# Effect of tolvaptan on the prognosis of patients with rapidly progressive autosomal dominant polycystic kidney disease: a prospective open-label study

**Authors:** Li Zhou, Wenge Li

PMC · DOI: 10.3389/fmed.2026.1739751 · Frontiers in Medicine · 2026-03-12

## TL;DR

This study shows that tolvaptan slows kidney growth in Chinese patients with a fast-progressing kidney disease and is well tolerated.

## Contribution

The study provides first large-scale local evidence supporting tolvaptan's efficacy in Chinese patients with rapidly progressive ADPKD.

## Key findings

- Tolvaptan significantly reduced total kidney volume growth in patients with rapidly progressive ADPKD.
- eGFR remained stable, and no major hepatic or renal toxicity was observed during treatment.
- The drug was well tolerated, with 60 mg and 45 mg being the most commonly used daily doses.

## Abstract

Although tolvaptan is internationally recognized for its therapeutic benefits in autosomal dominant polycystic kidney disease (ADPKD) and has been referenced in the 2020 Chinese Clinical Practice Guidelines, it has yet to be approved in China due to limited large-scale local evidence.

A two-year, prospective, single-center, open-label trial was conducted to assess the efficacy and safety of tolvaptan in patients with rapidly progressive ADPKD. The primary endpoint was the change in total kidney volume (TKV), while secondary endpoints included changes in eGFR and evaluation of safety and tolerability.

Eighty-nine patients were enrolled 80% had a family history of ADPKD, 40% had polycystic liver disease and 65.6% were diagnosed with hypertension. A proportion of patients also presented with renal insufficiency and vascular complications. Baseline laboratory tests showed a decreased median red blood cell count and elevated concentrations of urinary albumin, urea, creatinine and uric acid. The most commonly used daily doses of tolvaptan were 60 mg (31.1%) and 45 mg (26.7%). After treatment, the mean TKV change rate for the left kidney was −70.2 ± 206.07 mL at 6 months and −47.84 ± 132.58 mL at 12 months; for the right kidney, the respective changes were −42.69 ± 209.40 mL and −8.57 ± 286.86 mL. eGFR remained stable, with no major hepatic/renal toxicity.

Tolvaptan effectively slowed kidney volume growth and was well tolerated in Chinese patients with rapidly progressive ADPKD.

## Linked entities

- **Chemicals:** tolvaptan (PubChem CID 216237)
- **Diseases:** autosomal dominant polycystic kidney disease (MONDO:0004691), polycystic liver disease (MONDO:0000447), renal insufficiency (MONDO:0001106)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** hepatic/renal toxicity (MESH:D056486), vascular complications (MESH:D003925), polycystic liver disease (MESH:C536330), hypertension (MESH:D006973), renal insufficiency (MESH:D051437), ADPKD (MESH:D016891)
- **Chemicals:** uric acid (MESH:D014527), creatinine (MESH:D003404), Tolvaptan (MESH:D000077602), urea (MESH:D014508)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC13017235/full.md

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Source: https://tomesphere.com/paper/PMC13017235