T-cell bispecific (TCB) therapies have demonstrated promising therapeutic efficacies for patients with relapsed/refractory multiple myeloma. However, responses are transient and essentially all patients eventually relapse. Cytokine release syndrome and other on-target off-tumor toxicities are common. Together, these challenges ask for new approaches to optimize treatment and to eventually understand resistance mechanisms. This phase 1 study (NCT04557150) investigated mode of action and resistance mechanisms of forimtamig, a novel GPRC5DxCD3 TCB. Biomarker analyses included deep phenotyping of patients' tumor and immune cells, functional T cell characterization, cytokine release, soluble B-cell maturation antigen kinetics and minimal residual disease evaluation. Biomarker data analysis assessed the impact of different TCB treatment approaches on T cell-mediated tumor killing dynamics: subcutaneous vs intravenous administration, weekly vs every 4 days step-up dosing, and low vs high target doses. A machine learning model revealed T-to-natural killer (NK)cell ratio in blood and bone marrow as a strong predictor of response. Single cell transcriptomics showed increased DNA repair and proliferation as major tumor hallmarks associated with resistance, while T cell dysfunction signatures were not predictive of response. T cells from non-responding patients showed an increased cytokine release when exposed to higher forimtamig exposure in an ex vivo setting. T cells from responding and non-responding patients were equally fit in killing tumor cells ex vivo. Our results highlight that forimtamig treatment optimization may be possible by boosting T cell numbers over NK cells, targeting tumor intrinsic resistance mechanisms or individualized dosing approach.
I. Dekhtiarenko, Jan Attig, I. Lelios et al.· Blood Advances· 0 citations
Tumor-draining lymph nodes serve as critical sites for the generation, maintenance and differentiation of stem-like CD8⁺ T cells during antitumor immune responses. Recent evidence has shown that delivering interleukin-2 to PD1⁺ stem-like CD8⁺ T cells using PD1-IL2v, an immunocytokine combining PD-1 blockade and IL-2R agonism, promotes their differentiation into potent effector cells with enhanced tumor-killing capacity. However, it remains unclear how targeted interleukin-2 therapies imprint early stem-like T-cell differentiation programs. Here, using single-cell transcriptomics and T-cell receptor sequencing in murine pancreatic tumor models, we demonstrate that PD1-IL2v induces an early bifurcation in the differentiation of stem-like CD8⁺ T cells within tumor-draining lymph nodes. We identify an effector-primed stem-like population characterized by the expression of interferon-response genes, natural killer cell receptor genes, and Cx3cr1, consistent with activation of interleukin-2 and STAT5-associated programs. Clonal tracking revealed substantial overlap between these lymph node-derived cells and intratumoral effector populations, supporting a developmental relationship between early priming in lymph nodes and downstream effector differentiation. In contrast, an alternative stem-like state that displayed features associated with T-cell exhaustion, including increased Tox expression, was observed upon PD-1 therapy. Together, these findings identify an early branch point in stem-like T-cell differentiation and provide mechanistic insight into how PD1-IL2v circumvents exhaustion pathways to preferentially generate functional antitumor immunity.