Secondary failure of platelet recovery in patients treated with high-dose thiotepa and busulfan followed by autologous stem cell transplantation.
Fumiya WadaMomoko NishikoriMasakatsu HishizawaMitsumasa WatanabeAkiko AibaToshiyuki KitanoYayoi ShimazuTakero ShindoTadakazu KondoAkifumi Takaori-KondoPublished in: International journal of hematology (2020)
Autologous stem cell transplantation (ASCT) with high-dose thiotepa and busulfan is a treatment option for patients with central nervous system (CNS) lymphoma. We report here the occurrence of secondary failure of platelet recovery (SFPR) in three out of 24 patients who received high-dose thiotepa and busulfan followed by ASCT. Although there was no obvious abnormality in the primary platelet engraftment as well as the recovery of other blood cells, they developed SFPR with a median time to onset of day 38, and the platelets gradually recovered over several months with steroid therapy. During the same period, there was no development of SFPR among 50 patients who received ASCT with a conditioning regimen of MEAM (ranimustine, etoposide, cytarabine, and melphalan) or high-dose melphalan. However, one of the two patients who received a conditioning regimen of busulfan and melphalan developed SFPR, suggesting that the use of a busulfan-based conditioning regimen may be one of the risk factors for SFPR. It is important to be aware of this possible adverse effect of ASCT with high-dose thiotepa and busulfan to ensure timely diagnosis and prevention of subsequent serious complications.
Keyphrases
- high dose
- stem cell transplantation
- low dose
- allogeneic hematopoietic stem cell transplantation
- cell therapy
- acute myeloid leukemia
- emergency department
- acute lymphoblastic leukemia
- diffuse large b cell lymphoma
- risk factors
- stem cells
- cell death
- adverse drug
- replacement therapy
- smoking cessation
- hematopoietic stem cell
- cord blood