<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-14T07:59:57Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/157959" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/157959</identifier><datestamp>2025-12-06T04:04:59Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478798</setSpec><setSpec>col_2072_478916</setSpec><setSpec>col_2072_478917</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Outcomes of Medicare-age eligible NHL patients receiving RIC allogeneic transplantation: a CIBMTR analysis</dc:title>
   <dc:creator>Shah, Nirav N.</dc:creator>
   <dc:creator>Ahn, Kwang Woo</dc:creator>
   <dc:creator>Litovich, Carlos</dc:creator>
   <dc:creator>Fenske, Timothy S.</dc:creator>
   <dc:creator>Ahmed, Sairah</dc:creator>
   <dc:creator>Battiwalla, Minoo</dc:creator>
   <dc:creator>Bejanyan, Nelli</dc:creator>
   <dc:creator>Dahi, Parastoo B.</dc:creator>
   <dc:creator>Bolaños Meade, Javier</dc:creator>
   <dc:creator>Chen, Andy I.</dc:creator>
   <dc:creator>Ciurea, Stefan O.</dc:creator>
   <dc:creator>Bachanova, Veronika</dc:creator>
   <dc:creator>DeFilipp,  Zachariah</dc:creator>
   <dc:creator>Epperla, Narendranath</dc:creator>
   <dc:creator>Farhadfar, Nosha</dc:creator>
   <dc:creator>Herrera, Alex F.</dc:creator>
   <dc:creator>Haverkos, Bradley M.</dc:creator>
   <dc:creator>Holmberg, Leona</dc:creator>
   <dc:creator>Hossain, Nasheed M.</dc:creator>
   <dc:creator>Kharfan-Dabaja, Mohamed A.</dc:creator>
   <dc:creator>Kenkre, Vaishalee P.</dc:creator>
   <dc:creator>Lazarus, Hillard M.</dc:creator>
   <dc:creator>Murthy, Hemant S.</dc:creator>
   <dc:creator>Nishihori, Taiga</dc:creator>
   <dc:creator>Rezvani, Andrew R.</dc:creator>
   <dc:creator>D'Souza, Anita</dc:creator>
   <dc:creator>Savani, Bipin N.</dc:creator>
   <dc:creator>Ulrickson, Matthew L.</dc:creator>
   <dc:creator>Waller, Edmund K.</dc:creator>
   <dc:creator>Sureda, Anna</dc:creator>
   <dc:creator>Smith, Sonali M.</dc:creator>
   <dc:creator>Hamadani, Mehdi</dc:creator>
   <dc:subject>Cèl·lules canceroses</dc:subject>
   <dc:subject>Malaltia de Hodgkin</dc:subject>
   <dc:subject>Cancer cells</dc:subject>
   <dc:subject>Hodgkin's disease</dc:subject>
   <dc:description>The application of allogeneic hematopoietic cell transplantation (allo-HCT) in non-Hodgkin lymphoma (NHL) patients ≥65 years in the United States is limited by lack of Medicare coverage for this indication. Using the Center for International Blood and Marrow Transplant Research (CIBMTR) database, we report allo-HCT outcomes of NHL patients aged ≥65 years (older cohort; n = 446) compared with a cohort of younger NHL patients aged 55-64 years (n = 1183). We identified 1629 NHL patients undergoing a first reduced-intensity conditioning (RIC) or nonmyeloablative conditioning allo-HCT from 2008 to 2015 in the United States. Cord blood or haploidentical transplants were excluded. The median age was 68 years (range 65-77) for the older cohort vs 60 years (range 55-64) in the younger cohort. The 4-year adjusted probabilities of nonrelapse mortality (NRM), relapse/progression (R/P), progression-free survival (PFS), and overall survival (OS) of the younger and older groups were 24% vs 30% (P = .03), 41% vs 42% (P = .82), 37% vs 31% (P = .03), and 51% vs 46% (P = .07), respectively. Using multivariate analysis, compared with the younger group, the older cohort was associated with increased NRM, but there was no difference between the 2 cohorts in terms of R/P, PFS, or OS. The most common cause of death was disease relapse in both groups. In NHL patients eligible for allo-HCT, there was no difference in OS between the 2 cohorts. Age alone should not determine allo-HCT eligibility in NHL, and Medicare should expand allo-HCT coverage to older adults.</dc:description>
   <dc:date>2020-04-29T05:50:32Z</dc:date>
   <dc:date>2020-04-29T05:50:32Z</dc:date>
   <dc:date>2018-04-23</dc:date>
   <dc:date>2020-04-29T05:50:32Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>2473-9529</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/157959</dc:identifier>
   <dc:identifier>696016</dc:identifier>
   <dc:identifier>29685953</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1182/bloodadvances.2018018531</dc:relation>
   <dc:relation>Blood Advances, 2018, vol. 2, num. 8, p. 933-940</dc:relation>
   <dc:relation>https://doi.org/10.1182/bloodadvances.2018018531</dc:relation>
   <dc:rights>(c) American Society of Hematology, 2018</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>8 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>American Society of Hematology</dc:publisher>
   <dc:source>Articles publicats en revistes (Ciències Clíniques)</dc:source>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>