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
192P - Use of biosimulation to predict homologous recombination deficiency and PARPi benefit in patients with ovarian, pancreatic, prostate and triple negative breast cancers
Presenter: Daniel Palmer
Session: Poster session 08
193P - Translational, PK, PD, and immunophenotyping analyses of tuvusertib + niraparib in a phase Ib open-label multicenter dose-escalation study in patients with advanced solid tumors (DDRiver Solid Tumors 301)
Presenter: Anthony Tolcher
Session: Poster session 08
195P - Preclinical efficacy of the trastuzumab duocarmazine SYD985 as monotherapy or in combination with the PARP inhibitor niraparib in HER2-expressing endometrial cancer
Presenter: Eva Colas
Session: Poster session 08
196P - Randomized phase II study of trabectedin/olaparib compared to physician’s choice in subjects with previously treated advanced or recurrent solid tumors harboring DNA repair deficiencies
Presenter: Richard Schlenk
Session: Poster session 08
197P - PRIME-ROSE: Merging clinical outcome data from DRUP-like clinical trials
Presenter: Tina Kringelbach
Session: Poster session 08
198P - Inavolisib in cancers with activating PIK3CA mutations: Results from the CRAFT trial
Presenter: Christoph Heilig
Session: Poster session 08
199P - Association of homologous recombination deficiency status with outcomes for ovarian cancer patients treated with olaparib, and exploration of other biomarkers of relapse and survival
Presenter: qingsheng xie
Session: Poster session 08
200P - Outcomes of patients (pts) with unfavourable, non-squamous cancer of unknown primary (CUP) progressing after induction chemotherapy (CTX) in the global, open-label, phase II CUPISCO study
Presenter: Tilmann Bochtler
Session: Poster session 08
201P - Efficacy of antibody drug conjugate (ADC) by mRNA expression of targeted genes in advanced solid tumors: SCRUM-Japan MONSTAR-SCREEN-2
Presenter: Takao Fujisawa
Session: Poster session 08