Eskazan Ahmet Emre, Sadri Sevil, Keskin Dilek, Ayer Mesut, Kantarcioglu Bulent, Demirel Naciye, Aydin Demet, Aydinli Fuat, Yokus Osman, Ozunal Isil Erdogan, Berk Selin, Yalniz Fevzi Firat, Elverdi Tugrul, Salihoglu Ayse, Ar Muhlis Cem, Ongoren Seniz, Baslar Zafer, Aydin Yildiz, Tuzuner Nukhet, Ozbek Ugur, Soysal Teoman
Division of Hematology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Department of Hematology, Haseki Training and Research Hospital, Istanbul, Turkey.
Clin Lymphoma Myeloma Leuk. 2017 Dec;17(12):804-811. doi: 10.1016/j.clml.2017.07.255. Epub 2017 Aug 4.
The molecular response at 3 months of the original imatinib (OI) in patients with chronic myeloid leukemia has prognostic significance; however, this has never been tested for generic imatinib (GI).
We evaluated the BCR-ABL1 [international reporting scale (IS)] transcript levels at 3 and 6 months to determine whether an early molecular response (EMR) had a prognostic effect on the outcome among chronic myeloid leukemia patients receiving GI. Ninety patients were divided into 2 groups, according to the imatinib they received, as OI (group A) and GI (group B).
Two groups were equally balanced for age, gender, Sokal risk score, and optimal response. The 2 groups did not differ in achieving an EMR at 3 months, and patients with EMR at 3 months had significantly superior complete cytogenetic response and major molecular response rates compared with patients who did not achieve an EMR in both groups. The percentage of an optimal response [BCR-ABL1 (IS), < 1%] and a warning response [BCR-ABL1 (IS), 1%-10%] at 6 months was 93% and 95% for groups A and B, respectively (P = .553). Patients with an optimal response (OR) at both 3 and 6 months had significantly superior event-free survival rates compared with patients without an OR in groups A and B.
The results of the present study have demonstrated most probably for the first time that an OR at 3 and 6 months in patients receiving either first-line GI and OI is clearly associated with greater response and event-free survival rates. Prospective randomized trials with larger numbers of patients and longer follow-up periods are needed to address the effect of EMR in patients receiving GI.
慢性髓性白血病患者使用原研伊马替尼(OI)3个月时的分子反应具有预后意义;然而,通用型伊马替尼(GI)尚未进行过此类测试。
我们评估了3个月和6个月时的BCR-ABL1[国际报告量表(IS)]转录水平,以确定早期分子反应(EMR)对接受GI治疗的慢性髓性白血病患者的预后是否有影响。90例患者根据所接受的伊马替尼分为两组,即OI组(A组)和GI组(B组)。
两组在年龄、性别、索卡尔风险评分和最佳反应方面均衡性相同。两组在3个月时达到EMR的情况无差异,3个月时达到EMR的患者与未达到EMR的患者相比,完全细胞遗传学反应率和主要分子反应率显著更高。A组和B组在6个月时最佳反应[BCR-ABL1(IS),<1%]和警示反应[BCR-ABL1(IS),1%-10%]的百分比分别为93%和95%(P = 0.553)。A组和B组中,3个月和6个月时均有最佳反应(OR)的患者与无OR的患者相比,无事件生存率显著更高。
本研究结果很可能首次表明,接受一线GI和OI治疗的患者在3个月和6个月时的OR与更好的反应率和无事件生存率明显相关。需要进行更多患者、更长随访期的前瞻性随机试验,以探讨EMR对接受GI治疗患者的影响。