No Correlation Between Proteinuria and Renal Function in Patients with Unresectable Hepatocellular Carcinoma Treated with Atezolizumab Plus Bevacizumab: ARISE Study
<b>Background:</b> Atezolizumab plus bevacizumab (Atezo + Bev) is the standard of care for treatment-naïve patients with unresectable hepatocellular carcinoma (uHCC). Proteinuria is a treatment-emergent adverse event that often leads to Bev interruption. However, the relationship between Bev-related proteinuria and renal dysfunction is unclear. We retrospectively investigated the impact of proteinuria after starting Atezo + Bev on renal function in patients with uHCC. <b>Methods:</b> We performed a single-arm retrospective study of patients with uHCC treated with Atezo + Bev between 25 September 2020 and 31 May 2022, at Kindai University Hospital, Japan. The impact of proteinuria on renal function during Atezo + Bev treatment was analyzed in terms of the correlation between changes in urine protein creatinine ratio (UPCR) and estimated glomerular filtration rate (eGFR) relative to baseline. <b>Results:</b> We analyzed data from 100 patients (median age 74 years; range 41-89; 75% male). During Atezo + Bev treatment, the median (interquartile range) maximum increase from baseline in UPCR was 0.39 (0.08 to 2.05) and the median maximum decline from baseline in eGFR was -7.5 (-20.5 to -3.0) mL/min/1.73 m<sup>2</sup>. The Pearson and Spearman correlation coefficients (95% confidence intervals) between these variables were -0.16 (-0.34 to 0.04) and -0.13 (-0.32 to 0.07), respectively. <b>Conclusions:</b> We found no correlation between the changes in UPCR and eGFR during Atezo + Bev treatment. Bev interruption criteria are based on the degree of proteinuria; however, our results suggest that proteinuria does not necessarily impair renal function. Physicians should consider the risk-benefit profile when deciding whether to discontinue Bev in patients who develop proteinuria during Atezo + Bev treatment.
Authors
- Satoru Hagiwara (ORCID: https://orcid.org/0000-0002-3412-4701)
- Naoshi Nishida (ORCID: https://orcid.org/0000-0002-9111-5668)
- Masatoshi Kudo (ORCID: https://orcid.org/0000-0002-4102-3474)
- Tetsutaro Hamano
- Hiroshi Ida (ORCID: https://orcid.org/0000-0002-0690-8218)
- Yasunori Minami (ORCID: https://orcid.org/0000-0001-7146-5954)
- Kazuomi Ueshima (ORCID: https://orcid.org/0000-0002-7577-5789)
- Tomoko Aoki (ORCID: https://orcid.org/0000-0002-9950-4553)
- R. Take
- Ai Tanaka (ORCID: https://orcid.org/0000-0002-5919-9726)
- Masahiro Takita
- M Morita (ORCID: https://orcid.org/0000-0003-4550-3691)
- Chizuko Watanabe
- Kentaro Asoh
- Hirokazu Chishina
Institutions
- Chugai Pharma (United States) (US)
- CTI Engineering (Japan) (JP)
- Kindai University (JP)
Publication Details
- Journal
- Cancers
- Published
- 2025-11-28
- DOI
- https://doi.org/10.3390/cancers17233826
- Primary Topic
- Hepatocellular Carcinoma Treatment and Prognosis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Kindai University
- Kanazawa University
- Chugai Pharmaceutical