Abstract 154P
Background
The gut microbiome may be potentially disrupted by commonly used drugs, such as proton pump inhibitors (PPI), with possible impact in the immunologic response to cancer therapies. In this work we aimed to assess the impact of taking PPI in the outcome of patients with non-metastatic nasopharyngeal carcinoma (NPHC), treated at an oncological center.
Methods
We conducted a retrospective and observational study that included newly diagnosed subjects with non-metastatic NPHC, diagnosed between October 2012 and November 2019, and treated in our centre with a curative strategy that included radiotherapy (RT). Demographic and clinical variables were evaluated and patients were categorized as taking PPI at baseline/initiated PPI before the start of RT or not. Oncologic outcomes evaluated included disease-free survival (DFS) and overall survival (OS). OS and DFS were evaluated by the Kaplan-Meier method and prognostic features were assessed by univariate and multivariate Cox regression.
Results
We included 83 patients, of which 56 (67.5%) were males and 60 (72.3%) had at least 45 years-old. Fifty-nine (71.1%) had stage ≥ III and 35 (42.2%) were treated only with chemoradiotherapy, while 14 (16.9%) also received neoadjuvant chemotherapy and 26 (31.3%) adjuvant chemotherapy. Twenty-three (27.7%) were taking PPI at baseline or initiated it before the start of RT. On the multivariate analysis age ≥ 45 years [HR 6.07 (95% CI: 1.36-27.06), p=0.018] and taking PPI [HR 2.66 (95% CI: 1.07-6.60), p=0.035] were associated with worst DFS. Concerning OS, age ≥ 45 years [HR 9.90 (95% CI: 1.24-79.11), p=0.031], stage ≥ III [HR 5.17 (95% CI: 1.11-23.98), p=0.036] and taking PPI [HR 4.14 (95% CI: 1.47-11.68), p=0.007] were associated with a worst outcome.
Conclusions
In our sample, taking PPI at baseline or initiate it before the start of RT was associated with worst prognosis in non-metastatic NPHC patients. Further studies are still needed to assess the impact of drugs with potential to disrupt the gut microbiome on the outcome of non-metastatic NPHC patients.
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
30P - Role of microRNA and CDKN2A/p16INK4a expression in the prognostication of oral squamous cell carcinoma
Presenter: Olha Burtyn
Session: Cocktail & Poster Display session
Resources:
Abstract
31P - Identification of proteins associated with mRNA processing and maturation by quantitative proteomic analysis in Indian cervical cancer patients
Presenter: Amrita Mukherjee
Session: Cocktail & Poster Display session
Resources:
Abstract
32P - Expression of STAT3 and hypoxia markers in repeatedly resected glioma patients
Presenter: Katerina Dvorakova
Session: Cocktail & Poster Display session
Resources:
Abstract
33P - Unraveling the mechanisms of cisplatin resistance in bladder organoid by single cell RNA sequencing
Presenter: Tingting Xie
Session: Cocktail & Poster Display session
Resources:
Abstract
34P - Functional diagnostics and ex-vivo screening of erlotinib and nintedanib in non-small cell lung carcinoma: Implications for multidrug resistance and personalized therapy
Presenter: Jelena Dinić
Session: Cocktail & Poster Display session
Resources:
Abstract
35P - Enhancing efficacy of the MEK inhibitor trametinib in KRAS-mutated colorectal cancer cells
Presenter: Lee Ellis
Session: Cocktail & Poster Display session
Resources:
Abstract
36P - Comparison of pelitinib, tepotinib or docetaxel efficacy according to the copy number or gene alteration status of EGFR, MET, HRAS, KRAS and NRAS genes
Presenter: Dae Young Zang
Session: Cocktail & Poster Display session
Resources:
Abstract
37P - NET-mediated radio-resistance in early-stage non-small cell lung cancer
Presenter: Malcolm Ryan
Session: Cocktail & Poster Display session
Resources:
Abstract
39P - The use of antibiotics or proton pump inhibitors and the response to intravesical Bacillus Calmette Guérin therapy in non-muscle-invasive bladder cancer
Presenter: João Barbosa Martins
Session: Cocktail & Poster Display session
Resources:
Abstract
40P - YAP1 promotes sorafenib resistance by activation of TGFβ signaling pathway
Presenter: Chit Lai Chee
Session: Cocktail & Poster Display session
Resources:
Abstract