Prognostic Significance of Pathologic Lymph Node Invasion in Metastatic Renal Cell Carcinoma in the Immunotherapy Era

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Prognostic Significance of Pathologic Lymph Node Invasion in Metastatic Renal Cell Carcinoma in the Immunotherapy Era. / Scheipner, Lukas; Barletta, Francesco; Cano Garcia, Cristina; Incesu, Reha-Baris; Morra, Simone; Baudo, Andrea; Assad, Anis; Tian, Zhe; Saad, Fred; Shariat, Shahrokh F; Briganti, Alberto; Chun, Felix K H; Tilki, Derya; Longo, Nicola; Carmignani, Luca; Pichler, Martin; Ahyai, Sascha; Karakiewicz, Pierre I.

in: ANN SURG ONCOL, Jahrgang 30, Nr. 13, 12.2023, S. 8780-8785.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Scheipner, L, Barletta, F, Cano Garcia, C, Incesu, R-B, Morra, S, Baudo, A, Assad, A, Tian, Z, Saad, F, Shariat, SF, Briganti, A, Chun, FKH, Tilki, D, Longo, N, Carmignani, L, Pichler, M, Ahyai, S & Karakiewicz, PI 2023, 'Prognostic Significance of Pathologic Lymph Node Invasion in Metastatic Renal Cell Carcinoma in the Immunotherapy Era', ANN SURG ONCOL, Jg. 30, Nr. 13, S. 8780-8785. https://doi.org/10.1245/s10434-023-14367-6

APA

Scheipner, L., Barletta, F., Cano Garcia, C., Incesu, R-B., Morra, S., Baudo, A., Assad, A., Tian, Z., Saad, F., Shariat, S. F., Briganti, A., Chun, F. K. H., Tilki, D., Longo, N., Carmignani, L., Pichler, M., Ahyai, S., & Karakiewicz, P. I. (2023). Prognostic Significance of Pathologic Lymph Node Invasion in Metastatic Renal Cell Carcinoma in the Immunotherapy Era. ANN SURG ONCOL, 30(13), 8780-8785. https://doi.org/10.1245/s10434-023-14367-6

Vancouver

Bibtex

@article{90e05d5f2a6c42bdb86c63d2e31f04d6,
title = "Prognostic Significance of Pathologic Lymph Node Invasion in Metastatic Renal Cell Carcinoma in the Immunotherapy Era",
abstract = "BACKGROUND: This study aimed to test the prognostic significance of pathologically confirmed lymph node invasion in metastatic renal cell carcinoma (mRCC) patients in this immunotherapy era.METHODS: Surgically treated mRCC patients were identified in the Surveillance, Epidemiology, and End Results (SEER) database between 2010 and 2018. Kaplan-Meier plots and multivariable Cox-regression models were fitted to test for differences in cancer-specific mortality (CSM) and overall mortality (OM) according to N stage (pN0 vs pN1 vs. pNx). Subgroup analyses addressing pN1 patients tested for CSM and OM differences according to postoperative systemic therapy status.RESULTS: Overall, 3149 surgically treated mRCC patients were identified. Of these patients, 443 (14%) were labeled as pN1, 812 (26%) as pN0, and 1894 (60%) as pNx. In Kaplan-Meier analyses, the median CSM-free survival was 15 months for pN1 versus 40 months for pN0 versus 35 months for pNx (P < 0.001). In multivariable Cox regression analyses, pN1 independently predicted higher CSM (hazard ratio [HR], 1.88; P < 0.01) and OM (HR, 1.95; P < 0.01) relative to pN0. In sensitivity analyses addressing pN1 patients, postoperative systemic therapy use independently predicted lower CSM (HR, 0.73; P < 0.01) and OM (HR, 0.71; P < 0.01).CONCLUSION: Pathologically confirmed lymph node invasion independently predicted higher CSM and OM for surgically treated mRCC patients. For pN1 mRCC patients, use of postoperative systemic therapy was associated with lower CSM and OM. Consequently, N stage should be considered for individual patient counseling and clinical decision-making. Consort diagram of the study population.",
keywords = "Humans, Carcinoma, Renal Cell/surgery, Prognosis, Kidney Neoplasms/surgery, Lymph Nodes/pathology, Lymph Node Excision, Immunotherapy",
author = "Lukas Scheipner and Francesco Barletta and {Cano Garcia}, Cristina and Reha-Baris Incesu and Simone Morra and Andrea Baudo and Anis Assad and Zhe Tian and Fred Saad and Shariat, {Shahrokh F} and Alberto Briganti and Chun, {Felix K H} and Derya Tilki and Nicola Longo and Luca Carmignani and Martin Pichler and Sascha Ahyai and Karakiewicz, {Pierre I}",
note = "{\textcopyright} 2023. The Author(s).",
year = "2023",
month = dec,
doi = "10.1245/s10434-023-14367-6",
language = "English",
volume = "30",
pages = "8780--8785",
journal = "ANN SURG ONCOL",
issn = "1068-9265",
publisher = "Springer New York",
number = "13",

}

RIS

TY - JOUR

T1 - Prognostic Significance of Pathologic Lymph Node Invasion in Metastatic Renal Cell Carcinoma in the Immunotherapy Era

AU - Scheipner, Lukas

AU - Barletta, Francesco

AU - Cano Garcia, Cristina

AU - Incesu, Reha-Baris

AU - Morra, Simone

AU - Baudo, Andrea

AU - Assad, Anis

AU - Tian, Zhe

AU - Saad, Fred

AU - Shariat, Shahrokh F

AU - Briganti, Alberto

AU - Chun, Felix K H

AU - Tilki, Derya

AU - Longo, Nicola

AU - Carmignani, Luca

AU - Pichler, Martin

AU - Ahyai, Sascha

AU - Karakiewicz, Pierre I

N1 - © 2023. The Author(s).

PY - 2023/12

Y1 - 2023/12

N2 - BACKGROUND: This study aimed to test the prognostic significance of pathologically confirmed lymph node invasion in metastatic renal cell carcinoma (mRCC) patients in this immunotherapy era.METHODS: Surgically treated mRCC patients were identified in the Surveillance, Epidemiology, and End Results (SEER) database between 2010 and 2018. Kaplan-Meier plots and multivariable Cox-regression models were fitted to test for differences in cancer-specific mortality (CSM) and overall mortality (OM) according to N stage (pN0 vs pN1 vs. pNx). Subgroup analyses addressing pN1 patients tested for CSM and OM differences according to postoperative systemic therapy status.RESULTS: Overall, 3149 surgically treated mRCC patients were identified. Of these patients, 443 (14%) were labeled as pN1, 812 (26%) as pN0, and 1894 (60%) as pNx. In Kaplan-Meier analyses, the median CSM-free survival was 15 months for pN1 versus 40 months for pN0 versus 35 months for pNx (P < 0.001). In multivariable Cox regression analyses, pN1 independently predicted higher CSM (hazard ratio [HR], 1.88; P < 0.01) and OM (HR, 1.95; P < 0.01) relative to pN0. In sensitivity analyses addressing pN1 patients, postoperative systemic therapy use independently predicted lower CSM (HR, 0.73; P < 0.01) and OM (HR, 0.71; P < 0.01).CONCLUSION: Pathologically confirmed lymph node invasion independently predicted higher CSM and OM for surgically treated mRCC patients. For pN1 mRCC patients, use of postoperative systemic therapy was associated with lower CSM and OM. Consequently, N stage should be considered for individual patient counseling and clinical decision-making. Consort diagram of the study population.

AB - BACKGROUND: This study aimed to test the prognostic significance of pathologically confirmed lymph node invasion in metastatic renal cell carcinoma (mRCC) patients in this immunotherapy era.METHODS: Surgically treated mRCC patients were identified in the Surveillance, Epidemiology, and End Results (SEER) database between 2010 and 2018. Kaplan-Meier plots and multivariable Cox-regression models were fitted to test for differences in cancer-specific mortality (CSM) and overall mortality (OM) according to N stage (pN0 vs pN1 vs. pNx). Subgroup analyses addressing pN1 patients tested for CSM and OM differences according to postoperative systemic therapy status.RESULTS: Overall, 3149 surgically treated mRCC patients were identified. Of these patients, 443 (14%) were labeled as pN1, 812 (26%) as pN0, and 1894 (60%) as pNx. In Kaplan-Meier analyses, the median CSM-free survival was 15 months for pN1 versus 40 months for pN0 versus 35 months for pNx (P < 0.001). In multivariable Cox regression analyses, pN1 independently predicted higher CSM (hazard ratio [HR], 1.88; P < 0.01) and OM (HR, 1.95; P < 0.01) relative to pN0. In sensitivity analyses addressing pN1 patients, postoperative systemic therapy use independently predicted lower CSM (HR, 0.73; P < 0.01) and OM (HR, 0.71; P < 0.01).CONCLUSION: Pathologically confirmed lymph node invasion independently predicted higher CSM and OM for surgically treated mRCC patients. For pN1 mRCC patients, use of postoperative systemic therapy was associated with lower CSM and OM. Consequently, N stage should be considered for individual patient counseling and clinical decision-making. Consort diagram of the study population.

KW - Humans

KW - Carcinoma, Renal Cell/surgery

KW - Prognosis

KW - Kidney Neoplasms/surgery

KW - Lymph Nodes/pathology

KW - Lymph Node Excision

KW - Immunotherapy

U2 - 10.1245/s10434-023-14367-6

DO - 10.1245/s10434-023-14367-6

M3 - SCORING: Journal article

C2 - 37815682

VL - 30

SP - 8780

EP - 8785

JO - ANN SURG ONCOL

JF - ANN SURG ONCOL

SN - 1068-9265

IS - 13

ER -