TY - JOUR
T1 - Hematopoietic Cell Transplantation for Acute Panmyelosis with Myelofibrosis
T2 - A Retrospective Study in Japan
AU - for the Adult Acute Myeloid Leukemia Working Group of the Japan Society for Hematopoietic Cell Transplantation
AU - Konuma, Takaaki
AU - Kondo, Tadakazu
AU - Kawata, Takahito
AU - Iwato, Koji
AU - Sato, Yuji
AU - Mori, Takehiko
AU - Ohashi, Kazuteru
AU - Nakazawa, Hideyuki
AU - Sugahara, Hiroyuki
AU - Ago, Hiroatsu
AU - Eto, Tetsuya
AU - Imamura, Yutaka
AU - Fukuda, Takahiro
AU - Kanda, Yoshinobu
AU - Atsuta, Yoshiko
AU - Yano, Shingo
N1 - Publisher Copyright:
© 2018
PY - 2019/1
Y1 - 2019/1
N2 - Acute panmyelosis with myelofibrosis (APMF) is a rare subtype of acute myeloid leukemia characterized by acute onset of cytopenias and bone marrow fibrosis in the absence of splenomegaly. Because the prognosis of APMF is extremely poor even after chemotherapy, hematopoietic cell transplantation (HCT) has been used to treat APMF. However, the outcome after HCT for APMF remains unclear. To evaluate the outcomes and prognostic factors after HCT as a therapeutic modality for APMF, we retrospectively analyzed the Japanese registration data of 40 APMF patients who received allogeneic and syngeneic HCT between 2005 and 2015. The median age at HCT was 53.5 years (range, 16 to 70). The disease status at HCT was first complete remission (CR1) in 13 patients (33%). The probability of overall survival and the cumulative incidence of relapse at 3 years were 24% and 59%, respectively. Univariate analysis identified that female sex and disease status CR1 at the time of HCT were significantly associated with higher overall survival. Although APMF patients have a poor long-term prognosis even after syngeneic and allogeneic HCT, these data suggested that allogeneic HCT offered a curative option for APMF.
AB - Acute panmyelosis with myelofibrosis (APMF) is a rare subtype of acute myeloid leukemia characterized by acute onset of cytopenias and bone marrow fibrosis in the absence of splenomegaly. Because the prognosis of APMF is extremely poor even after chemotherapy, hematopoietic cell transplantation (HCT) has been used to treat APMF. However, the outcome after HCT for APMF remains unclear. To evaluate the outcomes and prognostic factors after HCT as a therapeutic modality for APMF, we retrospectively analyzed the Japanese registration data of 40 APMF patients who received allogeneic and syngeneic HCT between 2005 and 2015. The median age at HCT was 53.5 years (range, 16 to 70). The disease status at HCT was first complete remission (CR1) in 13 patients (33%). The probability of overall survival and the cumulative incidence of relapse at 3 years were 24% and 59%, respectively. Univariate analysis identified that female sex and disease status CR1 at the time of HCT were significantly associated with higher overall survival. Although APMF patients have a poor long-term prognosis even after syngeneic and allogeneic HCT, these data suggested that allogeneic HCT offered a curative option for APMF.
KW - Acute myelofibrosis
KW - Acute myeloid leukemia
KW - Acute myelosclerosis
KW - Acute panmyelosis with myelofibrosis
KW - Hematopoietic cell transplantation
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U2 - 10.1016/j.bbmt.2018.08.006
DO - 10.1016/j.bbmt.2018.08.006
M3 - Article
C2 - 30103016
AN - SCOPUS:85053309440
SN - 1083-8791
VL - 25
SP - e23-e27
JO - Biology of Blood and Marrow Transplantation
JF - Biology of Blood and Marrow Transplantation
IS - 1
ER -