Abstract 2015P
Background
Antibody drug conjugate (ADC) therapy using enfortumab-vedotin (EV) that targets nectin-4 increased progression-free as well as overall survival of patients with metastatic bladder cancer (BC) dramatically. However, the expression of nectin-4 on the tumor cells is not in all patients sufficient for an effective therapy with EV. In addition, the expression on metastases as the target lesions is even lower and often differed compared to primary tumors. Therefore, analysis of nectin-4 in blood from patients could be helpful to select patients for EV therapy and to monitor therapy response. The aim of this study was to analyze the diagnostic, prognostic and predictive value of nectin-4 in serum of BC patients.
Methods
Serum samples from 92 patients with BC (pTa=22, pT1=18, pT2=18, pT3=21, pT4=13) were obtained before surgery or before and during EV monotherapy or EV combination therapy with pembrolizumab (n=10). Nectin-4 was quantified by using an ELISA kit (Abcam, Germany). Statistical analysis was performed to test possible correlations with histopathological parameters using Mann-Whitney-U test or Kruskal-Wallis test. In addition, nectin-4-was quantified at different time points in patients who received EV therapy in first, second or third line settings.
Results
Nectin-4 concentration is significantly associated with T-category (p=0.0073) and increased with increasing T-category. Patients with lymph node metastases (pN+) at time of surgery exhibited significantly higher nectin-4 concentrations compared to those without metastases (pN-) (p=0.004). A trend of higher concentrations was observed in higher grades. Nectin-4 was detected in all metastatic patients before EV therapy and rose continuously during therapy in most cases. Correlation analysis with response will be presented at the congress as re-staging is currently ongoing.
Conclusions
To our knowledge, this is the first report on detection of nectin-4 in serum from patients with bladder cancer. Invasiveness and metastasis are associated with increased serum nectin-4 concentrations. nectin-4 in serum and the dynamic changes during therapy could be useful markers for therapy optimization. However, its predictive value has to be evaluated in larger studies considering mono- and combination therapies.
Clinical trial identification
Editorial acknowledgement
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
252P - Evolution of breast cancer biological subtypes between pre-treatment biopsy and residual disease after neoadjuvant therapy
Presenter: Katarzyna Pogoda
Session: Poster session 13
253P - Single-cell RNA sequencing reveals tumor heterogeneity and potential mechanisms of response/resistance in breast cancer treated with neoadjuvant therapy
Presenter: Marcela Carausu
Session: Poster session 13
254P - IHC and GEX biomarkers and their prognostic and treatment predictive role in the neoadjuvant treatment of breast cancer
Presenter: Hani Saghir
Session: Poster session 13
255P - Predicting early recurrence in breast cancer patients undergoing neo-adjuvant chemotherapy through MRI-radiomics analysis
Presenter: Anna D'Angelo
Session: Poster session 13
256P - Protein signature of tertiary lymphoid structure predicts efficacy of neoadjuvant chemotherapy in triple-negative breast cancer
Presenter: Shuling Zhou
Session: Poster session 13
257P - Spatial predictors of pathologic complete response to neoadjuvant chemotherapy using imaging mass cytometry in the IMMUcan TNBC cohort
Presenter: Andrea Joaquin Garcia
Session: Poster session 13
258P - Correlation between pathological complete response (pCR) following neoadjuvant docetaxel, carboplatin and trastuzumab (TCH) with or without pertuzumab (TCHP) and PAM50 subtypes in HER2(+) early breast cancer (eBC)
Presenter: Coralia Bueno Muiño
Session: Poster session 13
1954P - 5-methylthioadenosine phosphorylase (MTAP) loss in clinically advanced uveal melanoma (CAUM): A comprehensive genomic profiling (CGP) study
Presenter: Nimisha Srivastava
Session: Poster session 13
1955P - Glycan-programmed T cell immunity: Effective adoptive T cell transfer in a CRC preclinical model
Presenter: Yong Miao
Session: Poster session 13