Nand Ranveer, Bryke Christine, Kroft Steven H, Divgi Ajit, Bredeson Christopher, Atallah Ehab
Division of Neoplastic Diseases and Related Disorders, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Leuk Res. 2009 Aug;33(8):1144-6. doi: 10.1016/j.leukres.2009.03.011. Epub 2009 Apr 25.
ETV6/ABL is a rare gene rearrangement that has rarely been detected in Philadelphia-negative chronic myeloproliferative disorders (C-MPD) and found to have tyrosine kinase activity similar to the BCR/ABL fusion protein. We describe a case of a 61-year-old female with a C-MPD associated with an ETV6/ABL gene rearrangement. She achieved complete cytogenetic remission on imatinib 400mg daily for 17 months, but then developed morphologic and cytogenetic relapse. After starting nilotinib 400mg orally twice daily, she achieved CCyR at 3, 6, and 11 months, suggesting that second-generation TKIs can result in favorable responses in patients with ETV6/ABL rearrangement who relapse after imatinib.
ETV6/ABL是一种罕见的基因重排,在费城阴性慢性骨髓增殖性疾病(C-MPD)中很少被检测到,并且发现其具有与BCR/ABL融合蛋白相似的酪氨酸激酶活性。我们描述了一例61岁女性C-MPD患者,其与ETV6/ABL基因重排相关。她接受每日400mg伊马替尼治疗17个月后达到完全细胞遗传学缓解,但随后出现形态学和细胞遗传学复发。在开始每日口服两次400mg尼罗替尼后,她在3个月、6个月和11个月时达到完全细胞遗传学缓解(CCyR),这表明第二代酪氨酸激酶抑制剂(TKIs)可使伊马替尼治疗后复发的ETV6/ABL重排患者产生良好反应。