TY - JOUR
T1 - High-Dose Chemotherapy with Autologous Stem Cell Transplantation in Primary Central Nervous System Lymphoma
T2 - Data From the Japan Society for Hematopoietic Cell Transplantation Registry
AU - for the Adult Lymphoma Working Group of the Japan Society for Hematopoietic Cell Transplantation
AU - Kondo, Eisei
AU - Ikeda, Takashi
AU - Izutsu, Koji
AU - Chihara, Dai
AU - Shimizu-Koresawa, Risa
AU - Fujii, Nobuharu
AU - Sakai, Tomoyuki
AU - Kondo, Tadakazu
AU - Kubo, Kohmei
AU - Kato, Yuichi
AU - Akasaka, Takashi
AU - Fukuda, Takahiro
AU - Ichinohe, Tatsuo
AU - Atsuta, Yoshiko
AU - Suzumiya, Junji
AU - Suzuki, Ritsuro
N1 - Funding Information:
We retrospectively analyzed clinical data collected through the Transplant Registry Unified Management Program (TRUMP)sponsored by the JSHCT and the Japanese Data Center for Hematopoietic Cell Transplantation [18,19]. The TRUMP collects pretreatment patient characteristics and renews data on survival and disease status annually using follow-up forms. The inclusion criteria in this retrospective analysis included patients with PCNSL who received a first HDT/ASCT between 2006 and 2015. The Institutional Review Board of the Kawasaki Medical School Hospital, where this study was carried out, approved this retrospective study. We thank all the physicians and data managers at the hospitals and centers who contributed valuable data on transplantation to the Japan Society for Hematopoietic Cell Transplantation registry. Financial disclosure: None. Conflict of interest statement: There are no conflicts of interest to report. Authorship statement: E.K. T.I. J.S. and R.S. participated actively in the study conception and design; N.F. T.I. T.S. T.K. K.K. and T.A. provided patient data; T.F. T.I. and Y.A. contributed to the administrative support of the study; E.K. conducted the data analysis and interpretation and wrote the first draft of the manuscript; E.K. K.I. D.C. and R.S.K. critically revised the manuscript; and all authors approved the final version.
Publisher Copyright:
© 2019 American Society for Blood and Marrow Transplantation
PY - 2019/5
Y1 - 2019/5
N2 - High-dose chemotherapy (HDT)with autologous stem cell transplantation (ASCT)has been shown to improve the prognosis of patients with central nervous system (CNS)lymphoma. We queried the Japan Society for Hematopoietic Cell Transplantation Registry for 2006 to 2015 to analyze the outcomes of 102 patients with primary CNS lymphoma (PCNSL)who underwent first HDT/ASCT. The median patient age was 54 years (range, 20 to 74 years), and 65 patients were treated in an upfront setting. With a median duration of follow-up of 44 months, the 5-year overall survival (OS)and progession-free survival (PFS)were 54.9% and 38.4%, respectively. There were no significant differences in OS and PFS between upfront and salvage HDT/ASCT. Because thiotepa, a key agent in HDT/ASCT for PCNSL, has been unavailable since 2011 in Japan, the HDT regimens used were not uniform. Thiotepa-containing HDT was received by 16 out of 32 patients before 2010, but by only 2 of 70 patients after 2011. Thiotepa-containing HDT was associated with better PFS (P =.019), lower relapse (P =.042), and a trend toward a survival benefit. In multivariate analysis, noncomplete remission at HDT/ASCT was an independent predictor for OS (hazard ratio [HR], 2.40; 95% confidence interval [CI], 1.25 to 4.58; P =.008)and thiotepa-containing HDT remained significant for PFS (HR,.42; 95% CI,.19 to.95; P =.038). These results confirm the activity of thiotepa-containing regimens.
AB - High-dose chemotherapy (HDT)with autologous stem cell transplantation (ASCT)has been shown to improve the prognosis of patients with central nervous system (CNS)lymphoma. We queried the Japan Society for Hematopoietic Cell Transplantation Registry for 2006 to 2015 to analyze the outcomes of 102 patients with primary CNS lymphoma (PCNSL)who underwent first HDT/ASCT. The median patient age was 54 years (range, 20 to 74 years), and 65 patients were treated in an upfront setting. With a median duration of follow-up of 44 months, the 5-year overall survival (OS)and progession-free survival (PFS)were 54.9% and 38.4%, respectively. There were no significant differences in OS and PFS between upfront and salvage HDT/ASCT. Because thiotepa, a key agent in HDT/ASCT for PCNSL, has been unavailable since 2011 in Japan, the HDT regimens used were not uniform. Thiotepa-containing HDT was received by 16 out of 32 patients before 2010, but by only 2 of 70 patients after 2011. Thiotepa-containing HDT was associated with better PFS (P =.019), lower relapse (P =.042), and a trend toward a survival benefit. In multivariate analysis, noncomplete remission at HDT/ASCT was an independent predictor for OS (hazard ratio [HR], 2.40; 95% confidence interval [CI], 1.25 to 4.58; P =.008)and thiotepa-containing HDT remained significant for PFS (HR,.42; 95% CI,.19 to.95; P =.038). These results confirm the activity of thiotepa-containing regimens.
KW - High-dose chemotherapy/autologous stem cell transplantation
KW - Primary central nervous system lymphoma
KW - Thiotepa
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UR - http://www.scopus.com/inward/citedby.url?scp=85061454892&partnerID=8YFLogxK
U2 - 10.1016/j.bbmt.2019.01.020
DO - 10.1016/j.bbmt.2019.01.020
M3 - Article
C2 - 30664936
AN - SCOPUS:85061454892
SN - 1083-8791
VL - 25
SP - 899
EP - 905
JO - Biology of Blood and Marrow Transplantation
JF - Biology of Blood and Marrow Transplantation
IS - 5
ER -