Superior Survival After Unrelated Allogeneic Stem Cell Transplantation With Low-Dose ATG Compared to Low-Dose TBI in Myeloablative Fludarabine/Busulfan-Based Regimen for MDS on Behalf of the Adult MDS Working Group of the JS']JSTCT

被引:0
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作者
Fujioka, Machiko [1 ,2 ]
Itonaga, Hidehiro [3 ]
Nakazawa, Hideyuki [4 ]
Nishida, Tetsuya [5 ]
Kataoka, Keisuke [6 ]
Ikeda, Takashi [7 ]
Kako, Shinichi [8 ]
Matsuoka, Ken-ichi [9 ]
Adachi, Koji [10 ]
Fujiwara, Shin-ichiro [11 ]
Aotsuka, Nobuyuki [12 ]
Kawakita, Toshiro [13 ]
Sakaida, Emiko [14 ]
Kanda, Yoshinobu [8 ,11 ]
Ichinohe, Tatsuo [15 ]
Atsuta, Yoshiko [16 ,17 ]
Miyazaki, Yasushi [2 ,18 ]
Ishiyama, Ken [19 ]
机构
[1] Sasebo City Gen Hosp, Dept Hematol, Sasebo, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Dept Hematol, Atom Bomb Dis & Hibakusha Med Unit, Nagasaki, Japan
[3] Nagasaki Univ Hosp, Transfus & Cell Therapy Unit, 1-7-1 Sakamoto, Nagasaki, Japan
[4] Shinshu Univ, Sch Med, Dept Hematol, Matsumoto, Japan
[5] Nagoya Daiichi Hosp, Dept Hematol, Japanese Red Cross Aichi Med Ctr, Nagoya, Japan
[6] Keio Univ, Sch Med, Dept Med, Div Hematol, Tokyo, Japan
[7] Shizuoka Canc Ctr, Div Hematol & Stem Cell Transplantat, Shizuoka, Japan
[8] Jichi Med Univ, Saitama Med Ctr, Div Hematol, Saitama, Japan
[9] Okayama Univ Hosp, Dept Hematol & Oncol, Okayama, Japan
[10] Natl Hosp Org, Dept Hematol & Oncol, Yonago Med Ctr, Yoneko, Japan
[11] Jichi Med Univ, Div Hematol, Shimotsuke, Japan
[12] Japanese Red Cross Soc Narita Hosp, Div Hematol Oncol, Narita, Japan
[13] NHO Kumamoto Med Ctr, Dept Hematol, Kumamoto, Japan
[14] Chiba Univ Hosp, Dept Hematol, Chiba, Japan
[15] Hiroshima Univ, Res Inst Radiat Biol & Med, Dept Hematol & Oncol, Hiroshima, Japan
[16] Japanese Data Ctr Hematopoiet Cell Transplantat, Nagakute, Japan
[17] Aichi Med Univ, Sch Med, Dept Registry Sci Transplant & Cellular Therapy, Nagakute, Japan
[18] Nagasaki Univ Hosp, Dept Hematol, Nagasaki, Japan
[19] Natl Ctr Global Hlth & Med, Ctr Hosp, Dept Hematol, Tokyo, Japan
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2025年 / 31卷 / 01期
基金
日本学术振兴会;
关键词
Myelodysplastic; syndrome; Allogeneic hematopoi-etic stem cell; transplantation; ATG; TBI; Unrelated donor; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; ACUTE MYELOID-LEUKEMIA; DAILY INTRAVENOUS BUSULFAN; RELAPSE-FREE SURVIVAL; MYELODYSPLASTIC SYNDROME; RETROSPECTIVE ANALYSIS; CONDITIONING REGIMEN; SOMATIC MUTATIONS; RISK-FACTORS;
D O I
10.1016/j.jtct.2024.09.026
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The fludarabine/intravenous busulfan 12.8 mg/kg (FB4) regimen is an effective conditioning regimen in allogeneic hematopoietic stem cell transplantation for myelodysplastic syndrome (MDS); however, limited data is available on the prognostic impact of FB4 with low-dose anti-thymoglobulin (ATG <= 5 mg/kg) or low-dose total body irradiation (TBI <= 4 Gy). Therefore, we retrospectively evaluated the outcomes in 280 adults with de novo MDS who underwent their first transplantation from an unrelated donor between 2009 and 2018. Median age was 61 years (range, 16 to 70 years). In the FB4 alone (FB4), FB4 plus ATG (FB4-ATG), and FB4 plus TBI (FB4-TBI) groups, 3-years overall survival (OS) rates were 39.9%, 64.8%, and 43.7%; 3-years nonrelapse mortality (NRM) were 32.1%, 22.1%, and 27.1%; and 3-years relapse incidences were 34.7%, 21.2%, and 28.9%, respectively. The multivariate analyses showed that FB4-ATG group significantly correlated with better OS (hazard Ratio [HR], 0.51; 95% confidence interval [CI], 0.27 to 0.95; P = .032) than FB4 group. FB4-ATG group tended to correlate with lower NRM (HR, 0.36; 95% CI, 0.13 to 1.06; P = .063) than FB4 group. In comparison with FB4-TBI group, FB4-ATG group showed better OS (HR 0.52, 95% CI 0.27 to 0.99, P = .049) and NRM (HR 0.034, 95% CI 0.11 to 0.92, P = .034). No significant differences were observed in OS and NRM between the FB4-TBI and FB4 groups. The present study demonstrated that the FB4 plus low-dose ATG regimen improved OS and NRM, but FB4 plus low-dose TBI regimen had no clear benefit over FB4 alone, in MDS patients who used unrelated donors.
引用
收藏
页码:18e1 / 18e12
页数:12
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