Abstract 156P
Background
Bispecific CD3 T cell engagers (TCEs) show promising antitumor activity in solid tumors, but resistance often develops. Resistance to immunotherapy is influenced by the tumor microenvironment (TME), including at metastatic sites. Liver metastases, for example, are linked to an immunotolerant TME and resistance. We aimed to determine if the location of metastatic sites correlates with outcomes in patients (pts) treated with TCEs.
Methods
Pts treated with a TCE for metastatic solid tumors at the Drug Development Department in Gustave Roussy were included. Clinical data were gathered during screening, and disease progression was evaluated using RECIST criteria. Target lesions (TL) progression was tracked when available. Overall survival (OS) and progression-free survival (PFS) were estimated via the Kaplan-Meier method, with multivariate analyses (MVA) conducted using a Cox regression model.
Results
The cohort included 127 pts (73 M, 57 W), with a median age of 60 years. The most common tumor types were prostate cancer (30%) and small cell lung cancer (19%). The most frequent metastatic sites were lymph nodes (69%), bones (43%), and liver (38%). MVA (on histology and metastatic sites) revealed that only liver metastases were associated with worse outcomes in both PFS (HR: 1.94, [1.19-3.17], p=0.001), with a median PFS of 58 and 89 days respectively, and OS (HR: 2.39, [1.28-4.48], p=0.007), with a median OS of 249 and 527 days respectively, independent of tumor type. Detailed data on TL progression were available for 50 pts, including 22 with at least one hepatic TL. Among these, 18 pts (79%) had at least two TLs, and 78% (14/18) exhibited a dissociated response, with 79% (11/14) showing progressive disease (PD) in the liver. Overall, 82% of pts with hepatic TL showed PD in the liver. Dissociated response tend to be more frequent in pts with liver metastases (79%) compared to those with at least two non-hepatic TL (56%) (OR : 3.7, [0.83;19.77], p=0.06).
Conclusions
In pts treated with TCEs, liver metastases are associated with poorer outcomes for both PFS and OS. Pts with liver metastases are more likely to exhibit a dissociated response to treatment, with progressive disease predominantly occurring in hepatic lesions.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
N. Herbel: Financial Interests, Personal, Full or part-time Employment: Viroxis Biotech. All other authors have declared no conflicts of interest.
Resources from the same session
53P - Novel ex-vivo manufacturing of transiently expressed armoured CAR T cells for glioblastoma
Presenter: Saket Srivastava
Session: Poster Display session
Resources:
Abstract
54P - Superior antitumor activities of fourth-generation CAR-T cells containing three costimulatory domains targeting GD2-positive tumors
Presenter: Jatuporn Sujjitjoon
Session: Poster Display session
Resources:
Abstract
55P - Engineering of chimeric cytokine receptors (CCR) to induce IL-7 signaling to CAR-T cells for solid tumor treatment
Presenter: Marta Soria Castellano
Session: Poster Display session
Resources:
Abstract
56P - Potent antitumor efficiency of CD19-CAR T cells self-secreting PD-L1 x CD3 BiTE against aggressive B-cell lymphoma
Presenter: Jatuporn Sujjitjoon
Session: Poster Display session
Resources:
Abstract
57P - SENDER™ Directed LNP Delivery of mRNA for In Situ generation of highly potent CAR T Cells
Presenter: Biao Ma
Session: Poster Display session
Resources:
Abstract
58P - Cardiovascular outcomes of novel CAR-T cell therapies: A meta-analysis of incidence, risk factors, and management of cardiotoxicity
Presenter: Hashim Talib Hashim
Session: Poster Display session
Resources:
Abstract
59P - Long term survival data from all recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) patients treated with MVX-ONCO-1 during open-labelled phase I and phase IIa clinical trials
Presenter: Nicolas Mach
Session: Poster Display session
Resources:
Abstract
60P - Innovative applications of neoantigens in dendritic cell-derived exosome (DEX) therapy and their impact on personalized cancer treatment
Presenter: Ramon Gutierrez
Session: Poster Display session
Resources:
Abstract
61P - Optimized protocol for the accelerated production of dendritic cell-derived exosomes (DEXs): Achieving speed without compromising efficacy
Presenter: Ramon Gutierrez
Session: Poster Display session
Resources:
Abstract
62P - Ecto-CRT induction of NKp46 surface expression increases osimertinib-resistant lung cancer’s sensitivity to NK cells
Presenter: Sumei Chen
Session: Poster Display session
Resources:
Abstract