Chromosomal deletion of 9p21 is linked to poor patient prognosis in papillary and clear cell kidney cancer

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Chromosomal deletion of 9p21 is linked to poor patient prognosis in papillary and clear cell kidney cancer. / Eichenauer, Till; Simmendinger, Luca; Kluth, Martina; Chirico, Victoria; Luebke, Andreas M; Höflmayer, Doris; Hinsch, Andrea; Jacobsen, Frank; Hube-Magg, Claudia; Möller-Koop, Christina; Dahlem, Roland; Fisch, Margit; Rink, Michael; Riechardt, Silke; Tsourlakis, Maria Christina; Büscheck, Franziska; Bernreuther, Christian; Clauditz, Till; Lebok, Patrick; Simon, Ronald; Sauter, Guido; Wilczak, Waldemar; Fraune, Christoph.

in: UROL ONCOL-SEMIN ORI, Jahrgang 38, Nr. 6, 06.2020, S. 605.e1-605.e8.

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@article{820b18d845ae41be8da363c0793fb206,
title = "Chromosomal deletion of 9p21 is linked to poor patient prognosis in papillary and clear cell kidney cancer",
abstract = "BACKGROUND: The ongoing approval of adjuvant systemic therapy in high-risk kidney tumor will increase the demand for prognostic assessment in these tumors. 9p21 deletion has been suggested as a possible prognostic feature in clear cell kidney cancer.MATERIAL AND METHODS: To learn more on the prognostic relevance of 9p21 deletions in clear cell and other kidney tumors, 1,809 kidney tumor specimens were analyzed by dual-labeling fluorescence in situ hybridization (FISH) with probes for 9p21 and centromere 9 in a tissue microarray format. Results were compared to histologic tumor type, pT stage, grade, and patient outcome.RESULTS: A total of 1,341 (74%) of tumor samples had interpretable FISH results. 9p21 deletion was found in 4.4% of 894 clear cell, 5.1% of 197 papillary, and 4.2% of 71 chromophobe carcinomas. 9p21 deletions were not found in 112 oncocytomas and in 21 clear cell tubulo-papillary cancers. In clear cell carcinomas, 9p deletions were associated with advanced stage (P = 0.009) and nodal metastasis (P = 0.0067), but not with ISUP grade (P = 0.1039) and distant metastasis (P = 0.4809). Also, in papillary carcinomas, 9p deletions were associated with advanced stage (P = 0.0008) and nodal metastasis (P = 0.0202) but not with ISUP grade (0.0904) and distant metastasis (P = 0.2022). Follow-up data were available for 789 clear cell and 177 papillary cancers. In both tumor entities, 9p21 deletions were associated with shortened overall survival, tumor-specific death, and progression-free survival in univariate analysis (P < 0.02 each). In a multivariate analysis, 9p21 deletion was an independent predictor of early tumor recurrence (P = 0.04).CONCLUSION: 9p21 deletions, 9p21 deletions identify a small subset of aggressive renal carcinomas. 9p deletion assessment may be clinically useful to identify high-risk renal cell carcinomas.",
author = "Till Eichenauer and Luca Simmendinger and Martina Kluth and Victoria Chirico and Luebke, {Andreas M} and Doris H{\"o}flmayer and Andrea Hinsch and Frank Jacobsen and Claudia Hube-Magg and Christina M{\"o}ller-Koop and Roland Dahlem and Margit Fisch and Michael Rink and Silke Riechardt and Tsourlakis, {Maria Christina} and Franziska B{\"u}scheck and Christian Bernreuther and Till Clauditz and Patrick Lebok and Ronald Simon and Guido Sauter and Waldemar Wilczak and Christoph Fraune",
note = "Copyright {\textcopyright} 2020 Elsevier Inc. All rights reserved.",
year = "2020",
month = jun,
doi = "10.1016/j.urolonc.2020.02.022",
language = "English",
volume = "38",
pages = "605.e1--605.e8",
journal = "UROL ONCOL-SEMIN ORI",
issn = "1078-1439",
publisher = "Elsevier Inc.",
number = "6",

}

RIS

TY - JOUR

T1 - Chromosomal deletion of 9p21 is linked to poor patient prognosis in papillary and clear cell kidney cancer

AU - Eichenauer, Till

AU - Simmendinger, Luca

AU - Kluth, Martina

AU - Chirico, Victoria

AU - Luebke, Andreas M

AU - Höflmayer, Doris

AU - Hinsch, Andrea

AU - Jacobsen, Frank

AU - Hube-Magg, Claudia

AU - Möller-Koop, Christina

AU - Dahlem, Roland

AU - Fisch, Margit

AU - Rink, Michael

AU - Riechardt, Silke

AU - Tsourlakis, Maria Christina

AU - Büscheck, Franziska

AU - Bernreuther, Christian

AU - Clauditz, Till

AU - Lebok, Patrick

AU - Simon, Ronald

AU - Sauter, Guido

AU - Wilczak, Waldemar

AU - Fraune, Christoph

N1 - Copyright © 2020 Elsevier Inc. All rights reserved.

PY - 2020/6

Y1 - 2020/6

N2 - BACKGROUND: The ongoing approval of adjuvant systemic therapy in high-risk kidney tumor will increase the demand for prognostic assessment in these tumors. 9p21 deletion has been suggested as a possible prognostic feature in clear cell kidney cancer.MATERIAL AND METHODS: To learn more on the prognostic relevance of 9p21 deletions in clear cell and other kidney tumors, 1,809 kidney tumor specimens were analyzed by dual-labeling fluorescence in situ hybridization (FISH) with probes for 9p21 and centromere 9 in a tissue microarray format. Results were compared to histologic tumor type, pT stage, grade, and patient outcome.RESULTS: A total of 1,341 (74%) of tumor samples had interpretable FISH results. 9p21 deletion was found in 4.4% of 894 clear cell, 5.1% of 197 papillary, and 4.2% of 71 chromophobe carcinomas. 9p21 deletions were not found in 112 oncocytomas and in 21 clear cell tubulo-papillary cancers. In clear cell carcinomas, 9p deletions were associated with advanced stage (P = 0.009) and nodal metastasis (P = 0.0067), but not with ISUP grade (P = 0.1039) and distant metastasis (P = 0.4809). Also, in papillary carcinomas, 9p deletions were associated with advanced stage (P = 0.0008) and nodal metastasis (P = 0.0202) but not with ISUP grade (0.0904) and distant metastasis (P = 0.2022). Follow-up data were available for 789 clear cell and 177 papillary cancers. In both tumor entities, 9p21 deletions were associated with shortened overall survival, tumor-specific death, and progression-free survival in univariate analysis (P < 0.02 each). In a multivariate analysis, 9p21 deletion was an independent predictor of early tumor recurrence (P = 0.04).CONCLUSION: 9p21 deletions, 9p21 deletions identify a small subset of aggressive renal carcinomas. 9p deletion assessment may be clinically useful to identify high-risk renal cell carcinomas.

AB - BACKGROUND: The ongoing approval of adjuvant systemic therapy in high-risk kidney tumor will increase the demand for prognostic assessment in these tumors. 9p21 deletion has been suggested as a possible prognostic feature in clear cell kidney cancer.MATERIAL AND METHODS: To learn more on the prognostic relevance of 9p21 deletions in clear cell and other kidney tumors, 1,809 kidney tumor specimens were analyzed by dual-labeling fluorescence in situ hybridization (FISH) with probes for 9p21 and centromere 9 in a tissue microarray format. Results were compared to histologic tumor type, pT stage, grade, and patient outcome.RESULTS: A total of 1,341 (74%) of tumor samples had interpretable FISH results. 9p21 deletion was found in 4.4% of 894 clear cell, 5.1% of 197 papillary, and 4.2% of 71 chromophobe carcinomas. 9p21 deletions were not found in 112 oncocytomas and in 21 clear cell tubulo-papillary cancers. In clear cell carcinomas, 9p deletions were associated with advanced stage (P = 0.009) and nodal metastasis (P = 0.0067), but not with ISUP grade (P = 0.1039) and distant metastasis (P = 0.4809). Also, in papillary carcinomas, 9p deletions were associated with advanced stage (P = 0.0008) and nodal metastasis (P = 0.0202) but not with ISUP grade (0.0904) and distant metastasis (P = 0.2022). Follow-up data were available for 789 clear cell and 177 papillary cancers. In both tumor entities, 9p21 deletions were associated with shortened overall survival, tumor-specific death, and progression-free survival in univariate analysis (P < 0.02 each). In a multivariate analysis, 9p21 deletion was an independent predictor of early tumor recurrence (P = 0.04).CONCLUSION: 9p21 deletions, 9p21 deletions identify a small subset of aggressive renal carcinomas. 9p deletion assessment may be clinically useful to identify high-risk renal cell carcinomas.

U2 - 10.1016/j.urolonc.2020.02.022

DO - 10.1016/j.urolonc.2020.02.022

M3 - SCORING: Journal article

C2 - 32241691

VL - 38

SP - 605.e1-605.e8

JO - UROL ONCOL-SEMIN ORI

JF - UROL ONCOL-SEMIN ORI

SN - 1078-1439

IS - 6

ER -