Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia

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 be...

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Veröffentlicht in:Annals of hematology 2021-10, Vol.100 (10), p.2479-2486
Hauptverfasser: Hara, Ryujiro, Onizuka, Makoto, Kikkawa, Eri, Shiraiwa, Sawako, Harada, Kaito, Aoyama, Yasuyuki, Ogiya, Daisuke, Toyosaki, Masako, Suzuki, Rikio, Machida, Sinichiro, Ohmachi, Ken, Ogawa, Yoshiaki, Kawada, Hiroshi, Matsushita, Hiromichi, Ando, Kiyoshi
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container_end_page 2486
container_issue 10
container_start_page 2479
container_title Annals of hematology
container_volume 100
creator Hara, Ryujiro
Onizuka, Makoto
Kikkawa, Eri
Shiraiwa, Sawako
Harada, Kaito
Aoyama, Yasuyuki
Ogiya, Daisuke
Toyosaki, Masako
Suzuki, Rikio
Machida, Sinichiro
Ohmachi, Ken
Ogawa, Yoshiaki
Kawada, Hiroshi
Matsushita, Hiromichi
Ando, Kiyoshi
description 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.
doi_str_mv 10.1007/s00277-021-04587-9
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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. 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subjects Hematology
Induction therapy
Inhibitor drugs
Leukemia
Medical prognosis
Medicine
Medicine & Public Health
Oncology
Original Article
Targeted cancer therapy
title Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia
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