Bristol Myers Squibb, Princeton, NJ, USA.
Bristol Myers Squibb, 3033 Science Park Rd, San Diego, CA, 92121, USA.
Dig Dis Sci. 2024 Jun;69(6):2044-2054. doi: 10.1007/s10620-024-08391-z. Epub 2024 Apr 3.
Ozanimod showed efficacy and safety in the phase 2 STEPSTONE study conducted in patients with moderately to severely active Crohn's disease.
This analysis assessed the effects of ozanimod on circulating lymphocytes in Crohn's disease.
Patients received ozanimod 0.92 mg for 12 weeks. Lymphocyte subtypes were evaluated using multicolor flow analysis on blood samples collected before treatment and on Week 12. Absolute lymphocyte count changes were analyzed by Wilcoxon signed rank tests. Disease activity changes and efficacy outcomes were evaluated at Week 12, and associations with lymphocyte subtype levels were assessed using Spearman's correlation and logistic regression.
Reductions in median total T, Th, and cytotoxic T cells occurred at Week 12 (45.4%-76.8%), with reductions in most subtypes of 47.5% to 91.3% (P < 0.001). CD8 terminally differentiated effector memory cells were largely unaffected (median change, - 19%; P = 0.44). Reductions in median total B cells occurred at Week 12 (76.7%), with reductions in subtypes of 71.4% to 81.7% (P < 0.001). Natural killer and monocyte cell counts were unchanged. Greater baseline levels and changes in nonswitched memory B cells were significantly associated with clinical, endoscopic, and histologic efficacy (P < 0.05, all comparisons).
Ozanimod reduced circulating levels of all B-cell and most T-cell subsets but not monocytes or natural killer cells. Key subsets relevant to immune surveillance were not reduced, supporting the low risk of infection and malignancy with ozanimod in chronic inflammatory diseases. Levels of nonswitched memory B cells were associated with efficacy, providing a potential marker for ozanimod response.
ClinicalTrials.gov: NCT02531113, EudraCT: 2015-002025-19.
奥扎莫德在中度至重度活动克罗恩病患者中进行的 2 期 STEPSTONE 研究中显示出疗效和安全性。
本分析评估奥扎莫德对克罗恩病循环淋巴细胞的影响。
患者接受奥扎莫德 0.92mg 治疗 12 周。在治疗前和第 12 周采集血样,用多色流式分析评估淋巴细胞亚群。采用 Wilcoxon 符号秩检验分析淋巴细胞计数的变化。在第 12 周评估疾病活动度变化和疗效结果,并使用 Spearman 相关和逻辑回归评估与淋巴细胞亚群水平的相关性。
第 12 周时,中位数总 T、Th 和细胞毒性 T 细胞减少(45.4%-76.8%),大多数亚型减少 47.5%至 91.3%(P<0.001)。CD8 终末分化效应记忆细胞基本不受影响(中位数变化,-19%;P=0.44)。第 12 周时中位数总 B 细胞减少(76.7%),各亚型减少 71.4%至 81.7%(P<0.001)。自然杀伤细胞和单核细胞计数无变化。基线水平较高且无转换记忆 B 细胞变化与临床、内镜和组织学疗效显著相关(P<0.05,所有比较)。
奥扎莫德降低了所有 B 细胞和大多数 T 细胞亚群的循环水平,但不降低单核细胞或自然杀伤细胞。与免疫监视相关的关键亚群未减少,支持奥扎莫德在慢性炎症性疾病中感染和恶性肿瘤的风险低。无转换记忆 B 细胞水平与疗效相关,为奥扎莫德反应提供了一个潜在的标志物。
ClinicalTrials.gov:NCT02531113,EudraCT:2015-002025-19。