TY - JOUR
T1 - Outcome of 93 patients with relapse or progression following allogeneic hematopoietic cell transplantation
AU - Kurosawa, Saiko
AU - Fukuda, Takahiro
AU - Tajima, Kinuko
AU - Saito, Bungo
AU - Fuji, Shigeo
AU - Yokoyama, Hiroki
AU - Kim, Sung Won
AU - Mori, Shin Ichiro
AU - Tanosaki, Ryuji
AU - Heike, Yuji
AU - Takaue, Yoichi
PY - 2009/12
Y1 - 2009/12
N2 - Relapse/progression after allogeneic hematopoietic cell transplantation (allo-HCT) remains the major cause of treatment failure. In this study, the subsequent clinical outcome was overviewed in 292 patients with leukemia/ myelodysplastic syndrome who received allo-HCT. Among them, 93 (32%) showed relapse/progression. Cohort 1 was chosen to receive no interventions with curative intent (n 5 25). Cohort 2 received reinduction chemotherapy and/or donor lymphocyte infusion (n 5 48), and Cohort 3 underwent a second allo-HCT (n 5 20). Sixty-three patients received reinduction chemotherapy, and 27 (43%) achieved subsequent complete remission (CR). The incidence of nonrelapse mortality (NRM) was similar among the three cohorts (4, 15, and 5%). The 1-year overall survival (OS) after relapse was significantly better in patients with a second HCT (58%) than in others (14%, Cohorts 1 and 2; P < .001). However, the 2-year OS did not differ between the two groups, which suggests that it is difficult to maintain CR after the second HCT. Multivariate analysis showed that reinduction chemotherapy, CR after intervention, second HCT, and longer time to post-transplant relapse were associated with improved survival. In conclusion, for patients with relapse after allo-HCT, successful reinduction chemotherapy and a second HCT may be effective for prolonging survival without excessive NRM. However, effective measures to prevent disease progression after a second HCT clearly need to be developed.
AB - Relapse/progression after allogeneic hematopoietic cell transplantation (allo-HCT) remains the major cause of treatment failure. In this study, the subsequent clinical outcome was overviewed in 292 patients with leukemia/ myelodysplastic syndrome who received allo-HCT. Among them, 93 (32%) showed relapse/progression. Cohort 1 was chosen to receive no interventions with curative intent (n 5 25). Cohort 2 received reinduction chemotherapy and/or donor lymphocyte infusion (n 5 48), and Cohort 3 underwent a second allo-HCT (n 5 20). Sixty-three patients received reinduction chemotherapy, and 27 (43%) achieved subsequent complete remission (CR). The incidence of nonrelapse mortality (NRM) was similar among the three cohorts (4, 15, and 5%). The 1-year overall survival (OS) after relapse was significantly better in patients with a second HCT (58%) than in others (14%, Cohorts 1 and 2; P < .001). However, the 2-year OS did not differ between the two groups, which suggests that it is difficult to maintain CR after the second HCT. Multivariate analysis showed that reinduction chemotherapy, CR after intervention, second HCT, and longer time to post-transplant relapse were associated with improved survival. In conclusion, for patients with relapse after allo-HCT, successful reinduction chemotherapy and a second HCT may be effective for prolonging survival without excessive NRM. However, effective measures to prevent disease progression after a second HCT clearly need to be developed.
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U2 - 10.1002/ajh.21555
DO - 10.1002/ajh.21555
M3 - Article
C2 - 19899134
AN - SCOPUS:73349090556
SN - 0361-8609
VL - 84
SP - 815
EP - 820
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 12
ER -