Acute Erythroid Leukemia Post-Chemo-Radiotherapy and Autologous Stem Cell Transplantation Due to Multiple Myeloma: Tracing the Paths to Leukemic Transformation.
Gábor MéhesAttila MokánszkiAnikó UjfalusiZsuzsanna HevessyZsófia MiltényiLajos GergelyJudit BedekovicsPublished in: International journal of molecular sciences (2024)
The clinical impact of therapy-related acute leukemias is increasing with the extension of cancer-related survival; however, the origins remain largely unknown. Acute erythroleukemia (AEL), a rare unfavorable type of myeloid neoplasia, may also develop secondary to cytotoxic therapy. The disorder is featured by specific genetic alterations, most importantly multi-allelic mutations of the TP53 gene. While AEL might appear as a part of the therapy-related MDS/AML, spectrum information regarding the genetic complexity and progression is largely missing. We present two AEL cases arising after cytotoxic therapy and melphalan-based myeloablation/autologous peripheral stem cell transplantation due to multiple myeloma (MM). As stated, multiple pathogenic TP53 variants were present unrelated to preexisting MM, in parallel with uninvolved/wild-type hemopoiesis. Potential mechanisms of leukemic transformation are discussed, which include (1) preexisting preneoplastic hemopoietic stem cells (HSC) serving as the common origin for both MM and AEL, (2) the generation and intramedullary survival of p53-deficient post-chemotherapy HSCs, (3) reinoculation of mobilized autologous TP53 mutated HSCs, and (4) melphalan treatment-related late-onset myelodysplasia/leukemia with newly acquired TP53 mutations.
Keyphrases
- stem cell transplantation
- high dose
- acute myeloid leukemia
- bone marrow
- late onset
- stem cells
- liver failure
- multiple myeloma
- cell therapy
- wild type
- drug induced
- copy number
- respiratory failure
- aortic dissection
- locally advanced
- squamous cell carcinoma
- healthcare
- early stage
- low dose
- mesenchymal stem cells
- photodynamic therapy
- climate change
- radiation therapy
- immune response
- combination therapy
- dendritic cells
- peripheral blood
- cord blood
- acute lymphoblastic leukemia
- replacement therapy
- genome wide identification