Yamada Minami, Miyamura Koichi, Fujiwara Tohru, Yokoyama Hisayuki, Tomiya Yasuo, Ishizawa Kenichi, Harigae Hideo, Kameoka Junichi, Sasaki Takeshi
Department of Rheumatology and Hematology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tohoku J Exp Med. 2004 Sep;204(1):79-84. doi: 10.1620/tjem.204.79.
We described here four patients diagnosed with Philadelphia chromosome positive (Ph+) leukemia, consisting of chronic myeloid leukemia (CML) (n=2) and Ph+ acute lymphoblastic leukemia (ALL) (n=2). All patients were treated with imatinib mesylate (300-400 mg/day) for the treatment of relapsed CML after allogeneic hematopoietic stem cell transplantation (SCT) (n=2), relapsed Ph+ ALL after SCT (n=1), and Ph+ ALL preceding SCT (n=1). Significant clinical and molecular responses were observed in all patients and three of them achieved sustained molecular remission. Imatinib was well tolerated and did not induce noticeable graft versus host disease although one patient presented severe skin rash (Grade III). Notably, serum cyclosporine A concentration increased after the initiation of imatinib treatment, probably through competitive inhibition of P450 3A4 isoenzyme. Our data suggest that imatinib in conjunction with SCT for the Ph+ leukemia may be a promising treatment strategy.
我们在此描述了4例诊断为费城染色体阳性(Ph+)白血病的患者,其中包括慢性髓性白血病(CML)(n = 2)和Ph+急性淋巴细胞白血病(ALL)(n = 2)。所有患者均接受甲磺酸伊马替尼(300 - 400 mg/天)治疗,用于治疗异基因造血干细胞移植(SCT)后复发的CML(n = 2)、SCT后复发的Ph+ ALL(n = 1)以及SCT前的Ph+ ALL(n = 1)。所有患者均观察到显著的临床和分子反应,其中3例实现了持续分子缓解。伊马替尼耐受性良好,尽管有1例患者出现严重皮疹(III级),但未诱发明显的移植物抗宿主病。值得注意的是,伊马替尼治疗开始后血清环孢素A浓度升高,可能是通过对P450 3A4同工酶的竞争性抑制。我们的数据表明,伊马替尼联合SCT治疗Ph+白血病可能是一种有前景的治疗策略。