{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,12]],"date-time":"2026-08-12T03:30:56Z","timestamp":1786505456418,"version":"build-2736575974"},"reference-count":39,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2026,5,24]],"date-time":"2026-05-24T00:00:00Z","timestamp":1779580800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,5,24]],"date-time":"2026-05-24T00:00:00Z","timestamp":1779580800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Br J Haematol"],"published-print":{"date-parts":[[2026,8]]},"abstract":"<jats:title>Summary<\/jats:title>\n                  <jats:p>\n                    T\u2010lymphoblastic lymphoma (T\u2010LBL) is an aggressive malignancy with a high relapse risk despite intensive therapy. The optimal transplant strategy remains uncertain. We retrospectively analysed 81 patients with T\u2010LBL undergoing haematopoietic stem cell transplantation (HSCT) (59 allogeneic [allo\u2010HSCT] and 22 autologous [auto\u2010HSCT]). Survival outcomes were evaluated using Kaplan\u2013Meier and competing\u2010risk methods. Multivariable Cox regression, propensity score matching and landmark analyses at 12\u2009months were performed. At 3\u2009years, overall survival (OS) was comparable between allo\u2010HSCT and auto\u2010HSCT (76.0% vs. 77.0%;\n                    <jats:italic>p<\/jats:italic>\n                    \u2009=\u20090.890), while progression\u2010free survival (PFS) was numerically higher following allo\u2010HSCT (77.0% vs. 58.7%;\n                    <jats:italic>p<\/jats:italic>\n                    \u2009=\u20090.141). The cumulative incidence of relapse tended to be lower after allo\u2010HSCT (18.6% vs. 30.5%;\n                    <jats:italic>p<\/jats:italic>\n                    \u2009=\u20090.129), with similar non\u2010relapse mortality. Landmark analyses suggested a time\u2010dependent pattern, with divergence in PFS beyond 12\u2009months. In multivariable analyses, allo\u2010HSCT (hazard ratio [HR] 0.34;\n                    <jats:italic>p<\/jats:italic>\n                    \u2009=\u20090.037) and complete remission at transplantation (HR 0.23;\n                    <jats:italic>p<\/jats:italic>\n                    \u2009=\u20090.001) were independently associated with improved PFS, highlighting disease status as a key determinant. Allo\u2010HSCT showed a trend towards improved disease control without increased non\u2010relapse mortality. This effect may be influenced by disease status at transplantation. Findings should be interpreted cautiously and require prospective validation.\n                  <\/jats:p>","DOI":"10.1111\/bjh.70581","type":"journal-article","created":{"date-parts":[[2026,5,25]],"date-time":"2026-05-25T04:11:09Z","timestamp":1779682269000},"page":"621-631","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Long\u2010term outcomes after allogeneic versus autologous haematopoietic stem cell transplantation for T\u2010lymphoblastic lymphoma"],"prefix":"10.1111","volume":"209","author":[{"ORCID":"https:\/\/orcid.org\/0009-0006-5392-1657","authenticated-orcid":false,"given":"Qian","family":"Cheng","sequence":"first","affiliation":[{"name":"Jiangsu Institute of Hematology, National Clinical Research Center for Hematologic Diseases The First Affiliated Hospital of Soochow University  Suzhou P. R. 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