Division of Internal Medicine, National Kidney and Transplant Institute, Quezon City, Philippines.
Division of Internal Medicine, National Kidney and Transplant Institute, Quezon City, Philippines.
Transplant Proc. 2024 Apr;56(3):738-741. doi: 10.1016/j.transproceed.2024.03.004. Epub 2024 Mar 26.
Treatment-free remission (TFR) in chronic myeloid leukemia (CML) is achieved when a patient who has discontinued tyrosine-kinase inhibitor treatment sustains major molecular response (MMR) and does not require restarting therapy. The feasibility of kidney transplantation (KT), and achieving TFR post-transplantation in patients with a pre-existing CML, are currently not well-studied.
We describe the clinical course of a 39-year-old Filipino woman with IgA nephropathy who developed CML during treatment. She received nilotinib 600 mg daily and was able to achieve MMR after 5 months. Eight years later, the patient sustained MMR; however, she ultimately underwent KT due to advancing kidney disease. Before the transplant, she was able to achieve deep molecular response. In anticipation of possible drug-to-drug interaction of nilotinib with tacrolimus and everolimus, a shared decision was made to discontinue nilotinib despite not fulfilling the criteria for TFR. Twelve months post-transplant, the patient remains in MMR without nilotinib. Good renal allograft function was maintained, and there were no signs of allograft rejection.
Attempting TFR may be feasible after KT in patients with low-risk chronic phase CML especially if good molecular response is obtained before the transplant. Data regarding the length at which TFR can be maintained after KT is still yet to be determined. In this regard, low-risk chronic phase CML in good disease control may not be considered a contraindication to KT.
慢性髓性白血病(CML)患者停止酪氨酸激酶抑制剂治疗后维持主要分子反应(MMR)且无需重新开始治疗时可实现无治疗缓解(TFR)。目前,对于已有 CML 的患者,进行肾移植(KT)的可行性以及移植后实现 TFR 的情况尚未得到充分研究。
我们描述了一名 39 岁菲律宾女性的临床病程,她患有 IgA 肾病并在治疗期间发生 CML。她接受了每天 600 毫克尼洛替尼治疗,5 个月后达到 MMR。8 年后,患者维持 MMR,但由于肾脏疾病进展,最终进行了 KT。在移植前,她达到了深度分子反应。由于担心尼洛替尼与他克莫司和依维莫司之间可能发生药物相互作用,尽管不符合 TFR 标准,但还是做出了停用尼洛替尼的共同决策。移植后 12 个月,患者仍处于 MMR 状态且未使用尼洛替尼。良好的肾移植功能得以维持,且无移植排斥迹象。
对于低危慢性期 CML 患者,尤其是在移植前获得良好分子反应的患者,在 KT 后尝试 TFR 可能是可行的。关于 KT 后 TFR 可维持的时间长度的数据仍有待确定。在这方面,控制良好的低危慢性期 CML 可能不被视为 KT 的禁忌症。