Triche Lisa, Yarbrough Angela, Roth Michael, Ying Anita, Wells Robert
MD Anderson Cancer Center, University of Texas, Houston, Texas, USA.
Pediatr Hematol Oncol. 2020 Aug;37(5):375-379. doi: 10.1080/08880018.2020.1751755. Epub 2020 Apr 29.
We report a patient who developed chronic myelogenous leukemia (CML) at 12 months of age. She was treated aggressively with stem cell transplant (SCT), interferon, donor lymphocytes and imatinib, with subsequent molecular progression. She received dasatinib, achieving a complete molecular response. Dasatinib was discontinued at 3 years but she had a molecular recurrence. Dasatinib was restarted and continued for 5 additional years with a second major molecular remission (MMR). While on dasatinib therapy she suffered growth failure and was treated with concurrent growth hormone (GH). After discontinuing dasatinib and GH, catch-up growth continues and she remains in MMR. Discontinuation of TKI therapy and the toxicity of long-term TKI therapy is discussed.
我们报告了一名在12个月大时患上慢性粒细胞白血病(CML)的患者。她接受了积极的干细胞移植(SCT)、干扰素、供体淋巴细胞和伊马替尼治疗,但随后出现分子进展。她接受了达沙替尼治疗,实现了完全分子缓解。达沙替尼在3年后停药,但她出现了分子复发。达沙替尼重新开始使用,并持续了另外5年,实现了第二次主要分子缓解(MMR)。在接受达沙替尼治疗期间,她出现了生长发育迟缓,并接受了生长激素(GH)联合治疗。停用达沙替尼和GH后,追赶生长持续,她仍处于MMR状态。本文讨论了酪氨酸激酶抑制剂(TKI)治疗的停药以及长期TKI治疗的毒性。