Lack of Effectiveness of Postchemotherapy Lymphadenectomy in Bladder Cancer Patients with Clinical Evidence of Metastatic Pelvic or Retroperitoneal Lymph Nodes Only: A Propensity Score-based Analysis.


Journal

European urology focus
ISSN: 2405-4569
Titre abrégé: Eur Urol Focus
Pays: Netherlands
ID NLM: 101665661

Informations de publication

Date de publication:
03 2019
Historique:
received: 25 03 2017
revised: 04 05 2017
accepted: 22 05 2017
pubmed: 30 7 2017
medline: 18 12 2019
entrez: 30 7 2017
Statut: ppublish

Résumé

Limited data is available on the role, and extent of, postchemotherapy lymphadenectomy (PC-LND) in patients with clinical evidence of pelvic (cN1-3) or retroperitoneal (RP) lymph node spread from urothelial bladder carcinoma. To compare the outcomes of operated versus nonoperated patients after first-line chemotherapy. Data from 34 centers was collected, totaling 522 patients, treated between January 2000 and June 2015. Criteria for patient selection were the following: bladder primary tumor, lymph node metastases (pelvic±RP) only, first-line platinum-based chemotherapy given. LND (with cystectomy) versus observation after first-line chemotherapy for metastatic urothelial bladder carcinoma. Overall survival (OS) was the primary endpoint. Multiple propensity score techniques were adopted, including 1:1 propensity score matching and inverse probability of treatment weighting. Additionally, the inverse probability of treatment weighting analysis was performed with the inclusion of the covariates, that is, with doubly robust estimation. Overall, 242 (46.4%) patients received PC-LND and 280 (53.6%) observation after chemotherapy. There were 177 (33.9%) and 345 (66.1%) patients with either RP or pelvic LND only, respectively. Doubly robust estimation-adjusted comparison was not significant for improved OS for PC-LND (hazard ratio [HR]: 0.86, 95% confidence interval [CI]: 0.56-1.31, p=0.479), confirmed by matched analysis (HR: 0.91, 95% CI: 0.60-1.36, p=0.628). This was also observed in the RP subgroup (HR: 1.12, 95% CI: 0.68-1.84). The retrospective nature of the data and the heterogeneous patient population were the major limitations. Although there were substantial differences between the two groups, after accounting for major confounders we report a nonsignificant OS difference with PC-LND compared with observation only. These findings may be hypothesis-generating for future prospective trials. We found no differences in survival by adding postchemotherapy lymphadenectomy in patients with pelvic or retroperitoneal lymph node metastatic bladder cancer. The indication to perform postchemotherapy lymphadenectomy in the most suitable patients requires additional studies.

Sections du résumé

BACKGROUND
Limited data is available on the role, and extent of, postchemotherapy lymphadenectomy (PC-LND) in patients with clinical evidence of pelvic (cN1-3) or retroperitoneal (RP) lymph node spread from urothelial bladder carcinoma.
OBJECTIVE
To compare the outcomes of operated versus nonoperated patients after first-line chemotherapy.
DESIGN, SETTING, AND PARTICIPANTS
Data from 34 centers was collected, totaling 522 patients, treated between January 2000 and June 2015. Criteria for patient selection were the following: bladder primary tumor, lymph node metastases (pelvic±RP) only, first-line platinum-based chemotherapy given.
INTERVENTION
LND (with cystectomy) versus observation after first-line chemotherapy for metastatic urothelial bladder carcinoma.
OUTCOME MEASURES AND STATISTICAL ANALYSIS
Overall survival (OS) was the primary endpoint. Multiple propensity score techniques were adopted, including 1:1 propensity score matching and inverse probability of treatment weighting. Additionally, the inverse probability of treatment weighting analysis was performed with the inclusion of the covariates, that is, with doubly robust estimation.
RESULTS AND LIMITATIONS
Overall, 242 (46.4%) patients received PC-LND and 280 (53.6%) observation after chemotherapy. There were 177 (33.9%) and 345 (66.1%) patients with either RP or pelvic LND only, respectively. Doubly robust estimation-adjusted comparison was not significant for improved OS for PC-LND (hazard ratio [HR]: 0.86, 95% confidence interval [CI]: 0.56-1.31, p=0.479), confirmed by matched analysis (HR: 0.91, 95% CI: 0.60-1.36, p=0.628). This was also observed in the RP subgroup (HR: 1.12, 95% CI: 0.68-1.84). The retrospective nature of the data and the heterogeneous patient population were the major limitations.
CONCLUSIONS
Although there were substantial differences between the two groups, after accounting for major confounders we report a nonsignificant OS difference with PC-LND compared with observation only. These findings may be hypothesis-generating for future prospective trials.
PATIENT SUMMARY
We found no differences in survival by adding postchemotherapy lymphadenectomy in patients with pelvic or retroperitoneal lymph node metastatic bladder cancer. The indication to perform postchemotherapy lymphadenectomy in the most suitable patients requires additional studies.

Identifiants

pubmed: 28753897
pii: S2405-4569(17)30125-6
doi: 10.1016/j.euf.2017.05.006
pmc: PMC5712487
mid: NIHMS901371
pii:
doi:

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

242-249

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2017 European Association of Urology. Published by Elsevier B.V. All rights reserved.

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Auteurs

Andrea Necchi (A)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy. Electronic address: andrea.necchi@istitutotumori.mi.it.

Luigi Mariani (L)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

Salvatore Lo Vullo (S)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

Evan Y Yu (EY)

University of Washington, Seattle, WA, USA.

Michael E Woods (ME)

University of North Carolina at Chapel Hill, Lineberger Comprehensive Cancer Center, NC, USA.

Yu-Ning Wong (YN)

Fox Chase Cancer Center, Philadelphia, PA, USA.

Lauren C Harshman (LC)

Dana-Farber Cancer Institute, Boston, MA, USA.

Ajjaj Alva (A)

University of Michigan, Ann Arbor, MI, USA.

Cora N Sternberg (CN)

San Camillo Forlanini Hospital, Rome, Italy.

Aristotelis Bamias (A)

University of Athens, Athens, Greece.

Petros Grivas (P)

Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.

Vadim S Koshkin (VS)

Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.

Florian Roghmann (F)

Ruhr-University Bochum, Marien Hospital Herne, Herne, Germany.

Jakub Dobruch (J)

Centre of Postgraduate Medical Education, European Health Centre Otwock, Poland.

Bernie J Eigl (BJ)

British Columbia Cancer Agency, Vancouver, BC, Canada.

Lucia Nappi (L)

British Columbia Cancer Agency, Vancouver, BC, Canada.

Matthew I Milowsky (MI)

University of North Carolina at Chapel Hill, Lineberger Comprehensive Cancer Center, NC, USA.

Guenter Niegisch (G)

Heinrich-Heine-University, Medical faculty, Department of Urology, Düsseldorf, Germany.

Sumanta K Pal (SK)

City of Hope Comprehensive Cancer Center, Duarte, CA, USA.

Ugo De Giorgi (U)

IRCCS Istituto Scientifico Romagnolo per lo studio e la Cura dei Tumori, Meldola, Italy.

Federica Recine (F)

IRCCS Istituto Scientifico Romagnolo per lo studio e la Cura dei Tumori, Meldola, Italy.

Ulka Vaishampayan (U)

Karmanos Cancer Institute, Detroit, MI, USA.

Dominik D Berthold (DD)

Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Daniel W Bowles (DW)

Denver Veterans Affairs Medical Center, Eastern Colorado Health Care System, Denver, CO, USA.

Jack Baniel (J)

Rabin Medical Center, Petach Tikva, Israel.

Christine Theodore (C)

Hospital Foch, Suresnes, France.

Sylvain Ladoire (S)

Center Georges-François Leclerc, Dijon, France.

Sandy Srinivas (S)

Stanford University School of Medicine, Stanford, CA, USA.

Neeraj Agarwal (N)

University of Utah, Salt Lake City, UT, USA.

Simon Crabb (S)

University of Southampton, Southampton, United Kingdom.

Srikala Sridhar (S)

Princess Margaret Hospital, University Health Network, Toronto, Canada.

Ali-Reza Golshayan (AR)

Medical University of South Carolina, Charleston, SC, USA.

Carsten Ohlmann (C)

Saarland University, Homburg, Germany.

Evanguelos Xylinas (E)

Cochin Hospital, Assistance-Publique Hôpitaux de Paris, Paris Descartes University, Paris, France.

Thomas Powles (T)

Barts Health and the Royal Free NHS Trust, Queen Mary University of London, London, UK.

Johnathan E Rosenberg (JE)

Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

Joaquim Bellmunt (J)

Dana-Farber Cancer Institute, Boston, MA, USA.

Bas van Rhijn (B)

The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Matthew D Galsky (MD)

Mount Sinai School of Medicine, Tisch Cancer Institute, New York, NY, USA.

Kees Hendricksen (K)

The Netherlands Cancer Institute, Amsterdam, The Netherlands.

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