Coffey David G, Ataca Atilla Pinar, Atilla Erden, Landgren Ola, Cowan Andrew J, Simon Sylvain, Pont Margot J, Comstock Melissa L, Hill Geoffrey R, Riddell Stanley R, Green Damian J
Myeloma Division, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL.
Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Blood. 2025 Jan 9;145(2):220-233. doi: 10.1182/blood.2024025231.
Chimeric antigen receptor (CAR) T cells and bispecific antibodies targeting B-cell maturation antigen (BCMA) have significantly advanced the treatment of relapsed and refractory multiple myeloma. Resistance to BCMA-targeting therapies, nonetheless, remains a significant challenge. BCMA shedding by γ-secretase is a known resistance mechanism, and preclinical studies suggest that inhibition may improve anti-BCMA therapy. Leveraging a phase 1 clinical trial of the γ-secretase inhibitor (GSI), crenigacestat, with anti-BCMA CAR T cells (FCARH143), we used single-nuclei RNA sequencing and assay for transposase-accessible chromatin sequencing to characterize the effects of GSI on the tumor microenvironment. The most significant impacts of GSI involved effects on monocytes, which are known to promote tumor growth. In addition to observing a reduction in the frequency of nonclassical monocytes, we also detected significant changes in gene expression, chromatin accessibility, and inferred cell-cell interactions after exposure to GSI. Although many genes with altered expression are associated with γ-secretase-dependent signaling, such as Notch, other pathways were affected, indicating GSI has far-reaching effects. Finally, we detected monoallelic deletion of the BCMA locus in some patients with prior exposure to anti-BCMA therapy, which significantly correlated with reduced progression-free survival (PFS; median PFS, 57 vs 861 days). GSIs are being explored in combination with the full spectrum of BCMA-targeting agents, and our results reveal widespread effects of GSI on both tumor and immune cell populations, providing insight into mechanisms for enhancing BCMA-directed therapies.
嵌合抗原受体(CAR)T细胞和靶向B细胞成熟抗原(BCMA)的双特异性抗体显著推动了复发难治性多发性骨髓瘤的治疗。然而,对靶向BCMA疗法的耐药性仍然是一个重大挑战。γ-分泌酶导致的BCMA脱落是一种已知的耐药机制,临床前研究表明抑制γ-分泌酶可能会改善抗BCMA治疗。利用γ-分泌酶抑制剂(GSI)克雷尼加司他与抗BCMA CAR T细胞(FCARH143)的1期临床试验,我们使用单核RNA测序和转座酶可及染色质测序分析来表征GSI对肿瘤微环境的影响。GSI最显著的影响涉及对单核细胞的作用,已知单核细胞可促进肿瘤生长。除了观察到非经典单核细胞频率降低外,我们还检测到暴露于GSI后基因表达、染色质可及性以及推断的细胞间相互作用发生了显著变化。尽管许多表达改变的基因与γ-分泌酶依赖性信号传导相关,如Notch,但其他途径也受到影响,表明GSI具有广泛的作用。最后,我们在一些先前接受过抗BCMA治疗的患者中检测到BCMA基因座的单等位基因缺失,这与无进展生存期(PFS)缩短显著相关(中位PFS,57天对861天)。目前正在探索将GSI与全谱靶向BCMA药物联合使用,我们的结果揭示了GSI对肿瘤和免疫细胞群体的广泛影响,为增强BCMA导向治疗的机制提供了见解。