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Hematopoietic stem cell transplantation from non-sibling matched family donors for patients with thalassemia major in Jordan
There are limited data on the outcome of patients with thalassemia receiving HSCT from non‐sibling matched family donors. Of the 341 patients with thalassemia major that underwent donor search at our center from January 2003 to December 2011, 236 (69.2%) had fully matched family donor of which 28 pa...
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Published in: | Pediatric transplantation 2016-02, Vol.20 (1), p.120-123 |
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creator | Hussein, Ayad Ahmed Al-Zaben, Abdulhadi Khattab, Eman Haroun, Anas Frangoul, Haydar |
description | There are limited data on the outcome of patients with thalassemia receiving HSCT from non‐sibling matched family donors. Of the 341 patients with thalassemia major that underwent donor search at our center from January 2003 to December 2011, 236 (69.2%) had fully matched family donor of which 28 patients (8.2%) had non‐sibling matched family donors identified. We report on seven patients with a median age of eight yr (4–21) who underwent myeloablative (n = 4) or RIC (n = 3) HSCT. The median age of the donors was 33 yr (4–47), three were parents, two first cousins, one paternal uncle, and one paternal aunt. All patients achieved primary neutrophil and platelet engraftment at a median of 18 (13–20) and 16 days (11–20), respectively. One patient developed grade II acute GVHD, and two patients developed limited chronic GVHD. One patient experienced secondary GF requiring a second transplant. At a median follow‐up of 69 months (7–110), all patients are alive and thalassemia free. Our data emphasize the need for extended family HLA typing for patients with thalassemia major in regions where there is high rate of consanguinity. Transplant from non‐sibling matched family donor can result in excellent outcome. |
doi_str_mv | 10.1111/petr.12622 |
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Of the 341 patients with thalassemia major that underwent donor search at our center from January 2003 to December 2011, 236 (69.2%) had fully matched family donor of which 28 patients (8.2%) had non‐sibling matched family donors identified. We report on seven patients with a median age of eight yr (4–21) who underwent myeloablative (n = 4) or RIC (n = 3) HSCT. The median age of the donors was 33 yr (4–47), three were parents, two first cousins, one paternal uncle, and one paternal aunt. All patients achieved primary neutrophil and platelet engraftment at a median of 18 (13–20) and 16 days (11–20), respectively. One patient developed grade II acute GVHD, and two patients developed limited chronic GVHD. One patient experienced secondary GF requiring a second transplant. At a median follow‐up of 69 months (7–110), all patients are alive and thalassemia free. Our data emphasize the need for extended family HLA typing for patients with thalassemia major in regions where there is high rate of consanguinity. Transplant from non‐sibling matched family donor can result in excellent outcome.</description><identifier>ISSN: 1397-3142</identifier><identifier>EISSN: 1399-3046</identifier><identifier>DOI: 10.1111/petr.12622</identifier><identifier>PMID: 26493691</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; beta-Thalassemia - genetics ; beta-Thalassemia - therapy ; Blood Platelets - cytology ; Child ; Child, Preschool ; Family ; Female ; Genotype ; hematopoietic stem cell transplantation ; Hematopoietic Stem Cell Transplantation - methods ; Histocompatibility Testing ; HLA Antigens - immunology ; Humans ; Jordan ; Male ; Middle Aged ; Neutrophils - cytology ; non-sibling donor ; Retrospective Studies ; thalassemia ; Tissue Donors ; Transplantation Conditioning ; Treatment Outcome ; Young Adult</subject><ispartof>Pediatric transplantation, 2016-02, Vol.20 (1), p.120-123</ispartof><rights>2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26493691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hussein, Ayad Ahmed</creatorcontrib><creatorcontrib>Al-Zaben, Abdulhadi</creatorcontrib><creatorcontrib>Khattab, Eman</creatorcontrib><creatorcontrib>Haroun, Anas</creatorcontrib><creatorcontrib>Frangoul, Haydar</creatorcontrib><title>Hematopoietic stem cell transplantation from non-sibling matched family donors for patients with thalassemia major in Jordan</title><title>Pediatric transplantation</title><addtitle>Pediatr Transplantation</addtitle><description>There are limited data on the outcome of patients with thalassemia receiving HSCT from non‐sibling matched family donors. Of the 341 patients with thalassemia major that underwent donor search at our center from January 2003 to December 2011, 236 (69.2%) had fully matched family donor of which 28 patients (8.2%) had non‐sibling matched family donors identified. We report on seven patients with a median age of eight yr (4–21) who underwent myeloablative (n = 4) or RIC (n = 3) HSCT. The median age of the donors was 33 yr (4–47), three were parents, two first cousins, one paternal uncle, and one paternal aunt. All patients achieved primary neutrophil and platelet engraftment at a median of 18 (13–20) and 16 days (11–20), respectively. One patient developed grade II acute GVHD, and two patients developed limited chronic GVHD. One patient experienced secondary GF requiring a second transplant. At a median follow‐up of 69 months (7–110), all patients are alive and thalassemia free. Our data emphasize the need for extended family HLA typing for patients with thalassemia major in regions where there is high rate of consanguinity. Transplant from non‐sibling matched family donor can result in excellent outcome.</description><subject>Adolescent</subject><subject>Adult</subject><subject>beta-Thalassemia - genetics</subject><subject>beta-Thalassemia - therapy</subject><subject>Blood Platelets - cytology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Family</subject><subject>Female</subject><subject>Genotype</subject><subject>hematopoietic stem cell transplantation</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>Histocompatibility Testing</subject><subject>HLA Antigens - immunology</subject><subject>Humans</subject><subject>Jordan</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neutrophils - cytology</subject><subject>non-sibling donor</subject><subject>Retrospective Studies</subject><subject>thalassemia</subject><subject>Tissue Donors</subject><subject>Transplantation Conditioning</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1397-3142</issn><issn>1399-3046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNo9kUFv1DAQhS0EoqVw4QcgH7mk2LFjJ0e0Ki1VoVW1wNGadSasS2Kntldlpf54vLulc5knzftGmnmEvOfslJf6NGOOp7xWdf2CHHPRdZVgUr3ca10JLusj8ialO8a4kq18TY5qJTuhOn5MHi9wghzm4DA7S1PGiVocR5oj-DSP4DNkFzwdYpioD75KbjU6_5sWzK6xpwNMbtzSPvgQEx1CpHMh0OdEH1xe07yGEVLCyUFh7srceXoZYg_-LXk1wJjw3VM_IT--nC0XF9XV9fnXxeerygnF6woHwRuJvViBVcy2IORg0Wre9o1mXKBtLNSD1F1XFKtVbxlwbEXbd5qvmDghHw975xjuN5iymVzaXQkewyYZrlXbKKmanfXDk3WzmrA3c3QTxK35_7Fi4AfDgxtx-zznzOyyMLsszD4Lc3O2vN2rwlQHxpX__n1mIP4xSgvdmF_fzw1fXi6-yZ_atOIfpnyObw</recordid><startdate>201602</startdate><enddate>201602</enddate><creator>Hussein, Ayad Ahmed</creator><creator>Al-Zaben, Abdulhadi</creator><creator>Khattab, Eman</creator><creator>Haroun, Anas</creator><creator>Frangoul, Haydar</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>7X8</scope></search><sort><creationdate>201602</creationdate><title>Hematopoietic stem cell transplantation from non-sibling matched family donors for patients with thalassemia major in Jordan</title><author>Hussein, Ayad Ahmed ; Al-Zaben, Abdulhadi ; Khattab, Eman ; Haroun, Anas ; Frangoul, Haydar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3612-ef3154ed3bac60c8a34fcec718d57013ec5ca2f4799c5c026dc0a1e838d971b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>beta-Thalassemia - genetics</topic><topic>beta-Thalassemia - therapy</topic><topic>Blood Platelets - cytology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Family</topic><topic>Female</topic><topic>Genotype</topic><topic>hematopoietic stem cell transplantation</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>Histocompatibility Testing</topic><topic>HLA Antigens - immunology</topic><topic>Humans</topic><topic>Jordan</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neutrophils - cytology</topic><topic>non-sibling donor</topic><topic>Retrospective Studies</topic><topic>thalassemia</topic><topic>Tissue Donors</topic><topic>Transplantation Conditioning</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hussein, Ayad Ahmed</creatorcontrib><creatorcontrib>Al-Zaben, Abdulhadi</creatorcontrib><creatorcontrib>Khattab, Eman</creatorcontrib><creatorcontrib>Haroun, Anas</creatorcontrib><creatorcontrib>Frangoul, Haydar</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hussein, Ayad Ahmed</au><au>Al-Zaben, Abdulhadi</au><au>Khattab, Eman</au><au>Haroun, Anas</au><au>Frangoul, Haydar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hematopoietic stem cell transplantation from non-sibling matched family donors for patients with thalassemia major in Jordan</atitle><jtitle>Pediatric transplantation</jtitle><addtitle>Pediatr Transplantation</addtitle><date>2016-02</date><risdate>2016</risdate><volume>20</volume><issue>1</issue><spage>120</spage><epage>123</epage><pages>120-123</pages><issn>1397-3142</issn><eissn>1399-3046</eissn><abstract>There are limited data on the outcome of patients with thalassemia receiving HSCT from non‐sibling matched family donors. Of the 341 patients with thalassemia major that underwent donor search at our center from January 2003 to December 2011, 236 (69.2%) had fully matched family donor of which 28 patients (8.2%) had non‐sibling matched family donors identified. We report on seven patients with a median age of eight yr (4–21) who underwent myeloablative (n = 4) or RIC (n = 3) HSCT. The median age of the donors was 33 yr (4–47), three were parents, two first cousins, one paternal uncle, and one paternal aunt. All patients achieved primary neutrophil and platelet engraftment at a median of 18 (13–20) and 16 days (11–20), respectively. One patient developed grade II acute GVHD, and two patients developed limited chronic GVHD. One patient experienced secondary GF requiring a second transplant. At a median follow‐up of 69 months (7–110), all patients are alive and thalassemia free. Our data emphasize the need for extended family HLA typing for patients with thalassemia major in regions where there is high rate of consanguinity. Transplant from non‐sibling matched family donor can result in excellent outcome.</abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>26493691</pmid><doi>10.1111/petr.12622</doi><tpages>4</tpages></addata></record> |
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subjects | Adolescent Adult beta-Thalassemia - genetics beta-Thalassemia - therapy Blood Platelets - cytology Child Child, Preschool Family Female Genotype hematopoietic stem cell transplantation Hematopoietic Stem Cell Transplantation - methods Histocompatibility Testing HLA Antigens - immunology Humans Jordan Male Middle Aged Neutrophils - cytology non-sibling donor Retrospective Studies thalassemia Tissue Donors Transplantation Conditioning Treatment Outcome Young Adult |
title | Hematopoietic stem cell transplantation from non-sibling matched family donors for patients with thalassemia major in Jordan |
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