Hospital Mutua de Terrassa, Barcelona, Spain.
Hospital Clínic Barcelona, Barcelona, Spain.
Leukemia. 2024 Dec;38(12):2636-2643. doi: 10.1038/s41375-024-02416-2. Epub 2024 Sep 27.
Hydroxyurea (HU) constitutes the first-line treatment in most patients with essential thrombocythemia (ET), but criteria for changing therapy are not clearly established. The prognostic value of complete hematological response (CHR) and resistance/intolerance to HU was assessed in 1080 patients from the Spanish Registry of ET, classified according to revised IPSET-Thrombosis stratification (Very low- n = 61, Low- n = 83, Intermediate- n = 261, and High-risk n = 675). With a median therapy duration of 5 years, CHR was registered in 720 (67%) patients (1-year probability 51%) and resistance/intolerance in 219 (20%) patients (5-years probability 13%). After correction by other risk factors, High-risk patients achieving CHR showed a reduced risk of arterial thrombosis (HR: 0.35, 95%CI: 0.2-0.6, p = 0.001) and a trend towards lower risk of venous thrombosis (HR: 0.45, 95%CI: 0.2-1.02, p = 0.06) whereas no association was observed for intermediate- or low-risk patients. In comparison with non-responders, intermediate- and high-risk patients achieving CHR had longer survival and lower myelofibrosis incidence. Development of resistance/intolerance to HU, mainly cytopenia, was associated with higher probability of myelofibrosis but no effect on survival or thrombotic risk was demonstrated. In conclusion, CHR with HU is associated with better outcomes and might be an early indicator for selecting candidates to second-line clinical trials.
羟基脲 (HU) 构成大多数原发性血小板增多症 (ET) 患者的一线治疗方法,但尚未明确确立改变治疗方法的标准。根据修订后的 IPSET-Thrombosis 分层标准(极低危 n = 61,低危 n = 83,中危 n = 261,高危 n = 675),对来自西班牙 ET 登记处的 1080 例患者的完全血液学反应 (CHR) 和对 HU 的耐药性/不耐受性的预后价值进行了评估。中位治疗持续时间为 5 年,720 例(67%)患者达到 CHR(1 年概率为 51%),219 例(20%)患者出现耐药性/不耐受(5 年概率为 13%)。在其他危险因素校正后,达到 CHR 的高危患者发生动脉血栓形成的风险降低(HR:0.35,95%CI:0.2-0.6,p = 0.001),静脉血栓形成的风险也呈下降趋势(HR:0.45,95%CI:0.2-1.02,p = 0.06),而中危或低危患者未观察到这种关联。与无反应者相比,达到 CHR 的中危和高危患者的生存时间更长,骨髓纤维化发生率更低。HU 耐药/不耐受的发展,主要是血细胞减少症,与更高的骨髓纤维化发生率相关,但对生存或血栓形成风险无影响。总之,HU 联合 CHR 可改善预后,可能是选择二线临床试验候选者的早期指标。