Evidence map›Paper›PMID 41377852›Full record

ArticleClinical kidney journal2025

Tolvaptan in Autosomal Dominant Polycystic Kidney Disease (ADPKD): a multicenter real life Italian experience.

Laura Econimo, Diego Toso, Giovambattista Capasso, Marco Guarneri, Silvia Lai, Matteo Rigato, Carmelita Marcantoni, Maurizio Garozzo, Vittoria Esposito, Raffaella Cravero and 5 more

Abstract read
In one paragraph

Article in Clinical kidney journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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

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

1 citing paper in PubMed.

  1. Review
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

15 authors.

Laura EconimoNephrology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia - ASST Spedali Civili of Brescia, Brescia, Italy.
Diego TosoNephrology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia - ASST Spedali Civili of Brescia, Brescia, Italy.ORCID https://orcid.org/0009-0005-3950-3777
Giovambattista CapassoBiogem, Institute of Molecular Biology and Genetics, Ariano Irpino, Italy.
Marco GuarneriNephrology and Dialysis Unit, University Hospital Policlinic Paolo Giaccone, Palermo, Italy.
Silvia LaiDepartment of Translational and Precision Medicine, Division of Nephrology, Policlinico Umberto I Hospital, Sapienza University of Rome, Rome, Italy.ORCID https://orcid.org/0000-0002-7199-2954
Matteo RigatoUOC Nephrology, Dialysis and Kidney transplantation - Ospedale S. Bortolo di Vicenza, AULSS8 - Veneto, Vicenza, Italy.
Carmelita MarcantoniDivision of Nephrology and Dialysis, University Hospital System Gaspare Rodolico - San Marco, Catania, Italy.
Maurizio GarozzoUOC Nephrology and Dialysis, Azienda Sanitaria Provinciale di Catania, Ospedale Santa Marta e Santa Venera, Acireale CT, Italy.ORCID https://orcid.org/0000-0002-4910-7859
Vittoria EspositoUnit of Nephrology, Istituti Clinici Scientifici Maugeri IRCCS, Pavia Italy.
Raffaella CraveroUOC Nephrology, Biella Hospital, Ponderano, Italy.
Giovanni StalloneNephrology, Dialysis and Transplantation Unit, Department of Medical and Surgical Sciences, University of Foggia, Foggia, Italy.
Tolvaptan Real Life Study Group
Federico AlbericiNephrology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia - ASST Spedali Civili of Brescia, Brescia, Italy.ORCID https://orcid.org/0000-0002-1686-5709
Francesco ScolariNephrology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia - ASST Spedali Civili of Brescia, Brescia, Italy.
Claudia IzziDMMT, University of Brescia, Brescia, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tolvaptan is the only disease-modifying treatment approved to slow kidney disease progression in autosomal dominant polycystic kidney disease (ADPKD). Data on tolvaptan in ADPKD outside of clinical trials are limited, usually deal with short-term observations and are characterized by a drop-out rate of 21%-56%. Methods: In this retrospective, observational, multicenter study enrolling 122 Italian patients with ADPKD and rapid progressive renal disease, we evaluated the tolerability and side effects of tolvaptan treatment in a real-life setting. A personalized treatment strategy, based on an accurate patient selection and a strict clinical and laboratory monitoring, was applied. Results: During a median follow-up of 34.0 (interquartile range 17.3; -46.5) months the overall adherence on tolvaptan was 82.0%. Permanent withdrawal was reported in 22/122 patients (18.0%) after a mean of 34.4 ± 18.0 months; the main reasons for drug permanent withdrawal were onset of kidney failure in 7/122 (5.7%), poor tolerance to aquaresis in 4/122 (3.3%), family planning in 3/122 (2.5%) and liver function test elevation in 2/122 patients (1.6%). Temporary discontinuation was observed in 35/122 patients (28.7%) and in most cases it was not related to drug side effects. In order to evaluate tolvaptan eligibility, historic estimated glomerular filtration rate decline was the most inclusive criteria (92.9%) when compared with Mayo Imaging Classification (89.7%) and Predicting Renal Outcome in Polycystic Kidney Disease (PROPKD) Score (22.6%). Conclusion: This real-life study confirms the feasibility, safety, and tolerability of tolvaptan treatment. In order to overcome the challenges of tolvaptan treatment, our experience suggests that a dedicated PKD team may play a key role in implementing strategies focused to reduce drop-out and achieve treatment success.

Indexed as

autosomal dominant polycystic kidney disease (ADPKD)rapid progressive renal diseasereal-life experiencetolerabilitytolvaptan

Identifiers

PMID41377852
PMCPMC12686815

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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.