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Published in: Annals of Surgical Oncology 6/2020

01-06-2020 | Prostate Cancer | Urologic Oncology

Facility-Level Variation in Pelvic Lymphadenectomy During Radical Prostatectomy and Effect on Overall Survival in Men with High-Risk Prostate Cancer

Authors: David F. Friedlander, MD, MPH, Marieke J. Krimphove, MD, Alexander P. Cole, MD, Karl H. Tully, MD, Stuart R. Lipsitz, ScD, Adam S. Kibel, MD, Kerry L. Kilbridge, MD, Quoc-Dien Trinh, MD

Published in: Annals of Surgical Oncology | Issue 6/2020

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Abstract

Purpose

This study was designed to examine facility-level variation in the extent of pelvic lymphadenectomy and to determine whether more extensive lymphadenectomy is associated with a survival benefit among men with localized high-risk prostate cancer.

Methods

Using data from the National Cancer Data Base, we identified 13,652 men with a high predicted probability of 10-year survival (≤ 65 years of age and Charlson Comorbidity Index score of 0) who underwent radical prostatectomy at 1023 facilities for biopsy-confirmed localized high-risk prostate cancer diagnosed between January 2004 and December 2011. Multilevel, multinomial logistic regression was fitted to predict facility-level probability of receiving different extents of lymphadenectomy. Inverse probability of treatment weighting-adjusted Cox regression model with Bonferroni correction was fitted to compare risk of overall mortality.

Results

Overall, 11,284 (82.7%), 1601 (11.7%), and 767 (5.6%) men who underwent radical prostatectomy underwent concomitant none/limited lymphadenectomy (0–9 lymph nodes), standard lymphadenectomy (10–16 lymph nodes), and extended lymphadenectomy (≥ 17 lymph nodes), respectively. Extended lymphadenectomy was not associated with a survival benefit relative to standard lymphadenectomy (hazard ratio [HR] 0.72, 95% confidence interval [CI] 0.48–1.23; p = 0.4) nor no/limited lymphadenectomy (HR 0.77, 95% CI 0.87–2.20; p = 0.29) at a median follow-up of 83.3 months. Risk-adjusted facility-level predicted probabilities of extended, standard, or no/limited lymphadenectomy ranged from 0.01 to 52.6%, 3.3–53.3%, and 17.8–96.3%, respectively.

Conclusions

We found significant facility-level variation in the extent of pelvic lymphadenectomy during radical prostatectomy despite no apparent survival benefit associated with more extensive lymphadenectomy. Further prospective data are needed to reevaluate the role of lymphadenectomy in the management of clinically localized prostate cancer.
Literature
1.
go back to reference Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015. CA Cancer J Clin. 2015;65(1):5–29.CrossRef Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015. CA Cancer J Clin. 2015;65(1):5–29.CrossRef
2.
go back to reference Mohler JL, Armstrong AJ, Bahnson RR, et al. Prostate cancer, Version 1.2016. J Natl Comprehensive Cancer Netw JNCCN. 2016;14(1):19–30.CrossRef Mohler JL, Armstrong AJ, Bahnson RR, et al. Prostate cancer, Version 1.2016. J Natl Comprehensive Cancer Netw JNCCN. 2016;14(1):19–30.CrossRef
3.
go back to reference Briganti A, Suardi N, Gallina A, Abdollah F, Montorsi F. Pelvic lymph node dissection in prostate cancer: the mystery is taking shape. Eur Urol. 2013;63(3):459–61.CrossRef Briganti A, Suardi N, Gallina A, Abdollah F, Montorsi F. Pelvic lymph node dissection in prostate cancer: the mystery is taking shape. Eur Urol. 2013;63(3):459–61.CrossRef
4.
go back to reference Touijer KA, Ahallal Y, Guillonneau BD. Indications for and anatomical extent of pelvic lymph node dissection for prostate cancer: practice patterns of uro-oncologists in North America. Urol Oncol. 2013;31(8):1517–21.CrossRef Touijer KA, Ahallal Y, Guillonneau BD. Indications for and anatomical extent of pelvic lymph node dissection for prostate cancer: practice patterns of uro-oncologists in North America. Urol Oncol. 2013;31(8):1517–21.CrossRef
5.
go back to reference Liss MA, Palazzi K, Stroup SP, Jabaji R, Raheem OA, Kane CJ. Outcomes and complications of pelvic lymph node dissection during robotic-assisted radical prostatectomy. World J Urol. 2013;31(3):481–8.CrossRef Liss MA, Palazzi K, Stroup SP, Jabaji R, Raheem OA, Kane CJ. Outcomes and complications of pelvic lymph node dissection during robotic-assisted radical prostatectomy. World J Urol. 2013;31(3):481–8.CrossRef
6.
go back to reference Koo KC, Tuliao P, Komninos C, et al. Prognostic impact of time to undetectable prostate-specific antigen in patients with positive surgical margins following radical prostatectomy. Ann Surg Oncol. 2015;22(2):693–700.CrossRef Koo KC, Tuliao P, Komninos C, et al. Prognostic impact of time to undetectable prostate-specific antigen in patients with positive surgical margins following radical prostatectomy. Ann Surg Oncol. 2015;22(2):693–700.CrossRef
7.
go back to reference Chang M, Sherman C, Klotz L, Nam R. 1346 A nested, case-control, matched study examining the significance of pelvic lymphadenectomy during radical prostatectomy. J Urol. 2013;189(4, Supplement):e549–50.CrossRef Chang M, Sherman C, Klotz L, Nam R. 1346 A nested, case-control, matched study examining the significance of pelvic lymphadenectomy during radical prostatectomy. J Urol. 2013;189(4, Supplement):e549–50.CrossRef
8.
go back to reference Daimon T, Miyajima A, Maeda T, et al. Does pelvic lymph node dissection improve the biochemical relapse-free survival in low-risk prostate cancer patients treated by laparoscopic radical prostatectomy? J Endourol. 2012;26(9):1199–202.CrossRef Daimon T, Miyajima A, Maeda T, et al. Does pelvic lymph node dissection improve the biochemical relapse-free survival in low-risk prostate cancer patients treated by laparoscopic radical prostatectomy? J Endourol. 2012;26(9):1199–202.CrossRef
9.
go back to reference Berglund RK, Sadetsky N, DuChane J, Carroll PR, Klein EA. Limited pelvic lymph node dissection at the time of radical prostatectomy does not affect 5-year failure rates for low, intermediate and high risk prostate cancer: results from CaPSURE. J Urol. 2007;177(2):526–9 (discussion 529–30) Berglund RK, Sadetsky N, DuChane J, Carroll PR, Klein EA. Limited pelvic lymph node dissection at the time of radical prostatectomy does not affect 5-year failure rates for low, intermediate and high risk prostate cancer: results from CaPSURE. J Urol. 2007;177(2):526–9 (discussion 529–30)
10.
go back to reference Schiavina R, Manferrari F, Garofalo M, et al. The extent of pelvic lymph node dissection correlates with the biochemical recurrence rate in patients with intermediate- and high-risk prostate cancer. BJU Int. 2011;108(8):1262–8.CrossRef Schiavina R, Manferrari F, Garofalo M, et al. The extent of pelvic lymph node dissection correlates with the biochemical recurrence rate in patients with intermediate- and high-risk prostate cancer. BJU Int. 2011;108(8):1262–8.CrossRef
11.
go back to reference Joslyn SA, Konety BR. Impact of extent of lymphadenectomy on survival after radical prostatectomy for prostate cancer. Urology. 2006;68(1):121–5.CrossRef Joslyn SA, Konety BR. Impact of extent of lymphadenectomy on survival after radical prostatectomy for prostate cancer. Urology. 2006;68(1):121–5.CrossRef
12.
go back to reference Chen Y-W, Mahal BAV, Ziehr DR, et al. Can pelvic lymph node dissection be omitted in intermediate-risk prostate cancer patients? A SEER-based comparative study using inverse-probability-of-treatment weighting. J Clin Oncol. 2015;33(7_suppl):95. Chen Y-W, Mahal BAV, Ziehr DR, et al. Can pelvic lymph node dissection be omitted in intermediate-risk prostate cancer patients? A SEER-based comparative study using inverse-probability-of-treatment weighting. J Clin Oncol. 2015;33(7_suppl):95.
13.
go back to reference Fossati N, Willemse P-PM, Van den Broeck T, et al. The benefits and harms of different extents of lymph node dissection during radical prostatectomy for prostate cancer: a systematic review. Eur Urol. 2017;72(1):84–109. Fossati N, Willemse P-PM, Van den Broeck T, et al. The benefits and harms of different extents of lymph node dissection during radical prostatectomy for prostate cancer: a systematic review. Eur Urol. 2017;72(1):84–109.
14.
go back to reference Hu JC, Prasad SM, Gu X, et al. Determinants of performing radical prostatectomy pelvic lymph node dissection and the number of lymph nodes removed in elderly men. Urology. 2011;77(2):402–6.CrossRef Hu JC, Prasad SM, Gu X, et al. Determinants of performing radical prostatectomy pelvic lymph node dissection and the number of lymph nodes removed in elderly men. Urology. 2011;77(2):402–6.CrossRef
15.
go back to reference Wang EH, Yu JB, Gross CP, et al. Variation in pelvic lymph node dissection among patients undergoing radical prostatectomy by hospital characteristics and surgical approach: results from the National Cancer Database. J Urol. 2015;193(3):820–5.CrossRef Wang EH, Yu JB, Gross CP, et al. Variation in pelvic lymph node dissection among patients undergoing radical prostatectomy by hospital characteristics and surgical approach: results from the National Cancer Database. J Urol. 2015;193(3):820–5.CrossRef
16.
go back to reference Feifer AH, Elkin EB, Lowrance WT, et al. Temporal trends and predictors of pelvic lymph node dissection in open or minimally invasive radical prostatectomy. Cancer. 2011;117(17):3933–42.CrossRef Feifer AH, Elkin EB, Lowrance WT, et al. Temporal trends and predictors of pelvic lymph node dissection in open or minimally invasive radical prostatectomy. Cancer. 2011;117(17):3933–42.CrossRef
17.
go back to reference Charlson M, Szatrowski TP, Peterson J, Gold J. Validation of a combined comorbidity index. J Clin Epidemiol. 1994;47(11):1245–51.CrossRef Charlson M, Szatrowski TP, Peterson J, Gold J. Validation of a combined comorbidity index. J Clin Epidemiol. 1994;47(11):1245–51.CrossRef
18.
go back to reference Cole AP, Trinh QD. Secondary data analysis: techniques for comparing interventions and their limitations. Curr Opin Urol. 2017;27(4):354–9.CrossRef Cole AP, Trinh QD. Secondary data analysis: techniques for comparing interventions and their limitations. Curr Opin Urol. 2017;27(4):354–9.CrossRef
19.
go back to reference Fossati N, Parker WP, Karnes RJ, et al. More extensive lymph node dissection at radical prostatectomy is associated with improved outcomes with salvage radiotherapy for rising prostate-specific antigen after surgery: a long-term, multi-institutional analysis. Eur Urol. 2018;74(2):134–7.CrossRef Fossati N, Parker WP, Karnes RJ, et al. More extensive lymph node dissection at radical prostatectomy is associated with improved outcomes with salvage radiotherapy for rising prostate-specific antigen after surgery: a long-term, multi-institutional analysis. Eur Urol. 2018;74(2):134–7.CrossRef
20.
go back to reference Rider JR, Sandin F, Andren O, Wiklund P, Hugosson J, Stattin P. Long-term outcomes among noncuratively treated men according to prostate cancer risk category in a nationwide, population-based study. Eur Urol. 2013;63(1):88–96.CrossRef Rider JR, Sandin F, Andren O, Wiklund P, Hugosson J, Stattin P. Long-term outcomes among noncuratively treated men according to prostate cancer risk category in a nationwide, population-based study. Eur Urol. 2013;63(1):88–96.CrossRef
21.
go back to reference Trock BJ, Han M, Freedland SJ, et al. Prostate cancer-specific survival following salvage radiotherapy vs observation in men with biochemical recurrence after radical prostatectomy. JAMA. 2008;299(23):2760–9.CrossRef Trock BJ, Han M, Freedland SJ, et al. Prostate cancer-specific survival following salvage radiotherapy vs observation in men with biochemical recurrence after radical prostatectomy. JAMA. 2008;299(23):2760–9.CrossRef
22.
go back to reference Thompson I, Thrasher JB, Aus G, et al. Guideline for the management of clinically localized prostate cancer: 2007 update. J Urol. 2007;177(6):2106–31.CrossRef Thompson I, Thrasher JB, Aus G, et al. Guideline for the management of clinically localized prostate cancer: 2007 update. J Urol. 2007;177(6):2106–31.CrossRef
23.
go back to reference Mottet N, Bellmunt J, Bolla M, et al. EAU-ESTRO-SIOG Guidelines on prostate cancer. Part 1: screening, diagnosis, and local treatment with curative intent. Eur Urol. 2017;71(4):618–29. Mottet N, Bellmunt J, Bolla M, et al. EAU-ESTRO-SIOG Guidelines on prostate cancer. Part 1: screening, diagnosis, and local treatment with curative intent. Eur Urol. 2017;71(4):618–29.
24.
go back to reference Mazzola C, Savage C, Ahallal Y, et al. Nodal counts during pelvic lymph node dissection for prostate cancer: an objective indicator of quality under the influence of very subjective factors. BJU Int. 2012;109(9):1323–8.CrossRef Mazzola C, Savage C, Ahallal Y, et al. Nodal counts during pelvic lymph node dissection for prostate cancer: an objective indicator of quality under the influence of very subjective factors. BJU Int. 2012;109(9):1323–8.CrossRef
25.
go back to reference Davies JD, Simons CM, Ruhotina N, Barocas DA, Clark PE, Morgan TM. Anatomic basis for lymph node counts as measure of lymph node dissection extent: a cadaveric study. Urology. 2013;81(2):358–63.CrossRef Davies JD, Simons CM, Ruhotina N, Barocas DA, Clark PE, Morgan TM. Anatomic basis for lymph node counts as measure of lymph node dissection extent: a cadaveric study. Urology. 2013;81(2):358–63.CrossRef
Metadata
Title
Facility-Level Variation in Pelvic Lymphadenectomy During Radical Prostatectomy and Effect on Overall Survival in Men with High-Risk Prostate Cancer
Authors
David F. Friedlander, MD, MPH
Marieke J. Krimphove, MD
Alexander P. Cole, MD
Karl H. Tully, MD
Stuart R. Lipsitz, ScD
Adam S. Kibel, MD
Kerry L. Kilbridge, MD
Quoc-Dien Trinh, MD
Publication date
01-06-2020
Publisher
Springer International Publishing
Published in
Annals of Surgical Oncology / Issue 6/2020
Print ISSN: 1068-9265
Electronic ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-019-08110-3

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