Department of Urology, Dokkyo Medical University Saitama Medical Center, Saitama, Japan.
Department of Urology, Dokkyo Medical University Saitama Medical Center, Saitama, Japan.
Transplant Proc. 2023 May;55(4):1074-1077. doi: 10.1016/j.transproceed.2023.03.058. Epub 2023 May 3.
For chronic myeloid leukemia (CML), a Philadelphia chromosome-positive myeloproliferative neoplasm, the introduction of tyrosine kinase inhibitors has transformed CML from a lethal disease into a manageable chronic disease with a close-to-normal life expectancy. Active malignancy is an absolute contraindication to kidney transplantation. However, it is controversial whether kidney transplantation can be safely performed in patients with a history of CML who are in remission. We describe the clinical course of a 64-year-old male patient with chronic kidney disease from diabetic nephropathy (DMN) who underwent living donor kidney transplantation. The patient was diagnosed with CML 15 years ago and promptly achieved cytogenetic and molecular biological remission after starting imatinib. After that, he continued imatinib treatment for 15 years and was in remission, but his chronic kidney disease from DMN gradually worsened. A preemptive living donor kidney transplant was performed in July 2020. Imatinib for CML was discontinued because the patient maintained deep molecular remission (DMR) of major molecular response for more than 15 years before kidney transplantation. After kidney transplantation, the transplanted kidney function remained good at approximate serum creatinine levels of 1.1 mg/dL without histopathologic rejection, and the 3 monthly BCR-ABL1 measurement results were negative and are in progress. Thus, he continues to maintain treatment-free remission status without imatinib for 26 months after renal transplantation. In conclusion, this result suggests that CML with long-lasting DMR on imatinib therapy can be considered an inactive malignancy and therefore a relative indication for kidney transplantation.
对于慢性髓性白血病(CML),一种费城染色体阳性的骨髓增殖性肿瘤,酪氨酸激酶抑制剂的引入已经将 CML 从一种致命疾病转变为一种可管理的慢性疾病,预期寿命接近正常。活动性恶性肿瘤是肾移植的绝对禁忌证。然而,对于处于缓解期的 CML 病史患者,肾移植是否可以安全进行仍存在争议。我们描述了一名 64 岁男性患者的临床经过,该患者患有糖尿病肾病(DMN)引起的慢性肾脏病,接受了活体供肾移植。该患者 15 年前被诊断为 CML,并在开始使用伊马替尼后迅速达到细胞遗传学和分子生物学缓解。此后,他继续接受伊马替尼治疗 15 年并处于缓解期,但他的 DMN 慢性肾脏病逐渐恶化。2020 年 7 月进行了抢先性活体供肾移植。由于患者在肾移植前已持续超过 15 年达到主要分子反应的深度分子缓解(DMR),因此停止了用于治疗 CML 的伊马替尼。肾移植后,移植肾功能保持良好,血清肌酐水平约为 1.1mg/dL,无组织病理学排斥反应,且每 3 个月的 BCR-ABL1 测量结果均为阴性,并在持续进行中。因此,他在肾移植后 26 个月继续保持无伊马替尼治疗的无治疗缓解状态。总之,这一结果表明,在伊马替尼治疗下持续存在 DMR 的 CML 可被视为非活动性恶性肿瘤,因此是肾移植的相对适应证。