738 Interim dose escalation of davoceticept, a conditional CD28 costimulator and dual checkpoint inhibitor, in combination with pembrolizumab in advanced malignancies (NEON-2)

• Published in: Journal for immunotherapy of cancer Vol. 10; no. Suppl 2; p. A771
• Main Authors: Lakhani, Nehal, Patnaik, Amita, McKean, Meredith, Gainor, Justin, Cathy Vo Buu, Enstrom, Amanda, Davies, Rupert, Dillon, Stacey, Zayed, Hany, Chisamore, Michael, Pluda, James Michael, Naumovski, Allison, Stanford, Peng
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group LTD 01-11-2022
• Subjects: Gastric cancer; Immunotherapy; Kidney cancer; Prostate cancer; Tumors
• ISSN: 2051-1426
• DOI: 10.1136/jitc-2022-SITC2022.0738

BackgroundPD-1/PD-L1 inhibitors (PD-(L)1i) have improved outcomes for many patients with advanced malignancies; however, most do not respond, or fail to achieve durable anti-tumor immunity. PD-1-mediated inhibition of T-cell effector function works primarily by inactivating the CD28 costimulatory signal. While PD-(L)1i can remove such inhibition, active CD28 costimulation is likely still required for optimal T-cell activation. Davoceticept is a variant CD80 vIgD-Fc fusion protein, engineered to provide PD-L1-dependent CD28 costimulation, while inhibiting PD-1 and CTLA-4. In NEON-1 (NCT04186637), davoceticept monotherapy was well-tolerated up to 10mg/kg, Q3W, and showed evidence of clinical activity in papillary renal cell carcinoma (RCC). A davoceticept + PD-1i approach is supported by preclinical models where combination treatment yielded tumor volume reductions beyond those seen with either monotherapy. Further, PD-1 inhibition may up-regulate PD-L1 in the tumor and sensitize it to PD–L1-dependent CD28 costimulation by davoceticept.MethodsNEON-2 is an open-label dose escalation and expansion study of davoceticept + pembrolizumab in adults with advanced solid tumors or lymphoma (NCT04920383). Eligibility includes tumors for which single agent PD-(L)1i are standard of care, are refractory/resistant to standard therapies, or have no standard or curative treatments available. The study employs a standard 3+3 dose-escalation design with 2 schedules of intravenous (IV) davoceticept: Q1W and Q3W. Pembrolizumab is given per label at 400mg IV Q6W. Study objectives include evaluation of safety and tolerability, identification of the recommended phase 2 dose(s) (RP2D), pharmacokinetic, pharmacodynamic, exploratory biomarker analyses, and preliminary efficacy.ResultsAs of June 2022, 19 subjects have been treated with davoceticept in dose escalation at 0.1 and 0.3mg/kg, Q1W and Q3W. Seven subjects experienced a total of 9 Grade 3+ treatment–related adverse events, including one Grade 5 cardiogenic shock in the 0.3mg/kg, Q3W cohort. Gr3+ immune-related adverse events were more common in subjects receiving 0.3 vs. 0.1mg/kg regimens of davoceticept, at 27.3% and 12.5%, respectively. Of 14 evaluable subjects, 1 confirmed partial response has been observed in a nivolumab-experienced subject with clear cell RCC. Additionally, tumor reductions have been noted in a second ongoing RCC subject, and in subjects with prostate cancer and serous peritoneal carcinoma. Fifty percent of evaluable subjects achieved a best response of stable disease.ConclusionsThe davoceticept + pembrolizumab combination has demonstrated preliminary anti-tumor activity in clear cell RCC, potentially by reversing resistance to PD-(L)1i. Dose escalation efforts will resume at 0.1mg/kg, Q1W and Q3W. Tumor-specific expansion cohorts will open once the RP2D/schedule of the combination treatment is identified.Trial RegistrationNCT04920383Ethics ApprovalThis study received ethics approval from the WCG IRB (Sarah Cannon; ID 20211877), Salus IRB (START Texas; ID START2021.28, START Midwest; ID STMW2021.18), and Mass General Brigham IRB (Massachusetts General Hospital; ID 2021P002079). All study subjects provided their informed consent to participate in this study.