Therapy-related myelodysplastic syndrome and acute myeloid leukemia after hematopoietic stem cell transplantation for lymphoma

Downloads

Download data is not yet available.
PDF (Tiếng Việt)     0    0

Abstract

Therapy - related myelodysplastic syndromes/acute myeloid leukemia (t-MDS/AML) are now considered a single entity, called therapy - related myeloid neoplasms base on the current World Health Organization classification. T-MDS/t-AML is a complication of primary malignancies including solid tumors and/or hematological neoplasms and/or non-hematological neoplasms (systemic lupus erythematosus,...) after exposure to chemotherapeutic drugs and/or radiation and/or immunosuppressant drugs. T-AML accounts for approximately 10-20% of total AML cases. Those diseases can be: Hodgkin Lymphoma, non-Hodgkin Lymphoma, acute lymphoblastic leukemia (ALL), sarcoma, ovarian and testicular cancer, autologous hematopoietic stem cell transplantation (HSCT). Several thousand autotransplants are performed each year for patients with relapsed lymphoma. Estimates of the incidence of therapy-related leukemia among these lymphoma and Hodgkin disease patients range between 1-14% at 3-15 years. The risk appears lower in patients undergoing autologous HSCT for breast cancer and myeloma. Important risk factors include age, extent of prior therapy, and exposure to certain agents before and during the transplant procedure. The current standard protocols for autologous HSCT include drugs that are known to be leukemogenic. In particular, alkylating agents (AAs) and topoisomerase II inhibitors (TIs) are associated with an increased risk for development of t-MDS/AML. They damage to normal hematopoietic stem cells and immune cells, leading to genetic mutations. The increased use of allogeneic HSCT with reducedintensity conditioning (RIC) regimens could improve outcomes for lymphoma patients who received higher dose of chemotherapy because of the lower toxicity of RIC regimens compared to standard myeloablative conditioning regimens.

https://doi.org/10.38103/jcmhch.2021.67.2

References

Daniel A. Arber, Attilio Orazi, Robert Hasserjian, Jürgen Thiele, Michael J. Borowitz, Michelle M. Le Beau, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 2016; 127 (20): 2391-2405.

Jingfang Sun, Linlin Qu, Zhengwu Guo, Wei Xu. Treatment-related acute myeloid leukemia with type D CBFB-MYH11 after chemotherapy in non-hodgkin lymphoma: a rare case report. Int J Clin Exp Med 2016; 9: 403-407.

Lucy A. Godley, Richard A. Larson. Therapyrelated Myeloid Leukemia. Semin Oncol 2008; 35(4): 418-429.

Smita Bhatia. Therapy-related myelodysplasia and acute myeloid leukemia, Semin Oncol 2013; 40(6): 667-675.

Dan Yang, Xiaorui Fu, Xudong Zhang, Wencai Li, Mingzhi Zhang. Therapy-related acute myeloid leukemia in patients with lymphoma: A report of four cases and review of the literature. Oncology Letters 2015; 10: 3261-3265.

S Yamasaki, R Suzuki, K Hatano, K Fukushima, H Lida, S Morishima, et al. Therapy-related acute myeloid leukemia and myelodysplastic syndrome after hematopoietic cell transplantation for lymphoma. Bone Marrow Transplantation 2017; 52: 969-976.

John Kuruvilla. The role of autologous and allogeneic stem cell transplantation in the management of indolent B-cell lymphoma. Blood 2016; 127 (17): 2093-2100.

Michael Zach Koontz, Sandra J. Horning, Raymond Balise, Peter L. Greenberg, Saul A. Rosenberg, Richard T. Hoppe, et al. Risk of therapy-related secondary leukemia in Hodgkin lymphoma: the Stanford University experience over three generations of clinical trials. J Clin Oncol 2013; 31: 592-598.

Delwail V, Jail JP, Colonna P, Andrieu JM. Fifteen-year secondary leukemia risk observed in 761 patients with Hodgkin’s disease prospectively treatd by MOPP or ABVD chemotherapy plus high-dose irradiation. Br J Haematol 2002; 118: 189-194.

Krishnan A, Bhatia S, Slovak ML, Arber DA, Niland JC, Nademanee A, et al. Predictors of therapy-related leukemia and myelodysplasia following autologous transplantation for lymphoma: an assessment of risk factors. Blood 2000; 95: 1588-1593.

Milligan DW, Ruiz De Elvira MC, Kolb HJ, Goldstone AH, Meloni G, Rohatiner AZ, et al. Secondary leukaemia and myelodysplasia after autografting for lymphoma: results from the EBMT. EBMT Lymphoma and Late Effects Working Parties. European Group for Blood and Marrow Transplantation. Br J Haematol 1999; 106: 1020-1026.

Bhatia S, Ramsay K, Steinbuch M, Dusenbery K, Shapiro R, Weisdorf D, et al. Malignant neoplasms following bone marrow transplatation. Blood 1996; 87: 3633-3639.

Friedberg JW, Neuberg D, Stone R, Alyea E, Jallow H, LaCase A, et al. Outcome of patients with myelodysplastic syndrome after autologous bone marrow transplantation for non-Hodgkin lymphoma. J Clin Oncol 1999; 17: 3128-3135.

Published 05-01-2025
Fulltext
PDF (Tiếng Việt)     0    0
Language
Issue No. 67 (2021)
Section Review
DOI 10.38103/jcmhch.2021.67.2
Keywords t-MDS/AML, ghép tế bào gốc tạo máu, u lympho t-MDS/AML, hematopoietic stem cell transplantation, lymphoma

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Copyright (c) 2021 Journal of Clinical Medicine Hue Central Hospital

Nghiem, N. D. D., & Triet, L. P. M. (2025). Therapy-related myelodysplastic syndrome and acute myeloid leukemia after hematopoietic stem cell transplantation for lymphoma. Journal of Clinical Medicine Hue Central Hospital, (67), 9–12. https://doi.org/10.38103/jcmhch.2021.67.2