Evidence map›Paper›PMID 34549085›Full record

ArticleTransplantation direct2021

Cancer After Pediatric Kidney Transplantation: A Long-term Single-center Experience in Japan.

Tomoo Yabuuchi, Kenichiro Miura, Satoru Shimizu, Naoto Kaneko, Kiyonobu Ishizuka, Shoichiro Kanda, Hiroko Chikamoto, Yuko Akioka, Mikiya Fujieda, Motoshi Hattori

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Article in Transplantation direct, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Tomoo YabuuchiDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Kenichiro MiuraDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Satoru ShimizuMedical Research Institute, Tokyo Women's Medical University, Tokyo, Japan.
Naoto KanekoDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Kiyonobu IshizukaDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Shoichiro KandaDepartment of Pediatrics, The University of Tokyo, Tokyo, Japan.
Hiroko ChikamotoDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Yuko AkiokaDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Tokyo, Japan.
Mikiya FujiedaDepartment of Pediatrics, Kochi Medical School, Kochi University, Kochi, Japan.
Motoshi HattoriDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe cancer incidence, types, and risk factors after pediatric kidney transplantation (KT) have been reported in the United States, Canada, Europe, Australia, and New Zealand. However, no information is available about cancer in pediatric KT recipients in Asian countries.

methodsChildren aged <20 y who underwent initial KT from 1983 to 2016 were analyzed. We compared the cancer incidence with that in the general Japanese population using standardized incidence ratio and examined posttransplant cancer risk using Cox proportional hazards models.

resultsA total of 356 children (median age, 11.7 y; interquartile range, 5.0-17.6) received KT with a follow-up period of 4466 person-years. The median age of cancer onset was 18.5 y (interquartile range, 8.0-32.3), and 13 cancers occurred in 12 patients (3.4%). Two patients died from cancer. The most common cancers were posttransplant lymphoproliferative disorders (PTLDs) (38.5%). The median time to PTLD and non-PTLD diagnosis after KT was 0.6 and 16.4 y, respectively. There was no occurrence of skin cancer. The posttransplant cancer incidence was 9.9 times higher than that in the general age-matched population (standardized incidence ratio = 9.9; 95% confidence interval, 4.80-18.39). The cumulative cancer incidence was 5.3% in 20 y after KT, which is lower than that reported in previous studies. We could not identify any risk factors for all cancer after KT in all patients, whereas subgroup analysis in 264 patients with available data of recipient Epstein-Barr virus serological status showed that recipient Epstein-Barr virus-negative serology was an independent risk factor for cancer development.

conclusionsThe incidence of cancer is higher in Japanese pediatric KT recipients than in the general population. The cumulative incidence of cancer after KT was lower in our population than that previously reported. This may be because there was no skin cancer observed in the Japanese pediatric KT recipients in our study.

Identifiers

PMID34549085
PMCPMC8440015

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