Indication and benefit of upfront hematopoietic stem cell transplantation for T-cell lymphoblastic lymphoma in the era of ALL-type induction therapies

Since the introduction of leukemia-type induction therapies for T-cell lymphoblastic lymphoma (T-LBL), improvements in the long-term outcomes of T-LBL have been reported. However, indications for and the appropriate timing of hematopoietic stem cell transplantation (HSCT) have not yet been establish...

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Published inScientific reports Vol. 10; no. 1; pp. 21418 - 8
Main Authors Morita-Fujita, Mari, Arai, Yasuyuki, Yoshioka, Satoshi, Ishikawa, Takayuki, Kanda, Junya, Kondo, Tadakazu, Akasaka, Takashi, Ueda, Yasunori, Imada, Kazunori, Moriguchi, Toshinori, Yago, Kazuhiro, Kitano, Toshiyuki, Yonezawa, Akihito, Nohgawa, Masaharu, Takaori-Kondo, Akifumi
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 08.12.2020
Nature Publishing Group
Nature Portfolio
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ISSN2045-2322
2045-2322
DOI10.1038/s41598-020-78334-x

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Summary:Since the introduction of leukemia-type induction therapies for T-cell lymphoblastic lymphoma (T-LBL), improvements in the long-term outcomes of T-LBL have been reported. However, indications for and the appropriate timing of hematopoietic stem cell transplantation (HSCT) have not yet been established. Therefore, we performed a multicenter retrospective cohort study of patients with T-LBL treated using leukemia-type initial therapies to compare the outcomes after HSCT at different disease stages. We enrolled 21 patients with T-LBL from a total of 11 centers, and all patients received hyper-CVAD as a leukemia-type initial regimen. HSCT was performed during the CR1/PR1 (standard disease) stage in 11 patients, while it was completed at a later or non-remission (advanced disease) stage in 10 patients. Following HSCT, the overall survival rate was significantly greater in standard disease than in advanced-disease patients (79.5% vs. 30.0% at 5 years; hazard ratio (HR) 5.97; p  = 0.03), with trend to the lower incidence of relapse in the former group (27.3% vs. 60.0% at 5 years; HR 2.29; p  = 0.19). A prognostic difference was not detected between cases treated with allogeneic and autologous HSCTs. Our study suggests that frontline HSCT may be a feasible treatment option for T-LBL, even in the era of leukemia-type initial therapy.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-020-78334-x