Abstract 194P
Background
The combination of Pembrolizumab and Lenvatinib shows synergy in treatment of advanced microsatellite stable (MSS) or proficient mismatch repair (pMMR) endometrial cancer, yet only one-third of patients achieve a lasting response. Research into microenvironmental factors seeks to identify markers to select suitable candidates for improved treatment results.
Methods
An open, non-randomized observational association study was conducted across six clinical centers in Siberia and the Far East. The study encompassed an expanded (third iteration of analysis) cohort of 32 patients diagnosed with advanced MSS/pMMR endometrial cancer. Tissue samples were subjected to TSA-associated multiplex immunofluorescence using Vectra 3 (Akoya) to quantify the ratio of CD8-to-CD20 lymphocytes.
Results
In patients who exhibited a positive response to the treatment, there was a notable increase in both the percentage of CD20+ B lymphocytes and the ratio of CD8-to-CD20 lymphocytes when compared to those who did not respond (responders: 0.26% (0.1–1.37%); non-responders: 0.07% (0.00–0.14%), p = 0.0034; responders: 1.45 arb. units (0.58–2.81); non-responders: 20.30 arb. units (3.42–42.08), p = 0.0001). The diagnostic accuracy of the ratio of CD8-to-CD20 lymphocytes was demonstrated by their sensitivity and specificity rates, which were 91.45% for both. Patients with a CD8-to-CD20 lymphocyte ratio of 3.45 or higher had an OR of 10.54 (95% CI: 2.65–37.14, p = 0.0001). Bootstrap validation confirmed minimal bias for the CD8-to-CD20 lymphocyte ratio. Patients with a CD8-to-CD20 lymphocyte ratio less than 3.45 demonstrated improved PFS (CD8-to-CD20 ratio <3.45 vs. ≥3.45: median PFS not reached vs. 6 months, p < 0.0001). However, these factors did not significantly affect overall survival (OS) (CD8-to-CD20 ratio <3.45 vs. ≥3.45: median OS not reached vs. 82 months, p = 0.0736).
Conclusions
The CD8-to-CD20 lymphocyte ratio may act as an effective surrogate marker for immunotargeted therapy in individuals with advanced MSS/pMMR endometrial cancer. The study was supported by the Russian Science Foundation (grant # 20-75-10033-P).
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Tomsk National Research Medical Center.
Funding
The study was supported by the Russian Science Foundation (grant # 20-75-10033-P).
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
122P - Practice patterns and treatment outcomes of molecular tumour board (MTB)-based personalized cancer therapies: A single-center experience
Presenter: Florian Moik
Session: Poster session 08
123P - Pan-cancer homologous recombination deficiency (HRD) evaluation in patients enrolled in a routine molecular screening program
Presenter: Paula Romero-Lozano
Session: Poster session 08
124P - Incidence of activating frameshift and nonsense mutations in clinically actionable oncogenes
Presenter: Sjors Kas
Session: Poster session 08
125P - Comparison of microarray and next-generation sequencing-based approaches for detection of homologous recombination deficiency
Presenter: Caleb Kidwell
Session: Poster session 08
126P - Genomic landscape and prognostic impact of HER2 low-expressing tumors
Presenter: Aditya Shreenivas
Session: Poster session 08
127P - Clinical utility of circulating tumor DNA (ctDNA) next generation sequencing (NGS) to inform treatment decisions for patients (pts) with advanced solid tumors
Presenter: Diego Gomez Puerto
Session: Poster session 08
128P - Whole blood transcriptomics identifies transcriptional patterns linked to outcomes in patients receiving immune checkpoint inhibitors
Presenter: Sara Hone Lopez
Session: Poster session 08
129P - Integrating large data to unveil vulnerabilities for patients with hot tumors resistant to checkpoint inhibition
Presenter: Anlin Li
Session: Poster session 08
130P - Ipilimumab plus nivolumab (Ipi+Nivo) in patients with tumors harboring high tumor mutational burden or load (TMB/TML-H): Results from the Drug Rediscovery Protocol (DRUP)
Presenter: Soemeya Haj Mohammad
Session: Poster session 08
131P - Systemic immune-inflammation index and overall survival with checkpoint inhibitors
Presenter: Oliver Kennedy
Session: Poster session 08