Abstract 152P
Background
There is no relevant data of real-time programmed cell death-ligand 1 (PD-L1) expression and initial treatment pattern in Chinese muscle invasive urothelial bladder carcinoma patients (MIUBC). Thus, the aim of this multi-center, prospective, epidemiological study was to investigate the prevalence of high PD-L1 expression along with clinical observation of initial treatment pattern in the Chinese MIUBC patients (NCT03433924).
Methods
The study enrolled newly diagnosed patients with MIUBC and treatment naïve. The PD-L1 expression was tested by VENTANA PD-L1 (SP263) Assay. High PD-L1 expression is defined as ≥25% tumor cell (TC) + or 1) Tumor associated immune cell (IC) area >1%: ≥25% IC+; 2) IC area=1%: 100% IC+. The primary outcome was prevalence of high PD-L1 expression. The secondary outcomes included the PD-L1 expression profile in TC and IC, initial treatment pattern and concordance of PD-L1 testing between hospital and central laboratories. Further, an exploratory study was carried out to investigate correlation of PD-L1 and the infiltration of CD8+ T cells.
Results
Overall, 248 MIUBC patients were enrolled from 17 hospitals in China and 229 patients with PD-L1 data were included. High PD-L1 expression was observed in 52.4% of patients. The high PD-L1 expression was positive in 59 patients of TC and 82 patients of IC. The overall concordance rate between hospital and central labs for high PD-L1 expression was 80.4% (37/46, kappa=0.57). With respect to initial treatment pattern, 83.2% patients received radical cystectomy, and 2.2% received partial cystectomy, while 14.6% received transurethral bladder resection only. Only 7.3% patients received peri-operative treatment. Further, the Spearman’s rank correlation coefficient for percentage of TC with membrane PD-L1 positivity and CD8+ T cells, the percentage of IC with PD-L1 positivity and CD8+ T cells was determined as 0.27 and 0.34 respectively.
Conclusions
Our study reported high PD-L1 expression (52.4%) in MIUBC patients. Also, PD-L1 expression showed weak and positive association with infiltrated CD8+ T cells.
Clinical trial identification
NCT03433924.
Editorial acknowledgement
Legal entity responsible for the study
Liqun Zhou.
Funding
AstraZeneca.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
167P - Genetic testing for prostate cancer: The Indian scenario
Presenter: Ganesh Bakshi
Session: Poster viewing 03
168P - Transcriptional profiling of metastatic hormone sensitive prostate cancer (mHSPC) and distinct features are associated with clinical outcome
Presenter: BYULA JEE
Session: Poster viewing 03
169P - Urine tumor DNA fragmentation profiles provided a novel biomarker for early detection of prostate cancer
Presenter: Nianzeng Xing
Session: Poster viewing 03
170P - Safety, efficacy and pharmacoeconomic implications of low dose abiraterone in prostate cancer
Presenter: Suryakanta Acharya
Session: Poster viewing 03
171P - Clinical significance of prostate volume and testosterone reduction on lower urinary tract symptoms in patients with prostate cancer undergoing androgen deprivation therapy
Presenter: Jin Cho
Session: Poster viewing 03
172P - Impact on management of non-metastatic prostate cancer biochemical recurrence with use of 68Ga PET-PSMA PET/CT scans in single-institution experience
Presenter: Pimchanok Tuitemwong
Session: Poster viewing 03
173P - Clinical outcomes in stratification subgroups in the ARASENS study in metastatic hormone-sensitive prostate cancer (mHSPC)
Presenter: Francis Parnis
Session: Poster viewing 03
175TiP - A prospective phase II study to investigate the efficacy and safety of olaparib plus abiraterone and prednisone combination therapy in mHSPC patients with HRR gene mutation
Presenter: Junlong Zhuang
Session: Poster viewing 03
186P - Degradation of BRCA2 expression by hyperthermia sensitizes HRD-negative (BRCA2 wild-type) ovarian cancer cells to niraparib
Presenter: Junyang Li
Session: Poster viewing 03