| Literature DB >> 36136227 |
Shiho Taniguchi1, Sae Utsumi1, Yu Kochi1, Yuki Taya2, Yasuo Mori3, Yu-Ichiro Semba1,4, Takeshi Sugio1, Kohta Miyawaki5, Yoshikane Kikushige4, Yuya Kunisaki4, Goichi Yoshimoto1, Akihiko Numata1, Koji Kato1, Naoyuki Uchida2, Takahiro Maeda5, Toshihiro Miyamoto1, Shuichi Taniguchi2, Koichi Akashi1.
Abstract
Donor-derived hematological malignancies have been recognized as rare but serious late complications in allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients. Most cases in the literature were diagnosed as myelodysplastic syndrome or acute leukemia, with very few malignant lymphoma reported. We herein present another case of donor-derived Burkitt lymphoma that occurred 9 years after allo-HSCT under continued administration of immunosuppressants for chronic graft-versus-host disease (GVHD). The patient achieved a partial response after rituximab-combined intensive chemotherapy. To reduce the risk of relapse and to avoid organ toxicities due to repeated chemotherapies, we performed upfront high-dose chemotherapy followed by stem cell rescue using donor-derived CD34+ cells, called pseudo-autologous HSCT (pASCT), and adjusted immunosuppressants appropriately. The patient remained disease-free for 23 months after pASCT without exacerbation of cGVHD. Although the observation period has been relatively short and longer follow-up is needed, pASCT may be a feasible option for donor-derived lymphoma even in patients with active cGVHD.Entities:
Keywords: Burkitt lymphoma; Donor; Hematopoietic stem cell transplantation; Next generation sequencing; Pseudo-autologous transplantation
Year: 2022 PMID: 36136227 DOI: 10.1007/s12185-022-03458-x
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.319