Robinson Sara, Levy Yair, Maisel Christopher, Tong Alex W
Department of Internal Medicine, Baylor University Medical Center, Dallas, Texas, USA.
BMJ Case Rep. 2014 Apr 12;2014:bcr2014203894. doi: 10.1136/bcr-2014-203894.
A 74-year-old man was previously diagnosed with BCR-ABL1-positive pre-B cell acute lymphoblastic leukaemia (pre-B ALL) based on bone marrow cytology, flow cytometry, cytogenetics and fluorescent in situ hybridisation findings. Following a highly complicated hospital course, the patient achieved cytogenetic remission by consolidated chemotherapy and the tyrosine kinase inhibitor dasatinib. He subsequently presented with relapsed pre-B ALL after 3 years in remission. In consideration of his challenging clinical history, he was started on concurrent ponatinib (45 mg daily) and bortezomib (1.3 mg/m(2) intravenous weekly). The major molecular response was achieved (<0.0893% BCR-ABL1 transcripts) after 3 months. Bone marrow now demonstrates a BCR-ABL1-negative, complete cytogenetic response. The patient continues to do well with mild thrombocytopenia and improved anaemia on bortezomib and 30 mg daily ponatinib. Our experience with a single patient suggests the feasibility of combined targeted therapy with ponatinib and bortezomib. This novel treatment approach achieved clinical remission with a manageable toxicity profile.
一名74岁男性此前根据骨髓细胞学、流式细胞术、细胞遗传学和荧光原位杂交结果被诊断为BCR-ABL1阳性前B细胞急性淋巴细胞白血病(前B-ALL)。经过一个极其复杂的住院过程,该患者通过强化化疗和酪氨酸激酶抑制剂达沙替尼实现了细胞遗传学缓解。缓解3年后,他随后出现前B-ALL复发。考虑到他具有挑战性的临床病史,开始让他同时服用波纳替尼(每日45毫克)和硼替佐米(1.3毫克/平方米,静脉注射,每周一次)。3个月后实现了主要分子反应(BCR-ABL1转录本<0.0893%)。现在骨髓显示出BCR-ABL1阴性的完全细胞遗传学反应。该患者在服用硼替佐米和每日30毫克波纳替尼的情况下,血小板减少症症状轻微且贫血有所改善,情况持续良好。我们对一名患者的经验表明,波纳替尼和硼替佐米联合靶向治疗是可行的。这种新颖的治疗方法实现了临床缓解,且毒性反应可控。