Adding melphalan to fludarabine and a myeloablative dose of busulfan improved survival after allogeneic hematopoietic stem cell transplantation in a propensity score-matched cohort of hematological malignancies

Fludarabine and a myeloablative dose of busulfan (Flu/Bu4) can improve prognosis after allogeneic hematopoietic stem cell transplantation (HSCT) with melphalan (Mel). We investigated the prognostic impact of adding Mel to Flu/Bu4 by comparing between Flu/Bu4/Mel and Flu/Bu4 groups. This study includ...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2021-07, Vol.56 (7), p.1691-1699
Hauptverfasser: Shimomura, Yoshimitsu, Hara, Masahiko, Yamamoto, Hisashi, Uchida, Naoyuki, Kawakita, Toshiro, Ashida, Takashi, Takada, Satoru, Ikeda, Takashi, Morishige, Satoshi, Maruyama, Yumiko, Wake, Atsushi, Ichinohe, Tatsuo, Fukuda, Takahiro, Takanashi, Minoko, Atsuta, Yoshiko, Ishikawa, Takayuki
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container_issue 7
container_start_page 1691
container_title Bone marrow transplantation (Basingstoke)
container_volume 56
creator Shimomura, Yoshimitsu
Hara, Masahiko
Yamamoto, Hisashi
Uchida, Naoyuki
Kawakita, Toshiro
Ashida, Takashi
Takada, Satoru
Ikeda, Takashi
Morishige, Satoshi
Maruyama, Yumiko
Wake, Atsushi
Ichinohe, Tatsuo
Fukuda, Takahiro
Takanashi, Minoko
Atsuta, Yoshiko
Ishikawa, Takayuki
description Fludarabine and a myeloablative dose of busulfan (Flu/Bu4) can improve prognosis after allogeneic hematopoietic stem cell transplantation (HSCT) with melphalan (Mel). We investigated the prognostic impact of adding Mel to Flu/Bu4 by comparing between Flu/Bu4/Mel and Flu/Bu4 groups. This study included 846 propensity score (PS)-matched patients who received either Flu/Bu4/Mel ( n  = 423) or Flu/Bu4 ( n  = 423) from 2394 patients enrolled in a multicenter prospective registry, from January 2010 to December 2016. The primary endpoint (5-year overall survival [OS]), and the prognostic impact of adding Mel was evaluated using Cox regression analysis. The study population median age was 58 (interquartile 50–64) years and 61.0% were male. Patient characteristics were well-balanced between groups. Five-year OS was 34.2% (95% confidence interval [CI]: 27.3–41.1%) and 30.1% (24.8–35.6%) in the Flu/Bu4/Mel and Flu/Bu4 groups, respectively (log-rank P  = 0.019). The adjusted hazard ratio of adding Mel was 0.77 (95% CI: 0.62–0.96) ( P  = 0.022) for the 5-year OS, and this attributed to a lower incidence of 5-year relapse (0.71, 0.56–0.90, P  = 0.005) and relapse associated mortality (0.73, 0.57–0.95, P  = 0.018). There was no statistical difference in 5-year non-relapse mortality between groups (log-rank P  = 0.855). Flu/Bu4/Mel was associated with better 5-year OS compared to Flu/Bu4 in a PS-matched cohort after allogeneic HSCT.
doi_str_mv 10.1038/s41409-021-01217-w
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We investigated the prognostic impact of adding Mel to Flu/Bu4 by comparing between Flu/Bu4/Mel and Flu/Bu4 groups. This study included 846 propensity score (PS)-matched patients who received either Flu/Bu4/Mel ( n  = 423) or Flu/Bu4 ( n  = 423) from 2394 patients enrolled in a multicenter prospective registry, from January 2010 to December 2016. The primary endpoint (5-year overall survival [OS]), and the prognostic impact of adding Mel was evaluated using Cox regression analysis. The study population median age was 58 (interquartile 50–64) years and 61.0% were male. Patient characteristics were well-balanced between groups. Five-year OS was 34.2% (95% confidence interval [CI]: 27.3–41.1%) and 30.1% (24.8–35.6%) in the Flu/Bu4/Mel and Flu/Bu4 groups, respectively (log-rank P  = 0.019). The adjusted hazard ratio of adding Mel was 0.77 (95% CI: 0.62–0.96) ( P  = 0.022) for the 5-year OS, and this attributed to a lower incidence of 5-year relapse (0.71, 0.56–0.90, P  = 0.005) and relapse associated mortality (0.73, 0.57–0.95, P  = 0.018). There was no statistical difference in 5-year non-relapse mortality between groups (log-rank P  = 0.855). 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Hara, Masahiko ; Yamamoto, Hisashi ; Uchida, Naoyuki ; Kawakita, Toshiro ; Ashida, Takashi ; Takada, Satoru ; Ikeda, Takashi ; Morishige, Satoshi ; Maruyama, Yumiko ; Wake, Atsushi ; Ichinohe, Tatsuo ; Fukuda, Takahiro ; Takanashi, Minoko ; Atsuta, Yoshiko ; Ishikawa, Takayuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-6e881216d3de8acd6b1ebfc204bac5aaa91a92f72248e8d70f3cbbfe8ec1a58c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>692/308/174</topic><topic>692/699/1541/1990</topic><topic>Busulfan</topic><topic>Care and treatment</topic><topic>Cell Biology</topic><topic>Confidence intervals</topic><topic>Dosage and administration</topic><topic>Fludarabine</topic><topic>Hematology</topic><topic>Hematopoietic stem cells</topic><topic>Internal Medicine</topic><topic>Leukemia</topic><topic>Lymphomas</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine &amp; 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We investigated the prognostic impact of adding Mel to Flu/Bu4 by comparing between Flu/Bu4/Mel and Flu/Bu4 groups. This study included 846 propensity score (PS)-matched patients who received either Flu/Bu4/Mel ( n  = 423) or Flu/Bu4 ( n  = 423) from 2394 patients enrolled in a multicenter prospective registry, from January 2010 to December 2016. The primary endpoint (5-year overall survival [OS]), and the prognostic impact of adding Mel was evaluated using Cox regression analysis. The study population median age was 58 (interquartile 50–64) years and 61.0% were male. Patient characteristics were well-balanced between groups. Five-year OS was 34.2% (95% confidence interval [CI]: 27.3–41.1%) and 30.1% (24.8–35.6%) in the Flu/Bu4/Mel and Flu/Bu4 groups, respectively (log-rank P  = 0.019). The adjusted hazard ratio of adding Mel was 0.77 (95% CI: 0.62–0.96) ( P  = 0.022) for the 5-year OS, and this attributed to a lower incidence of 5-year relapse (0.71, 0.56–0.90, P  = 0.005) and relapse associated mortality (0.73, 0.57–0.95, P  = 0.018). There was no statistical difference in 5-year non-relapse mortality between groups (log-rank P  = 0.855). Flu/Bu4/Mel was associated with better 5-year OS compared to Flu/Bu4 in a PS-matched cohort after allogeneic HSCT.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33658646</pmid><doi>10.1038/s41409-021-01217-w</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0393-4066</orcidid><orcidid>https://orcid.org/0000-0003-1410-0830</orcidid><orcidid>https://orcid.org/0000-0003-4404-2870</orcidid><orcidid>https://orcid.org/0000-0001-5952-5926</orcidid><orcidid>https://orcid.org/0000-0003-3976-5230</orcidid><orcidid>https://orcid.org/0000-0003-1018-9508</orcidid></addata></record>
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ispartof Bone marrow transplantation (Basingstoke), 2021-07, Vol.56 (7), p.1691-1699
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1476-5365
language eng
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source EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects 692/308/174
692/699/1541/1990
Busulfan
Care and treatment
Cell Biology
Confidence intervals
Dosage and administration
Fludarabine
Hematology
Hematopoietic stem cells
Internal Medicine
Leukemia
Lymphomas
Medical prognosis
Medicine
Medicine & Public Health
Melphalan
Mortality
Patient outcomes
Population studies
Public Health
Regression analysis
Statistical analysis
Stem cell transplantation
Stem Cells
Survival
Transplantation
title Adding melphalan to fludarabine and a myeloablative dose of busulfan improved survival after allogeneic hematopoietic stem cell transplantation in a propensity score-matched cohort of hematological malignancies
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