Incidence of malignancy after pediatric kidney transplantation: a single-center experience over the past three decades in Japan View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2021-09-27

AUTHORS

Yujiro Aoki, Hiroyuki Satoh, Yuko Hamasaki, Riku Hamada, Ryoko Harada, Hiroshi Hataya, Kenji Ishikura, Masaki Muramatsu, Seiichiro Shishido, Ken Sakai

ABSTRACT

BackgroundMalignancy after kidney transplantation (KT) is one of the most serious post-transplant complications. This study aimed to investigate the incidence, type, and outcomes of malignancy after pediatric KT.MethodsWe performed a retrospective cohort study on pediatric kidney transplant recipients aged 18 years or younger who received their first transplant between 1975 and 2009.ResultsAmong the 375 children who underwent KT, 212 were male (56.5%) and 163 were female (43.5%) (median age at KT, 9.6 years [interquartile range {IQR}] 5.8–12.9 years). The incidence of malignancy was 5.6% (n = 21). The cumulative incidences of cancer were 0.8%, 2.5%, 2.8%, 4.2%, 5.5%, and 15.6% at 1, 5, 10, 15, 20, and 30 years post-transplantation, respectively. Of 375 patients, 12 (3.2%) had solid cancer and nine (2.4%) had lymphoproliferative malignancy. The median age at the first malignancy was 21.3 years (IQR 11.5–33.3 years). The median times from transplant to diagnosis were 22.3 years (IQR 12.3–26.6 years) for solid cancer and 2.2 years (IQR 0.6–2.8) for lymphoproliferative malignancies. During follow-up, five recipients died due to malignancy. The causes of death were hepatocellular carcinoma in one patient, squamous cell carcinoma in the transplanted kidney in one patient, malignant schwannoma in one patient, and Epstein-Barr virus-related lymphoma in two patients. The mortality rate was 0.79 per 1000 person-years (95% confidence interval 0.38, 1.85).ConclusionsEarly diagnosis and treatment of malignancies in transplant recipients is an important challenge. Therefore, enhanced surveillance and continued vigilance for malignancy following KT are necessary. More... »

PAGES

294-302

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10157-021-02143-3

DOI

http://dx.doi.org/10.1007/s10157-021-02143-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1141419999

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/34580806


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