Outcomes of subsequent neoplasms after umbilical cord blood transplantation in Europe.

Author:

Rafii Hanadi1ORCID,Ruggeri Annalisa2,kenzey chantal1,Sanz Jaime3,Peffault de Latour Régis4,Esquirol Albert5ORCID,Michel Gerard6,Chevallier Patrice7,Rubio Marie-Thérèse8,Cornelissen Jan J9,Michallet Mauricette10,Volt Fernanda1,Rivera Franco Monica Magdalena11,Scigliuolo Graziana Maria12,Cappelli Barbara13,ROCHA VANDERSON14,Gluckman Eliane11

Affiliation:

1. Monacord, Centre scientifique de Monaco, Monaco

2. Eurocord, Institut de Recherche de Saint-Louis (IRSL), APHP, France

3. Hospital Universitario La Fe, Valencia, Spain

4. Saint-Louis, Paris, France

5. Hospital de la Santa Creu i Sant Pau, IIB-Sant Pau, and Jose Carreras Leukemia Research Institutes. Universitat Autonoma of Barcelona, Barcelona, Spain

6. CHU Timone Enfants and Aix-Marseille University, Marseille, France

7. CHU Hotel-Dieu, Nantes, France

8. CHRU Nancy, Vandoeuvre les Nancy, France

9. Erasmus MC, Cancer Institute, Rotterdam, Netherlands

10. Centre Léon Bérard, Lyon, France

11. Eurocord, IRSL, Paris, France

12. Eurocord, Paris, France

13. Eurocord , Paris, France

14. University of Sao Paulo, Sao Paulo, Brazil

Abstract

Subsequent neoplasms (SNs) compromise long-term survivors after hematopoietic cell transplantion. We performed a retrospective analysis of SNs in a cohort of 10358 recipients of umbilical cord blood transplantation (UCBT) reported to Eurocord/EBMT registries from 1988 to 2018. A total of 233 patients developed SNs. Median age at UCBT was 31 years (y) (0.3-69), and 84 were pediatric patients. Indications for UCBT were malignant hematological diseases in 199 patients (85%). Three groups of SNs were observed. Post-transplant lymphoproliferative disorders (PTLD) were reported in 145 patients in a median of 4 months after UCBT. Of these, 9/145 patients died from relapse, 83/145 from PTLD, and 24/145 from transplant-related causes. At last follow-up, 29/145 were alive; 5y-overall survival (OS) after PTLD diagnosis was 21±3%. Acute leukemia / myelodysplasia (AL/MDS) was diagnosed in 23 patients in a median of 28 months after UCBT and included 3 donor-cell AL. Four of 23 patients died from relapse of primary disease, 8/23 from progression of SNs, and 4/23 from TRM. Seven patients were alive at last follow-up; 5y-OS after AL/MDS diagnosis was 36±10%. Solid tumors (ST) were reported in 65 patients in a median of 54 months after UCBT. Most common tumor sites were lung, thyroid, bone and soft tissue. A total of 33/65 patients died (26 due to ST, 6 to relapse of primary disease, 1 cause missing). At last follow-up, 32/65 patients were alive; 5y-OS after the diagnosis of ST was 51±6%. In conclusion, despite their poor outcomes, SNs that occur after UCBT are extremely rare. Identification of associated risk factors and early detection may help to improve OS.

Publisher

American Society of Hematology

Subject

Hematology

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