| Literature DB >> 31713653 |
Kiyotaka Izumi1, Junya Kanda2, Momoko Nishikori1, Yasuyuki Arai1, Takayuki Ishikawa3, Satoshi Yoshioka3, Yasunori Ueda4, Takeshi Maeda4, Akihito Yonezawa5, Naoyuki Anzai6, Toshinori Moriguchi7, Kazunori Imada8, Takashi Akasaka9, Masaharu Nohgawa10, Mitsuru Itoh11, Akiko Aiba12, Hiroko Tsunemine13, Mitsumasa Watanabe14, Tadakazu Kondo1, Akifumi Takaori-Kondo1.
Abstract
Allogeneic hematopoietic stem cell transplantation (allo-SCT) has been considered as a potentially curative treatment option for refractory or relapsed diffuse large B cell lymphoma (DLBCL) patients. However, there is little information available, especially for Japanese patients and in cord blood transplantation (CBT). We aimed to determine treatment outcomes of allo-SCT for DLBCL in the Kyoto Stem Cell Transplantation Group, a multi-institutional joint research group. Sixty-eight DLBCL patients who underwent their first allo-SCT between 2003 and 2016 were included. The median time from diagnosis to transplantation was 13.5 months. Thirty-one patients were in CR/PR at transplantation. Twenty-seven patients underwent CBT. The median follow-up for survivors was 44.2 months. Four-year overall survival (OS) and relapse-free survival (RFS) rates were 23% (95% CI, 13-35%) and 20% (95% CI, 11-31%), respectively. Cumulative incidences of non-relapse mortality and relapse were 23% and 57%, respectively. Patients in CR/PR at allo-SCT had better OS (4-year, 46% vs 4%, P < 0.001) and RFS (4-year, 36% vs 7%, P = 0.005). The source of the stem cell did not significantly affect OS (4-year, bone marrow vs cord blood vs peripheral blood, 28.6% vs 27.2% vs 6.5%, P = 0.193). In multivariate analysis, non-remission status at SCT associated with inferior OS and RFS. Duration from diagnosis to transplantation of less than 1 year associated with inferior RFS. Allo-SCT, including CBT, may be a promising therapeutic modality for DLBCL patients who have good disease control at transplantation.Entities:
Keywords: Allo-SCT; Cord blood transplantation; Diffuse large B cell lymphoma; Treatment outcome
Mesh:
Year: 2019 PMID: 31713653 DOI: 10.1007/s00277-019-03835-3
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673