AI Article Synopsis

  • The introduction of tyrosine kinase inhibitors transformed chronic myeloid leukemia (CML) from a deadly disease into a manageable condition, allowing patients to live with a near-normal life expectancy.
  • A 64-year-old male with a history of CML who achieved long-term remission underwent a successful living donor kidney transplant due to chronic kidney disease caused by diabetic nephropathy.
  • Post-transplant, the patient maintained good kidney function and continued to be CML-free for 26 months without the need for imatinib, suggesting CML in sustained remission may be considered safe for kidney transplantation.

Article Abstract

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.

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Source
http://dx.doi.org/10.1016/j.transproceed.2023.03.058DOI Listing

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