Survival of metastatic renal cell carcinoma patients continues to improve over time, even in targeted therapy era

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Survival of metastatic renal cell carcinoma patients continues to improve over time, even in targeted therapy era. / Marchioni, Michele; Bandini, Marco; Pompe, Raisa S; Tian, Zhe; Martel, Tristan; Kapoor, Anil; Cindolo, Luca; Berardinelli, Francesco; Briganti, Alberto; Shariat, Shahrokh F; Schips, Luigi; Karakiewicz, Pierre I.

in: INT UROL NEPHROL, Jahrgang 49, Nr. 12, 12.2017, S. 2143-2149.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Marchioni, M, Bandini, M, Pompe, RS, Tian, Z, Martel, T, Kapoor, A, Cindolo, L, Berardinelli, F, Briganti, A, Shariat, SF, Schips, L & Karakiewicz, PI 2017, 'Survival of metastatic renal cell carcinoma patients continues to improve over time, even in targeted therapy era', INT UROL NEPHROL, Jg. 49, Nr. 12, S. 2143-2149. https://doi.org/10.1007/s11255-017-1703-y

APA

Marchioni, M., Bandini, M., Pompe, R. S., Tian, Z., Martel, T., Kapoor, A., Cindolo, L., Berardinelli, F., Briganti, A., Shariat, S. F., Schips, L., & Karakiewicz, P. I. (2017). Survival of metastatic renal cell carcinoma patients continues to improve over time, even in targeted therapy era. INT UROL NEPHROL, 49(12), 2143-2149. https://doi.org/10.1007/s11255-017-1703-y

Vancouver

Bibtex

@article{21d52e9b27f64cbcbf208cce442c9e42,
title = "Survival of metastatic renal cell carcinoma patients continues to improve over time, even in targeted therapy era",
abstract = "OBJECTIVE: To examine the effect of diagnosis year, defined as contemporary (2010-2014), intermediate (2006-2009) and historical (2001-2005) on cancer-specific mortality (CSM) in patients with metastatic renal cell carcinoma (mRCC).METHODS: Within Surveillance, Epidemiology, and End Results registry (2001-2014), we identified patients with mRCC. Cumulative incidence and competing risks regression (CRR) models examined CSM, after accounting for other-cause mortality. Finally, we performed subgroup analyses according to histological subtype: clear-cell mRCC (ccmRCC) versus non-ccmRCC.RESULTS: We identified 15,444 patients with mRCC. Of those, 41.0, 28.7 and 30.3% were diagnosed, respectively, in the contemporary, intermediate and historical years. Of all, 47.1, 5.3 and 47.6% were, respectively, ccmRCC, non-ccmRCC and other mRCC histological variants [sarcomatoid mRCC, cyst-associated mRCC, collecting duct carcinoma and mRCC not otherwise specified (NOS)]. Overall, 24-month CSM rates were, respectively, 61.0, 63.7 and 67.3% in contemporary, intermediate and historical patients. In all patients, multivariable CRR models exhibited higher CSM in intermediate (HR 1.11; p < 0.001) and historical patients (HR 1.24; p < 0.001) than in contemporary patients. Multivariable CRR models focusing on ccmRCC yielded virtually the same results. However, multivariable CRR models focusing on non-ccmRCC showed no CSM differences according to diagnosis year (all p ≥ 0.3).CONCLUSION: The introduction of new therapeutic agents resulted in CSM-free survival improvement over study time. However, this effect exclusively applies to patients with ccmRCC, but not to those with non-ccmRCC. This observation is in agreement with established efficacy of systemic therapies for ccmRCC, but lesser efficacy of these agents for non-ccmRCC.",
keywords = "Journal Article",
author = "Michele Marchioni and Marco Bandini and Pompe, {Raisa S} and Zhe Tian and Tristan Martel and Anil Kapoor and Luca Cindolo and Francesco Berardinelli and Alberto Briganti and Shariat, {Shahrokh F} and Luigi Schips and Karakiewicz, {Pierre I}",
year = "2017",
month = dec,
doi = "10.1007/s11255-017-1703-y",
language = "English",
volume = "49",
pages = "2143--2149",
journal = "INT UROL NEPHROL",
issn = "0301-1623",
publisher = "Springer Netherlands",
number = "12",

}

RIS

TY - JOUR

T1 - Survival of metastatic renal cell carcinoma patients continues to improve over time, even in targeted therapy era

AU - Marchioni, Michele

AU - Bandini, Marco

AU - Pompe, Raisa S

AU - Tian, Zhe

AU - Martel, Tristan

AU - Kapoor, Anil

AU - Cindolo, Luca

AU - Berardinelli, Francesco

AU - Briganti, Alberto

AU - Shariat, Shahrokh F

AU - Schips, Luigi

AU - Karakiewicz, Pierre I

PY - 2017/12

Y1 - 2017/12

N2 - OBJECTIVE: To examine the effect of diagnosis year, defined as contemporary (2010-2014), intermediate (2006-2009) and historical (2001-2005) on cancer-specific mortality (CSM) in patients with metastatic renal cell carcinoma (mRCC).METHODS: Within Surveillance, Epidemiology, and End Results registry (2001-2014), we identified patients with mRCC. Cumulative incidence and competing risks regression (CRR) models examined CSM, after accounting for other-cause mortality. Finally, we performed subgroup analyses according to histological subtype: clear-cell mRCC (ccmRCC) versus non-ccmRCC.RESULTS: We identified 15,444 patients with mRCC. Of those, 41.0, 28.7 and 30.3% were diagnosed, respectively, in the contemporary, intermediate and historical years. Of all, 47.1, 5.3 and 47.6% were, respectively, ccmRCC, non-ccmRCC and other mRCC histological variants [sarcomatoid mRCC, cyst-associated mRCC, collecting duct carcinoma and mRCC not otherwise specified (NOS)]. Overall, 24-month CSM rates were, respectively, 61.0, 63.7 and 67.3% in contemporary, intermediate and historical patients. In all patients, multivariable CRR models exhibited higher CSM in intermediate (HR 1.11; p < 0.001) and historical patients (HR 1.24; p < 0.001) than in contemporary patients. Multivariable CRR models focusing on ccmRCC yielded virtually the same results. However, multivariable CRR models focusing on non-ccmRCC showed no CSM differences according to diagnosis year (all p ≥ 0.3).CONCLUSION: The introduction of new therapeutic agents resulted in CSM-free survival improvement over study time. However, this effect exclusively applies to patients with ccmRCC, but not to those with non-ccmRCC. This observation is in agreement with established efficacy of systemic therapies for ccmRCC, but lesser efficacy of these agents for non-ccmRCC.

AB - OBJECTIVE: To examine the effect of diagnosis year, defined as contemporary (2010-2014), intermediate (2006-2009) and historical (2001-2005) on cancer-specific mortality (CSM) in patients with metastatic renal cell carcinoma (mRCC).METHODS: Within Surveillance, Epidemiology, and End Results registry (2001-2014), we identified patients with mRCC. Cumulative incidence and competing risks regression (CRR) models examined CSM, after accounting for other-cause mortality. Finally, we performed subgroup analyses according to histological subtype: clear-cell mRCC (ccmRCC) versus non-ccmRCC.RESULTS: We identified 15,444 patients with mRCC. Of those, 41.0, 28.7 and 30.3% were diagnosed, respectively, in the contemporary, intermediate and historical years. Of all, 47.1, 5.3 and 47.6% were, respectively, ccmRCC, non-ccmRCC and other mRCC histological variants [sarcomatoid mRCC, cyst-associated mRCC, collecting duct carcinoma and mRCC not otherwise specified (NOS)]. Overall, 24-month CSM rates were, respectively, 61.0, 63.7 and 67.3% in contemporary, intermediate and historical patients. In all patients, multivariable CRR models exhibited higher CSM in intermediate (HR 1.11; p < 0.001) and historical patients (HR 1.24; p < 0.001) than in contemporary patients. Multivariable CRR models focusing on ccmRCC yielded virtually the same results. However, multivariable CRR models focusing on non-ccmRCC showed no CSM differences according to diagnosis year (all p ≥ 0.3).CONCLUSION: The introduction of new therapeutic agents resulted in CSM-free survival improvement over study time. However, this effect exclusively applies to patients with ccmRCC, but not to those with non-ccmRCC. This observation is in agreement with established efficacy of systemic therapies for ccmRCC, but lesser efficacy of these agents for non-ccmRCC.

KW - Journal Article

U2 - 10.1007/s11255-017-1703-y

DO - 10.1007/s11255-017-1703-y

M3 - SCORING: Journal article

C2 - 28932952

VL - 49

SP - 2143

EP - 2149

JO - INT UROL NEPHROL

JF - INT UROL NEPHROL

SN - 0301-1623

IS - 12

ER -