Prognostic factors for survival in children who relapsed after allogeneic hematopoietic stem cell transplantation for acute leukemia

Background Post‐transplant relapse has a dismal prognosis in children with acute leukemia undergoing allogeneic hematopoietic stem cell transplantation (allo‐HSCT). Data on risk factors, treatment options, and outcomes are limited. Procedure In this retrospective multicenter study in which a questio...

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Veröffentlicht in:Pediatric transplantation 2021-08, Vol.25 (5), p.e13942-n/a
Hauptverfasser: Hazar, Volkan, Tezcan Karasu, Gülsün, Öztürk, Gülyüz, Küpesiz, Alphan, Aksoylar, Serap, Özbek, Namık, Uygun, Vedat, İleri, Talia, Okur, Fatma Visal, Koçak, Ülker, Kılıç, Suar Çakı, Akçay, Arzu, Güler, Elif, Kansoy, Savaş, Karakükcü, Musa, Bayram, İbrahim, Aksu, Tekin, Yeşilipek, Akif, Karagün, Barbaros Şahin, Yılmaz, Şebnem, Ertem, Mehmet, Uçkan, Duygu, Fışgın, Tunç, Gürsel, Orhan, Yaman, Yöntem, Bozkurt, Ceyhun, Gökçe, Müge
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container_issue 5
container_start_page e13942
container_title Pediatric transplantation
container_volume 25
creator Hazar, Volkan
Tezcan Karasu, Gülsün
Öztürk, Gülyüz
Küpesiz, Alphan
Aksoylar, Serap
Özbek, Namık
Uygun, Vedat
İleri, Talia
Okur, Fatma Visal
Koçak, Ülker
Kılıç, Suar Çakı
Akçay, Arzu
Güler, Elif
Kansoy, Savaş
Karakükcü, Musa
Bayram, İbrahim
Aksu, Tekin
Yeşilipek, Akif
Karagün, Barbaros Şahin
Yılmaz, Şebnem
Ertem, Mehmet
Uçkan, Duygu
Fışgın, Tunç
Gürsel, Orhan
Yaman, Yöntem
Bozkurt, Ceyhun
Gökçe, Müge
description Background Post‐transplant relapse has a dismal prognosis in children with acute leukemia undergoing allogeneic hematopoietic stem cell transplantation (allo‐HSCT). Data on risk factors, treatment options, and outcomes are limited. Procedure In this retrospective multicenter study in which a questionnaire was sent to all pediatric transplant centers reporting relapse after allo‐HSCT for a cohort of 938 children with acute leukemia, we analyzed 255 children with relapse of acute leukemia after their first allo‐HSCT. Results The median interval from transplantation to relapse was 180 days, and the median follow‐up from relapse to the last follow‐up was 1844 days. The 3‐year overall survival (OS) rate was 12.0%. The main cause of death was disease progression or subsequent relapse (82.6%). The majority of children received salvage treatment with curative intent without a second HSCT (67.8%), 22.0% of children underwent a second allo‐HSCT, and 10.2% received palliative therapy. Isolated extramedullary relapse (hazard ratio (HR): 0.607, P = .011) and relapse earlier than 365 days post‐transplantation (HR: 2.101, P 
doi_str_mv 10.1111/petr.13942
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Data on risk factors, treatment options, and outcomes are limited. Procedure In this retrospective multicenter study in which a questionnaire was sent to all pediatric transplant centers reporting relapse after allo‐HSCT for a cohort of 938 children with acute leukemia, we analyzed 255 children with relapse of acute leukemia after their first allo‐HSCT. Results The median interval from transplantation to relapse was 180 days, and the median follow‐up from relapse to the last follow‐up was 1844 days. The 3‐year overall survival (OS) rate was 12.0%. The main cause of death was disease progression or subsequent relapse (82.6%). The majority of children received salvage treatment with curative intent without a second HSCT (67.8%), 22.0% of children underwent a second allo‐HSCT, and 10.2% received palliative therapy. Isolated extramedullary relapse (hazard ratio (HR): 0.607, P = .011) and relapse earlier than 365 days post‐transplantation (HR: 2.101, P &lt; .001 for 0‐180 days; HR: 1.522, P = .041 for 181‐365 days) were found in multivariate analysis to be significant prognostic factors for outcome. The type of salvage therapy in chemosensitive relapse was identified as a significant prognostic factor for OS. Conclusion A salvage approach with curative intent may be considered for patients with post‐transplant relapse, even if they relapse in the first year post‐transplantation. For sustainable remission, a second allo‐HSCT may be recommended for patients who achieve complete remission after reinduction treatment.</description><identifier>ISSN: 1397-3142</identifier><identifier>EISSN: 1399-3046</identifier><identifier>DOI: 10.1111/petr.13942</identifier><identifier>PMID: 33320995</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Acute Disease ; acute leukemia ; Adolescent ; Child ; Child, Preschool ; Children ; Combined Modality Therapy ; Female ; Follow-Up Studies ; Hematopoietic Stem Cell Transplantation - methods ; Hematopoietic stem cells ; Humans ; Infant ; Infant, Newborn ; Leukemia ; Leukemia - diagnosis ; Leukemia - mortality ; Leukemia - therapy ; Male ; Medical prognosis ; Multivariate analysis ; Patients ; post‐transplant relapse ; Prognosis ; Recurrence ; Remission ; Remission (Medicine) ; Retrospective Studies ; Risk factors ; Salvage Therapy ; Stem cell transplantation ; Survival Analysis ; Transplantation, Homologous ; treatment ; Turkey - epidemiology ; Young Adult</subject><ispartof>Pediatric transplantation, 2021-08, Vol.25 (5), p.e13942-n/a</ispartof><rights>2020 Wiley Periodicals LLC</rights><rights>2020 Wiley Periodicals LLC.</rights><rights>2021 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3572-5cbd477f3b29666c42eafbc8a9c86a744267f092413cc05418949f20dbc120c23</citedby><cites>FETCH-LOGICAL-c3572-5cbd477f3b29666c42eafbc8a9c86a744267f092413cc05418949f20dbc120c23</cites><orcidid>0000-0003-0841-1667 ; 0000-0003-3257-7798 ; 0000-0002-1407-2334 ; 0000-0002-4640-6159 ; 0000-0001-9268-8858 ; 0000-0002-7678-5524 ; 0000-0002-4514-8637</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpetr.13942$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpetr.13942$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33320995$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hazar, Volkan</creatorcontrib><creatorcontrib>Tezcan Karasu, Gülsün</creatorcontrib><creatorcontrib>Öztürk, Gülyüz</creatorcontrib><creatorcontrib>Küpesiz, Alphan</creatorcontrib><creatorcontrib>Aksoylar, Serap</creatorcontrib><creatorcontrib>Özbek, Namık</creatorcontrib><creatorcontrib>Uygun, Vedat</creatorcontrib><creatorcontrib>İleri, Talia</creatorcontrib><creatorcontrib>Okur, Fatma Visal</creatorcontrib><creatorcontrib>Koçak, Ülker</creatorcontrib><creatorcontrib>Kılıç, Suar Çakı</creatorcontrib><creatorcontrib>Akçay, Arzu</creatorcontrib><creatorcontrib>Güler, Elif</creatorcontrib><creatorcontrib>Kansoy, Savaş</creatorcontrib><creatorcontrib>Karakükcü, Musa</creatorcontrib><creatorcontrib>Bayram, İbrahim</creatorcontrib><creatorcontrib>Aksu, Tekin</creatorcontrib><creatorcontrib>Yeşilipek, Akif</creatorcontrib><creatorcontrib>Karagün, Barbaros Şahin</creatorcontrib><creatorcontrib>Yılmaz, Şebnem</creatorcontrib><creatorcontrib>Ertem, Mehmet</creatorcontrib><creatorcontrib>Uçkan, Duygu</creatorcontrib><creatorcontrib>Fışgın, Tunç</creatorcontrib><creatorcontrib>Gürsel, Orhan</creatorcontrib><creatorcontrib>Yaman, Yöntem</creatorcontrib><creatorcontrib>Bozkurt, Ceyhun</creatorcontrib><creatorcontrib>Gökçe, Müge</creatorcontrib><creatorcontrib>Turkish Pediatric Bone Marrow Transplantation Study Group</creatorcontrib><creatorcontrib>the Turkish Pediatric Bone Marrow Transplantation Study Group</creatorcontrib><title>Prognostic factors for survival in children who relapsed after allogeneic hematopoietic stem cell transplantation for acute leukemia</title><title>Pediatric transplantation</title><addtitle>Pediatr Transplant</addtitle><description>Background Post‐transplant relapse has a dismal prognosis in children with acute leukemia undergoing allogeneic hematopoietic stem cell transplantation (allo‐HSCT). Data on risk factors, treatment options, and outcomes are limited. Procedure In this retrospective multicenter study in which a questionnaire was sent to all pediatric transplant centers reporting relapse after allo‐HSCT for a cohort of 938 children with acute leukemia, we analyzed 255 children with relapse of acute leukemia after their first allo‐HSCT. Results The median interval from transplantation to relapse was 180 days, and the median follow‐up from relapse to the last follow‐up was 1844 days. The 3‐year overall survival (OS) rate was 12.0%. The main cause of death was disease progression or subsequent relapse (82.6%). The majority of children received salvage treatment with curative intent without a second HSCT (67.8%), 22.0% of children underwent a second allo‐HSCT, and 10.2% received palliative therapy. Isolated extramedullary relapse (hazard ratio (HR): 0.607, P = .011) and relapse earlier than 365 days post‐transplantation (HR: 2.101, P &lt; .001 for 0‐180 days; HR: 1.522, P = .041 for 181‐365 days) were found in multivariate analysis to be significant prognostic factors for outcome. The type of salvage therapy in chemosensitive relapse was identified as a significant prognostic factor for OS. Conclusion A salvage approach with curative intent may be considered for patients with post‐transplant relapse, even if they relapse in the first year post‐transplantation. For sustainable remission, a second allo‐HSCT may be recommended for patients who achieve complete remission after reinduction treatment.</description><subject>Acute Disease</subject><subject>acute leukemia</subject><subject>Adolescent</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>Hematopoietic stem cells</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Leukemia</subject><subject>Leukemia - diagnosis</subject><subject>Leukemia - mortality</subject><subject>Leukemia - therapy</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Multivariate analysis</subject><subject>Patients</subject><subject>post‐transplant relapse</subject><subject>Prognosis</subject><subject>Recurrence</subject><subject>Remission</subject><subject>Remission (Medicine)</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Salvage Therapy</subject><subject>Stem cell transplantation</subject><subject>Survival Analysis</subject><subject>Transplantation, Homologous</subject><subject>treatment</subject><subject>Turkey - epidemiology</subject><subject>Young Adult</subject><issn>1397-3142</issn><issn>1399-3046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1rFTEUhoMotlY3_gAJuCnC1HzNZLKUUj-gYJG6DpnMSW9qJhmTTEv3_nBn7q0uXHg271k85-HAi9BrSs7oOu9nqPmMciXYE3S8pmo4Ed3T_S4bTgU7Qi9KuSWEdqIXz9ER55wRpdpj9Osqp5uYSvUWO2NrygW7lHFZ8p2_MwH7iO3OhzFDxPe7hDMEMxcYsXEVMjYhpBuIsJ7vYDI1zcnDJisVJmwhBFyziWUOJlZTfYp7vbFLBRxg-QGTNy_RM2dCgVePeYK-f7y4Pv_cXH799OX8w2VjeStZ09phFFI6PjDVdZ0VDIwbbG-U7TsjhWCddEQxQbm1pBW0V0I5RsbBUkYs4yfo9OCdc_q5QKl68mX70URIS9FMSNIxJQhd0bf_oLdpyXH9TrO2balkst-odwfK5lRKBqfn7CeTHzQleutGb93ofTcr_OZRuQwTjH_RP2WsAD0A9z7Aw39U-uri-ttB-ht0mpvJ</recordid><startdate>202108</startdate><enddate>202108</enddate><creator>Hazar, Volkan</creator><creator>Tezcan Karasu, Gülsün</creator><creator>Öztürk, Gülyüz</creator><creator>Küpesiz, Alphan</creator><creator>Aksoylar, Serap</creator><creator>Özbek, Namık</creator><creator>Uygun, Vedat</creator><creator>İleri, Talia</creator><creator>Okur, Fatma Visal</creator><creator>Koçak, Ülker</creator><creator>Kılıç, Suar Çakı</creator><creator>Akçay, Arzu</creator><creator>Güler, Elif</creator><creator>Kansoy, Savaş</creator><creator>Karakükcü, Musa</creator><creator>Bayram, İbrahim</creator><creator>Aksu, Tekin</creator><creator>Yeşilipek, Akif</creator><creator>Karagün, Barbaros Şahin</creator><creator>Yılmaz, Şebnem</creator><creator>Ertem, Mehmet</creator><creator>Uçkan, Duygu</creator><creator>Fışgın, Tunç</creator><creator>Gürsel, Orhan</creator><creator>Yaman, Yöntem</creator><creator>Bozkurt, Ceyhun</creator><creator>Gökçe, Müge</creator><general>Wiley Subscription Services, Inc</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0841-1667</orcidid><orcidid>https://orcid.org/0000-0003-3257-7798</orcidid><orcidid>https://orcid.org/0000-0002-1407-2334</orcidid><orcidid>https://orcid.org/0000-0002-4640-6159</orcidid><orcidid>https://orcid.org/0000-0001-9268-8858</orcidid><orcidid>https://orcid.org/0000-0002-7678-5524</orcidid><orcidid>https://orcid.org/0000-0002-4514-8637</orcidid></search><sort><creationdate>202108</creationdate><title>Prognostic factors for survival in children who relapsed after allogeneic hematopoietic stem cell transplantation for acute leukemia</title><author>Hazar, Volkan ; Tezcan Karasu, Gülsün ; Öztürk, Gülyüz ; Küpesiz, Alphan ; Aksoylar, Serap ; Özbek, Namık ; Uygun, Vedat ; İleri, Talia ; Okur, Fatma Visal ; Koçak, Ülker ; Kılıç, Suar Çakı ; Akçay, Arzu ; Güler, Elif ; Kansoy, Savaş ; Karakükcü, Musa ; Bayram, İbrahim ; Aksu, Tekin ; Yeşilipek, Akif ; Karagün, Barbaros Şahin ; Yılmaz, Şebnem ; Ertem, Mehmet ; Uçkan, Duygu ; Fışgın, Tunç ; Gürsel, Orhan ; Yaman, Yöntem ; Bozkurt, Ceyhun ; Gökçe, Müge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3572-5cbd477f3b29666c42eafbc8a9c86a744267f092413cc05418949f20dbc120c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acute Disease</topic><topic>acute leukemia</topic><topic>Adolescent</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>Hematopoietic stem cells</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Leukemia</topic><topic>Leukemia - diagnosis</topic><topic>Leukemia - mortality</topic><topic>Leukemia - therapy</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Multivariate analysis</topic><topic>Patients</topic><topic>post‐transplant relapse</topic><topic>Prognosis</topic><topic>Recurrence</topic><topic>Remission</topic><topic>Remission (Medicine)</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Salvage Therapy</topic><topic>Stem cell transplantation</topic><topic>Survival Analysis</topic><topic>Transplantation, Homologous</topic><topic>treatment</topic><topic>Turkey - epidemiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hazar, Volkan</creatorcontrib><creatorcontrib>Tezcan Karasu, Gülsün</creatorcontrib><creatorcontrib>Öztürk, Gülyüz</creatorcontrib><creatorcontrib>Küpesiz, Alphan</creatorcontrib><creatorcontrib>Aksoylar, Serap</creatorcontrib><creatorcontrib>Özbek, Namık</creatorcontrib><creatorcontrib>Uygun, Vedat</creatorcontrib><creatorcontrib>İleri, Talia</creatorcontrib><creatorcontrib>Okur, Fatma Visal</creatorcontrib><creatorcontrib>Koçak, Ülker</creatorcontrib><creatorcontrib>Kılıç, Suar Çakı</creatorcontrib><creatorcontrib>Akçay, Arzu</creatorcontrib><creatorcontrib>Güler, Elif</creatorcontrib><creatorcontrib>Kansoy, Savaş</creatorcontrib><creatorcontrib>Karakükcü, Musa</creatorcontrib><creatorcontrib>Bayram, İbrahim</creatorcontrib><creatorcontrib>Aksu, Tekin</creatorcontrib><creatorcontrib>Yeşilipek, Akif</creatorcontrib><creatorcontrib>Karagün, Barbaros Şahin</creatorcontrib><creatorcontrib>Yılmaz, Şebnem</creatorcontrib><creatorcontrib>Ertem, Mehmet</creatorcontrib><creatorcontrib>Uçkan, Duygu</creatorcontrib><creatorcontrib>Fışgın, Tunç</creatorcontrib><creatorcontrib>Gürsel, Orhan</creatorcontrib><creatorcontrib>Yaman, Yöntem</creatorcontrib><creatorcontrib>Bozkurt, Ceyhun</creatorcontrib><creatorcontrib>Gökçe, Müge</creatorcontrib><creatorcontrib>Turkish Pediatric Bone Marrow Transplantation Study Group</creatorcontrib><creatorcontrib>the Turkish Pediatric Bone Marrow Transplantation Study Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hazar, Volkan</au><au>Tezcan Karasu, Gülsün</au><au>Öztürk, Gülyüz</au><au>Küpesiz, Alphan</au><au>Aksoylar, Serap</au><au>Özbek, Namık</au><au>Uygun, Vedat</au><au>İleri, Talia</au><au>Okur, Fatma Visal</au><au>Koçak, Ülker</au><au>Kılıç, Suar Çakı</au><au>Akçay, Arzu</au><au>Güler, Elif</au><au>Kansoy, Savaş</au><au>Karakükcü, Musa</au><au>Bayram, İbrahim</au><au>Aksu, Tekin</au><au>Yeşilipek, Akif</au><au>Karagün, Barbaros Şahin</au><au>Yılmaz, Şebnem</au><au>Ertem, Mehmet</au><au>Uçkan, Duygu</au><au>Fışgın, Tunç</au><au>Gürsel, Orhan</au><au>Yaman, Yöntem</au><au>Bozkurt, Ceyhun</au><au>Gökçe, Müge</au><aucorp>Turkish Pediatric Bone Marrow Transplantation Study Group</aucorp><aucorp>the Turkish Pediatric Bone Marrow Transplantation Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic factors for survival in children who relapsed after allogeneic hematopoietic stem cell transplantation for acute leukemia</atitle><jtitle>Pediatric transplantation</jtitle><addtitle>Pediatr Transplant</addtitle><date>2021-08</date><risdate>2021</risdate><volume>25</volume><issue>5</issue><spage>e13942</spage><epage>n/a</epage><pages>e13942-n/a</pages><issn>1397-3142</issn><eissn>1399-3046</eissn><abstract>Background Post‐transplant relapse has a dismal prognosis in children with acute leukemia undergoing allogeneic hematopoietic stem cell transplantation (allo‐HSCT). Data on risk factors, treatment options, and outcomes are limited. Procedure In this retrospective multicenter study in which a questionnaire was sent to all pediatric transplant centers reporting relapse after allo‐HSCT for a cohort of 938 children with acute leukemia, we analyzed 255 children with relapse of acute leukemia after their first allo‐HSCT. Results The median interval from transplantation to relapse was 180 days, and the median follow‐up from relapse to the last follow‐up was 1844 days. The 3‐year overall survival (OS) rate was 12.0%. The main cause of death was disease progression or subsequent relapse (82.6%). The majority of children received salvage treatment with curative intent without a second HSCT (67.8%), 22.0% of children underwent a second allo‐HSCT, and 10.2% received palliative therapy. Isolated extramedullary relapse (hazard ratio (HR): 0.607, P = .011) and relapse earlier than 365 days post‐transplantation (HR: 2.101, P &lt; .001 for 0‐180 days; HR: 1.522, P = .041 for 181‐365 days) were found in multivariate analysis to be significant prognostic factors for outcome. The type of salvage therapy in chemosensitive relapse was identified as a significant prognostic factor for OS. Conclusion A salvage approach with curative intent may be considered for patients with post‐transplant relapse, even if they relapse in the first year post‐transplantation. For sustainable remission, a second allo‐HSCT may be recommended for patients who achieve complete remission after reinduction treatment.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33320995</pmid><doi>10.1111/petr.13942</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-0841-1667</orcidid><orcidid>https://orcid.org/0000-0003-3257-7798</orcidid><orcidid>https://orcid.org/0000-0002-1407-2334</orcidid><orcidid>https://orcid.org/0000-0002-4640-6159</orcidid><orcidid>https://orcid.org/0000-0001-9268-8858</orcidid><orcidid>https://orcid.org/0000-0002-7678-5524</orcidid><orcidid>https://orcid.org/0000-0002-4514-8637</orcidid></addata></record>
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1399-3046
language eng
recordid cdi_proquest_miscellaneous_2470629401
source Access via Wiley Online Library; MEDLINE
subjects Acute Disease
acute leukemia
Adolescent
Child
Child, Preschool
Children
Combined Modality Therapy
Female
Follow-Up Studies
Hematopoietic Stem Cell Transplantation - methods
Hematopoietic stem cells
Humans
Infant
Infant, Newborn
Leukemia
Leukemia - diagnosis
Leukemia - mortality
Leukemia - therapy
Male
Medical prognosis
Multivariate analysis
Patients
post‐transplant relapse
Prognosis
Recurrence
Remission
Remission (Medicine)
Retrospective Studies
Risk factors
Salvage Therapy
Stem cell transplantation
Survival Analysis
Transplantation, Homologous
treatment
Turkey - epidemiology
Young Adult
title Prognostic factors for survival in children who relapsed after allogeneic hematopoietic stem cell transplantation for acute leukemia
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