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. 2018 Aug 8;58(3):107–121. doi: 10.3960/jslrt.18011

Table 6. Previous reports of ATL development after allo-HSCT and organ transplantation.

Year ATL Development of ATL Age, sex Transplantation Recipient
HTLV-1
Donor
HTLV-1
Immune suppression Therapy for ATL Outcome
Tamaki et al. 2006 ATL 2 months 63, F BMT + + CSP/PSL Irradiation of 3060 cGy and
rapid reduction of
immunosuppressive agents
32months
alive
Nakamizo et al. 2011 ATL 6 years 46, F BMT + + CSP Whole brain irradiation and
localised irradiation
27 months
alive
Kitamura et al. 2017 ATL 16 months 52, M BMT + - FK/PSL PSL Several
months,
PD
Kawano and
Yoshizumi et al.
2006 ATL 6 months 39, F Liver trp + + FK/PSL Discontinuation of immune
suppression agents
15 days
dead
Kawano and
Yoshizumi et al.
2006 ATL 2 years 45, M Liver trp + + FK/PSL Chemotherapy
LSG 15 ③
3 months
dead
Kawano and
Yoshizumi et al.
2006 ATL 9 months 67, M Liver trp + + FK/PSL Chemotherapy
CHOP① and CHOV-VMMV③
5 months
dead
Yoshizumi et al. 2012 ATL 4 years 48, M Liver trp - + CSP/PSL Chemotherapy 15 months
dead
Iiona et al. 2013 ATL 2 years 59, M Liver trp - + FK/PSL Chemotherapy 27 months
dead
Zanke et al. 1989 ATL 2 years 43, M Renal trp n.d. n.d. CSP/PSL Chemotherapy
CVP④
20 months
alive
Tsurumi et al. 1992 ATL 4 years 32, M Renal trp + - CSP/
mizoribine
Chemotherapy
CHOP⑥, KM2210
13 months
alive
Willizms et al. 1994 ATL 13 years 42, M Renal trp n.d. n.d. Azathioprine/PSL No treatment 1 day
dead
Jenks et al. 1995 ATL 9 months 61, M Renal trp + - CSP/azathioprine/PSL Chemotherapy
CHOP①
5 days
dead
Mouri et al. 2000 ATL 3 years 49, F Renal trp n.d. n.d. FK/
azathioprine/PSL
Chemotherapy
CHOP①
1month
dead
Ichikawa et al. 2000 ATL 10 years 42, M Renal trp - n.d. CSP/azathioprine/PSL Chemotherapy
CHOP+radiation
3months
dead
Glowacka et al. 2013 ATL 2 years 59, M Liver trp - + FK PSL alive
Glowacka et al. 2013 ATL 3 years 28, M Renal trp - n.d. FK/MMF PSL alive

In the present and previous reports of ATL development after allo-HSCT and organ transplantation (renal or liver transplantation), three cases were after allo-HSCT and 13 cases were after organ transplantation, including six cases after renal transplantation and five cases after liver transplantation. The majority of the cases were recipient-derived ATL, except for ATL development after allo-HSCT. Rapid development and progression were characteristic of ATL development after allo-HSCT and organ transplantation. At our institution, two HTLV-1 carriers who underwent allo-HSCT and renal transplantation did not develop ATL or HAM during careful follow-up.