Hirose Yuka, Kiyoi Hitoshi, Iwai Masanori, Yokozawa Toshiya, Ito Masafumi, Naoe Tomoki
Department of Infectious Diseases, Nagoya University School of Medicine, Japan.
Int J Hematol. 2002 Nov;76(4):349-53. doi: 10.1007/BF02982695.
The prognosis of patients with chronic myeloid leukemia in blastic crisis (CML-BC) remains extremely poor, and multiagent chemotherapy regimens commonly used to treat acute leukemia offer only short-term benefits. Therefore, the advent of the novel molecularly targeted anticancer agent imatinib mesylate is a breakthrough in CML therapy. We present a CML patient in megakaryoblastic crisis with severe myelofibrosis, who was treated with imatinib at a dosage of 400 mg/day and achieved complete remission together with a marked regression of myelofibrosis after 1 month. The effect of imatinib on the long-term prognosis remains unclear, although the agent is clearly a promising drug for treating CML-BC even in cases of myelofibrosis.
慢性粒细胞白血病急变期(CML-BC)患者的预后仍然极差,常用于治疗急性白血病的多药化疗方案仅能带来短期益处。因此,新型分子靶向抗癌药物甲磺酸伊马替尼的出现是CML治疗的一项突破。我们报告一例巨核细胞急变期伴严重骨髓纤维化的CML患者,该患者接受了每日400毫克剂量的伊马替尼治疗,1个月后实现完全缓解,同时骨髓纤维化明显消退。尽管伊马替尼显然是治疗CML-BC的一种有前景的药物,即使在存在骨髓纤维化的情况下也是如此,但其对长期预后的影响仍不清楚。