Kerry Madison
Washington University in St. Louis
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European Urology | 2015
Sabine Brookman-May; Matthias May; Ingmar Wolff; Richard Zigeuner; Georg C. Hutterer; Luca Cindolo; Luigi Schips; Ottavio De Cobelli; Bernardo Rocco; Cosimo De Nunzio; Andrea Tubaro; I. Coman; Michael C. Truss; Orietta Dalpiaz; Bogdan Feciche; Robert S. Figenshau; Kerry Madison; Manuel Sánchez-Chapado; Maria del Carmen Santiago Martin; L. Salzano; G. Lotrecchiano; Stefan Zastrow; Manfred P. Wirth; Petros Sountoulides; Shahrokh F. Shariat; Raphaela Waidelich; Christian Stief; Sven Gunia
BACKGROUND The current TNM system for renal cell carcinoma (RCC) merges perirenal fat invasion (PFI) and renal vein invasion (RVI) as stage pT3a despite limited evidence concerning their prognostic equivalence. In addition, the prognostic value of PFI compared to pT1-pT2 tumors remains controversial. OBJECTIVE To analyze the prognostic significance of PFI, RVI, and tumor size in pT1-pT3a RCC. DESIGN, SETTING, AND PARTICIPANTS Data for 7384 pT1a-pT3a RCC patients were pooled from 12 centers. Patients were grouped according to stages and PFI/RVI presence as follows: pT1-2N0M0 (n=6137; 83.1%), pT3aN0M0 + PFI (n=1036; 14%), and pT3aN0M0 (RVI ± PFI; n=211; 2.9%). INTERVENTION Radical nephrectomy or nephron-sparing surgery (NSS) (1992-2010). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS Cancer-specific survival was estimated using the Kaplan-Meier method. Univariate and multivariate Cox proportional-hazards regression models, as well as sensitivity and discrimination analyses, were used to evaluate the impact of clinicopathologic parameters on cancer-specific mortality (CSM). RESULTS AND LIMITATIONS Compared to stage pT1-2, patients with stage pT3a RCC were significantly more often male (59.4% vs 53.1%) and older (64.9 vs 62.1 yr), more often had clear cell RCC (85.2% vs 77.7%), Fuhrman grade 3-4 (29.4% vs 13.4%), and tumor size >7 cm (39.1% vs 13%), and underwent NSS less often (7.5% vs 36.6%; all p<0.001). According to multivariate analysis, CSM was significantly higher for the PFI and RVI ± PFI groups compared to pT1-2 patients (hazard ratio [HR] 1.94 and 2.12, respectively; p<0.001), whereas patients with PFI only and RVI ± PFI did not differ (HR 1.17; p=0.316). Tumor size instead enhanced CSM by 7% per cm in stage pT3a (HR 1.07; p<0.001) with a 7 cm cutoff yielding the highest prediction accuracy. CONCLUSIONS Since the prognostic impact of PFI and RVI on CSM seems to be comparable, merging both as stage pT3a RCC might be justified. Enhanced prognostic discrimination of stage pT3a RCC appears to be possible by applying a tumor size cutoff of 7 cm within an alternative staging system. PATIENT SUMMARY Prognosis prediction for patients with localized renal cell carcinoma up to stage pT3a can be enhanced by including tumor size with a cutoff of 7 cm as an additional parameter in the TNM classification system.
Urologic Oncology-seminars and Original Investigations | 2014
Matthias May; Luca Cindolo; Richard Zigeuner; Ottavio De Cobelli; Bernardo Rocco; Cosimo De Nunzio; Andrea Tubaro; I. Coman; Michael C. Truss; Orietta Dalpiaz; Ingmar Wolff; Bogdan Feciche; Fabian Fenske; Martin Pichler; Luigi Schips; Robert S. Figenshau; Kerry Madison; M. Sánchez-Chapado; Maria del Carmen Santiago Martin; L. Salzano; G. Lotrecchiano; Raphaela Waidelich; Christian G. Stief; Petros Sountoulides; Sabine Brookman-May
OBJECTIVES To analyze clinicopathological features and survival of surgically treated patients with renal cell carcinoma (RCC) ≥ 80 years of age in comparison with patients between the ages of 60 and 70 years. MATERIALS AND METHODS The data for 2,516 patients with a median follow-up of 57 months were retrieved from a multinational database (Collaborative Research on Renal Neoplasms Association [CORONA]), including data for 6,234 consecutive patients with RCC after radical or partial nephrectomy. Comparative analysis of clinicopathological features of 241 octogenarians (3.9% of the database) and 2,275 reference patients between the ages of 60 and 70 years (36.5%) was performed. Multivariable regression analysis adjusted for competing risks was applied to identify the effect of advanced age on cancer-specific mortality (CSM) and other-cause mortality (OCM). Furthermore, instrumental variable analysis was employed to reduce residual confounding by unmeasured parameters. RESULTS Significantly more women were present (50% vs. 40%, P = 0.004), and significantly less often nephron-sparing surgery was performed in octogenarians compared with the reference group (11% vs. 20%, P<0.001). Although median tumor size and stages did not significantly defer, older patients less often had advanced or metastatic disease (N+/M1) (4.6% vs. 9.6%, P = 0.009). On multivariable analysis, higher CSM (hazard ratio = 1.48, P = 0.042) and OCM rates (hazard ratio = 4.32, P<0.001) were detectable in octogenarians (c-indices = 0.85 and 0.72, respectively). Integration of the variable age group in multivariable models significantly increased the predictive accuracy regarding OCM (6%, P<0.001), but not for CSM. Limitations are based on the retrospective study design. CONCLUSIONS Octogenarian patients with RCC significantly differ in clinical features and display significantly higher CSM and OCM rates in comparison with their younger counterparts.
Urologe A | 2014
Matthias May; Richard Zigeuner; Atiqullah Aziz; Luca Cindolo; Christian Gilfrich; Luigi Schips; De Cobelli O; Bernardo Rocco; De Nunzio C; A. Tubaro; I. Coman; Bogdan Feciche; Michael C. Truss; B. Hoschke; Orietta Dalpiaz; Stoltze A; Fabian Fenske; Hans-Martin Fritsche; Thomas F. Chromecki; Steffen Lebentrau; Robert S. Figenshau; Kerry Madison; M. Sánchez-Chapado; Del Carmen Santiago Martin M; L. Salzano; G. Lotrecchiano; Steven Joniau; Raphaela Waidelich; Christian G. Stief; Sabine Brookman-May
BACKGROUND The chromophobe subtype represents the third most common histological subtype of renal cell carcinoma (chRCC). Due to the rarity of this subtype only one publication regarding the specific analysis of clinical and histopathological criteria as well as survival analysis of more than 200 patients with chRCC is known to date. MATERIALS AND METHODS A total of 6,234 RCC patients from 11 centres who were treated by (partial) nephrectomy are contained in the database of this multinational study. Of the patients 259 were diagnosed with chRCC (4.2 %) and thus formed the study group for this retrospective investigation. These subjects were compared to 4,994 patients with a clear cell subtype (80.1 %) with respect to clinical and histopathological criteria. The independent influence of the chromophobe subtype regarding tumor-specific survival and overall survival was determined using analysis by Cox proportional hazards regression models. The median follow-up was 59 months (interquartile range 29-106 months). RESULTS The chRCC patients were significantly younger (60 vs. 63.2 years, p < 0.001), more often female (50 vs. 41 %, p = 0.005) and showed simultaneous distant metastases to a lesser extent (3.5 vs. 7.1 %, p = 0.023) compared to patients with a clear cell subtype. Despite a comparable median tumor size a ≥ pT3 tumor stage was diagnosed in only 24.7 % of the patients compared to of 30.5 % in patients with a clear cell subtype (p = 0.047). In addition to the clinical criteria of age, sex and distant metastases, the histological variables pTN stage, grade and tumor size showed a significant influence on tumor-specific and overall survival. However, in the multivariable Cox regression analysis no independent effect on tumor-specific mortality (HR 0.88, p = 0.515) and overall mortality (HR 1.00, p = 0.998) due to the histological subtype was found (c-index 0.86 and 0.77, respectively). CONCLUSIONS Patients with chRCC and clear cell RCC differ significantly concerning the distribution of clinical and histopathological criteria. Patients with chRCC present with less advanced tumors which leads to better tumor-specific survival rates in general; however, this advantage could not be verified after adjustment for the established risk factors.
Urologe A | 2013
Matthias May; Richard Zigeuner; Atiqullah Aziz; Luca Cindolo; Christian Gilfrich; Luigi Schips; O. De Cobelli; Bernardo Rocco; C. De Nunzio; Andrea Tubaro; I. Coman; Bogdan Feciche; Michael C. Truss; B. Hoschke; Orietta Dalpiaz; A. Stoltze; Fabian Fenske; Hans Martin Fritsche; Thomas F. Chromecki; S. Lebentrau; Robert S. Figenshau; Kerry Madison; M. Sánchez-Chapado; M. del Carmen Santiago Martin; L. Salzano; G. Lotrecchiano; Steven Joniau; Raphaela Waidelich; Christian G. Stief; Sabine Brookman-May
BACKGROUND The chromophobe subtype represents the third most common histological subtype of renal cell carcinoma (chRCC). Due to the rarity of this subtype only one publication regarding the specific analysis of clinical and histopathological criteria as well as survival analysis of more than 200 patients with chRCC is known to date. MATERIALS AND METHODS A total of 6,234 RCC patients from 11 centres who were treated by (partial) nephrectomy are contained in the database of this multinational study. Of the patients 259 were diagnosed with chRCC (4.2 %) and thus formed the study group for this retrospective investigation. These subjects were compared to 4,994 patients with a clear cell subtype (80.1 %) with respect to clinical and histopathological criteria. The independent influence of the chromophobe subtype regarding tumor-specific survival and overall survival was determined using analysis by Cox proportional hazards regression models. The median follow-up was 59 months (interquartile range 29-106 months). RESULTS The chRCC patients were significantly younger (60 vs. 63.2 years, p < 0.001), more often female (50 vs. 41 %, p = 0.005) and showed simultaneous distant metastases to a lesser extent (3.5 vs. 7.1 %, p = 0.023) compared to patients with a clear cell subtype. Despite a comparable median tumor size a ≥ pT3 tumor stage was diagnosed in only 24.7 % of the patients compared to of 30.5 % in patients with a clear cell subtype (p = 0.047). In addition to the clinical criteria of age, sex and distant metastases, the histological variables pTN stage, grade and tumor size showed a significant influence on tumor-specific and overall survival. However, in the multivariable Cox regression analysis no independent effect on tumor-specific mortality (HR 0.88, p = 0.515) and overall mortality (HR 1.00, p = 0.998) due to the histological subtype was found (c-index 0.86 and 0.77, respectively). CONCLUSIONS Patients with chRCC and clear cell RCC differ significantly concerning the distribution of clinical and histopathological criteria. Patients with chRCC present with less advanced tumors which leads to better tumor-specific survival rates in general; however, this advantage could not be verified after adjustment for the established risk factors.
Urologe A | 2014
Matthias May; Richard Zigeuner; Atiqullah Aziz; Luca Cindolo; Christian Gilfrich; Luigi Schips; O. De Cobelli; Bernardo Rocco; C. De Nunzio; A. Tubaro; I. Coman; Bogdan Feciche; Michael C. Truss; B. Hoschke; Orietta Dalpiaz; A. Stoltze; Fabian Fenske; Hans Martin Fritsche; Thomas F. Chromecki; S. Lebentrau; Robert S. Figenshau; Kerry Madison; M. Sánchez-Chapado; M. del Carmen Santiago Martin; L. Salzano; G. Lotrecchiano; Steven Joniau; Raphaela Waidelich; Christian G. Stief; Sabine Brookman-May
BACKGROUND The chromophobe subtype represents the third most common histological subtype of renal cell carcinoma (chRCC). Due to the rarity of this subtype only one publication regarding the specific analysis of clinical and histopathological criteria as well as survival analysis of more than 200 patients with chRCC is known to date. MATERIALS AND METHODS A total of 6,234 RCC patients from 11 centres who were treated by (partial) nephrectomy are contained in the database of this multinational study. Of the patients 259 were diagnosed with chRCC (4.2 %) and thus formed the study group for this retrospective investigation. These subjects were compared to 4,994 patients with a clear cell subtype (80.1 %) with respect to clinical and histopathological criteria. The independent influence of the chromophobe subtype regarding tumor-specific survival and overall survival was determined using analysis by Cox proportional hazards regression models. The median follow-up was 59 months (interquartile range 29-106 months). RESULTS The chRCC patients were significantly younger (60 vs. 63.2 years, p < 0.001), more often female (50 vs. 41 %, p = 0.005) and showed simultaneous distant metastases to a lesser extent (3.5 vs. 7.1 %, p = 0.023) compared to patients with a clear cell subtype. Despite a comparable median tumor size a ≥ pT3 tumor stage was diagnosed in only 24.7 % of the patients compared to of 30.5 % in patients with a clear cell subtype (p = 0.047). In addition to the clinical criteria of age, sex and distant metastases, the histological variables pTN stage, grade and tumor size showed a significant influence on tumor-specific and overall survival. However, in the multivariable Cox regression analysis no independent effect on tumor-specific mortality (HR 0.88, p = 0.515) and overall mortality (HR 1.00, p = 0.998) due to the histological subtype was found (c-index 0.86 and 0.77, respectively). CONCLUSIONS Patients with chRCC and clear cell RCC differ significantly concerning the distribution of clinical and histopathological criteria. Patients with chRCC present with less advanced tumors which leads to better tumor-specific survival rates in general; however, this advantage could not be verified after adjustment for the established risk factors.
Urologe - Ausgabe A | 2014
Matthias May; Richard Zigeuner; Atiqullah Aziz; Luca Cindolo; Christian Gilfrich; Luigi Schips; O. De Cobelli; Bernardo Rocco; C. De Nunzio; A. Tubaro; I. Coman; Bogdan Feciche; Michael C. Truss; B. Hoschke; Orietta Dalpiaz; A. Stoltze; Fabian Fenske; Hans Martin Fritsche; Thomas F. Chromecki; S. Lebentrau; Robert S. Figenshau; Kerry Madison; M. Sánchez-Chapado; M. del Carmen Santiago Martin; L. Salzano; G. Lotrecchiano; Steven Joniau; Raphaela Waidelich; Christian G. Stief; Sabine Brookman-May
BACKGROUND The chromophobe subtype represents the third most common histological subtype of renal cell carcinoma (chRCC). Due to the rarity of this subtype only one publication regarding the specific analysis of clinical and histopathological criteria as well as survival analysis of more than 200 patients with chRCC is known to date. MATERIALS AND METHODS A total of 6,234 RCC patients from 11 centres who were treated by (partial) nephrectomy are contained in the database of this multinational study. Of the patients 259 were diagnosed with chRCC (4.2 %) and thus formed the study group for this retrospective investigation. These subjects were compared to 4,994 patients with a clear cell subtype (80.1 %) with respect to clinical and histopathological criteria. The independent influence of the chromophobe subtype regarding tumor-specific survival and overall survival was determined using analysis by Cox proportional hazards regression models. The median follow-up was 59 months (interquartile range 29-106 months). RESULTS The chRCC patients were significantly younger (60 vs. 63.2 years, p < 0.001), more often female (50 vs. 41 %, p = 0.005) and showed simultaneous distant metastases to a lesser extent (3.5 vs. 7.1 %, p = 0.023) compared to patients with a clear cell subtype. Despite a comparable median tumor size a ≥ pT3 tumor stage was diagnosed in only 24.7 % of the patients compared to of 30.5 % in patients with a clear cell subtype (p = 0.047). In addition to the clinical criteria of age, sex and distant metastases, the histological variables pTN stage, grade and tumor size showed a significant influence on tumor-specific and overall survival. However, in the multivariable Cox regression analysis no independent effect on tumor-specific mortality (HR 0.88, p = 0.515) and overall mortality (HR 1.00, p = 0.998) due to the histological subtype was found (c-index 0.86 and 0.77, respectively). CONCLUSIONS Patients with chRCC and clear cell RCC differ significantly concerning the distribution of clinical and histopathological criteria. Patients with chRCC present with less advanced tumors which leads to better tumor-specific survival rates in general; however, this advantage could not be verified after adjustment for the established risk factors.
The Journal of Urology | 2012
Youssef S. Tanagho; Gerald L. Andriole; Alethea Paradis; Kerry Madison; Gurdarshan S. Sandhu; J. Esteban Varela; Brian M. Benway
World Journal of Urology | 2013
Matthias May; Atiqullah Aziz; Richard Zigeuner; Thomas F. Chromecki; Luca Cindolo; Luigi Schips; Ottavio De Cobelli; Bernardo Rocco; Cosimo De Nunzio; Andrea Tubaro; I. Coman; Michael C. Truss; Orietta Dalpiaz; B. Hoschke; Christian Gilfrich; Bogdan Feciche; Anette Stoltze; Fabian Fenske; Hans Martin Fritsche; Robert S. Figenshau; Kerry Madison; M. Sánchez-Chapado; Maria del Carmen Santiago Martin; L. Salzano; G. Lotrecchiano; Steven Joniau; Raphaela Waidelich; Christian G. Stief; Sabine Brookman-May
The Journal of Urology | 2014
Atiqullah Aziz; Matthias May; Richard Zigeuner; Martin Pichler; Thomas F. Chromecki; Luca Cindolo; Luigi Schips; Ottavio De Cobelli; Bernardo Rocco; Cosimo De Nunzio; Andrea Tubaro; Ioan Coman; Michael C. Truss; Orietta Dalpiaz; B. Hoschke; Christian Gilfrich; Bogdan Feciche; Fabian Fenske; Petros Sountoulides; Robert S. Figenshau; Kerry Madison; Manuel Sánchez-Chapado; Maria del Carmen Santiago Martin; Wolf F. Wieland; L. Salzano; G. Lotrecchiano; Raphaela Waidelich; Christian G. Stief; Sabine Brookman-May
Ejso | 2016
Ingmar Wolff; Matthias May; B. Hoschke; Richard Zigeuner; Luca Cindolo; Georg C. Hutterer; Luigi Schips; O. De Cobelli; Bernardo Rocco; C. De Nunzio; Andrea Tubaro; I. Coman; Bogdan Feciche; Michael C. Truss; Orietta Dalpiaz; Robert S. Figenshau; Kerry Madison; M. Sánchez-Chapado; M.D.C. Santiago Martin; L. Salzano; G. Lotrecchiano; Shahrokh F. Shariat; Markus Hohenfellner; Raphaela Waidelich; Christian G. Stief; Kelly E. Miller; Sascha Pahernik; Sabine Brookman-May