Literature DB >> 30828868

Frequency, characteristics, and outcome of PTLD after allo-SCT: A multicenter study from the Spanish group of blood and marrow transplantation (GETH).

Irene García-Cadenas1, Lucrecia Yáñez2, Isidro Jarque3, Rodrigo Martino1, Jose Antonio Pérez-Simón4, David Valcárcel5, Jaime Sanz3, Arantxa Bermúdez2, Cristina Muñoz6, Cristina Calderón-Cabrera4, Estefania García7, Laura Alonso5, Maria Suárez-Lledó8, Marta González Vicent9, Inmaculada Heras10, Mª Cruz Viguria11, Montserrat Batlle12, Lourdes Vázquez13, Javier López14, Carlos Solano15.   

Abstract

Post-transplant lymphoproliferative disorder (PTLD) is an infrequent complication of allogeneic stem cell transplant (allo-SCT). AIMS: To estimate the frequency and management of PTLD in Spain and to identify prognostic factors influencing outcomes.
METHODS: Multicenter, retrospective analysis of allo-SCT performed in 14 transplant units over a 15-year period.
RESULTS: 102 PTLD were diagnosed among 12 641 allo-SCT, leading to an estimated frequency of 0.8%. PTLD was diagnosed at a median of 106 days after SCT. Eighty-seven cases (85%) were diagnosed between 2007 and 2013. At diagnosis, 22% and 17% of the patients had gastrointestinal tract and CNS involvement. Eighty-seven (85%) received rituximab treatment, alone or in combination with immunosuppression reduction, with an ORR of 50.6%. With a median follow-up for survivors of 58 months, the 2-year overall survival (OS) was 33% and the PTLD-related mortality 45%. Age ≥ 40 years, malignant underlying disease, non-response to rituximab, and severe thrombocytopenia or lymphocytopenia at PTLD diagnosis were associated with worse overall survival.
CONCLUSIONS: Only a small proportion of allografted patients were diagnosed a PTLD. Its clinical course was highly aggressive, and prognosis poor, especially in those failing rituximab. The prognostic impact found of the platelet, and lymphocyte count at diagnosis requires further confirmation.
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  EBV; PTLD; allo-SCT; infection; rituximab

Mesh:

Substances:

Year:  2019        PMID: 30828868     DOI: 10.1111/ejh.13226

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  3 in total

Review 1.  Epstein-Barr virus posttransplant lymphoproliferative disorder: update on management and outcomes.

Authors:  Julian Lindsay; Jad Othman; Madeleine R Heldman; Monica A Slavin
Journal:  Curr Opin Infect Dis       Date:  2021-12-01       Impact factor: 4.915

2.  Refractory Epstein-Barr Virus (EBV)-Related Post-transplant Lymphoproliferative Disease: Cure by Combined Brentuximab Vedotin and Allogeneic EBV-Specific T-Lymphocytes.

Authors:  Thomas Mika; Katharina Strate; Swetlana Ladigan; Clemens Aigner; Uwe Schlegel; Iris Tischoff; Sabine Tischer-Zimmermann; Britta Eiz-Vesper; Britta Maecker-Kolhoff; Roland Schroers
Journal:  Front Med (Lausanne)       Date:  2019-12-18

3.  Characteristics, management, and outcome of pediatric patients with post-transplant lymphoproliferative disease-A 20 years' experience from Austria.

Authors:  Anna Füreder; Gabriele Kropshofer; Martin Benesch; Michael Dworzak; Sabine Greil; Wolf-Dietrich Huber; Holger Hubmann; Anita Lawitschka; Georg Mann; Ina Michel-Behnke; Thomas Müller-Sacherer; Herbert Pichler; Ingrid Simonitsch-Klupp; Wolfgang Schwinger; Zsolt Szepfalusi; Roman Crazzolara; Andishe Attarbaschi
Journal:  Cancer Rep (Hoboken)       Date:  2021-03-23
  3 in total

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