Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Centre for Trials Research, Cardiff University, Cardiff, United Kingdom.
Blood. 2023 Nov 16;142(20):1697-1707. doi: 10.1182/blood.2023020630.
Addition of gemtuzumab ozogamicin (GO) to induction chemotherapy improves outcomes in older patients with acute myeloid leukemia (AML), but it is uncertain whether a fractionated schedule provides additional benefit to a single dose. We randomized 852 older adults (median age, 68-years) with AML/high-risk myelodysplasia to GO on day 1 (GO1) or on days 1 and 4 (GO2) of course 1 induction. The median follow-up period was 50.2 months. Although complete remission (CR) rates after course 1 did not significantly differ between arms (GO2, 63%; GO1, 57%; odds ratio [OR], 0.78; P = .08), there were significantly more patients who achieved CR with a measurable residual disease (MRD)<0.1% (50% vs 41%; OR, 0.72; P = .027). This differential MRD reduction with GO2 varied across molecular subtypes, being greatest for IDH mutations. The 5-year overall survival (OS) was 29% for patients in the GO2 arm and 24% for those in the GO1 arm (hazard ratio [HR], 0.89; P = .14). In a sensitivity analysis excluding patients found to have adverse cytogenetics or TP53 mutations, the 5-year OS was 33% for GO2 and 26% for GO1 (HR, 0.83; P = .045). In total, 228 (27%) patients received an allogeneic transplantation in first remission. Posttransplant OS was superior in the GO2 arm (HR, 0.67; P = .033); furthermore, the survival advantage from GO2 in the sensitivity analysis was lost when data of patients were censored at transplantation. In conclusion, GO2 was associated with a greater reduction in MRD and improved survival in older adults with nonadverse risk genetics. This benefit from GO2 was dependent on allogeneic transplantation to translate the better leukemia clearance into improved survival. This trial was registered at www.isrctn.com as #ISRCTN 31682779.
添加吉妥珠单抗奥佐米星(GO)到诱导化疗可改善老年急性髓系白血病(AML)患者的结局,但分次给药方案是否比单次剂量更有优势尚不确定。我们将 852 例年龄≥68 岁的 AML/高危骨髓增生异常综合征患者随机分配至第 1 天(GO1)或第 1 天和第 4 天(GO2)接受 GO 诱导治疗。中位随访时间为 50.2 个月。尽管第 1 疗程后的完全缓解(CR)率在两组间无显著差异(GO2 组 63%,GO1 组 57%,比值比 [OR],0.78;P =.08),但有更多患者达到 MRD<0.1%的完全缓解(GO2 组 50%,GO1 组 41%;OR,0.72;P =.027)。GO2 导致的这种 MRD 降低在不同的分子亚型间存在差异,在 IDH 突变的患者中最为显著。GO2 组和 GO1 组的 5 年总生存(OS)率分别为 29%和 24%(风险比 [HR],0.89;P =.14)。在排除了具有不良细胞遗传学或 TP53 突变的患者后进行敏感性分析,GO2 组和 GO1 组的 5 年 OS 率分别为 33%和 26%(HR,0.83;P =.045)。总共 228(27%)例患者在首次缓解期接受了异基因移植。GO2 组的移植后 OS 更优(HR,0.67;P =.033);此外,当在移植时对患者的数据进行删失时,GO2 带来的生存优势在敏感性分析中消失。总之,GO2 与老年非不良风险遗传学患者的 MRD 降低和生存改善相关。GO2 的获益依赖于异基因移植,以将更好的白血病清除转化为更好的生存。该试验在 www.isrctn.com 上注册,编号为 ISRCTN31682779。