Abou Dalle Iman, Labopin Myriam, Kröger Nicolaus, Schroeder Thomas, Finke Jürgen, Stelljes Matthias, Neubauer Andreas, Blaise Didier, Yakoub-Agha Ibrahim, Salmenniemi Urpu, Forcade Edouard, Itäla-Remes Maija, Dreger Peter, Bug Gesine, Passweg Jakob, Heuser Michael, Choi Goda, Brissot Eolia, Giebel Sebastian, Nagler Arnon, Ciceri Fabio, Bazarbachi Ali, Mohty Mohamad
Bone Marrow Transplantation Program, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Department of Haematology, Hopital Saint-Antoine, INSERM, Paris, France.
Bone Marrow Transplant. 2023 Jul;58(7):784-790. doi: 10.1038/s41409-023-01961-1. Epub 2023 Apr 11.
Pre-transplant detectable measurable residual disease (MRD) is still associated with high risk of relapse and poor outcomes in acute myeloid leukemia (AML). We aimed at evaluating the impact of disease burden on prediction of relapse and survival in patients receiving allogeneic hematopoietic cell transplantation (allo-HCT) in first remission (CR1). We identified a total of 3202 adult AML patients, of these 1776 patients were in CR1 and MRD positive and 1426 patients were primary refractory at time of transplant. After a median follow-up of 24.4 months, non-relapse mortality and relapse rate were significantly higher in the primary refractory group compared to the CR1 MRD positive group (Hazards Ratio (HR) = 1.82 (95% CI: 1.47-2.24) p < 0.001 and HR = 1.54 (95% CI: 1.34-1.77), p < 0.001), respectively. Leukemia-free survival (LFS) and overall survival (OS) were significantly worse in the primary refractory group (HR = 1.61 (95% CI: 1.44-1.81), p < 0.001 and HR = 1.71 (95% CI: 1.51-1.94), p < 0.001, respectively). Our real-life data suggest that patients in CR1 and MRD positive at time of transplant could still be salvaged by allo-HCT with a 2-year OS of 63%, if negative MRD cannot be obtained and their outcomes are significantly better than patients transplanted with active disease.
移植前可检测到的微小残留病(MRD)在急性髓系白血病(AML)中仍与高复发风险和不良预后相关。我们旨在评估疾病负担对首次缓解期(CR1)接受异基因造血细胞移植(allo-HCT)患者复发和生存预测的影响。我们共纳入了3202例成年AML患者,其中1776例患者处于CR1且MRD阳性,1426例患者在移植时为原发难治性。中位随访24.4个月后,原发难治组的非复发死亡率和复发率显著高于CR1 MRD阳性组(风险比(HR)分别为1.82(95%置信区间:1.47-2.24),p<0.001和HR = 1.54(95%置信区间:1.34-1.77),p<0.001)。原发难治组的无白血病生存期(LFS)和总生存期(OS)明显更差(HR分别为1.61(95%置信区间:1.44-1.81),p<0.001和HR = 1.71(95%置信区间:1.51-1.94),p<0.001)。我们的真实数据表明,移植时处于CR1且MRD阳性的患者如果无法获得MRD阴性结果,仍可通过allo-HCT挽救,其2年总生存率为63%,且其预后明显优于移植时患有活动性疾病的患者。