Giordano Ugo, Piekarska Agnieszka, Prejzner Witold, Gil Lidia, Zaucha Jan Maciej, Kujawska Joanna, Dybko Zuzanna, Dudek Krzysztof, Giebel Sebastian, Dybko Jarosław
Department and Clinic of Endocrinology and Internal Medicine, Wrocław University Hospital, 50-367 Wroclaw, Poland.
Department of Hematology and Transplantology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Biomedicines. 2025 Jan 11;13(1):163. doi: 10.3390/biomedicines13010163.
: The implementation of tyrosine kinase inhibitors (TKIs) in the treatment of chronic myeloid leukemia (CML) has brought a significant improvement in the prognosis for CML patients and a decrease in the number of patients requiring allogeneic hematopoietic stem cell transplantation (allo-HCT). Nevertheless, the impact of TKIs on allo-HCT outcomes has not been thoroughly explored. : The main endpoint of our research was to assess the impact of prior TKI treatment on acute graft-versus-host disease (aGvHD) and chronic graft-versus-host disease (cGvHD). : In our retrospective analysis, we included 240 patients treated between 1993 and 2013 and divided them into three groups according to the therapy administered prior to haploidentical, matched-related, or matched-unrelated donor allo-HCT (imatinib group = 41, dasatinib/nilotinib group = 28, TKI-naïve group = 171). : Both the cumulative incidence of aGvHD ( = 0.044) and cGvHD ( < 0.001) in individuals receiving second-generation TKIs (2G-TKIs) prior to allo-HCT were decreased compared to patients receiving no TKIs or imatinib (IMA) (40.7% vs. 61.4% vs. 70.7%, = 0.044; 25.0% vs. 76.4% vs. 51.2%, < 0.001, respectively). In the case of the 2G-TKI cohort, the number of low-grade aGvHD and cGvHD was significantly lower compared to the IMA and TKI-naïve groups ( = 0.018, = 0.004; < 0.001 versus TKI-naïve, respectively). In terms of 3-year overall survival (OS), there were no important variations between TKI-naïve, IMA, and 2G-TKI (55% vs. 49.9% vs. 69.6%, = 0.740). : The results of our study suggest that TKI treatment prior to allo-HCT may have a protective impact on immune-mediated outcomes.
酪氨酸激酶抑制剂(TKIs)在慢性髓性白血病(CML)治疗中的应用显著改善了CML患者的预后,并减少了需要接受异基因造血干细胞移植(allo-HCT)的患者数量。然而,TKIs对allo-HCT结果的影响尚未得到充分探索。
我们研究的主要终点是评估既往TKI治疗对急性移植物抗宿主病(aGvHD)和慢性移植物抗宿主病(cGvHD)的影响。
在我们的回顾性分析中,纳入了1993年至2013年间接受治疗的240例患者,并根据单倍体相合、亲缘匹配或非亲缘匹配供体allo-HCT之前所接受的治疗将他们分为三组(伊马替尼组 = 41例,达沙替尼/尼洛替尼组 = 28例,未接受TKI治疗组 = 171例)。
与未接受TKI治疗或伊马替尼(IMA)的患者相比,allo-HCT前接受第二代TKIs(2G-TKIs)治疗的患者中,aGvHD(P = 0.044)和cGvHD(P < 0.001)的累积发生率均有所降低(分别为40.7% 对61.4% 对70.7%,P = 0.044;25.0% 对76.4% 对51.2%,P < 0.001)。在2G-TKI队列中,与IMA组和未接受TKI治疗组相比,轻度aGvHD和cGvHD的病例数显著减少(P = 0.018,P = 0.004;与未接受TKI治疗组相比,P < 0.001)。在3年总生存期(OS)方面,未接受TKI治疗组、IMA组和2G-TKI组之间没有显著差异(55% 对49.9% 对69.6%,P = 0.740)。
我们的研究结果表明,allo-HCT前的TKI治疗可能对免疫介导的结果具有保护作用。