PD-L1 and PD1 expression in post-transplantation lymphoproliferative disease (PTLD) of childhood and adolescence: An inter- and intra-individual descriptive study covering the whole spectrum of PTLD categories.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
08 2019
Historique:
received: 23 05 2019
revised: 20 06 2019
accepted: 20 06 2019
pubmed: 4 7 2019
medline: 15 8 2020
entrez: 4 7 2019
Statut: ppublish

Résumé

Therapy of children with post-transplantation lymphoproliferative disorder (PTLD) after hematopoietic stem cell (HSCT) and solid organ transplantation (SOT) can be challenging. In this retrospective study, we investigated PD-L1 and PD1 expression in all PTLD categories of childhood and adolescence to see whether checkpoint inhibition with PD-L1/PD1 inhibitors may serve as a therapy option. We included 21 patients aged 19 years or younger (at date of transplant) with PTLD following SOT or HSCT having adequate tumor samples available (n = 29). Using immunohistochemistry, we evaluated PD-L1/PD1 expression on both tumor cells and cells of the microenvironment in all samples. Availability of consecutively matched tumor samples during 6 of 21 patients' disease courses also allowed an intra-individual assessment of PD-L1/PD1 expression. We observed lower PD-L1 and higher PD1 expression in non-destructive lesions, and higher PD-L1 and lower PD1 expression in polymorphic and, in particular, in monomorphic PTLD, mostly diffuse large B-cell lymphomas (DLBCL, n = 10/21). The amount of PD-L1- and PD1-positive cells changed in the opposite way in sequential biopsies of the same individual correlating well with the PTLD category. This is the first comprehensive pediatric study assessing PD-L1 and PD1 expression on tumor cells and in the microenvironment of PTLD including not only monomorphic, but also non-destructive early lesions. PD-L1 expression of the tumor cells inversely correlated with PD1 expression in surrounding tissues, with the highest expression in DLBCL. Since PTLD can be therapeutically challenging, our results indicate a potential efficacy of checkpoint inhibitors if standard immune- and/or chemotherapy fail or are impossible. We therefore recommend routine staining of PD-L1 and PD1 in all PTLD categories.

Identifiants

pubmed: 31269329
doi: 10.1002/cam4.2394
pmc: PMC6712474
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4656-4668

Informations de copyright

© 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Ana-Iris Schiefer (AI)

Department of Pathology, Medical University of Vienna, Vienna, Austria.

Elisabeth Salzer (E)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
CeMM, Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.

Anna Füreder (A)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Zsolt Szepfalusi (Z)

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Thomas Müller-Sacherer (T)

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Wolf-Dietrich Huber (WD)

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Ina Michel-Behnke (I)

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Cardiology, Pediatric Heart Center, Medical University of Vienna, Vienna, Austria.

Anita Lawitschka (A)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Herbert Pichler (H)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Georg Mann (G)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Caroline Hutter (C)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Ingrid Simonitsch-Klupp (I)

Department of Pathology, Medical University of Vienna, Vienna, Austria.

Andishe Attarbaschi (A)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

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Classifications MeSH