Breccia M, Diverio D, Pane F, Nanni M, Russo E, Biondo F, Frustaci A, Gentilini F, Alimena G
Department of Cellular Biotechnologies and Hematology, University La Sapienza, Rome, Italy.
Leuk Res. 2006 Dec;30(12):1577-9. doi: 10.1016/j.leukres.2006.03.011. Epub 2006 Apr 19.
Imatinib has become the gold standard therapy for Ph(+) CML, as it induces complete cytogenetic remission (CCR) in 75-90% of patients in chronic phase (CP), and up to 40% of these patients obtain at least a 3 log reduction of BCR/ABL transcript [Kantarjian HM, Cortes JE, O'Brien S, Luthra R, Giles F, Verstovsek S, et al. Long-term survival benefit and improved complete cytogenetic and molecular response rates with imatinib mesylate in Philadelphia chromosome-positive chronic-phase chronic myeloid leukemia after failure of interferon-alpha. Blood. 2004;104:1979-1988]. However, it is not yet stated whether continued therapy is required to maintain this response or whether imatinib may be discontinued after confirmation of a prolonged complete molecular remission (CMR). We here report on a Ph(+) CML case in long lasting CCR following interferon-alpha treatment (IFN) which reached CMR with imatinib but soon relapsed at molecular level after this latter drug discontinuation; we considered the present observation also in the light of previously reported data.
伊马替尼已成为Ph(+)慢性髓性白血病(CML)的金标准疗法,因为它能使75%至90%的慢性期(CP)患者实现完全细胞遗传学缓解(CCR),其中高达40%的患者BCR/ABL转录本至少降低3个对数级[Kantarjian HM, Cortes JE, O'Brien S, Luthra R, Giles F, Verstovsek S等。甲磺酸伊马替尼治疗α干扰素治疗失败后的费城染色体阳性慢性期慢性髓性白血病的长期生存获益及完全细胞遗传学和分子反应率的改善。《血液》。2004年;104:1979 - 1988]。然而,尚未阐明是否需要持续治疗以维持这种反应,或者在确认长期完全分子缓解(CMR)后伊马替尼是否可以停用。我们在此报告一例经α干扰素治疗(IFN)后处于长期CCR的Ph(+) CML病例,该病例使用伊马替尼达到CMR,但在停用该药物后很快在分子水平复发;我们结合先前报道的数据对目前的观察结果进行了分析。