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Outcome of donor lymphocyte infusion after allogeneic hematopoietic stem cell transplantation in relapsed myelodysplastic syndrome
Allogeneic hematopoietic stem cell transplantation (HSCT) improves outcomes for myelodysplastic syndrome (MDS) patients, but relapse rates remain high, and postrelapse treatment options are limited. Therefore, this study aimed to identify the factors contributing to the response to donor lymphocyte...
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creator | Marumo, Atsushi Nagata, Yasunobu Fujioka, Machiko Kurosawa, Shuhei Najima, Yuho Sakaida, Emiko Doki, Noriko Fukushima, Kentaro Ota, Shuichi Shono, Katsuhiro Ito, Ayumu Uchida, Naoyuki Nishida, Tetsuya Sawa, Masashi Tsunemine, Hiroko Matsuoka, Ken-ichi Makoto, Onizuka Kanda, Yoshinobu Fukuda, Takahiro Atsuta, Yoshiko Itonaga, Hidehiro |
description | Allogeneic hematopoietic stem cell transplantation (HSCT) improves outcomes for myelodysplastic syndrome (MDS) patients, but relapse rates remain high, and postrelapse treatment options are limited. Therefore, this study aimed to identify the factors contributing to the response to donor lymphocyte infusion (DLI) in relapsed MDS patients post-HSCT.
This study included 107 patients with relapsed and DLI-treated MDS who underwent their first HSCT between 2002 and 2022 and were registered in the Transplant Registry Unified Program. Univariate and multivariate survival analyses were conducted using log-rank tests and Cox proportional hazards models. Overall survival (OS) and response rates to DLI were also analyzed.
The 1-year OS was 30.0% and univariate analysis identified poor prognostic factors: age ≥58 years (P = 0.003), complex karyotype (P = 0.026), hematologic relapse (P = 0.026) and early relapse (P = 0.004). Azacitidine plus DLI also improved prognosis (P < 0.001). Multivariate analysis confirmed age ≥58 years, hematologic relapse, and early relapse as poor prognostic factors. The adjusted OS for patients aged ≥58 years who relapsed |
doi_str_mv | 10.1016/j.jcyt.2024.09.006 |
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This study included 107 patients with relapsed and DLI-treated MDS who underwent their first HSCT between 2002 and 2022 and were registered in the Transplant Registry Unified Program. Univariate and multivariate survival analyses were conducted using log-rank tests and Cox proportional hazards models. Overall survival (OS) and response rates to DLI were also analyzed.
The 1-year OS was 30.0% and univariate analysis identified poor prognostic factors: age ≥58 years (P = 0.003), complex karyotype (P = 0.026), hematologic relapse (P = 0.026) and early relapse (P = 0.004). Azacitidine plus DLI also improved prognosis (P < 0.001). Multivariate analysis confirmed age ≥58 years, hematologic relapse, and early relapse as poor prognostic factors. The adjusted OS for patients aged ≥58 years who relapsed <110 days post-transplant showed that the 1-year OS in patients with cytogenetic/molecular relapse was 43.6%, compared to 9.4% for those with hematologic relapse. Acute graft-versus-host disease (GVHD) occurred in 62.3% of patients, and chronic GVHD in 30.8%, with manageable outcomes.
DLI may improve OS in younger patients, those with cytogenetic/molecular relapse, and those with late relapse. Despite the risk of GVHD, its impact on prognosis is minimal. Given the limited treatment options, DLI should be considered for relapsed MDS patients post-HSCT.</description><identifier>ISSN: 1465-3249</identifier><identifier>ISSN: 1477-2566</identifier><identifier>EISSN: 1477-2566</identifier><identifier>DOI: 10.1016/j.jcyt.2024.09.006</identifier><identifier>PMID: 39503682</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>azacitidine ; donor lymphocyte infusion ; hematopoietic stem cell transplantation ; myelodysplastic syndrome ; relapse</subject><ispartof>Cytotherapy (Oxford, England), 2024-10</ispartof><rights>2024 International Society for Cell & Gene Therapy</rights><rights>Copyright © 2024 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1522-6038155359695bf5fda034879058b738016107a2c41d546834bb701e209e2de53</cites><orcidid>0000-0002-1661-8273 ; 0000-0001-6426-6770 ; 0000-0001-5952-5926 ; 0000-0003-4404-2870 ; 0000-0001-6849-9117 ; 0000-0002-8661-3179 ; 0000-0001-5681-6357</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1465324924008843$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39503682$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marumo, Atsushi</creatorcontrib><creatorcontrib>Nagata, Yasunobu</creatorcontrib><creatorcontrib>Fujioka, Machiko</creatorcontrib><creatorcontrib>Kurosawa, Shuhei</creatorcontrib><creatorcontrib>Najima, Yuho</creatorcontrib><creatorcontrib>Sakaida, Emiko</creatorcontrib><creatorcontrib>Doki, Noriko</creatorcontrib><creatorcontrib>Fukushima, Kentaro</creatorcontrib><creatorcontrib>Ota, Shuichi</creatorcontrib><creatorcontrib>Shono, Katsuhiro</creatorcontrib><creatorcontrib>Ito, Ayumu</creatorcontrib><creatorcontrib>Uchida, Naoyuki</creatorcontrib><creatorcontrib>Nishida, Tetsuya</creatorcontrib><creatorcontrib>Sawa, Masashi</creatorcontrib><creatorcontrib>Tsunemine, Hiroko</creatorcontrib><creatorcontrib>Matsuoka, Ken-ichi</creatorcontrib><creatorcontrib>Makoto, Onizuka</creatorcontrib><creatorcontrib>Kanda, Yoshinobu</creatorcontrib><creatorcontrib>Fukuda, Takahiro</creatorcontrib><creatorcontrib>Atsuta, Yoshiko</creatorcontrib><creatorcontrib>Itonaga, Hidehiro</creatorcontrib><title>Outcome of donor lymphocyte infusion after allogeneic hematopoietic stem cell transplantation in relapsed myelodysplastic syndrome</title><title>Cytotherapy (Oxford, England)</title><addtitle>Cytotherapy</addtitle><description>Allogeneic hematopoietic stem cell transplantation (HSCT) improves outcomes for myelodysplastic syndrome (MDS) patients, but relapse rates remain high, and postrelapse treatment options are limited. Therefore, this study aimed to identify the factors contributing to the response to donor lymphocyte infusion (DLI) in relapsed MDS patients post-HSCT.
This study included 107 patients with relapsed and DLI-treated MDS who underwent their first HSCT between 2002 and 2022 and were registered in the Transplant Registry Unified Program. Univariate and multivariate survival analyses were conducted using log-rank tests and Cox proportional hazards models. Overall survival (OS) and response rates to DLI were also analyzed.
The 1-year OS was 30.0% and univariate analysis identified poor prognostic factors: age ≥58 years (P = 0.003), complex karyotype (P = 0.026), hematologic relapse (P = 0.026) and early relapse (P = 0.004). Azacitidine plus DLI also improved prognosis (P < 0.001). Multivariate analysis confirmed age ≥58 years, hematologic relapse, and early relapse as poor prognostic factors. The adjusted OS for patients aged ≥58 years who relapsed <110 days post-transplant showed that the 1-year OS in patients with cytogenetic/molecular relapse was 43.6%, compared to 9.4% for those with hematologic relapse. Acute graft-versus-host disease (GVHD) occurred in 62.3% of patients, and chronic GVHD in 30.8%, with manageable outcomes.
DLI may improve OS in younger patients, those with cytogenetic/molecular relapse, and those with late relapse. Despite the risk of GVHD, its impact on prognosis is minimal. Given the limited treatment options, DLI should be considered for relapsed MDS patients post-HSCT.</description><subject>azacitidine</subject><subject>donor lymphocyte infusion</subject><subject>hematopoietic stem cell transplantation</subject><subject>myelodysplastic syndrome</subject><subject>relapse</subject><issn>1465-3249</issn><issn>1477-2566</issn><issn>1477-2566</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kLuO1jAQhS0EYi_wAhTIJU2CL7GTSDRotcBKK20DteXYE9a_HDvYDlJanhyHf6Gkmhn5nDOeD6E3lLSUUPn-1J7MXlpGWNeSsSVEPkOXtOv7hgkpnx-9FA1n3XiBrnI-EcLIMIiX6IKPgnA5sEv062ErJi6A44xtDDFhvy_rY6zBgF2Yt-xiwHoukLD2Pn6HAM7gR1h0iWt0UOqUCyzYgPe4JB3y6nUouhxGF3ACr9cMFi87-Gj34zn_ce3Bprr6FXoxa5_h9VO9Rt8-3X69-dLcP3y-u_l43xgqGGsk4QMVgotRjmKaxWw14d3Qj0QMU8-HSoSSXjPTUSs6OfBumnpCgZERmAXBr9G7c-6a4o8NclGLy8evdYC4ZcUp6-R4MKtSdpaaFHNOMKs1uUWnXVGiDvbqpA726mCvyKgq-2p6-5S_TQvYf5a_sKvgw1kA9cqfDpLKxkEwYF0CU5SN7n_5vwEYSpfQ</recordid><startdate>20241017</startdate><enddate>20241017</enddate><creator>Marumo, Atsushi</creator><creator>Nagata, Yasunobu</creator><creator>Fujioka, Machiko</creator><creator>Kurosawa, Shuhei</creator><creator>Najima, Yuho</creator><creator>Sakaida, Emiko</creator><creator>Doki, Noriko</creator><creator>Fukushima, Kentaro</creator><creator>Ota, Shuichi</creator><creator>Shono, Katsuhiro</creator><creator>Ito, Ayumu</creator><creator>Uchida, Naoyuki</creator><creator>Nishida, Tetsuya</creator><creator>Sawa, Masashi</creator><creator>Tsunemine, Hiroko</creator><creator>Matsuoka, Ken-ichi</creator><creator>Makoto, Onizuka</creator><creator>Kanda, Yoshinobu</creator><creator>Fukuda, Takahiro</creator><creator>Atsuta, Yoshiko</creator><creator>Itonaga, Hidehiro</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1661-8273</orcidid><orcidid>https://orcid.org/0000-0001-6426-6770</orcidid><orcidid>https://orcid.org/0000-0001-5952-5926</orcidid><orcidid>https://orcid.org/0000-0003-4404-2870</orcidid><orcidid>https://orcid.org/0000-0001-6849-9117</orcidid><orcidid>https://orcid.org/0000-0002-8661-3179</orcidid><orcidid>https://orcid.org/0000-0001-5681-6357</orcidid></search><sort><creationdate>20241017</creationdate><title>Outcome of donor lymphocyte infusion after allogeneic hematopoietic stem cell transplantation in relapsed myelodysplastic syndrome</title><author>Marumo, Atsushi ; 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Therefore, this study aimed to identify the factors contributing to the response to donor lymphocyte infusion (DLI) in relapsed MDS patients post-HSCT.
This study included 107 patients with relapsed and DLI-treated MDS who underwent their first HSCT between 2002 and 2022 and were registered in the Transplant Registry Unified Program. Univariate and multivariate survival analyses were conducted using log-rank tests and Cox proportional hazards models. Overall survival (OS) and response rates to DLI were also analyzed.
The 1-year OS was 30.0% and univariate analysis identified poor prognostic factors: age ≥58 years (P = 0.003), complex karyotype (P = 0.026), hematologic relapse (P = 0.026) and early relapse (P = 0.004). Azacitidine plus DLI also improved prognosis (P < 0.001). Multivariate analysis confirmed age ≥58 years, hematologic relapse, and early relapse as poor prognostic factors. The adjusted OS for patients aged ≥58 years who relapsed <110 days post-transplant showed that the 1-year OS in patients with cytogenetic/molecular relapse was 43.6%, compared to 9.4% for those with hematologic relapse. Acute graft-versus-host disease (GVHD) occurred in 62.3% of patients, and chronic GVHD in 30.8%, with manageable outcomes.
DLI may improve OS in younger patients, those with cytogenetic/molecular relapse, and those with late relapse. Despite the risk of GVHD, its impact on prognosis is minimal. Given the limited treatment options, DLI should be considered for relapsed MDS patients post-HSCT.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>39503682</pmid><doi>10.1016/j.jcyt.2024.09.006</doi><orcidid>https://orcid.org/0000-0002-1661-8273</orcidid><orcidid>https://orcid.org/0000-0001-6426-6770</orcidid><orcidid>https://orcid.org/0000-0001-5952-5926</orcidid><orcidid>https://orcid.org/0000-0003-4404-2870</orcidid><orcidid>https://orcid.org/0000-0001-6849-9117</orcidid><orcidid>https://orcid.org/0000-0002-8661-3179</orcidid><orcidid>https://orcid.org/0000-0001-5681-6357</orcidid></addata></record> |
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subjects | azacitidine donor lymphocyte infusion hematopoietic stem cell transplantation myelodysplastic syndrome relapse |
title | Outcome of donor lymphocyte infusion after allogeneic hematopoietic stem cell transplantation in relapsed myelodysplastic syndrome |
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