Do urinary mast cell mediators predict immune response to BCG in patients with primary high‐grade non‐muscle invasive bladder cancer?

Background Mast cells play a critical role in cancer‐associated immunity. We aimed to determine the predictive value of urinary mast cell mediators in patients with non‐muscle invasive bladder cancer (NMIBC) treated with Bacillus Calmette‐Guérin (BCG) immunotherapy. Methods In this prospective study...

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Veröffentlicht in:International journal of clinical practice (Esher) 2021-05, Vol.75 (5), p.e13959-n/a
Hauptverfasser: Simsekoglu, Muhammed Fatih, Kaleler, Islim, Onal, Bulent, Demirdag, Cetin, Citgez, Sinharib, Uslu, Ezel, Erozenci, Ahmet, Talat, Zubeyr
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container_issue 5
container_start_page e13959
container_title International journal of clinical practice (Esher)
container_volume 75
creator Simsekoglu, Muhammed Fatih
Kaleler, Islim
Onal, Bulent
Demirdag, Cetin
Citgez, Sinharib
Uslu, Ezel
Erozenci, Ahmet
Talat, Zubeyr
description Background Mast cells play a critical role in cancer‐associated immunity. We aimed to determine the predictive value of urinary mast cell mediators in patients with non‐muscle invasive bladder cancer (NMIBC) treated with Bacillus Calmette‐Guérin (BCG) immunotherapy. Methods In this prospective study, 19 patients who received immunotherapy because of NMIBC (Group 1) and 19 healthy participants (Group 2) were enrolled. Urine samples were collected to assay N‐methylhistamine, histamine, and tryptase levels immediately before the first BCG instillation, immediately after the third and sixth instillations, and 4 weeks after the sixth instillation in Group 1 and at a single visit in Group 2. The changes in urinary markers because of BCC response, BCG instillation, and the presence of NMIBC were assessed. Results The average age was 56.1 ± 10.5 years in Group 1 and 52.6 ± 9.7 years in Group 2. Fourteen patients had high‐grade Ta tumours and five had T1 tumours. While 12 patients had responded to the BCG, seven patients did not respond to the BCG. There was no correlation between mast cell mediators and BCG response. The N‐methylhistamine and histamine levels significantly increased with the onset of immunotherapy, and N‐methylhistamine levels significantly decreased when immunotherapy was terminated (P 
doi_str_mv 10.1111/ijcp.13959
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We aimed to determine the predictive value of urinary mast cell mediators in patients with non‐muscle invasive bladder cancer (NMIBC) treated with Bacillus Calmette‐Guérin (BCG) immunotherapy. Methods In this prospective study, 19 patients who received immunotherapy because of NMIBC (Group 1) and 19 healthy participants (Group 2) were enrolled. Urine samples were collected to assay N‐methylhistamine, histamine, and tryptase levels immediately before the first BCG instillation, immediately after the third and sixth instillations, and 4 weeks after the sixth instillation in Group 1 and at a single visit in Group 2. The changes in urinary markers because of BCC response, BCG instillation, and the presence of NMIBC were assessed. Results The average age was 56.1 ± 10.5 years in Group 1 and 52.6 ± 9.7 years in Group 2. Fourteen patients had high‐grade Ta tumours and five had T1 tumours. While 12 patients had responded to the BCG, seven patients did not respond to the BCG. There was no correlation between mast cell mediators and BCG response. The N‐methylhistamine and histamine levels significantly increased with the onset of immunotherapy, and N‐methylhistamine levels significantly decreased when immunotherapy was terminated (P &lt; .05). The pre‐BCG estimated marginal mean values of N‐methylhistamine were significantly higher in Group 1 than in Group 2 (P &lt; .05). Conclusions Our study is the first to identify the changes in mast cell mediators with the onset of immunotherapy and in presence of bladder cancer. However, these mediators cannot predict patients’ response to immunotherapy.</description><identifier>ISSN: 1368-5031</identifier><identifier>EISSN: 1742-1241</identifier><identifier>DOI: 10.1111/ijcp.13959</identifier><identifier>PMID: 33369059</identifier><language>eng</language><publisher>England: Hindawi Limited</publisher><subject>Administration, Intravesical ; Aged ; BCG Vaccine - therapeutic use ; Bladder cancer ; Cancer ; Histamine ; Humans ; Immune response ; Immunity ; Immunotherapy ; Invasiveness ; Mast Cells ; Middle Aged ; Neoplasm Recurrence, Local ; Prospective Studies ; Tryptase ; Tumors ; Urinary Bladder Neoplasms - drug therapy</subject><ispartof>International journal of clinical practice (Esher), 2021-05, Vol.75 (5), p.e13959-n/a</ispartof><rights>2020 John Wiley &amp; Sons Ltd</rights><rights>2020 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2021 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3939-cfd366960483446fa7b2e0c80a67ce8a7eaf187d187ea03ba02bc18f9a57e4de3</citedby><cites>FETCH-LOGICAL-c3939-cfd366960483446fa7b2e0c80a67ce8a7eaf187d187ea03ba02bc18f9a57e4de3</cites><orcidid>0000-0002-8912-9155 ; 0000-0002-2712-7955 ; 0000-0003-0540-2693 ; 0000-0003-0645-4129 ; 0000-0003-3925-0851 ; 0000-0001-7577-7955 ; 0000-0002-3897-2951 ; 0000-0002-6389-5353</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fijcp.13959$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fijcp.13959$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33369059$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Simsekoglu, Muhammed Fatih</creatorcontrib><creatorcontrib>Kaleler, Islim</creatorcontrib><creatorcontrib>Onal, Bulent</creatorcontrib><creatorcontrib>Demirdag, Cetin</creatorcontrib><creatorcontrib>Citgez, Sinharib</creatorcontrib><creatorcontrib>Uslu, Ezel</creatorcontrib><creatorcontrib>Erozenci, Ahmet</creatorcontrib><creatorcontrib>Talat, Zubeyr</creatorcontrib><title>Do urinary mast cell mediators predict immune response to BCG in patients with primary high‐grade non‐muscle invasive bladder cancer?</title><title>International journal of clinical practice (Esher)</title><addtitle>Int J Clin Pract</addtitle><description>Background Mast cells play a critical role in cancer‐associated immunity. We aimed to determine the predictive value of urinary mast cell mediators in patients with non‐muscle invasive bladder cancer (NMIBC) treated with Bacillus Calmette‐Guérin (BCG) immunotherapy. Methods In this prospective study, 19 patients who received immunotherapy because of NMIBC (Group 1) and 19 healthy participants (Group 2) were enrolled. Urine samples were collected to assay N‐methylhistamine, histamine, and tryptase levels immediately before the first BCG instillation, immediately after the third and sixth instillations, and 4 weeks after the sixth instillation in Group 1 and at a single visit in Group 2. The changes in urinary markers because of BCC response, BCG instillation, and the presence of NMIBC were assessed. Results The average age was 56.1 ± 10.5 years in Group 1 and 52.6 ± 9.7 years in Group 2. Fourteen patients had high‐grade Ta tumours and five had T1 tumours. While 12 patients had responded to the BCG, seven patients did not respond to the BCG. There was no correlation between mast cell mediators and BCG response. The N‐methylhistamine and histamine levels significantly increased with the onset of immunotherapy, and N‐methylhistamine levels significantly decreased when immunotherapy was terminated (P &lt; .05). The pre‐BCG estimated marginal mean values of N‐methylhistamine were significantly higher in Group 1 than in Group 2 (P &lt; .05). Conclusions Our study is the first to identify the changes in mast cell mediators with the onset of immunotherapy and in presence of bladder cancer. 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We aimed to determine the predictive value of urinary mast cell mediators in patients with non‐muscle invasive bladder cancer (NMIBC) treated with Bacillus Calmette‐Guérin (BCG) immunotherapy. Methods In this prospective study, 19 patients who received immunotherapy because of NMIBC (Group 1) and 19 healthy participants (Group 2) were enrolled. Urine samples were collected to assay N‐methylhistamine, histamine, and tryptase levels immediately before the first BCG instillation, immediately after the third and sixth instillations, and 4 weeks after the sixth instillation in Group 1 and at a single visit in Group 2. The changes in urinary markers because of BCC response, BCG instillation, and the presence of NMIBC were assessed. Results The average age was 56.1 ± 10.5 years in Group 1 and 52.6 ± 9.7 years in Group 2. Fourteen patients had high‐grade Ta tumours and five had T1 tumours. While 12 patients had responded to the BCG, seven patients did not respond to the BCG. There was no correlation between mast cell mediators and BCG response. The N‐methylhistamine and histamine levels significantly increased with the onset of immunotherapy, and N‐methylhistamine levels significantly decreased when immunotherapy was terminated (P &lt; .05). The pre‐BCG estimated marginal mean values of N‐methylhistamine were significantly higher in Group 1 than in Group 2 (P &lt; .05). Conclusions Our study is the first to identify the changes in mast cell mediators with the onset of immunotherapy and in presence of bladder cancer. 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subjects Administration, Intravesical
Aged
BCG Vaccine - therapeutic use
Bladder cancer
Cancer
Histamine
Humans
Immune response
Immunity
Immunotherapy
Invasiveness
Mast Cells
Middle Aged
Neoplasm Recurrence, Local
Prospective Studies
Tryptase
Tumors
Urinary Bladder Neoplasms - drug therapy
title Do urinary mast cell mediators predict immune response to BCG in patients with primary high‐grade non‐muscle invasive bladder cancer?
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