Unfavorable Cancer-specific Survival After Neoadjuvant Chemotherapy and Radical Cystectomy in Patients With Bladder Cancer and Squamous Cell Variant: A Multi-institutional Study.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
10 2020
Historique:
received: 17 11 2019
revised: 13 01 2020
accepted: 30 01 2020
pubmed: 8 3 2020
medline: 19 8 2021
entrez: 8 3 2020
Statut: ppublish

Résumé

Nonurothelial carcinoma (UC) malignancies have traditionally been considered to have a more aggressive clinical course, and little is known about their response to neoadjuvant therapy. We examined the effect of neoadjuvant chemotherapy (NAC) on a large population of patients with bladder cancer (BCa) with different histologic variants (HVs). We relied on a retrospective, multicenter database of 2858 patients with BCa who had undergone radical cystectomy with or without NAC from 1990 to 2017. Pure and mixed HVs were grouped into 6 categories: squamous cell carcinoma (SCC; n = 283; 45%), other subtypes (n = 95; 15%), micropapillary (n = 85; 14%), adenocarcinoma (n = 65; 10%), small cell (n = 54; 8.6%), and sarcomatous (n = 47; 7.6%). Kaplan-Meier and Cox regression analyses were used to examine cancer-specific survival (CSS) according to the HV, using pure UC as the reference. Logistic regression models were used to examine the odds of clinical-to-pathologic downstaging after NAC according to the HV. Overall, we identified 2229 cases of pure UC and 629 cases of BCa with HVs at radical cystectomy. Of the 450 NAC-treated patients, only those patients with SCC (n = 44; 9.8%) had had worse CSS (median CSS, 33 vs. 116 months; P < .001) and higher mortality rates (hazard ratio, 2.1; P = .03) compared with those with pure UC (n = 328; 72.9%). The results of the analyses were also confirmed when the pure and mixed cases were considered separately. After adjusting for NAC, only SCC showed a lower rate of clinical-to-pathologic downstaging (odds ratio, 0.4; P = .03) compared with UC. SCC was the HV exhibiting the lowest effect of NAC in terms of activity and CSS. Compared with pure UC, SCC seemed to be insensitive to traditional NAC regimens.

Sections du résumé

BACKGROUND
Nonurothelial carcinoma (UC) malignancies have traditionally been considered to have a more aggressive clinical course, and little is known about their response to neoadjuvant therapy. We examined the effect of neoadjuvant chemotherapy (NAC) on a large population of patients with bladder cancer (BCa) with different histologic variants (HVs).
PATIENTS AND METHODS
We relied on a retrospective, multicenter database of 2858 patients with BCa who had undergone radical cystectomy with or without NAC from 1990 to 2017. Pure and mixed HVs were grouped into 6 categories: squamous cell carcinoma (SCC; n = 283; 45%), other subtypes (n = 95; 15%), micropapillary (n = 85; 14%), adenocarcinoma (n = 65; 10%), small cell (n = 54; 8.6%), and sarcomatous (n = 47; 7.6%). Kaplan-Meier and Cox regression analyses were used to examine cancer-specific survival (CSS) according to the HV, using pure UC as the reference. Logistic regression models were used to examine the odds of clinical-to-pathologic downstaging after NAC according to the HV.
RESULTS
Overall, we identified 2229 cases of pure UC and 629 cases of BCa with HVs at radical cystectomy. Of the 450 NAC-treated patients, only those patients with SCC (n = 44; 9.8%) had had worse CSS (median CSS, 33 vs. 116 months; P < .001) and higher mortality rates (hazard ratio, 2.1; P = .03) compared with those with pure UC (n = 328; 72.9%). The results of the analyses were also confirmed when the pure and mixed cases were considered separately. After adjusting for NAC, only SCC showed a lower rate of clinical-to-pathologic downstaging (odds ratio, 0.4; P = .03) compared with UC.
CONCLUSIONS
SCC was the HV exhibiting the lowest effect of NAC in terms of activity and CSS. Compared with pure UC, SCC seemed to be insensitive to traditional NAC regimens.

Identifiants

pubmed: 32144050
pii: S1558-7673(20)30033-1
doi: 10.1016/j.clgc.2020.01.007
pmc: PMC8491463
mid: NIHMS1732104
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e543-e556

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA221745
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Références

Oncogene. 2014 Sep 18;33(38):4632-42
pubmed: 24141770
Eur Urol Focus. 2017 Dec;3(6):577-583
pubmed: 28753816
Hum Pathol. 2007 May;38(5):741-6
pubmed: 17306328
Urol Oncol. 2019 Jun;37(6):353.e17-353.e24
pubmed: 30704959
Cancer. 2007 Aug 15;110(4):764-9
pubmed: 17614317
BJU Int. 2019 Oct;124(4):665-671
pubmed: 30801918
Urology. 2005 Nov;66(5):1122-6
pubmed: 16286151
Cancer Med. 2016 Feb;5(2):192-9
pubmed: 26679712
Eur Urol. 2020 Apr;77(4):439-446
pubmed: 31708296
Cancer. 2019 May 1;125(9):1449-1458
pubmed: 30620387
Urol Oncol. 2013 Nov;31(8):1650-5
pubmed: 22608543
N Engl J Med. 2003 Aug 28;349(9):859-66
pubmed: 12944571
Eur Urol. 2016 Jul;70(1):106-119
pubmed: 26996659
Oncotarget. 2014 Nov 30;5(22):11576-87
pubmed: 25344912
Eur Urol Oncol. 2021 Jun;4(3):510-514
pubmed: 31395481
J Urol. 2012 Jan;187(1):74-9
pubmed: 22088332
Clin Transl Radiat Oncol. 2018 Dec 12;15:38-41
pubmed: 30656221
World J Urol. 2018 Feb;36(2):231-240
pubmed: 29127452
Eur Urol Focus. 2019 Jan;5(1):104-108
pubmed: 28753857
Clin Genitourin Cancer. 2018 Apr;16(2):e437-e442
pubmed: 29154041
Eur Urol Oncol. 2020 Aug;3(4):509-514
pubmed: 31411987
Semin Cancer Biol. 2018 Feb;48:91-103
pubmed: 28467889
Eur Urol. 2020 Apr;77(4):548-556
pubmed: 31959546
Eur Urol. 2017 Jul;72(1):54-60
pubmed: 28040351
Nat Rev Clin Oncol. 2017 Apr;14(4):221-234
pubmed: 27874062
Cancer. 2017 Nov 15;123(22):4346-4355
pubmed: 28743155
Cancer Discov. 2016 Feb;6(2):202-16
pubmed: 26645196
Clin Genitourin Cancer. 2019 Jun;17(3):e672-e677
pubmed: 31097390

Auteurs

Marco Bandini (M)

Urological Research Institute, Unit of Urology, IRCCS Ospedale San Raffaele, Vita-Salute San Raffaele University, Milan, Italy. Electronic address: bandini.marco@hsr.it.

Filippo Pederzoli (F)

Urological Research Institute, Unit of Urology, IRCCS Ospedale San Raffaele, Vita-Salute San Raffaele University, Milan, Italy.

Russell Madison (R)

Foundation Medicine, Cambridge, MA.

Alberto Briganti (A)

Urological Research Institute, Unit of Urology, IRCCS Ospedale San Raffaele, Vita-Salute San Raffaele University, Milan, Italy.

Jeffrey S Ross (JS)

Foundation Medicine, Cambridge, MA; Upstate Medical University, Syracuse, NY.

Günter Niegisch (G)

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

Evan Y Yu (EY)

Fred Hutchinson Cancer Research Center, University of Washington, Seattle, WA.

Aristotelis Bamias (A)

National and Kapodistrian University of Athens, Athens, Greece.

Neeraj Agarwal (N)

Huntsman Cancer Institute, University of Utah, Salt Lake, UT.

Srikala S Sridhar (SS)

Cancer Clinical Research Unit, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.

Jonathan E Rosenberg (JE)

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

Joaquim Bellmunt (J)

Bladder Cancer Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.

Sumanta Kumar Pal (SK)

City of Hope Comprehensive Cancer Center, Duarte, CA.

Matthew D Galsky (MD)

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

Roberta Lucianò (R)

Department of Pathology, Ospedale San Raffaele, Milan, Italy.

Andrea Gallina (A)

Urological Research Institute, Unit of Urology, IRCCS Ospedale San Raffaele, Vita-Salute San Raffaele University, Milan, Italy.

Andrea Salonia (A)

Urological Research Institute, Unit of Urology, IRCCS Ospedale San Raffaele, Vita-Salute San Raffaele University, Milan, Italy.

Francesco Montorsi (F)

Urological Research Institute, Unit of Urology, IRCCS Ospedale San Raffaele, Vita-Salute San Raffaele University, Milan, Italy.

Siraj M Ali (SM)

Foundation Medicine, Cambridge, MA.

Jon H Chung (JH)

Foundation Medicine, Cambridge, MA.

Andrea Necchi (A)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

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