Outcome of allogeneic hematopoietic stem cell transplantation for T-cell lymphoblastic leukemia/lymphoma: A single-center study. (September 2021)
- Record Type:
- Journal Article
- Title:
- Outcome of allogeneic hematopoietic stem cell transplantation for T-cell lymphoblastic leukemia/lymphoma: A single-center study. (September 2021)
- Main Title:
- Outcome of allogeneic hematopoietic stem cell transplantation for T-cell lymphoblastic leukemia/lymphoma: A single-center study
- Authors:
- Yasuda, Shunichiro
Najima, Yuho
Konishi, Tatsuya
Yamada, Yuta
Nagata, Akihito
Takezaki, Toshiaki
Kaito, Satoshi
Kurosawa, Shuhei
Sakaguchi, Masahiro
Harada, Kaito
Shingai, Naoki
Yoshioka, Kosuke
Inamoto, Kyoko
Mukae, Junichi
Toya, Takashi
Igarashi, Aiko
Shimizu, Hiroaki
Kobayashi, Takeshi
Kakihana, Kazuhiko
Sakamaki, Hisashi
Kawamata, Norihiko
Ohashi, Kazuteru
Doki, Noriko - Abstract:
- Highlights: Allo-HSCT outcomes for T-ALL/LBL and Ph-negative B-ALL were analyzed and compared. Allo-HSCT outcomes for T-ALL/LBL were comparable to those for Ph-negative B-ALL. Regardless of the disease entity, achieving CR at allo-HSCT could decrease relapse. Regardless of the disease entity, achieving CR at allo-HSCT leads to a favorable OS. Advances in treatment strategies before allo-HSCT can improve T-ALL/LBL outcomes. Abstract: Although the indications for allogeneic hematopoietic stem cell transplantation (allo-HSCT) as a treatment for T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) and Philadelphia chromosome (Ph)-negative B-cell acute lymphoblastic leukemia (B-ALL) are similar, few studies have compared its outcomes for T-ALL/LBL and Ph-negative B-ALL. The clinical data of 28 patients with T-ALL, 16 with T-LBL, and 99 with Ph-negative B-ALL who underwent the first allo-HSCT from 2000 to 2019 were retrospectively analyzed. Complete remission (CR) rates at allo-HSCT were 79 %, 63 %, and 75 % for T-ALL, T-LBL, and B-ALL, respectively; the 3-year overall survival (OS) rates were 55.7 %, 56.2 %, and 58.6 %, respectively ( p = 0.92). Univariate analysis revealed that disease subtypes were not significantly associated with OS (B-ALL vs. T-ALL: hazard ratio [HR]=0.89, p = 0.70; T-LBL vs. T-ALL: HR=0.87, p = 0.75), and CR at allo-HSCT was the only prognostic factor for OS (HR=0.25, p < 0.001). Multivariate analysis demonstrated that CR at allo-HSCT was the onlyHighlights: Allo-HSCT outcomes for T-ALL/LBL and Ph-negative B-ALL were analyzed and compared. Allo-HSCT outcomes for T-ALL/LBL were comparable to those for Ph-negative B-ALL. Regardless of the disease entity, achieving CR at allo-HSCT could decrease relapse. Regardless of the disease entity, achieving CR at allo-HSCT leads to a favorable OS. Advances in treatment strategies before allo-HSCT can improve T-ALL/LBL outcomes. Abstract: Although the indications for allogeneic hematopoietic stem cell transplantation (allo-HSCT) as a treatment for T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) and Philadelphia chromosome (Ph)-negative B-cell acute lymphoblastic leukemia (B-ALL) are similar, few studies have compared its outcomes for T-ALL/LBL and Ph-negative B-ALL. The clinical data of 28 patients with T-ALL, 16 with T-LBL, and 99 with Ph-negative B-ALL who underwent the first allo-HSCT from 2000 to 2019 were retrospectively analyzed. Complete remission (CR) rates at allo-HSCT were 79 %, 63 %, and 75 % for T-ALL, T-LBL, and B-ALL, respectively; the 3-year overall survival (OS) rates were 55.7 %, 56.2 %, and 58.6 %, respectively ( p = 0.92). Univariate analysis revealed that disease subtypes were not significantly associated with OS (B-ALL vs. T-ALL: hazard ratio [HR]=0.89, p = 0.70; T-LBL vs. T-ALL: HR=0.87, p = 0.75), and CR at allo-HSCT was the only prognostic factor for OS (HR=0.25, p < 0.001). Multivariate analysis demonstrated that CR at allo-HSCT was the only predictor of OS (HR=0.24, p < 0.001). In all three disease subtypes, patients in CR at allo-HSCT tended to have a lower cumulative incidence of relapse than did those in non-CR (T-ALL: 13.6 % vs. 50.0 %, p = 0.10; T-LBL: 20.0 % vs. 50.0 %, p = 0.21; B-ALL: 10.0 % vs. 56.0 %, p < 0.01). Thus, the outcomes of allo-HSCT for T-ALL/LBL were comparable to those of Ph-negative B-ALL. Irrespective of the disease subtypes, achieving CR before allo-HSCT was associated with a favorable OS. Further advances in chemotherapy before allo-HSCT and defining the optimal timing of allo-HSCT would improve the prognosis of patients with T-ALL/LBL. … (more)
- Is Part Of:
- Leukemia research. Volume 108(2021)
- Journal:
- Leukemia research
- Issue:
- Volume 108(2021)
- Issue Display:
- Volume 108, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 108
- Issue:
- 2021
- Issue Sort Value:
- 2021-0108-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-09
- Subjects:
- Allo-HSCT allogeneic hematopoietic stem cell transplantation -- T-ALL T-cell acute lymphoblastic leukemia -- T-LBL T-cell lymphoblastic lymphoma -- Ph Philadelphia chromosome -- B-ALL B-cell acute lymphoblastic leukemia -- CR complete remission, OS, overall survival -- HR hazard ratio -- NHL non-Hodgkin lymphoma -- CY cyclophosphamide -- TBI total body irradiation -- GVHD graft-versus-host disease -- aGVHD acute graft-versus-host disease -- PFS progression-free survival -- CIR cumulative incidence of relapse -- NRM non-relapse mortality -- CMV cytomegalovirus -- VZV varicella-zoster virus -- HHV-6 human herpesvirus 6 -- CI confidence interval
T-cell lymphoblastic leukemia -- T-cell lymphoblastic lymphoma -- Allogeneic hematopoietic stem cell transplantation
Leukemia -- Periodicals
Leukemia -- Periodicals
Leucémie -- Périodiques
Leukemia
Periodicals
Electronic journals
Electronic journals
616.9941905 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01452126 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.leukres.2021.106627 ↗
- Languages:
- English
- ISSNs:
- 0145-2126
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- Legaldeposit
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