Abstract 39P
Background
Drugs with potential to disrupt the microbiome and therefore the immune system, such as antibiotics (ATB) and/or proton pump inhibitors (PPI), have been associated with a negative impact in several oncologic treatments. Here we aimed to evaluate the impact of ATB and PPI in the outcome of non-muscle-invasive bladder cancer (NMIBC) treated with intravesical Bacillus Calmette-Guérin (BCG).
Methods
We conducted a retrospective observational study including patients with NMIBC who underwent transurethral resection of a bladder tumor (TURBT), followed by intravesical BCG therapy, at our institution, between 2013 and 2018. We categorized patients as receiving ATB in the previous 2 months before BCG initiation and baseline use of PPI. Oncologic outcomes such as recurrence-free survival (RFS) and progression-free survival (PFS) were analyzed.
Results
Forty-nine patients were enrolled and their mean age was 67.2 years and 41 (83.7%) were males. Concerning NMIBC 16 (32.7%) had Ta disease while 33 (67.3%) had T1. Twenty-five (51.0%) patients took ATB prior to intravesical BCG therapy and 10 (20.4%) were taking PPI at baseline. During the follow-up period 15 (30.6%) patients had disease recurrence and 8 (16.3%) progression. Previous ATB intake was not associated with differences in RFS (3-year RFS: 79.8% with ATB vs 73.3% without; log rank, p=0.348) or PFS (3-year PFS: 87.8% with ATB vs 95.5% without; log rank, p=0.451). Concerning PPI intake, there were no significant differences in RFS, however there was a non-significant trend for worst outcome in those taking PPI at baseline (3-year RFS: 57.1% with PPI vs 81.5% without; log rank, p=0.083). Concerning PFS, there were no differences for PPI intake between the two groups (3-year PFS: 90.0% with PPI vs 92.1% without; log rank, p=0.118).
Conclusions
PPI or ATB intake was not associated with worst oncologic outcomes after intravesical BCG treatment. Further studies are needed to better understand the association between these drugs and NMIBC prognosis.
Editorial acknowledgement
Clinical trial identification
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
125P - Combination of navitoclax with alpelisib and trametinib to synergistically impair cell viability in high-grade ovarian cancer
Presenter: Lisa Wozelka-Oltjan
Session: Cocktail & Poster Display session
Resources:
Abstract
126P - Effect of sequential antitumoral treatment with immune checkpoint blockade and tyrosine kinase inhibitors in hepatocellular carcinoma
Presenter: Vincenza Ciaramella
Session: Cocktail & Poster Display session
Resources:
Abstract
127P - Novel bone-targeting of activatable sirolimus for targeted therapy of bone-resident cancers
Presenter: Alistare Sadra
Session: Cocktail & Poster Display session
Resources:
Abstract
128P - Network medicine approach identifies small molecule drugs as immune checkpoint inhibitors repurposable for rectal cancer
Presenter: Faheem Ahmed
Session: Cocktail & Poster Display session
Resources:
Abstract
129P - Repurposing existing therapies for adrenal cancer: Unlocking new possibilities
Presenter: Anupama Samantasinghar
Session: Cocktail & Poster Display session
Resources:
Abstract
130P - Restoration of the mutant p53 protein upon treatment with small molecule modulators
Presenter: Elvina Gilyazova
Session: Cocktail & Poster Display session
Resources:
Abstract
131P - Trop 2 and its overexpression in metastatic colorectal cancer patients (mCRCp): Biological, clinical and therapeutic implications
Presenter: Andrea Mancuso Petricca
Session: Cocktail & Poster Display session
Resources:
Abstract
132P - Novel small molecule modulators for activation of mutant tumor suppressor p53
Presenter: Damir Davletshin
Session: Cocktail & Poster Display session
Resources:
Abstract
133P - Cytotoxic efficacy of artificial vesicles obtained from CAR-T cells by ultrasonication
Presenter: Ekaterina Zmievskaya
Session: Cocktail & Poster Display session
Resources:
Abstract
134P - Doxorubicin and olaparib (OLA) synergism in high-grade serous ovarian (HGOC) and triple-negative breast cancer (TNBC) cell lines with olaparib-resistance
Presenter: Jose Alejandro Perez Fidalgo
Session: Cocktail & Poster Display session
Resources:
Abstract