Stimulus MDS-US Trial in Progress: Evaluating Sabatolimab in Combination with Hypomethylating Agents (HMAs) in Patients with Intermediate-, High-, or Very High-Risk Myelodysplastic Syndrome (MDS)

Abstract

Background Patients with intermediate-, high-, or very-high-risk myelodysplastic syndrome (I/H/vHR-MDS) need durable treatment options with favorable tolerability. Sabatolimab (MBG453) is a novel immunotherapy targeting TIM-3, an immuno-myeloid regulator expressed on immune and leukemic stem cells, but not on normal hematopoietic stem cells. Patients with higher-risk MDS experience poor outcomes and limited treatment options. HMAs are approved for the frontline management of higher-risk MDS, but 50% of HMA-treated patients experience primary failure, and most responders progress within 2 years. Novel therapies that provide improved durable outcomes with favorable safety profiles are needed for these patients. In a phase Ib study (NCT03066648), sabatolimab+HMAs demonstrated an encouraging safety-tolerability profile and emerging durable responses in patients with higher-risk MDS (64% overall response rate and approximately 84% of patients still in response after 6 months). Sabatolimab is being studied in multiple phase I-III trials within the STIMULUS program. We present the STIMULUS MDS-US trial, designed to further assess the safety and efficacy of sabatolimab+HMAs, including an oral HMA. Study Design and Methods: STIMULUS MDS-US (NCT04878432) is a nonrandomized, single-arm, open-label, phase II study evaluating the safety and efficacy of sabatolimab in combination with FDA-approved HMAs of the investigator's choice in patients with MDS in the United States. A 12-month extension phase will continue investigating safety and efficacy after 24 months of treatment. The planned enrollment is estimated to be 90 patients. The trial is currently enrolling. Eligible patients are aged ≥18 years and have treatment-naive, higher-risk MDS (IPSS-R intermediate- or high/very high-risk) not suitable for intensive chemotherapy or hematopoietic stem cell transplant. Patients will receive IV sabatolimab 800 mg on day 8 (D8; or once between D5-8 to coincide with partner HMA administration) of each 28-day cycle for 24 months plus the investigator's choice of the following HMAs: oral decitabine (Inqovi®, decitabine 35 mg and cedazuridine 100 mg, D1-5); IV decitabine (20 mg/m2, D1-5); or IV or subcutaneous azacitidine (75 mg/m2, D1-7 or D1-5+8-9). Primary end points are incidence and severity of adverse events (AEs) and serious AEs. Secondary endpoints are complete remission (CR) rate (according to International Working Group for the Prognosis for MDS), progression-free survival, overall survival, leukemia-free survival, percentage of patients with CR, marrow CR and/or partial remission, duration of CR, time to CR, and percentage of patients with improvement in red blood cell/platelet transfusion independence. Figure 1View largeDownload PPTFigure 1View largeDownload PPT Close modal