Abstract Multiple myeloma (MM) remains an incurable hematologic malignancy characterized by inevitable relapse and progressively therapy-resistant disease, despite the widespread use of combination regimens and autologous stem cell transplantation (ASCT). While only ∼30% of patients achieve a complete response following initial therapy and ∼40-50% with ASCT, the durability of these responses is limited, underscoring the persistence of highly drug-refractory cellular subpopulations. Increasing evidence implicates multiple myeloma stem-like cells (MMSLCs), a CD138-/ALDH+ phenotype enriched for self-renewal, metabolic plasticity, and intrinsic chemoresistance, as key drivers of relapse. Aldehyde dehydrogenases (ALDHs) promote MM survival by detoxifying cytotoxic aldehydes and sustaining retinoic acid-dependent stemness pathways, making them attractive therapeutic targets. We report the development and characterization of KS100, a novel pan-ALDH inhibitor, which potently eliminates both bulk MM cells and MMSLC populations in treatment-naïve and treatment-resistant models in vitro and in vivo. KS100 significantly reduces clonogenic growth, exhausts the ALDH-high compartment, and synergizes with standard MM therapies, including proteasome inhibitors and IMiDs, even in models with established resistance. These findings demonstrate that ALDH inhibition disrupts a universal resistance mechanism and position KS100 as a promising therapeutic strategy to eradicate stem-like reservoirs and improve long-term disease control in MM. Citation Format: Michael J. Ingling, Robert Chitren, Krishne Gowda, Shantu Amin, Subash C. Jonnalagadda, Tulin Budak-Alpdogan, Manoj Pandey. Aldehyde dehydrogenase inhibition as a strategy to overcome drug-refractory multiple myeloma abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5721.
Ingling et al. (Fri,) studied this question.