishek" last="Srivastava">Abhishek Srivastava</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Department of Urology, Montefiore Medical Center</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Shariat, Shahrokh F" sort="Shariat, Shahrokh F" uniqKey="Shariat S" first="Shahrokh F." last="Shariat">Shahrokh F. Shariat</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>3 aut.</sZ>
<sZ>16 aut.</sZ>
<sZ>29 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="05">
<s1>Department of Urology, Medical University of Vienna</s1>
<s2>Vienna</s2>
<s3>AUT</s3>
<sZ>3 aut.</sZ>
<sZ>18 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Strieker, Phillip D" sort="Strieker, Phillip D" uniqKey="Strieker P" first="Phillip D." last="Strieker">Phillip D. Strieker</name>
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<inist:fA14 i1="06">
<s1>Prostate Cancer Centre, St. Vincent's Clinic</s1>
<s2>Sydney</s2>
<s3>AUS</s3>
<sZ>4 aut.</sZ>
<sZ>25 aut.</sZ>
<sZ>26 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Ahlering, Thomas" sort="Ahlering, Thomas" uniqKey="Ahlering T" first="Thomas" last="Ahlering">Thomas Ahlering</name>
<affiliation>
<inist:fA14 i1="07">
<s1>Department of Urology, University of California-Irvine School of Medicine</s1>
<s2>Irvine, CA</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>22 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Eden, Christopher G" sort="Eden, Christopher G" uniqKey="Eden C" first="Christopher G." last="Eden">Christopher G. Eden</name>
<affiliation>
<inist:fA14 i1="08">
<s1>Department of Urology, Royal Surrey County Hospital</s1>
<s2>Guildford</s2>
<s3>GBR</s3>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Wiklund, Peter N" sort="Wiklund, Peter N" uniqKey="Wiklund P" first="Peter N." last="Wiklund">Peter N. Wiklund</name>
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<inist:fA14 i1="02">
<s1>Department of Molecular Medicine and Surgery, Karolinska Institutet</s1>
<s2>Stockholm</s2>
<s3>SWE</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>14 aut.</sZ>
<sZ>15 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Sanchez Salas, Rafael" sort="Sanchez Salas, Rafael" uniqKey="Sanchez Salas R" first="Rafael" last="Sanchez-Salas">Rafael Sanchez-Salas</name>
<affiliation>
<inist:fA14 i1="09">
<s1>Department of Urology, L'Institut Mutualiste Montsouris</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Mottrie, Alexandre" sort="Mottrie, Alexandre" uniqKey="Mottrie A" first="Alexandre" last="Mottrie">Alexandre Mottrie</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Department of Urology, Onze-Lieve-Vrouwziekenhuis Hospital</s1>
<s2>Aalst</s2>
<s3>BEL</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Lee, David" sort="Lee, David" uniqKey="Lee D" first="David" last="Lee">David Lee</name>
<affiliation>
<inist:fA14 i1="11">
<s1>Department of Urology, University of Pennsylvania</s1>
<s2>Philadelphia, PA</s2>
<s3>USA</s3>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Neal, David E" sort="Neal, David E" uniqKey="Neal D" first="David E." last="Neal">David E. Neal</name>
<affiliation>
<inist:fA14 i1="12">
<s1>Department of Uro-oncology, University of Cambridge</s1>
<s2>Cambridge</s2>
<s3>GBR</s3>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="13">
<s1>Uro-oncology Research Group, Cancer Research UK, Cambridge Research Institute</s1>
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<s3>GBR</s3>
<sZ>11 aut.</sZ>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Ghavamian, Reza" sort="Ghavamian, Reza" uniqKey="Ghavamian R" first="Reza" last="Ghavamian">Reza Ghavamian</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Department of Urology, Montefiore Medical Center</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Nyirady, Peter" sort="Nyirady, Peter" uniqKey="Nyirady P" first="Peter" last="Nyirady">Peter Nyirady</name>
<affiliation>
<inist:fA14 i1="14">
<s1>Department of Urology, Semmelweis University</s1>
<s2>Budapest</s2>
<s3>HUN</s3>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Nilsson, Andreas" sort="Nilsson, Andreas" uniqKey="Nilsson A" first="Andreas" last="Nilsson">Andreas Nilsson</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Molecular Medicine and Surgery, Karolinska Institutet</s1>
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<s3>SWE</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>14 aut.</sZ>
<sZ>15 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Carlsson, Stefan" sort="Carlsson, Stefan" uniqKey="Carlsson S" first="Stefan" last="Carlsson">Stefan Carlsson</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Molecular Medicine and Surgery, Karolinska Institutet</s1>
<s2>Stockholm</s2>
<s3>SWE</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>14 aut.</sZ>
<sZ>15 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Xylinas, Evanguelos" sort="Xylinas, Evanguelos" uniqKey="Xylinas E" first="Evanguelos" last="Xylinas">Evanguelos Xylinas</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>3 aut.</sZ>
<sZ>16 aut.</sZ>
<sZ>29 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Loidl, Wolfgang" sort="Loidl, Wolfgang" uniqKey="Loidl W" first="Wolfgang" last="Loidl">Wolfgang Loidl</name>
<affiliation>
<inist:fA14 i1="15">
<s1>Department of Urology, St. Vincent's Hospital</s1>
<s2>Linz</s2>
<s3>AUT</s3>
<sZ>17 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Seitz, Christian" sort="Seitz, Christian" uniqKey="Seitz C" first="Christian" last="Seitz">Christian Seitz</name>
<affiliation>
<inist:fA14 i1="05">
<s1>Department of Urology, Medical University of Vienna</s1>
<s2>Vienna</s2>
<s3>AUT</s3>
<sZ>3 aut.</sZ>
<sZ>18 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Schramek, Paul" sort="Schramek, Paul" uniqKey="Schramek P" first="Paul" last="Schramek">Paul Schramek</name>
<affiliation>
<inist:fA14 i1="16">
<s1>Department of Urology, Saint John of God Hospital</s1>
<s2>Vienna</s2>
<s3>AUT</s3>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Roehrborn, Claus" sort="Roehrborn, Claus" uniqKey="Roehrborn C" first="Claus" last="Roehrborn">Claus Roehrborn</name>
<affiliation>
<inist:fA14 i1="17">
<s1>Department of Urology, University of Texas Southwestern Medical Center</s1>
<s2>Dallas, TX</s2>
<s3>USA</s3>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Cathelineau, Xavier" sort="Cathelineau, Xavier" uniqKey="Cathelineau X" first="Xavier" last="Cathelineau">Xavier Cathelineau</name>
<affiliation>
<inist:fA14 i1="09">
<s1>Department of Urology, L'Institut Mutualiste Montsouris</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Skarecky, Douglas" sort="Skarecky, Douglas" uniqKey="Skarecky D" first="Douglas" last="Skarecky">Douglas Skarecky</name>
<affiliation>
<inist:fA14 i1="07">
<s1>Department of Urology, University of California-Irvine School of Medicine</s1>
<s2>Irvine, CA</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>22 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Shaw, Greg" sort="Shaw, Greg" uniqKey="Shaw G" first="Greg" last="Shaw">Greg Shaw</name>
<affiliation>
<inist:fA14 i1="13">
<s1>Uro-oncology Research Group, Cancer Research UK, Cambridge Research Institute</s1>
<s2>Cambridge</s2>
<s3>GBR</s3>
<sZ>11 aut.</sZ>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Warren, Anne" sort="Warren, Anne" uniqKey="Warren A" first="Anne" last="Warren">Anne Warren</name>
<affiliation>
<inist:fA14 i1="18">
<s1>Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust</s1>
<s2>Cambridge</s2>
<s3>GBR</s3>
<sZ>24 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Delprado, Warick J" sort="Delprado, Warick J" uniqKey="Delprado W" first="Warick J." last="Delprado">Warick J. Delprado</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Prostate Cancer Centre, St. Vincent's Clinic</s1>
<s2>Sydney</s2>
<s3>AUS</s3>
<sZ>4 aut.</sZ>
<sZ>25 aut.</sZ>
<sZ>26 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Haynes, Anne Marie" sort="Haynes, Anne Marie" uniqKey="Haynes A" first="Anne-Marie" last="Haynes">Anne-Marie Haynes</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Prostate Cancer Centre, St. Vincent's Clinic</s1>
<s2>Sydney</s2>
<s3>AUS</s3>
<sZ>4 aut.</sZ>
<sZ>25 aut.</sZ>
<sZ>26 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Steyerberg, Ewout" sort="Steyerberg, Ewout" uniqKey="Steyerberg E" first="Ewout" last="Steyerberg">Ewout Steyerberg</name>
<affiliation>
<inist:fA14 i1="19">
<s1>Department of Public Health, Erasmus MC-University Medical Center Rotterdam</s1>
<s2>Rotterdam</s2>
<s3>NLD</s3>
<sZ>27 aut.</sZ>
<sZ>28 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Roobol, Monique J" sort="Roobol, Monique J" uniqKey="Roobol M" first="Monique J." last="Roobol">Monique J. Roobol</name>
<affiliation>
<inist:fA14 i1="19">
<s1>Department of Public Health, Erasmus MC-University Medical Center Rotterdam</s1>
<s2>Rotterdam</s2>
<s3>NLD</s3>
<sZ>27 aut.</sZ>
<sZ>28 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Tewari, Ashutosh K" sort="Tewari, Ashutosh K" uniqKey="Tewari A" first="Ashutosh K." last="Tewari">Ashutosh K. Tewari</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital</s1>
<s2>New York, NY</s2>
<s3>USA</s3>
<sZ>3 aut.</sZ>
<sZ>16 aut.</sZ>
<sZ>29 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
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<series>
<title level="j" type="main">European urology</title>
<title level="j" type="abbreviated">Eur. urol.</title>
<idno type="ISSN">0302-2838</idno>
<imprint>
<date when="2014">2014</date>
</imprint>
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<title level="j" type="main">European urology</title>
<title level="j" type="abbreviated">Eur. urol.</title>
<idno type="ISSN">0302-2838</idno>
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<term>Comparative study</term>
<term>Endoscopic surgery</term>
<term>Human</term>
<term>Laparoscopic surgery</term>
<term>Laparoscopy</term>
<term>Nephrology</term>
<term>Prostatectomy</term>
<term>Rate</term>
<term>Robotics</term>
<term>Surgical margin</term>
<term>Telemedicine</term>
<term>Treatment</term>
<term>Urology</term>
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<keywords scheme="Pascal" xml:lang="fr">
<term>Marge chirurgicale</term>
<term>Etude comparative</term>
<term>Chirurgie endoscopique</term>
<term>Taux</term>
<term>Prostatectomie</term>
<term>Coeliochirurgie</term>
<term>Robotique</term>
<term>Homme</term>
<term>Laparoscopie</term>
<term>Télémédecine</term>
<term>Néphrologie</term>
<term>Urologie</term>
<term>Traitement</term>
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<front>
<div type="abstract" xml:lang="en">Background: Positive surgical margins (PSMs) are a known risk factor for biochemical recurrence in patients with prostate cancer (PCa) and are potentially affected by surgical technique and volume. Objective: To investigate whether radical prostatectomy (RP) modality and volume affect PSM rates. Design, setting, and participants: Fourteen institutions in Europe, the United States, and Australia were invited to participate in this study, all of which retrospectively provided margins data on 9778 open RP, 4918 laparoscopic RP, and 7697 robotic RP patients operated on between January 2000 and October 2011. Outcome measurements and statistical analyses: The outcome measure was PSM rate. Multivariable logistic regression analyses and propensity score methods identified odds ratios for risk of a PSM for one modality compared with another, after adjustment for age, preoperative prostate-specific antigen, postoperative Gleason score, pathologic stage, and year of surgery. Classic adjustment using standard covariates was also implemented to compare PSM rates based on center volume for each minimally invasive surgical cohort. Results and limitations: Open RP patients had higher-risk PCa at time of surgery on average and were operated on earlier in the study time period on average, compared with minimally invasive cohorts. Crude margin rates were lowest for robotic RP (13.8%), intermediate for laparoscopic RP (16.3%), and highest for open RP (22.8%); significant differences persisted, although were ameliorated, after statistical adjustments. Lower-volume centers had increased risks of PSM compared with the highest-volume center for both laparoscopic RP and robotic RP. The study is limited by its nonrandomized nature; missing data across covariates, especially year of surgery in many of the open cohort cases; lack of standardized histologic processing and central pathology review; and lack of information regarding potential confounders such as patient comorbidity, nerve-sparing status, lymph node status, tumor volume, and individual surgeon caseload.</div>
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<s0>Background: Positive surgical margins (PSMs) are a known risk factor for biochemical recurrence in patients with prostate cancer (PCa) and are potentially affected by surgical technique and volume. Objective: To investigate whether radical prostatectomy (RP) modality and volume affect PSM rates. Design, setting, and participants: Fourteen institutions in Europe, the United States, and Australia were invited to participate in this study, all of which retrospectively provided margins data on 9778 open RP, 4918 laparoscopic RP, and 7697 robotic RP patients operated on between January 2000 and October 2011. Outcome measurements and statistical analyses: The outcome measure was PSM rate. Multivariable logistic regression analyses and propensity score methods identified odds ratios for risk of a PSM for one modality compared with another, after adjustment for age, preoperative prostate-specific antigen, postoperative Gleason score, pathologic stage, and year of surgery. Classic adjustment using standard covariates was also implemented to compare PSM rates based on center volume for each minimally invasive surgical cohort. Results and limitations: Open RP patients had higher-risk PCa at time of surgery on average and were operated on earlier in the study time period on average, compared with minimally invasive cohorts. Crude margin rates were lowest for robotic RP (13.8%), intermediate for laparoscopic RP (16.3%), and highest for open RP (22.8%); significant differences persisted, although were ameliorated, after statistical adjustments. Lower-volume centers had increased risks of PSM compared with the highest-volume center for both laparoscopic RP and robotic RP. The study is limited by its nonrandomized nature; missing data across covariates, especially year of surgery in many of the open cohort cases; lack of standardized histologic processing and central pathology review; and lack of information regarding potential confounders such as patient comorbidity, nerve-sparing status, lymph node status, tumor volume, and individual surgeon caseload.</s0>
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<NO>PASCAL 14-0223163 INIST</NO>
<ET>A Multinational, Multi-institutional Study Comparing Positive Surgical Margin Rates Among 22 393 Open, Laparoscopic, and Robot-assisted Radical Prostatectomy Patients</ET>
<AU>SOORIAKUMARAN (Prasanna); SRIVASTAVA (Abhishek); SHARIAT (Shahrokh F.); STRIEKER (Phillip D.); AHLERING (Thomas); EDEN (Christopher G.); WIKLUND (Peter N.); SANCHEZ-SALAS (Rafael); MOTTRIE (Alexandre); LEE (David); NEAL (David E.); GHAVAMIAN (Reza); NYIRADY (Peter); NILSSON (Andreas); CARLSSON (Stefan); XYLINAS (Evanguelos); LOIDL (Wolfgang); SEITZ (Christian); SCHRAMEK (Paul); ROEHRBORN (Claus); CATHELINEAU (Xavier); SKARECKY (Douglas); SHAW (Greg); WARREN (Anne); DELPRADO (Warick J.); HAYNES (Anne-Marie); STEYERBERG (Ewout); ROOBOL (Monique J.); TEWARI (Ashutosh K.)</AU>
<AF>Surgical Intervention Trials Unit, Nuffield Department of Surgical Sciences, University of Oxford/Oxford/Royaume-Uni (1 aut.); Department of Molecular Medicine and Surgery, Karolinska Institutet/Stockholm/Suède (1 aut., 7 aut., 14 aut., 15 aut.); Department of Urology, Montefiore Medical Center/New York, NY/Etats-Unis (2 aut., 12 aut.); Department of Urology, Weill Cornell Medical College-New York Presbyterian Hospital/New York, NY/Etats-Unis (3 aut., 16 aut., 29 aut.); Department of Urology, Medical University of Vienna/Vienna/Autriche (3 aut., 18 aut.); Prostate Cancer Centre, St. Vincent's Clinic/Sydney/Australie (4 aut., 25 aut., 26 aut.); Department of Urology, University of California-Irvine School of Medicine/Irvine, CA/Etats-Unis (5 aut., 22 aut.); Department of Urology, Royal Surrey County Hospital/Guildford/Royaume-Uni (6 aut.); Department of Urology, L'Institut Mutualiste Montsouris/Paris/France (8 aut., 21 aut.); Department of Urology, Onze-Lieve-Vrouwziekenhuis Hospital/Aalst/Belgique (9 aut.); Department of Urology, University of Pennsylvania/Philadelphia, PA/Etats-Unis (10 aut.); Department of Uro-oncology, University of Cambridge/Cambridge/Royaume-Uni (11 aut.); Uro-oncology Research Group, Cancer Research UK, Cambridge Research Institute/Cambridge/Royaume-Uni (11 aut., 23 aut.); Department of Urology, Semmelweis University/Budapest/Hongrie (13 aut.); Department of Urology, St. Vincent's Hospital/Linz/Autriche (17 aut.); Department of Urology, Saint John of God Hospital/Vienna/Autriche (19 aut.); Department of Urology, University of Texas Southwestern Medical Center/Dallas, TX/Etats-Unis (20 aut.); Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust/Cambridge/Royaume-Uni (24 aut.); Department of Public Health, Erasmus MC-University Medical Center Rotterdam/Rotterdam/Pays-Bas (27 aut., 28 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>European urology; ISSN 0302-2838; Coden EUURAV; Royaume-Uni; Da. 2014; Vol. 66; No. 3; Pp. 450-456; Bibl. 27 ref.</SO>
<LA>Anglais</LA>
<EA>Background: Positive surgical margins (PSMs) are a known risk factor for biochemical recurrence in patients with prostate cancer (PCa) and are potentially affected by surgical technique and volume. Objective: To investigate whether radical prostatectomy (RP) modality and volume affect PSM rates. Design, setting, and participants: Fourteen institutions in Europe, the United States, and Australia were invited to participate in this study, all of which retrospectively provided margins data on 9778 open RP, 4918 laparoscopic RP, and 7697 robotic RP patients operated on between January 2000 and October 2011. Outcome measurements and statistical analyses: The outcome measure was PSM rate. Multivariable logistic regression analyses and propensity score methods identified odds ratios for risk of a PSM for one modality compared with another, after adjustment for age, preoperative prostate-specific antigen, postoperative Gleason score, pathologic stage, and year of surgery. Classic adjustment using standard covariates was also implemented to compare PSM rates based on center volume for each minimally invasive surgical cohort. Results and limitations: Open RP patients had higher-risk PCa at time of surgery on average and were operated on earlier in the study time period on average, compared with minimally invasive cohorts. Crude margin rates were lowest for robotic RP (13.8%), intermediate for laparoscopic RP (16.3%), and highest for open RP (22.8%); significant differences persisted, although were ameliorated, after statistical adjustments. Lower-volume centers had increased risks of PSM compared with the highest-volume center for both laparoscopic RP and robotic RP. The study is limited by its nonrandomized nature; missing data across covariates, especially year of surgery in many of the open cohort cases; lack of standardized histologic processing and central pathology review; and lack of information regarding potential confounders such as patient comorbidity, nerve-sparing status, lymph node status, tumor volume, and individual surgeon caseload.</EA>
<CC>002B14</CC>
<FD>Marge chirurgicale; Etude comparative; Chirurgie endoscopique; Taux; Prostatectomie; Coeliochirurgie; Robotique; Homme; Laparoscopie; Télémédecine; Néphrologie; Urologie; Traitement</FD>
<FG>Endoscopie</FG>
<ED>Surgical margin; Comparative study; Endoscopic surgery; Rate; Prostatectomy; Laparoscopic surgery; Robotics; Human; Laparoscopy; Telemedicine; Nephrology; Urology; Treatment</ED>
<EG>Endoscopy</EG>
<SD>Margen quirúrgica; Estudio comparativo; Cirugía endoscópica; Tasa; Prostatectomía; Cirugía laparoscopica; Robótica; Hombre; Laparoscopia; Telemedicina; Nefrología; Urología; Tratamiento</SD>
<LO>INIST-16847.354000504835110130</LO>
<ID>14-0223163</ID>
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   |texte=   A Multinational, Multi-institutional Study Comparing Positive Surgical Margin Rates Among 22 393 Open, Laparoscopic, and Robot-assisted Radical Prostatectomy Patients
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