The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery
Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An internat...
Ausführliche Beschreibung
Autor*in: |
Bigot, Pierre [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2015 |
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Anmerkung: |
© Springer-Verlag Berlin Heidelberg 2015 |
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Übergeordnetes Werk: |
Enthalten in: World journal of urology - Berlin : Springer, 1983, 34(2015), 3 vom: 07. Juli, Seite 347-352 |
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Übergeordnetes Werk: |
volume:34 ; year:2015 ; number:3 ; day:07 ; month:07 ; pages:347-352 |
Links: |
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DOI / URN: |
10.1007/s00345-015-1634-0 |
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Katalog-ID: |
SPR004316096 |
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100 | 1 | |a Bigot, Pierre |e verfasserin |4 aut | |
245 | 1 | 4 | |a The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery |
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520 | |a Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. | ||
650 | 4 | |a Nephron sparing surgery |7 (dpeaa)DE-He213 | |
650 | 4 | |a Papillary renal cell carcinoma |7 (dpeaa)DE-He213 | |
650 | 4 | |a Oncologic outcomes |7 (dpeaa)DE-He213 | |
700 | 1 | |a Bernhard, Jean-Christophe |4 aut | |
700 | 1 | |a Gill, Inderbir S. |4 aut | |
700 | 1 | |a Vuong, Nam Son |4 aut | |
700 | 1 | |a Verhoest, Grégory |4 aut | |
700 | 1 | |a Flamand, Vincent |4 aut | |
700 | 1 | |a Reix, Boris |4 aut | |
700 | 1 | |a Suer, Evren |4 aut | |
700 | 1 | |a Gökce, Ilker |4 aut | |
700 | 1 | |a Beauval, Jean Baptiste |4 aut | |
700 | 1 | |a Nouhaud, François Xavier |4 aut | |
700 | 1 | |a Eto, Masatoshi |4 aut | |
700 | 1 | |a Baco, Eduard |4 aut | |
700 | 1 | |a Matsugasumi, Toru |4 aut | |
700 | 1 | |a Chowaniec, Yvonne |4 aut | |
700 | 1 | |a Rigaud, Jérôme |4 aut | |
700 | 1 | |a Lenormand, Claire |4 aut | |
700 | 1 | |a Pfister, Christian |4 aut | |
700 | 1 | |a Hetet, Jean François |4 aut | |
700 | 1 | |a Ploussard, Guillaume |4 aut | |
700 | 1 | |a Roupret, Morgan |4 aut | |
700 | 1 | |a Léon, Priscilla |4 aut | |
700 | 1 | |a Bakri, Adnan El |4 aut | |
700 | 1 | |a Larré, Stéphane |4 aut | |
700 | 1 | |a Tillou, Xavier |4 aut | |
700 | 1 | |a Doerfler, Arnaud |4 aut | |
700 | 1 | |a Descazeaud, Aurélien |4 aut | |
700 | 1 | |a Koutlidis, Nicolas |4 aut | |
700 | 1 | |a Schneider, Alexandre |4 aut | |
700 | 1 | |a Sebe, Philippe |4 aut | |
700 | 1 | |a Ingels, Alexandre |4 aut | |
700 | 1 | |a Azzouzi, Abdel Rahmène |4 aut | |
700 | 1 | |a Soulié, Michel |4 aut | |
700 | 1 | |a Méjean, Arnaud |4 aut | |
700 | 1 | |a Bensalah, Karim |4 aut | |
700 | 1 | |a Patard, Jean-Jacques |4 aut | |
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10.1007/s00345-015-1634-0 doi (DE-627)SPR004316096 (SPR)s00345-015-1634-0-e DE-627 ger DE-627 rakwb eng Bigot, Pierre verfasserin aut The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. Nephron sparing surgery (dpeaa)DE-He213 Papillary renal cell carcinoma (dpeaa)DE-He213 Oncologic outcomes (dpeaa)DE-He213 Bernhard, Jean-Christophe aut Gill, Inderbir S. aut Vuong, Nam Son aut Verhoest, Grégory aut Flamand, Vincent aut Reix, Boris aut Suer, Evren aut Gökce, Ilker aut Beauval, Jean Baptiste aut Nouhaud, François Xavier aut Eto, Masatoshi aut Baco, Eduard aut Matsugasumi, Toru aut Chowaniec, Yvonne aut Rigaud, Jérôme aut Lenormand, Claire aut Pfister, Christian aut Hetet, Jean François aut Ploussard, Guillaume aut Roupret, Morgan aut Léon, Priscilla aut Bakri, Adnan El aut Larré, Stéphane aut Tillou, Xavier aut Doerfler, Arnaud aut Descazeaud, Aurélien aut Koutlidis, Nicolas aut Schneider, Alexandre aut Sebe, Philippe aut Ingels, Alexandre aut Azzouzi, Abdel Rahmène aut Soulié, Michel aut Méjean, Arnaud aut Bensalah, Karim aut Patard, Jean-Jacques aut Enthalten in World journal of urology Berlin : Springer, 1983 34(2015), 3 vom: 07. Juli, Seite 347-352 (DE-627)254910874 (DE-600)1463303-6 1433-8726 nnns volume:34 year:2015 number:3 day:07 month:07 pages:347-352 https://dx.doi.org/10.1007/s00345-015-1634-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 3 07 07 347-352 |
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10.1007/s00345-015-1634-0 doi (DE-627)SPR004316096 (SPR)s00345-015-1634-0-e DE-627 ger DE-627 rakwb eng Bigot, Pierre verfasserin aut The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. Nephron sparing surgery (dpeaa)DE-He213 Papillary renal cell carcinoma (dpeaa)DE-He213 Oncologic outcomes (dpeaa)DE-He213 Bernhard, Jean-Christophe aut Gill, Inderbir S. aut Vuong, Nam Son aut Verhoest, Grégory aut Flamand, Vincent aut Reix, Boris aut Suer, Evren aut Gökce, Ilker aut Beauval, Jean Baptiste aut Nouhaud, François Xavier aut Eto, Masatoshi aut Baco, Eduard aut Matsugasumi, Toru aut Chowaniec, Yvonne aut Rigaud, Jérôme aut Lenormand, Claire aut Pfister, Christian aut Hetet, Jean François aut Ploussard, Guillaume aut Roupret, Morgan aut Léon, Priscilla aut Bakri, Adnan El aut Larré, Stéphane aut Tillou, Xavier aut Doerfler, Arnaud aut Descazeaud, Aurélien aut Koutlidis, Nicolas aut Schneider, Alexandre aut Sebe, Philippe aut Ingels, Alexandre aut Azzouzi, Abdel Rahmène aut Soulié, Michel aut Méjean, Arnaud aut Bensalah, Karim aut Patard, Jean-Jacques aut Enthalten in World journal of urology Berlin : Springer, 1983 34(2015), 3 vom: 07. Juli, Seite 347-352 (DE-627)254910874 (DE-600)1463303-6 1433-8726 nnns volume:34 year:2015 number:3 day:07 month:07 pages:347-352 https://dx.doi.org/10.1007/s00345-015-1634-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 3 07 07 347-352 |
allfields_unstemmed |
10.1007/s00345-015-1634-0 doi (DE-627)SPR004316096 (SPR)s00345-015-1634-0-e DE-627 ger DE-627 rakwb eng Bigot, Pierre verfasserin aut The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. Nephron sparing surgery (dpeaa)DE-He213 Papillary renal cell carcinoma (dpeaa)DE-He213 Oncologic outcomes (dpeaa)DE-He213 Bernhard, Jean-Christophe aut Gill, Inderbir S. aut Vuong, Nam Son aut Verhoest, Grégory aut Flamand, Vincent aut Reix, Boris aut Suer, Evren aut Gökce, Ilker aut Beauval, Jean Baptiste aut Nouhaud, François Xavier aut Eto, Masatoshi aut Baco, Eduard aut Matsugasumi, Toru aut Chowaniec, Yvonne aut Rigaud, Jérôme aut Lenormand, Claire aut Pfister, Christian aut Hetet, Jean François aut Ploussard, Guillaume aut Roupret, Morgan aut Léon, Priscilla aut Bakri, Adnan El aut Larré, Stéphane aut Tillou, Xavier aut Doerfler, Arnaud aut Descazeaud, Aurélien aut Koutlidis, Nicolas aut Schneider, Alexandre aut Sebe, Philippe aut Ingels, Alexandre aut Azzouzi, Abdel Rahmène aut Soulié, Michel aut Méjean, Arnaud aut Bensalah, Karim aut Patard, Jean-Jacques aut Enthalten in World journal of urology Berlin : Springer, 1983 34(2015), 3 vom: 07. Juli, Seite 347-352 (DE-627)254910874 (DE-600)1463303-6 1433-8726 nnns volume:34 year:2015 number:3 day:07 month:07 pages:347-352 https://dx.doi.org/10.1007/s00345-015-1634-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 3 07 07 347-352 |
allfieldsGer |
10.1007/s00345-015-1634-0 doi (DE-627)SPR004316096 (SPR)s00345-015-1634-0-e DE-627 ger DE-627 rakwb eng Bigot, Pierre verfasserin aut The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. Nephron sparing surgery (dpeaa)DE-He213 Papillary renal cell carcinoma (dpeaa)DE-He213 Oncologic outcomes (dpeaa)DE-He213 Bernhard, Jean-Christophe aut Gill, Inderbir S. aut Vuong, Nam Son aut Verhoest, Grégory aut Flamand, Vincent aut Reix, Boris aut Suer, Evren aut Gökce, Ilker aut Beauval, Jean Baptiste aut Nouhaud, François Xavier aut Eto, Masatoshi aut Baco, Eduard aut Matsugasumi, Toru aut Chowaniec, Yvonne aut Rigaud, Jérôme aut Lenormand, Claire aut Pfister, Christian aut Hetet, Jean François aut Ploussard, Guillaume aut Roupret, Morgan aut Léon, Priscilla aut Bakri, Adnan El aut Larré, Stéphane aut Tillou, Xavier aut Doerfler, Arnaud aut Descazeaud, Aurélien aut Koutlidis, Nicolas aut Schneider, Alexandre aut Sebe, Philippe aut Ingels, Alexandre aut Azzouzi, Abdel Rahmène aut Soulié, Michel aut Méjean, Arnaud aut Bensalah, Karim aut Patard, Jean-Jacques aut Enthalten in World journal of urology Berlin : Springer, 1983 34(2015), 3 vom: 07. Juli, Seite 347-352 (DE-627)254910874 (DE-600)1463303-6 1433-8726 nnns volume:34 year:2015 number:3 day:07 month:07 pages:347-352 https://dx.doi.org/10.1007/s00345-015-1634-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 3 07 07 347-352 |
allfieldsSound |
10.1007/s00345-015-1634-0 doi (DE-627)SPR004316096 (SPR)s00345-015-1634-0-e DE-627 ger DE-627 rakwb eng Bigot, Pierre verfasserin aut The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2015 Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. Nephron sparing surgery (dpeaa)DE-He213 Papillary renal cell carcinoma (dpeaa)DE-He213 Oncologic outcomes (dpeaa)DE-He213 Bernhard, Jean-Christophe aut Gill, Inderbir S. aut Vuong, Nam Son aut Verhoest, Grégory aut Flamand, Vincent aut Reix, Boris aut Suer, Evren aut Gökce, Ilker aut Beauval, Jean Baptiste aut Nouhaud, François Xavier aut Eto, Masatoshi aut Baco, Eduard aut Matsugasumi, Toru aut Chowaniec, Yvonne aut Rigaud, Jérôme aut Lenormand, Claire aut Pfister, Christian aut Hetet, Jean François aut Ploussard, Guillaume aut Roupret, Morgan aut Léon, Priscilla aut Bakri, Adnan El aut Larré, Stéphane aut Tillou, Xavier aut Doerfler, Arnaud aut Descazeaud, Aurélien aut Koutlidis, Nicolas aut Schneider, Alexandre aut Sebe, Philippe aut Ingels, Alexandre aut Azzouzi, Abdel Rahmène aut Soulié, Michel aut Méjean, Arnaud aut Bensalah, Karim aut Patard, Jean-Jacques aut Enthalten in World journal of urology Berlin : Springer, 1983 34(2015), 3 vom: 07. Juli, Seite 347-352 (DE-627)254910874 (DE-600)1463303-6 1433-8726 nnns volume:34 year:2015 number:3 day:07 month:07 pages:347-352 https://dx.doi.org/10.1007/s00345-015-1634-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 34 2015 3 07 07 347-352 |
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Enthalten in World journal of urology 34(2015), 3 vom: 07. Juli, Seite 347-352 volume:34 year:2015 number:3 day:07 month:07 pages:347-352 |
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Enthalten in World journal of urology 34(2015), 3 vom: 07. Juli, Seite 347-352 volume:34 year:2015 number:3 day:07 month:07 pages:347-352 |
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Nephron sparing surgery Papillary renal cell carcinoma Oncologic outcomes |
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Bigot, Pierre @@aut@@ Bernhard, Jean-Christophe @@aut@@ Gill, Inderbir S. @@aut@@ Vuong, Nam Son @@aut@@ Verhoest, Grégory @@aut@@ Flamand, Vincent @@aut@@ Reix, Boris @@aut@@ Suer, Evren @@aut@@ Gökce, Ilker @@aut@@ Beauval, Jean Baptiste @@aut@@ Nouhaud, François Xavier @@aut@@ Eto, Masatoshi @@aut@@ Baco, Eduard @@aut@@ Matsugasumi, Toru @@aut@@ Chowaniec, Yvonne @@aut@@ Rigaud, Jérôme @@aut@@ Lenormand, Claire @@aut@@ Pfister, Christian @@aut@@ Hetet, Jean François @@aut@@ Ploussard, Guillaume @@aut@@ Roupret, Morgan @@aut@@ Léon, Priscilla @@aut@@ Bakri, Adnan El @@aut@@ Larré, Stéphane @@aut@@ Tillou, Xavier @@aut@@ Doerfler, Arnaud @@aut@@ Descazeaud, Aurélien @@aut@@ Koutlidis, Nicolas @@aut@@ Schneider, Alexandre @@aut@@ Sebe, Philippe @@aut@@ Ingels, Alexandre @@aut@@ Azzouzi, Abdel Rahmène @@aut@@ Soulié, Michel @@aut@@ Méjean, Arnaud @@aut@@ Bensalah, Karim @@aut@@ Patard, Jean-Jacques @@aut@@ |
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Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. 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Bigot, Pierre |
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Bigot, Pierre misc Nephron sparing surgery misc Papillary renal cell carcinoma misc Oncologic outcomes The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery |
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The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery Nephron sparing surgery (dpeaa)DE-He213 Papillary renal cell carcinoma (dpeaa)DE-He213 Oncologic outcomes (dpeaa)DE-He213 |
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The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery |
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Bigot, Pierre Bernhard, Jean-Christophe Gill, Inderbir S. Vuong, Nam Son Verhoest, Grégory Flamand, Vincent Reix, Boris Suer, Evren Gökce, Ilker Beauval, Jean Baptiste Nouhaud, François Xavier Eto, Masatoshi Baco, Eduard Matsugasumi, Toru Chowaniec, Yvonne Rigaud, Jérôme Lenormand, Claire Pfister, Christian Hetet, Jean François Ploussard, Guillaume Roupret, Morgan Léon, Priscilla Bakri, Adnan El Larré, Stéphane Tillou, Xavier Doerfler, Arnaud Descazeaud, Aurélien Koutlidis, Nicolas Schneider, Alexandre Sebe, Philippe Ingels, Alexandre Azzouzi, Abdel Rahmène Soulié, Michel Méjean, Arnaud Bensalah, Karim Patard, Jean-Jacques |
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subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery |
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The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery |
abstract |
Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. © Springer-Verlag Berlin Heidelberg 2015 |
abstractGer |
Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. © Springer-Verlag Berlin Heidelberg 2015 |
abstract_unstemmed |
Objectives To evaluate the oncological outcomes of papillary renal cell carcinoma (pRCC) following nephron sparing surgery (NSS) and to determine whether the subclassification type of pRCC could be a prognostic factor for recurrence, progression, and specific death. Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. Tumor stage superior to pT1 was the only prognostic factor for CFS (HR 3.5; p = 0.03). Conclusion Histological subtyping of pRCC has no impact on oncologic outcomes after nephron sparing surgery. In this selected population of pRCC tumors, we found that tumor stage is the only prognostic factor for cancer-free survival. © Springer-Verlag Berlin Heidelberg 2015 |
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3 |
title_short |
The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery |
url |
https://dx.doi.org/10.1007/s00345-015-1634-0 |
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Bernhard, Jean-Christophe Gill, Inderbir S. Vuong, Nam Son Verhoest, Grégory Flamand, Vincent Reix, Boris Suer, Evren Gökce, Ilker Beauval, Jean Baptiste Nouhaud, François Xavier Eto, Masatoshi Baco, Eduard Matsugasumi, Toru Chowaniec, Yvonne Rigaud, Jérôme Lenormand, Claire Pfister, Christian Hetet, Jean François Ploussard, Guillaume Roupret, Morgan Léon, Priscilla Bakri, Adnan El Larré, Stéphane Tillou, Xavier Doerfler, Arnaud Descazeaud, Aurélien Koutlidis, Nicolas Schneider, Alexandre Sebe, Philippe Ingels, Alexandre Azzouzi, Abdel Rahmène Soulié, Michel Méjean, Arnaud Bensalah, Karim Patard, Jean-Jacques |
author2Str |
Bernhard, Jean-Christophe Gill, Inderbir S. Vuong, Nam Son Verhoest, Grégory Flamand, Vincent Reix, Boris Suer, Evren Gökce, Ilker Beauval, Jean Baptiste Nouhaud, François Xavier Eto, Masatoshi Baco, Eduard Matsugasumi, Toru Chowaniec, Yvonne Rigaud, Jérôme Lenormand, Claire Pfister, Christian Hetet, Jean François Ploussard, Guillaume Roupret, Morgan Léon, Priscilla Bakri, Adnan El Larré, Stéphane Tillou, Xavier Doerfler, Arnaud Descazeaud, Aurélien Koutlidis, Nicolas Schneider, Alexandre Sebe, Philippe Ingels, Alexandre Azzouzi, Abdel Rahmène Soulié, Michel Méjean, Arnaud Bensalah, Karim Patard, Jean-Jacques |
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up_date |
2024-07-04T00:38:30.843Z |
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Materials and methods An international multicentre retrospective study involving 19 institutions and the French network for research on kidney cancer was conducted after IRB approval. We analyzed data of all patients with pRCC who were treated by NSS between 2004 and 2014. Results We included 486 patients. Tumors were type 1 pRCC in 369 (76 %) cases and type 2 pRCC in 117 (24 %) cases. After a mean follow-up of 35 (1–120) months, 8 (1.6 %) patients experienced a local recurrence, 12 (1.5 %) had a metastatic progression, 24 (4.9 %) died, and 7 (1.4 %) died from cancer. Patients with type I pRCC had more grade II (66.3 vs. 46.1 %; p < 0.001) and less grade III (20 vs. 41 %; p < 0.001) tumors. Three-year estimated cancer-free survival (CFS) rate for type 1 pRCC was 96.5 % and for type 2 pRCC was 95.1 % (p = 0.894), respectively. Three-year estimated cancer-specific survival rate for type 1 pRCC was 98.4 % and for type 2 pRCC was 97.3 % (p = 0.947), respectively. 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|
score |
7.401101 |