TY - JOUR
T1 - Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia
AU - Hara, Ryujiro
AU - Onizuka, Makoto
AU - Kikkawa, Eri
AU - Shiraiwa, Sawako
AU - Harada, Kaito
AU - Aoyama, Yasuyuki
AU - Ogiya, Daisuke
AU - Toyosaki, Masako
AU - Suzuki, Rikio
AU - Machida, Sinichiro
AU - Ohmachi, Ken
AU - Ogawa, Yoshiaki
AU - Kawada, Hiroshi
AU - Matsushita, Hiromichi
AU - Ando, Kiyoshi
N1 - Funding Information:
We would like to thank Editage (www.editage.com) for English language editing. The results of this study were presented in part at the 76th Japanese Society of Hematology Annual Meeting in Osaka, Japan, 2014, and at the 40th Annual Meeting of the Japan Society for Hematopoietic Cell Transplantation in Hokkaido, Japan, 2018.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2021/10
Y1 - 2021/10
N2 - The prognosis of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) has improved dramatically. Although measurable residual disease (MRD) kinetics during pretransplant treatment has been recently reported to correlate with patient outcomes, it is unclear whether prognosis is better if the MRD falls below the detection sensitivity soon after induction therapy. We retrospectively analyzed data of 37 Ph + ALL patients who were treated with autologous or allogeneic stem cell transplantation (auto-SCT, allo-SCT) at our institute from 2003 to 2019. Based on MRD kinetics, patients were divided into three groups: early responders (MRD became negative after induction therapy [n = 10, 27.0%]); late responders (MRD remained positive after induction therapy and became negative just before SCT [n = 12, 32.4%]); and poor responders (MRD was positive until just before SCT [n = 15, 40.5%]). The 5-year disease-free survival (DFS) rates for the three groups were 80.0%, 60.0%, and 29.9%, respectively (P = 0.037). The 5-year overall survival rates were not significantly different. The 5-year relapse rates were 0.0%, 31.7%, and 49.5%, respectively (P = 0.045). Non-relapse mortality (NRM) rates were similar among the three groups. Subgroup analysis for the cases that received posttransplantation tyrosine kinase inhibitor maintenance therapy revealed that DFS was similarly dependent on MRD kinetics (P = 0.022). This study clarified that MRD kinetics was a significant prognosticator for DFS and relapse rate in Ph + ALL.
AB - The prognosis of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) has improved dramatically. Although measurable residual disease (MRD) kinetics during pretransplant treatment has been recently reported to correlate with patient outcomes, it is unclear whether prognosis is better if the MRD falls below the detection sensitivity soon after induction therapy. We retrospectively analyzed data of 37 Ph + ALL patients who were treated with autologous or allogeneic stem cell transplantation (auto-SCT, allo-SCT) at our institute from 2003 to 2019. Based on MRD kinetics, patients were divided into three groups: early responders (MRD became negative after induction therapy [n = 10, 27.0%]); late responders (MRD remained positive after induction therapy and became negative just before SCT [n = 12, 32.4%]); and poor responders (MRD was positive until just before SCT [n = 15, 40.5%]). The 5-year disease-free survival (DFS) rates for the three groups were 80.0%, 60.0%, and 29.9%, respectively (P = 0.037). The 5-year overall survival rates were not significantly different. The 5-year relapse rates were 0.0%, 31.7%, and 49.5%, respectively (P = 0.045). Non-relapse mortality (NRM) rates were similar among the three groups. Subgroup analysis for the cases that received posttransplantation tyrosine kinase inhibitor maintenance therapy revealed that DFS was similarly dependent on MRD kinetics (P = 0.022). This study clarified that MRD kinetics was a significant prognosticator for DFS and relapse rate in Ph + ALL.
KW - Dasatinib
KW - Hematopoietic stem cell transplantation
KW - Imatinib
KW - Measurable residual disease
KW - Philadelphia chromosome-positive acute lymphoblastic leukemia
KW - Tyrosine kinase inhibitor
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U2 - 10.1007/s00277-021-04587-9
DO - 10.1007/s00277-021-04587-9
M3 - Article
C2 - 34247299
AN - SCOPUS:85110640488
SN - 0939-5555
VL - 100
SP - 2479
EP - 2486
JO - Annals of Hematology
JF - Annals of Hematology
IS - 10
ER -