{
  "abstract": "Background T cell checkpoint blockade has revolutionized cancer treatment, however, transformative clinical responses continue to be observed in only a subset of patients and tumor indications. Inherently, the finite capacity of a patient’s immune system to recognize tumor mutations as foreign antigens is a well-established factor limiting the benefit of immunotherapy. Diacylglycerol kinases zeta (DGKζ) and alpha, are expressed in T cells and play a key role modulating the intensity of T cell receptor (TCR) signaling. Through phosphorylation of the critical secondary messenger diacylglycerol (DAG) to form phosphatidic acid, DGKs act as intracellular checkpoints attenuating T cell activation and limiting recognition of tumor antigens. Preclinically, BAY2965501 has been shown to inhibit DGKζ enhancing T cell activation and resistance to immune suppression. These effects lead to improved anti-tumor activity in vitro and in vivo syngeneic mouse tumor models as a monotherapy and in combination with anti-PD-1. Thus, selective blocking of DGKζ could represent an attractive strategy to overcome the limitations of first generation immunotherapies.Methods BAY2965501 is being investigated in a FIH dose-escalation and expansion study ( NCT05614102) to evaluate safety, pharmacokinetics and pharmacodynamics, in patients with solid tumors as a monotherapy and in combination with anti-PD-1 antibody pembrolizumab. In addition, a major objective of the study is to establish proof of mechanism (PoM) and determine if DGKζ inhibition has the potential to expand anti-tumor immune responses in patients. To achieve this, the ability of BAY2965501 to enhance TCR signaling, increase T cell function and activation along with modulating the TCR repertoire was evaluated in peripheral blood (n=>100) and tumors (n=>25) across >100 patients in monotherapy and PD-1 combination cohorts.Results Treatment with BAY2965501 achieved exposures above the preclinically defined EC50 necessary for immunologically relevant enhancement of T cell function. This resulted in a dose dependent modulation of TCR signaling as measured by increased ERK phosphorylation and cytokine production in ex vivo assays. Peripherally, patients also showed >2-fold increase in in-situ T cell activation (Ki67+) compared to baseline levels. BAY2965501-induced T cell activation coincided with expansion of newly detected T cell clones both in monotherapy and anti-PD-1 combination as measured by TCRseq. In evaluable paired biopsies, >50% of patients demonstrated >2-fold increase of T cell infiltration/activation confirming DGK inhibition dependent changes in anti-tumor immunity.Conclusions BAY2965501 demonstrates pharmacodynamic PoM in monotherapy and combination, providing evidence that specific inhibition of DGKζ in patients is sufficient to modulate anti-tumor immunity.Acknowledgements Acknowledgments: BAY2965501 DGKz trial 21948 investigators and their patients that participated in the trial and provided samples for this analysisEthics Approval Data from This abstract was collected as part of clinical study NCT05614102 and has received regulatory approval from respective countries and IRBs of respective institutions participating in the trial",
  "authors": [
    {
      "affiliations": [
        "Bayer, Whippany, NJ, USA"
      ],
      "name": "David Schaer"
    },
    {
      "affiliations": [
        "Bayer AG, Wuppertal, Germany"
      ],
      "name": "Konstantin Lang"
    },
    {
      "affiliations": [
        "Bayer AG, Berlin, Germany"
      ],
      "name": "Helge G Roider"
    },
    {
      "affiliations": [
        "Bayer AG, Berlin, Germany"
      ],
      "name": "Stefanie Reif"
    },
    {
      "affiliations": [
        "Bayer AG, Berlin, Germany"
      ],
      "name": "Bart Ploeger"
    },
    {
      "affiliations": [
        "Bayer AG, Berlin, Germany"
      ],
      "name": "Nicole Schubert"
    },
    {
      "affiliations": [
        "Bayer, Whippany, NJ, USA"
      ],
      "name": "David Balli"
    },
    {
      "affiliations": [
        "Bayer AG, Berlin, Germany"
      ],
      "name": "Anke Weispfenning"
    },
    {
      "affiliations": [
        "Bayer AG, Berlin, Germany"
      ],
      "name": "Janine Noth"
    },
    {
      "affiliations": [
        "Bayer, Whippany, NJ, USA"
      ],
      "name": "Teresa Lunt"
    },
    {
      "affiliations": [
        "Bayer, Whippany, NJ, USA"
      ],
      "name": "Jasminka Cormarkovic-dragovic"
    },
    {
      "affiliations": [
        "Bayer, Mississauga, ON, Canada"
      ],
      "name": "Kristen Armstrong"
    },
    {
      "affiliations": [
        "Bayer, Mississauga, ON, Canada"
      ],
      "name": "Stephanie Lapointe"
    },
    {
      "affiliations": [
        "Bayer, Mississauga, ON, Canada"
      ],
      "name": "Annabelle Chow"
    },
    {
      "affiliations": [
        "Bayer, Cambridge, MA, USA"
      ],
      "name": "Yuko Ishii"
    },
    {
      "affiliations": [
        "Bayer AG, Basel, Switzerland"
      ],
      "name": "Christoph Mancao"
    },
    {
      "affiliations": [
        "Seoul National University Bundang Hospital, Seongnam, Republic of Korea"
      ],
      "name": "Keun-Wook Lee"
    },
    {
      "affiliations": [
        "National Cancer Center East, Chiba, Japan"
      ],
      "name": "Toshihiko Doi"
    },
    {
      "affiliations": [
        "Samsung Medical Center, Seoul, Republic of Korea"
      ],
      "name": "Seung Tae Kim"
    },
    {
      "affiliations": [
        "14Vall d’Hebron University Hospital and Vall d’Hebron Institute of Oncology, Barcelona, Spain"
      ],
      "name": "Enriqueta Felip"
    },
    {
      "affiliations": [
        "START – Barcelona HM Nou Delfos, Barcelona, Spain"
      ],
      "name": "Tatiana Hernandez-Guerrero"
    },
    {
      "affiliations": [
        "Clinica Universidad de Navarra and Cima and University of Oxford, Pamplona, Navarra, Spain"
      ],
      "name": "Ignacio Melero"
    },
    {
      "affiliations": [
        "University Hospital Antwerp (UZ Antwerp), Edegem, Belgium"
      ],
      "name": "Hans Prenen"
    },
    {
      "affiliations": [
        "University of Oxford, Oxford, UK"
      ],
      "name": "Mark R Middleton"
    },
    {
      "affiliations": [
        "Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea"
      ],
      "name": "Hye Ryun Kim"
    },
    {
      "affiliations": [
        "START Cancer Center, San Antonio, TX, USA"
      ],
      "name": "Kyriakos P Papadopoulos"
    },
    {
      "affiliations": [
        "START, Madrid, Spain"
      ],
      "name": "Ramon Yarza"
    },
    {
      "affiliations": [
        "Royal Marsden Hospital, Sutton, UK"
      ],
      "name": "Anna Minchom"
    },
    {
      "affiliations": [
        "Sarah Cannon Research Institute at HealthONE, Denver, CO, USA"
      ],
      "name": "Jason T Henry"
    },
    {
      "affiliations": [
        "Newcastle University, Newcastle, UK"
      ],
      "name": "Ruth Plummer"
    },
    {
      "affiliations": [
        "Bayer AG, Berlin, Germany"
      ],
      "name": "Dennis Kirchhoff"
    },
    {
      "affiliations": [
        "University of Birmingham, Berlin, Germany"
      ],
      "name": "Leila Khoja"
    }
  ],
  "title": "588 Selective inhibition of Diacylglycerol kinase zeta exhibits increased T cell activation and anti-tumor immunity, demonstrating pharmacodynamic proof of mechanism in the FIH trial of BAY2965501",
  "uid": "04da8885-10c9-5ff9-a8ba-d8955cd64845"
}