Non-Hodgkin lymphoma after liver and kidney transplantation in children. Experience from one center.


Journal

Advances in clinical and experimental medicine : official organ Wroclaw Medical University
ISSN: 1899-5276
Titre abrégé: Adv Clin Exp Med
Pays: Poland
ID NLM: 101138582

Informations de publication

Date de publication:
Feb 2020
Historique:
pubmed: 11 3 2020
medline: 29 7 2020
entrez: 11 3 2020
Statut: ppublish

Résumé

Post-transplantation lymphoproliferative disorder (PTLD) is a complication of organ transplantation and a life-threatening condition. Children who underwent organ transplantation are at risk of developing lymphoproliferative disorders and, among them, non-Hodgkin lymphoma (NHL) is the most serious. The objective of this study was to describe the clinical course of NHL after liver and kidney transplantation. Retrospective analysis of medical records of children who underwent liver/kidney transplantation and developed NHL. Nine children were identified, all girls, 6 after liver and 3 after kidney transplantations. Age at transplantation ranged from 1 year to 13 years (median: 4 years), while age at lymphoma diagnosis from 4 to 17 years (median: 12 years). Time from transplantation to lymphoma diagnosis ranged from 7 months to 12 years (median: 9 years). All but 1 patient developed mature B-cell lymphoma, 4 children - diffuse large B-cell lymphoma (DLBCL), 2 children - Burkitt's lymphoma, 1 child - mature B-cell leukemia, 1 child - Burkitt-like lymphoma, while 1 patient was diagnosed with T-cell lymphoblastic lymphoma. High levels of Epstein-Barr virus (EBV) DNA were found in blood of 3 patients, and EBV in tissue samples was detected in 4 patients. Six patients presented with stage III and 2 with stage IV disease. Two patients had graft involvement. Three children received chemotherapy according to R-CHOP, 3 LMB protocol (2 with addition of rituximab), while 1 received CHOP and 5 courses of COP. T-cell lymphoma patient was treated with Euro-LB protocol. Six out of 8 treated patients are alive with a median follow-up of 6 years. Two children died from disease progression during treatment and 1 from cerebral herniation before starting therapy. All patients experienced at least 1 toxic episode of grade 3 and 4 according to Common Toxicity Criteria Adverse Event (CTCAE). Complications of chemotherapy were manageable and there were no transplanted organ failures. Our study provides further data on the treatment and outcome of monomorphic PTLD and indicates that it is feasible to treat solid organ recipients with multiagent chemotherapy.

Sections du résumé

BACKGROUND BACKGROUND
Post-transplantation lymphoproliferative disorder (PTLD) is a complication of organ transplantation and a life-threatening condition. Children who underwent organ transplantation are at risk of developing lymphoproliferative disorders and, among them, non-Hodgkin lymphoma (NHL) is the most serious.
OBJECTIVES OBJECTIVE
The objective of this study was to describe the clinical course of NHL after liver and kidney transplantation.
MATERIAL AND METHODS METHODS
Retrospective analysis of medical records of children who underwent liver/kidney transplantation and developed NHL.
RESULTS RESULTS
Nine children were identified, all girls, 6 after liver and 3 after kidney transplantations. Age at transplantation ranged from 1 year to 13 years (median: 4 years), while age at lymphoma diagnosis from 4 to 17 years (median: 12 years). Time from transplantation to lymphoma diagnosis ranged from 7 months to 12 years (median: 9 years). All but 1 patient developed mature B-cell lymphoma, 4 children - diffuse large B-cell lymphoma (DLBCL), 2 children - Burkitt's lymphoma, 1 child - mature B-cell leukemia, 1 child - Burkitt-like lymphoma, while 1 patient was diagnosed with T-cell lymphoblastic lymphoma. High levels of Epstein-Barr virus (EBV) DNA were found in blood of 3 patients, and EBV in tissue samples was detected in 4 patients. Six patients presented with stage III and 2 with stage IV disease. Two patients had graft involvement. Three children received chemotherapy according to R-CHOP, 3 LMB protocol (2 with addition of rituximab), while 1 received CHOP and 5 courses of COP. T-cell lymphoma patient was treated with Euro-LB protocol. Six out of 8 treated patients are alive with a median follow-up of 6 years. Two children died from disease progression during treatment and 1 from cerebral herniation before starting therapy. All patients experienced at least 1 toxic episode of grade 3 and 4 according to Common Toxicity Criteria Adverse Event (CTCAE). Complications of chemotherapy were manageable and there were no transplanted organ failures.
CONCLUSIONS CONCLUSIONS
Our study provides further data on the treatment and outcome of monomorphic PTLD and indicates that it is feasible to treat solid organ recipients with multiagent chemotherapy.

Identifiants

pubmed: 32154678
doi: 10.17219/acem/112605
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

197-202

Auteurs

Bożenna Dembowska-Bagińska (B)

Department of Oncology, Children's Memorial Health Institute, Warszawa, Poland.

Anna Wakulińska (A)

Department of Oncology, Children's Memorial Health Institute, Warszawa, Poland.

Iwona Daniluk (I)

Department of Oncology, Children's Memorial Health Institute, Warszawa, Poland.

Joanna Teisseyre (J)

Department of Pediatric Surgery and Organ Transplantation, Children's Memorial Health Institute, Warszawa, Poland.

Irena Jankowska (I)

Department of Gastroenterology, Children's Memorial Health Institute, Warszawa, Poland.

Piotr Czubkowski (P)

Department of Gastroenterology, Children's Memorial Health Institute, Warszawa, Poland.

Ryszard Grenda (R)

Department of Nephrology, Kidney Transplantation and Hypertension, Children's Memorial Health Institute, Warszawa, Poland.

Wioletta Jarmużek (W)

Department of Nephrology, Kidney Transplantation and Hypertension, Children's Memorial Health Institute, Warszawa, Poland.

Wiesława Grajkowska (W)

Department of Pathology, Children's Memorial Health Institute, Warszawa, Poland.

Jagoda Małdyk (J)

Department of Pathology, Medical University of Warsaw, Poland.

Piotr Kaliciński (P)

Department of Pediatric Surgery and Organ Transplantation, Children's Memorial Health Institute, Warszawa, Poland.

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