Iurlo A, Cattaneo D, Consonni D, Castagnetti F, Miggiano M C, Binotto G, Bonifacio M, Rege-Cambrin G, Tiribelli M, Lunghi F, Gozzini A, Pregno P, Abruzzese E, Capodanno I, Bucelli C, Pizzuti M, Artuso S, Iezza M, Scalzulli E, La Barba G, Maggi A, Russo S, Elena C, Scortechini A R, Tafuri A, Latagliata R, Caocci G, Bocchia M, Galimberti S, Luciano L, Fava C, Foà R, Saglio G, Rosti G, Breccia M
Hematology Division, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Front Pharmacol. 2023 Mar 23;14:1154377. doi: 10.3389/fphar.2023.1154377. eCollection 2023.
TKIs long-term treatment in CML may lead to persistent adverse events (AEs) that can promote relevant morbidity and mortality. Consequently, TKIs dose reduction is often used to prevent AEs. However, data on its impact on successful treatment-free remission (TFR) are quite scarce. We conducted a retrospective study on the outcome of CML subjects who discontinued low-dose TKIs from 54 Italian hematology centers participating in the Campus CML network. Overall, 1.785 of 5.108 (35.0%) regularly followed CML patients were treated with low-dose TKIs, more frequently due to relevant comorbidities or AEs (1.288, 72.2%). TFR was attempted in 248 (13.9%) subjects, all but three while in deep molecular response (DMR). After a median follow-up of 24.9 months, 172 (69.4%) patients were still in TFR. TFR outcome was not influenced by gender, Sokal/ELTS risk scores, prior interferon, number and last type of TKI used prior to treatment cessation, DMR degree, reason for dose reduction or median TKIs duration. Conversely, TFR probability was significantly better in the absence of resistance to any prior TKI. In addition, patients with a longer DMR duration before TKI discontinuation (i.e., >6.8 years) and those with an e14a2 transcript type showed a trend towards prolonged TFR. It should also be emphasized that only 30.6% of our cases suffered from molecular relapse, less than reported during full-dose TKI treatment. The use of low-dose TKIs does not appear to affect the likelihood of achieving a DMR and thus trying a treatment withdrawal, but might even promote the TFR rate.
酪氨酸激酶抑制剂(TKIs)用于慢性粒细胞白血病(CML)的长期治疗可能会导致持续的不良事件(AE),进而增加相关的发病率和死亡率。因此,TKIs减量常常被用于预防不良事件。然而,关于其对无治疗缓解(TFR)成功与否影响的数据却相当匮乏。我们对参与校园CML网络的54家意大利血液学中心中停用低剂量TKIs的CML患者的结局进行了一项回顾性研究。总体而言,5108例规律随访的CML患者中有1785例(35.0%)接受了低剂量TKIs治疗,更多是由于相关合并症或不良事件(1288例,72.2%)。248例(13.9%)患者尝试进行TFR,除3例患者外,其余均处于深度分子反应(DMR)状态。经过24.9个月的中位随访,172例(69.4%)患者仍处于TFR状态。TFR结局不受性别、索卡尔/欧洲白血病网络(ELTS)风险评分、既往干扰素使用情况、停药前使用的TKI数量及最后一种类型、DMR程度、减量原因或TKIs中位疗程的影响。相反,对任何既往TKI均无耐药性的患者,其TFR概率显著更高。此外,在停用TKI前DMR持续时间较长(即>6.8年)的患者以及具有e14a2转录本类型的患者显示出TFR延长的趋势。还应强调的是,我们的病例中只有30.6%发生分子复发,低于全剂量TKI治疗期间报告的比例。使用低剂量TKIs似乎不会影响实现DMR并因此尝试停药的可能性,但甚至可能提高TFR率。