Evidence map›Paper›PMID 35011990›Full record

ArticleJournal of clinical medicine2022

Everolimus Reduces Cancer Incidence and Improves Patient and Graft Survival Rates after Kidney Transplantation: A Multi-Center Study.

Ryoichi Imamura, Ryo Tanaka, Ayumu Taniguchi, Shigeaki Nakazawa, Taigo Kato, Kazuaki Yamanaka, Tomoko Namba-Hamano, Yoichi Kakuta, Toyofumi Abe, Koichi Tsutahara and 3 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Special Issue: New Advances in Kidney Transplantation.Journal of clinical medicine · 2022
    Article
4 · The record

Corrections and comments

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

13 authors.

Ryoichi ImamuraDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-8782-9852
Ryo TanakaDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Ayumu TaniguchiDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Shigeaki NakazawaDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Taigo KatoDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Kazuaki YamanakaDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Tomoko Namba-HamanoDepartment of Nephrology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Yoichi KakutaOsaka General Medical Center, Department of Urology, Osaka 558-8558, Japan.
Toyofumi AbeDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Koichi TsutaharaOsaka General Medical Center, Department of Urology, Osaka 558-8558, Japan.
Tetsuya TakaoOsaka General Medical Center, Department of Urology, Osaka 558-8558, Japan.
Hidefumi KishikawaDepartment of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya 662-0918, Japan.
Norio NonomuraDepartment of Urology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kidney transplantation can prevent renal failure and associated complications in patients with end-stage renal disease. Despite the good quality of life, de novo cancers after kidney transplantation are a major complication impacting survival and there is an urgent need to establish immunosuppressive protocols to prevent de novo cancers. We conducted a multi-center retrospective study of 2002 patients who underwent kidney transplantation between 1965 and 2020 to examine patient and graft survival rates and cumulative cancer incidence in the following groups categorized based on specific induction immunosuppressive therapies: group 1, antiproliferative agents and steroids; group 2, calcineurin inhibitors (CNIs), antiproliferative agents and steroids; group 3, CNIs, mycophenolate mofetil, and steroids; and group 4, mammalian target of rapamycin inhibitors including everolimus, CNIs, mycophenolate mofetil, and steroids. The patient and graft survival rates were significantly higher in groups 3 and 4. The cumulative cancer incidence rate significantly increased with the use of more potent immunosuppressants, and the time to develop cancer was shorter. Only one patient in group 4 developed de novo cancer. Potent immunosuppressants might improve graft survival rate while inducing de novo cancer after kidney transplantation. Our data also suggest that everolimus might suppress cancer development after kidney transplantation.

Indexed as

cumulative incidencede novo cancereverolimuskidney transplantationmammalian target of rapamycinsurvival

Identifiers

PMID35011990
PMCPMC8746009

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.