Evidence map›Paper›PMID 33575935›Full record

Observational studyClinical and experimental nephrology2021

Safety and effectiveness of everolimus in maintenance kidney transplant patients in the real-world setting: results from a 2-year post-marketing surveillance study in Japan.

Naomi Hayase, Mariko Yamada, Shuhei Kaneko, Yoko Watanabe

Open access · hybridAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Clinical and experimental nephrology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% of its field
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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 1 country.

Naomi HayaseNovartis Pharma K.K. Medical Division, 23-1, Toranomon 1-chome, Minato-ku, Tokyo, 105-6333, Japan. naomi.hayase@novartis.com.
Mariko YamadaPatient Safety Japan Re-Examination Department, Novartis Pharma K.K., Tokyo, Japan.
Shuhei KanekoBiostatistics Pharma, Integrated Biostatistics Japan, Clinical Development & Analytics Japan, Novartis Pharma K.K., Tokyo, Japan.
Yoko WatanabeImmunology, Hepatology & Dermatology Clinical Development Department, Clinical Development & Analytics Japan, Novartis Pharma K.K., Tokyo, Japan.
Novartis (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundData on real-world use of everolimus (EVR) in Japanese maintenance kidney transplant (KTx) patients are limited. This post-marketing surveillance study was conducted to assess the safety and effectiveness of EVR, and identify factors affecting renal impairment.

methodsAdult maintenance KTx patients were enrolled within 14 days of initiating EVR. Patient medical data were collected using electronic data capture case report forms at 6 months, 1, and 2 years after initiating EVR, or at discontinuation.

resultsAll patients receiving EVR in Japan during the surveillance period were enrolled (N = 263). Mean time from transplantation to EVR initiation was 75.7 months. Decreased renal function (31.56%) was the primary reason for initiating EVR. In combination with EVR, the mean daily dose of tacrolimus and cyclosporine could be reduced to ~ 79 and ~ 64%, by 2 years, respectively. Incidences of serious adverse events and adverse drug reactions were 15.97 and 49.43%, respectively. Two-year graft survival rate was 95.82% and low in patients with baseline estimated glomerular filtration rate (eGFR; modification of diet in renal disease) < 30 mL/min/1.73 m

conclusionsNo new safety concerns for the use of EVR in adult maintenance KTx patients were identified. Early EVR initiation may be considered in these patients before renal function deterioration occurs.

Indexed as

AdultAgedCyclosporineDrug Therapy, CombinationEverolimusFemaleGraft RejectionGraft SurvivalHumansImmunosuppressive AgentsJapanKidney TransplantationMaleMiddle AgedProduct Surveillance, PostmarketingTacrolimusCyclosporineEverolimusImmunosuppressive AgentsTacrolimusEverolimusMaintenance kidney transplant patientsObservational studyPost-marketing surveillanceRenal impairment

Identifiers

PMID33575935
PMCPMC8106613
OpenAlexW3128618311

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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.