Allogeneic hematopoietic stem cell transplantation for adult patients with mixed phenotype acute leukemia: results of a matched-pair analysis
Adult patients with mixed phenotype acute leukemia (MPAL) have a poor prognosis, and the therapeutic role of allogeneic stem cell transplantation (allo‐SCT) for MPAL remains to be elucidated. Thus, we retrospectively assessed the efficacy of allo‐SCT for MPAL. Eighteen patients with MPAL were identi...
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Veröffentlicht in: | European journal of haematology 2015-11, Vol.95 (5), p.455-460 |
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creator | Shimizu, Hiroaki Saitoh, Takayuki Machida, Shinichiro Kako, Shinichi Doki, Noriko Mori, Takehiko Sakura, Toru Kanda, Yoshinobu Kanamori, Heiwa Miyawaki, Shuichi Okamoto, Shinichiro |
description | Adult patients with mixed phenotype acute leukemia (MPAL) have a poor prognosis, and the therapeutic role of allogeneic stem cell transplantation (allo‐SCT) for MPAL remains to be elucidated. Thus, we retrospectively assessed the efficacy of allo‐SCT for MPAL. Eighteen patients with MPAL were identified from the transplant outcome database of Kanto Study Group for Cell Therapy (KSGCT). We also selected 215 patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) as control cohorts using an optimal matching method. The 5‐yr overall survival (OS) rate of patients with MPAL was 48.1%, and patients in remission at the time of transplant showed significantly better survival than those not in remission (5‐yr OS: 71.8% vs. 0%, P = 0.001). No significant differences were seen in OS when stratifying patients according to immunophenotype, cytogenetic abnormalities, or the type of induction therapy. The 5‐yr OS rate of patients with MPAL was not significantly different compared with AML control patients (48.1% vs. 48.1%; P = 0.855) or ALL control patients (48.1% vs. 37.8%; P = 0.426). These results suggested that allo‐SCT is an effective treatment for MPAL, especially early in the disease course, and innovative transplant approaches are warranted to improve the transplant outcome of patients with MPAL who are not in remission. |
doi_str_mv | 10.1111/ejh.12516 |
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Thus, we retrospectively assessed the efficacy of allo‐SCT for MPAL. Eighteen patients with MPAL were identified from the transplant outcome database of Kanto Study Group for Cell Therapy (KSGCT). We also selected 215 patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) as control cohorts using an optimal matching method. The 5‐yr overall survival (OS) rate of patients with MPAL was 48.1%, and patients in remission at the time of transplant showed significantly better survival than those not in remission (5‐yr OS: 71.8% vs. 0%, P = 0.001). No significant differences were seen in OS when stratifying patients according to immunophenotype, cytogenetic abnormalities, or the type of induction therapy. The 5‐yr OS rate of patients with MPAL was not significantly different compared with AML control patients (48.1% vs. 48.1%; P = 0.855) or ALL control patients (48.1% vs. 37.8%; P = 0.426). These results suggested that allo‐SCT is an effective treatment for MPAL, especially early in the disease course, and innovative transplant approaches are warranted to improve the transplant outcome of patients with MPAL who are not in remission.</description><identifier>ISSN: 0902-4441</identifier><identifier>EISSN: 1600-0609</identifier><identifier>DOI: 10.1111/ejh.12516</identifier><identifier>PMID: 25605541</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; allogeneic hematopoietic stem cell transplantation ; Allografts ; Databases, Factual ; Disease-Free Survival ; Female ; Hematopoietic Stem Cell Transplantation ; Humans ; Leukemia, Biphenotypic, Acute - genetics ; Leukemia, Biphenotypic, Acute - mortality ; Leukemia, Biphenotypic, Acute - therapy ; Leukemia, Myeloid, Acute - genetics ; Leukemia, Myeloid, Acute - mortality ; Leukemia, Myeloid, Acute - therapy ; Male ; matched-pair analysis ; Middle Aged ; mixed phenotype acute leukemia ; outcomes ; Philadelphia chromosome ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy ; Survival Rate ; Unrelated Donors</subject><ispartof>European journal of haematology, 2015-11, Vol.95 (5), p.455-460</ispartof><rights>2015 John Wiley & Sons A/S. 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Thus, we retrospectively assessed the efficacy of allo‐SCT for MPAL. Eighteen patients with MPAL were identified from the transplant outcome database of Kanto Study Group for Cell Therapy (KSGCT). We also selected 215 patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) as control cohorts using an optimal matching method. The 5‐yr overall survival (OS) rate of patients with MPAL was 48.1%, and patients in remission at the time of transplant showed significantly better survival than those not in remission (5‐yr OS: 71.8% vs. 0%, P = 0.001). No significant differences were seen in OS when stratifying patients according to immunophenotype, cytogenetic abnormalities, or the type of induction therapy. The 5‐yr OS rate of patients with MPAL was not significantly different compared with AML control patients (48.1% vs. 48.1%; P = 0.855) or ALL control patients (48.1% vs. 37.8%; P = 0.426). These results suggested that allo‐SCT is an effective treatment for MPAL, especially early in the disease course, and innovative transplant approaches are warranted to improve the transplant outcome of patients with MPAL who are not in remission.</description><subject>Adolescent</subject><subject>Adult</subject><subject>allogeneic hematopoietic stem cell transplantation</subject><subject>Allografts</subject><subject>Databases, Factual</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Humans</subject><subject>Leukemia, Biphenotypic, Acute - genetics</subject><subject>Leukemia, Biphenotypic, Acute - mortality</subject><subject>Leukemia, Biphenotypic, Acute - therapy</subject><subject>Leukemia, Myeloid, Acute - genetics</subject><subject>Leukemia, Myeloid, Acute - mortality</subject><subject>Leukemia, Myeloid, Acute - therapy</subject><subject>Male</subject><subject>matched-pair analysis</subject><subject>Middle Aged</subject><subject>mixed phenotype acute leukemia</subject><subject>outcomes</subject><subject>Philadelphia chromosome</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</subject><subject>Survival Rate</subject><subject>Unrelated Donors</subject><issn>0902-4441</issn><issn>1600-0609</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1uFSEYhonR2GN14Q0YlrqYFhgGOu6app5jc1IT40_ihjDwjUPLDFNg0p6L8J6lnrY72RDI8z5feEHoLSVHtKxjuBqOKGuoeIZWVBBSEUHa52hFWsIqzjk9QK9SuiKEsJbKl-iANYI0Dacr9OfU-_AbJnAGDzDqHObgIJdTyjBiA97jHPWUZq-nrLMLE-5DxNouPuO5XMCUE751ecCjuwOL5wGmkHczYG2WDNjDcg2j0x9xhFRCCYcea1xGmQFsNWtXbJP2u-TSa_Si1z7Bm4f9EH3_dP7tbFNtv6w_n51uK8PrWlQnXBioJZENkbQXBDoKba95bxg3VreMSd5BaaYxzFombd11Bk7AslYI3bD6EL3fe-cYbhZIWY0u3b9VTxCWpKhkrGU1F6SgH_aoiSGlCL2aoxt13ClK1H37qrSv_rVf2HcP2qUbwT6Rj3UX4HgP3DoPu_-b1PnF5lFZ7ROu_MfdU0LHayVkLRv183KtLte_vrabH1t1Uf8FDuChGw</recordid><startdate>201511</startdate><enddate>201511</enddate><creator>Shimizu, Hiroaki</creator><creator>Saitoh, Takayuki</creator><creator>Machida, Shinichiro</creator><creator>Kako, Shinichi</creator><creator>Doki, Noriko</creator><creator>Mori, Takehiko</creator><creator>Sakura, Toru</creator><creator>Kanda, Yoshinobu</creator><creator>Kanamori, Heiwa</creator><creator>Miyawaki, Shuichi</creator><creator>Okamoto, Shinichiro</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201511</creationdate><title>Allogeneic hematopoietic stem cell transplantation for adult patients with mixed phenotype acute leukemia: results of a matched-pair analysis</title><author>Shimizu, Hiroaki ; Saitoh, Takayuki ; Machida, Shinichiro ; Kako, Shinichi ; Doki, Noriko ; Mori, Takehiko ; Sakura, Toru ; Kanda, Yoshinobu ; Kanamori, Heiwa ; Miyawaki, Shuichi ; Okamoto, Shinichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4336-846ce37075071f60eb1e9fa4fc24cda92274be1115c2dd27d3bbce8ed2966a523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>allogeneic hematopoietic stem cell transplantation</topic><topic>Allografts</topic><topic>Databases, Factual</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Humans</topic><topic>Leukemia, Biphenotypic, Acute - genetics</topic><topic>Leukemia, Biphenotypic, Acute - mortality</topic><topic>Leukemia, Biphenotypic, Acute - therapy</topic><topic>Leukemia, Myeloid, Acute - genetics</topic><topic>Leukemia, Myeloid, Acute - mortality</topic><topic>Leukemia, Myeloid, Acute - therapy</topic><topic>Male</topic><topic>matched-pair analysis</topic><topic>Middle Aged</topic><topic>mixed phenotype acute leukemia</topic><topic>outcomes</topic><topic>Philadelphia chromosome</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</topic><topic>Survival Rate</topic><topic>Unrelated Donors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shimizu, Hiroaki</creatorcontrib><creatorcontrib>Saitoh, Takayuki</creatorcontrib><creatorcontrib>Machida, Shinichiro</creatorcontrib><creatorcontrib>Kako, Shinichi</creatorcontrib><creatorcontrib>Doki, Noriko</creatorcontrib><creatorcontrib>Mori, Takehiko</creatorcontrib><creatorcontrib>Sakura, Toru</creatorcontrib><creatorcontrib>Kanda, Yoshinobu</creatorcontrib><creatorcontrib>Kanamori, Heiwa</creatorcontrib><creatorcontrib>Miyawaki, Shuichi</creatorcontrib><creatorcontrib>Okamoto, Shinichiro</creatorcontrib><creatorcontrib>Kanto Study Group for Cell Therapy (KSGCT)</creatorcontrib><creatorcontrib>Kanto Study Group for Cell Therapy (KSGCT)</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimizu, Hiroaki</au><au>Saitoh, Takayuki</au><au>Machida, Shinichiro</au><au>Kako, Shinichi</au><au>Doki, Noriko</au><au>Mori, Takehiko</au><au>Sakura, Toru</au><au>Kanda, Yoshinobu</au><au>Kanamori, Heiwa</au><au>Miyawaki, Shuichi</au><au>Okamoto, Shinichiro</au><aucorp>Kanto Study Group for Cell Therapy (KSGCT)</aucorp><aucorp>Kanto Study Group for Cell Therapy (KSGCT)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Allogeneic hematopoietic stem cell transplantation for adult patients with mixed phenotype acute leukemia: results of a matched-pair analysis</atitle><jtitle>European journal of haematology</jtitle><addtitle>Eur J Haematol</addtitle><date>2015-11</date><risdate>2015</risdate><volume>95</volume><issue>5</issue><spage>455</spage><epage>460</epage><pages>455-460</pages><issn>0902-4441</issn><eissn>1600-0609</eissn><abstract>Adult patients with mixed phenotype acute leukemia (MPAL) have a poor prognosis, and the therapeutic role of allogeneic stem cell transplantation (allo‐SCT) for MPAL remains to be elucidated. Thus, we retrospectively assessed the efficacy of allo‐SCT for MPAL. Eighteen patients with MPAL were identified from the transplant outcome database of Kanto Study Group for Cell Therapy (KSGCT). We also selected 215 patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) as control cohorts using an optimal matching method. The 5‐yr overall survival (OS) rate of patients with MPAL was 48.1%, and patients in remission at the time of transplant showed significantly better survival than those not in remission (5‐yr OS: 71.8% vs. 0%, P = 0.001). No significant differences were seen in OS when stratifying patients according to immunophenotype, cytogenetic abnormalities, or the type of induction therapy. The 5‐yr OS rate of patients with MPAL was not significantly different compared with AML control patients (48.1% vs. 48.1%; P = 0.855) or ALL control patients (48.1% vs. 37.8%; P = 0.426). These results suggested that allo‐SCT is an effective treatment for MPAL, especially early in the disease course, and innovative transplant approaches are warranted to improve the transplant outcome of patients with MPAL who are not in remission.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25605541</pmid><doi>10.1111/ejh.12516</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult allogeneic hematopoietic stem cell transplantation Allografts Databases, Factual Disease-Free Survival Female Hematopoietic Stem Cell Transplantation Humans Leukemia, Biphenotypic, Acute - genetics Leukemia, Biphenotypic, Acute - mortality Leukemia, Biphenotypic, Acute - therapy Leukemia, Myeloid, Acute - genetics Leukemia, Myeloid, Acute - mortality Leukemia, Myeloid, Acute - therapy Male matched-pair analysis Middle Aged mixed phenotype acute leukemia outcomes Philadelphia chromosome Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy Survival Rate Unrelated Donors |
title | Allogeneic hematopoietic stem cell transplantation for adult patients with mixed phenotype acute leukemia: results of a matched-pair analysis |
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