{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T07:14:54Z","timestamp":1789974894859,"version":"4.0.1"},"reference-count":22,"publisher":"American Society of Clinical Oncology (ASCO)","issue":"25","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JCO"],"published-print":{"date-parts":[[2013,9,1]]},"abstract":"<jats:sec>\n                    <jats:title>Purpose<\/jats:title>\n                    <jats:p>To analyze outcomes of hematopoietic cell transplantation (HCT) in T-cell non-Hodgkin lymphoma.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Patients and Methods<\/jats:title>\n                    <jats:p>Outcomes of 241 patients (112 anaplastic large-cell lymphoma, 102 peripheral T-cell lymphoma not otherwise specified, 27 angioimmunoblastic T-cell lymphoma) undergoing autologous HCT (autoHCT; n = 115; median age, 43 years) or allogeneic HCT (alloHCT; n = 126; median age, 38 years) were analyzed. Primary outcomes were nonrelapse mortality (NRM), relapse\/progression, progression-free survival (PFS), and overall survival (OS). Patient, disease, and HCT-related variables were analyzed in multivariate Cox proportional hazard models to determine association with outcomes.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>AutoHCT recipients were more likely in first complete remission (CR1; 35% v 14%; P = .001) and with chemotherapy-sensitive disease (86% v 60%; P &lt; .001), anaplastic large-cell histology (53% v 40%; P = .04), and two or fewer lines of prior therapy (65% v 44%; P &lt; .001) compared with alloHCT recipients. Three-year PFS and OS of autoHCT recipients beyond CR1 were 42% and 53%, respectively. Among alloHCT recipients who received transplantations beyond CR1, 31% remained progression-free at 3 years, despite being more heavily pretreated and with more refractory disease. NRM was 3.5-fold higher (95% CI, 1.80 to 6.99; P &lt; .001) for alloHCT. In multivariate analysis, chemotherapy sensitivity (hazard ratio [HR], 1.8; 95% CI, 1.16 to 2.87) and two or fewer lines of pretransplantation therapy (HR, 5.02; 95% CI, 2.15 to 11.72) were prognostic of survival.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>These data describe the roles of autoHCT and alloHCT in T-cell non-Hodgkin lymphoma and suggest greater effectiveness earlier in the disease course, and limited utility in multiply relapsed disease. Notably, autoHCT at relapse may be a potential option for select patients, particularly those with anaplastic large-cell lymphoma histology.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1200\/jco.2012.46.0188","type":"journal-article","created":{"date-parts":[[2013,7,30]],"date-time":"2013-07-30T00:12:23Z","timestamp":1375143143000},"page":"3100-3109","source":"Crossref","is-referenced-by-count":208,"title":["Hematopoietic Cell Transplantation for Systemic Mature T-Cell Non-Hodgkin Lymphoma"],"prefix":"10.1200","volume":"31","author":[{"given":"Sonali M.","family":"Smith","sequence":"first","affiliation":[{"name":"Sonali M. Smith, University of Chicago Hospitals, Chicago, IL; Linda J. Burns, University of Minnesota Medical Center, Minneapolis; David J. Inwards, Mayo Clinic Rochester, Rochester, MN; Koen van Besien, Weill Cornell Medical College; Peter H. Wiernik, Continuum Cancer Centers of New York at St Luke's-Roosevelt Hospital and Beth Israel Medical Center, New York City; Mitchell S. Cairo, New York Medical College, Valhalla, NY; Jennifer LeRademacher, Wensheng He, and Parameswaran N. Hari, Center for..."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Linda J.","family":"Burns","sequence":"additional","affiliation":[{"name":"Sonali M. Smith, University of Chicago Hospitals, Chicago, IL; Linda J. Burns, University of Minnesota Medical Center, Minneapolis; David J. Inwards, Mayo Clinic Rochester, Rochester, MN; Koen van Besien, Weill Cornell Medical College; Peter H. Wiernik, Continuum Cancer Centers of New York at St Luke's-Roosevelt Hospital and Beth Israel Medical Center, New York City; Mitchell S. Cairo, New York Medical College, Valhalla, NY; Jennifer LeRademacher, Wensheng He, and Parameswaran N. Hari, Center for..."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Koen","family":"van Besien","sequence":"additional","affiliation":[{"name":"Sonali M. Smith, University of Chicago Hospitals, Chicago, IL; Linda J. Burns, University of Minnesota Medical Center, Minneapolis; David J. Inwards, Mayo Clinic Rochester, Rochester, MN; Koen van Besien, Weill Cornell Medical College; Peter H. Wiernik, Continuum Cancer Centers of New York at St Luke's-Roosevelt Hospital and Beth Israel Medical Center, New York City; Mitchell S. Cairo, New York Medical College, Valhalla, NY; Jennifer LeRademacher, Wensheng He, and Parameswaran N. Hari, Center for..."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer","family":"LeRademacher","sequence":"additional","affiliation":[{"name":"Sonali M. Smith, University of Chicago Hospitals, Chicago, IL; Linda J. Burns, University of Minnesota Medical Center, Minneapolis; David J. Inwards, Mayo Clinic Rochester, Rochester, MN; Koen van Besien, Weill Cornell Medical College; Peter H. Wiernik, Continuum Cancer Centers of New York at St Luke's-Roosevelt Hospital and Beth Israel Medical Center, New York City; Mitchell S. Cairo, New York Medical College, Valhalla, NY; Jennifer LeRademacher, Wensheng He, and Parameswaran N. Hari, Center for..."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wensheng","family":"He","sequence":"additional","affiliation":[{"name":"Sonali M. Smith, University of Chicago Hospitals, Chicago, IL; Linda J. Burns, University of Minnesota Medical Center, Minneapolis; David J. Inwards, Mayo Clinic Rochester, Rochester, MN; Koen van Besien, Weill Cornell Medical College; Peter H. Wiernik, Continuum Cancer Centers of New York at St Luke's-Roosevelt Hospital and Beth Israel Medical Center, New York City; Mitchell S. Cairo, New York Medical College, Valhalla, NY; Jennifer LeRademacher, Wensheng He, and Parameswaran N. 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