Efficacy and safety of autologous hematopoietic cell transplantation in elderly patients with multiple myeloma: a retrospective national multi-site cohort study
We aimed to test the efficacy and toxicity of autologous hematopoietic cell transplant (HCT) in Multiple Myeloma (MM) patients aged ≥65 years compared to patients aged 60–64. Two hundred twenty consecutive patients (age ≥65, n = 87) with MM aged 60 and above, who underwent HCT as part of an upfront...
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Veröffentlicht in: | Annals of hematology 2017-02, Vol.96 (2), p.271-278 |
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creator | Cohen, Yael C Zuckerman, Tsila Yeshurun, Moshe Perez, Galit Magen, Hila Henig, Israel Levi, Itai Shargian, Liat Trestman, Svetlana Rouvio, Uri Naparstek, Elizabeth Ganon-Elazar, Eti Avivi, Irit Ram, Ron |
description | We aimed to test the efficacy and toxicity of autologous hematopoietic cell transplant (HCT) in Multiple Myeloma (MM) patients aged ≥65 years compared to patients aged 60–64. Two hundred twenty consecutive patients (age ≥65,
n
= 87) with MM aged 60 and above, who underwent HCT as part of an upfront MM treatment, at four Israeli centers between 2000 and 2014 were included. A melphalan dose of 200 mg/m
2
was more frequent in the 60–64 age group vs. the ≥65 age group (77 vs. 57%,
p
= 0.002). There were no differences between groups in median day of neutrophil engraftment, incidence of infections, grades 3–4 mucositis, cardiovascular events, or non-relapse mortality at 100 days post HCT (4.7, vs. 5%,
p
= 0.9). A similar rate of improvement in response level was observed (36, vs. 35%,
p
= 0.87). At 3 years post HCT progression-free survival (PFS) was higher in the 60–64 age group (42 vs. 29%,
p
= 0.04); however, it was no longer so after adjustment for disease status prior to HCT (
p
= 0.49). In a Multivariate analysis, melphalan doses and age did not predict PFS. There was no difference in overall survival (OS) between age groups (
p
= 0.2). We conclude that toxicity profile, response, PFS, and OS of HCT in aged ≥65 patients with myeloma is similar to patients aged 60–64. |
doi_str_mv | 10.1007/s00277-016-2882-9 |
format | Article |
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n
= 87) with MM aged 60 and above, who underwent HCT as part of an upfront MM treatment, at four Israeli centers between 2000 and 2014 were included. A melphalan dose of 200 mg/m
2
was more frequent in the 60–64 age group vs. the ≥65 age group (77 vs. 57%,
p
= 0.002). There were no differences between groups in median day of neutrophil engraftment, incidence of infections, grades 3–4 mucositis, cardiovascular events, or non-relapse mortality at 100 days post HCT (4.7, vs. 5%,
p
= 0.9). A similar rate of improvement in response level was observed (36, vs. 35%,
p
= 0.87). At 3 years post HCT progression-free survival (PFS) was higher in the 60–64 age group (42 vs. 29%,
p
= 0.04); however, it was no longer so after adjustment for disease status prior to HCT (
p
= 0.49). In a Multivariate analysis, melphalan doses and age did not predict PFS. There was no difference in overall survival (OS) between age groups (
p
= 0.2). We conclude that toxicity profile, response, PFS, and OS of HCT in aged ≥65 patients with myeloma is similar to patients aged 60–64.</description><identifier>ISSN: 0939-5555</identifier><identifier>EISSN: 1432-0584</identifier><identifier>DOI: 10.1007/s00277-016-2882-9</identifier><identifier>PMID: 28039512</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aged ; Cohort Studies ; Female ; Hematology ; Hematopoietic Stem Cell Transplantation - adverse effects ; Hematopoietic Stem Cell Transplantation - mortality ; Hematopoietic Stem Cell Transplantation - trends ; Humans ; Israel - epidemiology ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Multiple Myeloma - diagnosis ; Multiple Myeloma - mortality ; Multiple Myeloma - therapy ; Oncology ; Original Article ; Retrospective Studies ; Survival Rate - trends ; Transplantation Conditioning - adverse effects ; Transplantation Conditioning - mortality ; Transplantation Conditioning - trends ; Transplantation, Autologous - adverse effects ; Transplantation, Autologous - mortality ; Transplantation, Autologous - trends ; Treatment Outcome</subject><ispartof>Annals of hematology, 2017-02, Vol.96 (2), p.271-278</ispartof><rights>Springer-Verlag Berlin Heidelberg 2016</rights><rights>Annals of Hematology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-96e2f99d9dc44753be49f4c716204500513a5567defeb4b928742be9d2042c5b3</citedby><cites>FETCH-LOGICAL-c372t-96e2f99d9dc44753be49f4c716204500513a5567defeb4b928742be9d2042c5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00277-016-2882-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00277-016-2882-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28039512$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cohen, Yael C</creatorcontrib><creatorcontrib>Zuckerman, Tsila</creatorcontrib><creatorcontrib>Yeshurun, Moshe</creatorcontrib><creatorcontrib>Perez, Galit</creatorcontrib><creatorcontrib>Magen, Hila</creatorcontrib><creatorcontrib>Henig, Israel</creatorcontrib><creatorcontrib>Levi, Itai</creatorcontrib><creatorcontrib>Shargian, Liat</creatorcontrib><creatorcontrib>Trestman, Svetlana</creatorcontrib><creatorcontrib>Rouvio, Uri</creatorcontrib><creatorcontrib>Naparstek, Elizabeth</creatorcontrib><creatorcontrib>Ganon-Elazar, Eti</creatorcontrib><creatorcontrib>Avivi, Irit</creatorcontrib><creatorcontrib>Ram, Ron</creatorcontrib><title>Efficacy and safety of autologous hematopoietic cell transplantation in elderly patients with multiple myeloma: a retrospective national multi-site cohort study</title><title>Annals of hematology</title><addtitle>Ann Hematol</addtitle><addtitle>Ann Hematol</addtitle><description>We aimed to test the efficacy and toxicity of autologous hematopoietic cell transplant (HCT) in Multiple Myeloma (MM) patients aged ≥65 years compared to patients aged 60–64. Two hundred twenty consecutive patients (age ≥65,
n
= 87) with MM aged 60 and above, who underwent HCT as part of an upfront MM treatment, at four Israeli centers between 2000 and 2014 were included. A melphalan dose of 200 mg/m
2
was more frequent in the 60–64 age group vs. the ≥65 age group (77 vs. 57%,
p
= 0.002). There were no differences between groups in median day of neutrophil engraftment, incidence of infections, grades 3–4 mucositis, cardiovascular events, or non-relapse mortality at 100 days post HCT (4.7, vs. 5%,
p
= 0.9). A similar rate of improvement in response level was observed (36, vs. 35%,
p
= 0.87). At 3 years post HCT progression-free survival (PFS) was higher in the 60–64 age group (42 vs. 29%,
p
= 0.04); however, it was no longer so after adjustment for disease status prior to HCT (
p
= 0.49). In a Multivariate analysis, melphalan doses and age did not predict PFS. There was no difference in overall survival (OS) between age groups (
p
= 0.2). We conclude that toxicity profile, response, PFS, and OS of HCT in aged ≥65 patients with myeloma is similar to patients aged 60–64.</description><subject>Aged</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Hematology</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Hematopoietic Stem Cell Transplantation - mortality</subject><subject>Hematopoietic Stem Cell Transplantation - trends</subject><subject>Humans</subject><subject>Israel - epidemiology</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Multiple Myeloma - diagnosis</subject><subject>Multiple Myeloma - mortality</subject><subject>Multiple Myeloma - therapy</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Retrospective Studies</subject><subject>Survival Rate - trends</subject><subject>Transplantation Conditioning - adverse effects</subject><subject>Transplantation Conditioning - mortality</subject><subject>Transplantation Conditioning - trends</subject><subject>Transplantation, Autologous - adverse effects</subject><subject>Transplantation, Autologous - mortality</subject><subject>Transplantation, Autologous - trends</subject><subject>Treatment Outcome</subject><issn>0939-5555</issn><issn>1432-0584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kc1u3SAQRlHUqLlJ-wDdVEhdkwIGY7qrovRHitRNukYYj3OJsHEBt_Lb5FFL4rTqpmxGYs58MDoIvWH0klGq3mdKuVKEspbwruNEn6ADEw0nVHbiBTpQ3Wgi6zlD5znfU8p4J_hLdMY72mjJ-AE9XI-jd9Zt2M4DznaEsuE4YruWGOJdXDM-wmRLXKKH4h12EAIuyc55CXYutvg4Yz9jCAOksOGl3sBcMv7lyxFPayh-CYCnDUKc7AdscYKSYl7AFf8T8PyUYMOOkuwLYBePMRWcyzpsr9DpaEOG18_1An3_dH179YXcfPv89erjDXGN4oXoFvio9aAHJ4SSTQ9Cj8Ip1nIqJKWSNVbKVg0wQi96zTsleA96qG3uZN9coHd77pLijxVyMfdxTfVj2bBOKqnaTqtKsZ1ydYWcYDRL8pNNm2HUPDoxuxNTnZhHJ0bXmbfPyWs_wfB34o-ECvAdyLU130H65-n_pv4GW9SbRA</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Cohen, Yael C</creator><creator>Zuckerman, Tsila</creator><creator>Yeshurun, Moshe</creator><creator>Perez, Galit</creator><creator>Magen, Hila</creator><creator>Henig, Israel</creator><creator>Levi, Itai</creator><creator>Shargian, Liat</creator><creator>Trestman, Svetlana</creator><creator>Rouvio, Uri</creator><creator>Naparstek, Elizabeth</creator><creator>Ganon-Elazar, Eti</creator><creator>Avivi, Irit</creator><creator>Ram, Ron</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20170201</creationdate><title>Efficacy and safety of autologous hematopoietic cell transplantation in elderly patients with multiple myeloma: a retrospective national multi-site cohort study</title><author>Cohen, Yael C ; Zuckerman, Tsila ; Yeshurun, Moshe ; Perez, Galit ; Magen, Hila ; Henig, Israel ; Levi, Itai ; Shargian, Liat ; Trestman, Svetlana ; Rouvio, Uri ; Naparstek, Elizabeth ; Ganon-Elazar, Eti ; Avivi, Irit ; Ram, Ron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-96e2f99d9dc44753be49f4c716204500513a5567defeb4b928742be9d2042c5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Hematology</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Hematopoietic Stem Cell Transplantation - mortality</topic><topic>Hematopoietic Stem Cell Transplantation - trends</topic><topic>Humans</topic><topic>Israel - epidemiology</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Multiple Myeloma - diagnosis</topic><topic>Multiple Myeloma - mortality</topic><topic>Multiple Myeloma - therapy</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Retrospective Studies</topic><topic>Survival Rate - trends</topic><topic>Transplantation Conditioning - adverse effects</topic><topic>Transplantation Conditioning - mortality</topic><topic>Transplantation Conditioning - trends</topic><topic>Transplantation, Autologous - adverse effects</topic><topic>Transplantation, Autologous - mortality</topic><topic>Transplantation, Autologous - trends</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cohen, Yael C</creatorcontrib><creatorcontrib>Zuckerman, Tsila</creatorcontrib><creatorcontrib>Yeshurun, Moshe</creatorcontrib><creatorcontrib>Perez, Galit</creatorcontrib><creatorcontrib>Magen, Hila</creatorcontrib><creatorcontrib>Henig, Israel</creatorcontrib><creatorcontrib>Levi, Itai</creatorcontrib><creatorcontrib>Shargian, Liat</creatorcontrib><creatorcontrib>Trestman, Svetlana</creatorcontrib><creatorcontrib>Rouvio, Uri</creatorcontrib><creatorcontrib>Naparstek, Elizabeth</creatorcontrib><creatorcontrib>Ganon-Elazar, Eti</creatorcontrib><creatorcontrib>Avivi, Irit</creatorcontrib><creatorcontrib>Ram, Ron</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Annals of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cohen, Yael C</au><au>Zuckerman, Tsila</au><au>Yeshurun, Moshe</au><au>Perez, Galit</au><au>Magen, Hila</au><au>Henig, Israel</au><au>Levi, Itai</au><au>Shargian, Liat</au><au>Trestman, Svetlana</au><au>Rouvio, Uri</au><au>Naparstek, Elizabeth</au><au>Ganon-Elazar, Eti</au><au>Avivi, Irit</au><au>Ram, Ron</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and safety of autologous hematopoietic cell transplantation in elderly patients with multiple myeloma: a retrospective national multi-site cohort study</atitle><jtitle>Annals of hematology</jtitle><stitle>Ann Hematol</stitle><addtitle>Ann Hematol</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>96</volume><issue>2</issue><spage>271</spage><epage>278</epage><pages>271-278</pages><issn>0939-5555</issn><eissn>1432-0584</eissn><abstract>We aimed to test the efficacy and toxicity of autologous hematopoietic cell transplant (HCT) in Multiple Myeloma (MM) patients aged ≥65 years compared to patients aged 60–64. Two hundred twenty consecutive patients (age ≥65,
n
= 87) with MM aged 60 and above, who underwent HCT as part of an upfront MM treatment, at four Israeli centers between 2000 and 2014 were included. A melphalan dose of 200 mg/m
2
was more frequent in the 60–64 age group vs. the ≥65 age group (77 vs. 57%,
p
= 0.002). There were no differences between groups in median day of neutrophil engraftment, incidence of infections, grades 3–4 mucositis, cardiovascular events, or non-relapse mortality at 100 days post HCT (4.7, vs. 5%,
p
= 0.9). A similar rate of improvement in response level was observed (36, vs. 35%,
p
= 0.87). At 3 years post HCT progression-free survival (PFS) was higher in the 60–64 age group (42 vs. 29%,
p
= 0.04); however, it was no longer so after adjustment for disease status prior to HCT (
p
= 0.49). In a Multivariate analysis, melphalan doses and age did not predict PFS. There was no difference in overall survival (OS) between age groups (
p
= 0.2). We conclude that toxicity profile, response, PFS, and OS of HCT in aged ≥65 patients with myeloma is similar to patients aged 60–64.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28039512</pmid><doi>10.1007/s00277-016-2882-9</doi><tpages>8</tpages></addata></record> |
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subjects | Aged Cohort Studies Female Hematology Hematopoietic Stem Cell Transplantation - adverse effects Hematopoietic Stem Cell Transplantation - mortality Hematopoietic Stem Cell Transplantation - trends Humans Israel - epidemiology Male Medicine Medicine & Public Health Middle Aged Multiple Myeloma - diagnosis Multiple Myeloma - mortality Multiple Myeloma - therapy Oncology Original Article Retrospective Studies Survival Rate - trends Transplantation Conditioning - adverse effects Transplantation Conditioning - mortality Transplantation Conditioning - trends Transplantation, Autologous - adverse effects Transplantation, Autologous - mortality Transplantation, Autologous - trends Treatment Outcome |
title | Efficacy and safety of autologous hematopoietic cell transplantation in elderly patients with multiple myeloma: a retrospective national multi-site cohort study |
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