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CD4+ T-cell reconstitution predicts survival outcomes after acute graft-versus-host-disease: a dual-center validation.
de Koning, Coco; Prockop, Susan; van Roessel, Ichelle; Kernan, Nancy; Klein, Elizabeth; Langenhorst, Jurgen; Szanto, Celina; Belderbos, Mirjam; Bierings, Marc; Boulad, Farid; Bresters, Dorine; Cancio, Maria; Curran, Kevin; Kollen, Wouter; O'Reilly, Richard; Scaradavou, Andromachi; Spitzer, Barbara; Versluijs, Birgitta; Huitema, Alwin; Lindemans, Caroline; Nierkens, Stefan; Boelens, Jaap Jan.
Afiliação
  • de Koning C; Center for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Prockop S; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • van Roessel I; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Kernan N; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Klein E; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Langenhorst J; Center for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Szanto C; Center for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Belderbos M; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Bierings M; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Boulad F; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Bresters D; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Cancio M; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Curran K; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Kollen W; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • O'Reilly R; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Scaradavou A; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Spitzer B; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Versluijs B; Pediatric Stem Cell Transplant and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Huitema A; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Lindemans C; Department of Clinical Pharmacy, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands; and.
  • Nierkens S; Department of Pharmacy & Pharmacology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Boelens JJ; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Blood ; 137(6): 848-855, 2021 02 11.
Article em En | MEDLINE | ID: mdl-33150379
ABSTRACT
Acute graft-versus-host-Disease (aGVHD) is a major cause of morbidity and mortality after allogeneic hematopoietic cell transplantation (HCT). We previously showed that early CD4+ T-cell immune reconstitution (IR; CD4+ IR) predicts survival after HCT. Here, we studied the relation between CD4+ IR and survival in patients developing aGVHD. Pediatric patients undergoing first allogeneic HCT at University Medical Center Utrecht (UMC)/Princess Máxima Center (PMC) or Memorial Sloan Kettering Cancer Center (MSK) were included. Primary outcomes were nonrelapse mortality (NRM) and overall survival (OS), stratified for aGVHD and CD4+ IR, defined as ≥50 CD4+ T cells per µL within 100 days after HCT or before aGVHD onset. Multivariate and time-to-event Cox proportional hazards models were applied, and 591 patients (UMC/PMC, n = 276; MSK, n = 315) were included. NRM in patients with grade 3 to 4 aGVHD with or without CD4+ IR within 100 days after HCT was 30% vs 80% (P = .02) at UMC/PMC and 5% vs 67% (P = .02) at MSK. This was associated with lower OS without CD4+ IR (UMC/PMC, 61% vs 20%; P = .04; MSK, 75% vs 33%; P = .12). Inadequate CD4+ IR before aGVHD onset was associated with significantly higher NRM (74% vs 12%; P < .001) and inferior OS (24% vs 78%; P < .001). In this retrospective analysis, we demonstrate that early CD4+ IR, a simple and robust marker predictive of outcomes after HCT, is associated with survival after moderate to severe aGVHD. This association must be confirmed prospectively but suggests strategies to improve T-cell recovery after HCT may influence survival in patients developing aGVHD.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T CD4-Positivos / Transplante de Células-Tronco Hematopoéticas / Contagem de Linfócito CD4 / Reconstituição Imune / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T CD4-Positivos / Transplante de Células-Tronco Hematopoéticas / Contagem de Linfócito CD4 / Reconstituição Imune / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article