Yoshimitsu Makoto, Fuji Shigeo, Utsunomiya Atae, Nakano Nobuaki, Ito Ayumu, Ito Yoshikiyo, Miyamoto Toshihiro, Suehiro Youko, Kawakita Toshiro, Moriuchi Yukiyoshi, Nakamae Hirohisa, Kanda Yoshinobu, Ichinohe Tatsuo, Fukuda Takahiro, Atsuta Yoshiko, Kato Koji
Department of Hematology and Rheumatology, Kagoshima University Hospital, Kagoshima, Japan.
Department of Hematology, Osaka International Cancer Center, Osaka, Japan.
Biol Blood Marrow Transplant. 2020 Apr;26(4):718-722. doi: 10.1016/j.bbmt.2019.12.004. Epub 2019 Dec 9.
Allogeneic hematopoietic stem cell transplantation (allo-HCT) is the only available curative treatment option for patients with aggressive adult T cell leukemia-lymphoma (ATL). Donor human T cell leukemia virus (HTLV) 1 seropositivity is a critical concern when choosing relative donors, as they are not usually recommended due solely to the occurrence of donor-derived ATL. A previous report suggested that allo-HCT with an HTLV-1-seropositive donor increased ATL-related mortality. We updated the risk assessment for choosing an HTLV-1-seropositive allo-HCT donor for ATL. Our current registry data, which include larger numbers of HTLV-1-seropositive donors and longer observation periods, revealed no significant difference in overall survival (hazard ratio [HR], 0.93; 95% confidence interval [CI], 0.70-1.24; P = .61) or cumulative incidence of either ATL-related (HR, 0.96; 95% CI, 0.64 to 1.45; P = .80) or non-ATL-related mortality (HR, 0.91; 95% CI, 0.61 to 1.37; P = .66). Similarly, when considering only patients with ATL in complete remission, there was no significant difference in overall survival (HR, 1.02; 95% CI, 0.70 to 1.49; P = .91) or cumulative incidence of either ATL-related (HR, 1.20; 95% CI, 0.66 to 2.20; P=0.54) or non-ATL-related mortality (HR, 0.86; 95% CI, 0.52-1.42; P = .66). These data indicate that selecting HTLV-1-seropositive donors might not be contraindicated for patients with ATL receiving allo-HCT if alternative donors are unavailable. Further risk assessment remains to be performed.
异基因造血干细胞移植(allo-HCT)是侵袭性成人T细胞白血病-淋巴瘤(ATL)患者唯一可用的治愈性治疗选择。供体人类T细胞白血病病毒(HTLV)1血清学阳性是选择亲属供体时的一个关键问题,因为仅由于供体来源的ATL的发生,通常不推荐选择此类供体。先前的一份报告表明,采用HTLV-1血清学阳性供体进行allo-HCT会增加ATL相关死亡率。我们更新了为ATL患者选择HTLV-1血清学阳性allo-HCT供体的风险评估。我们目前的登记数据包括更多数量的HTLV-1血清学阳性供体和更长的观察期,结果显示总体生存率(风险比[HR],0.93;95%置信区间[CI],0.70-1.24;P = 0.61)或ATL相关(HR,0.96;95% CI,0.64至1.45;P = 0.80)或非ATL相关死亡率(HR,0.91;95% CI,0.61至1.37;P = 0.66)的累积发生率均无显著差异。同样,仅考虑处于完全缓解期的ATL患者时,总体生存率(HR,1.02;95% CI,0.70至1.49;P = 0.91)或ATL相关(HR,1.20;95% CI,0.66至2.20;P = 0.54)或非ATL相关死亡率(HR,0.86;95% CI,0.52-1.42;P = 0.66)的累积发生率也无显著差异。这些数据表明,如果没有其他供体可供选择,对于接受allo-HCT的ATL患者,选择HTLV-1血清学阳性供体可能并非禁忌。仍有待进行进一步的风险评估。