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. 2025 Jul 25;25(1):1220.
doi: 10.1186/s12885-025-14654-3.

Impact of first-line tyrosine kinase inhibitor selection on survival outcomes with second-line nivolumab in metastatic renal cell carcinoma

Affiliations

Impact of first-line tyrosine kinase inhibitor selection on survival outcomes with second-line nivolumab in metastatic renal cell carcinoma

Omer Faruk Kuzu et al. BMC Cancer. .

Abstract

Introduction: Access to first-line immune checkpoint inhibitor (ICI) combinations in metastatic renal cell carcinoma (mRCC) remains limited in many low- and middle-income countries. Consequently, tyrosine kinase inhibitors (TKIs) are still widely used. This study investigates the impact of first-line sunitinib versus pazopanib on survival outcomes with second-line nivolumab.

Methods: We conducted a retrospective analysis of 245 patients with mRCC from the Turkish Oncology Group Kidney Cancer Consortium Database. Patients received first-line sunitinib or pazopanib, followed by second-line nivolumab. Primary endpoints were time to treatment failure (TTF) and overall survival (OS). Subgroup analyses were performed based on IMDC risk classification and presence of sarcomatoid features.

Results: A total of 245 patients who were treated with sunitinib or pazopanib monotherapy as first-line treatment followed by nivolumab as second-line treatment were included in this study. Median TTF following nivolumab initiation was similar between prior sunitinib and pazopanib groups (7.79 vs 7.72 months; p = 0.892). Median OS-2 was 27.21 months with prior sunitinib and 18.92 months with prior pazopanib (p = 0.496). In patients with sarcomatoid features (n = 20), those pretreated with pazopanib demonstrated numerically longer OS-2 compared to sunitinib (p = 0.023), although the small sample size limits definitive conclusions.

Conclusion: No significant differences in survival outcomes were observed between first-line sunitinib and pazopanib before nivolumab in mRCC. In the small subgroup with sarcomatoid features, pazopanib pre-treatment was associated with a numerically longer survival. These findings warrant cautious interpretation and further prospective validation, especially in resource-constrained settings.

Keywords: Metastatic renal cell cancer; Nivolumab; Pazopanib; Sunitinib.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: The study was approved by the Ankara University Faculty Ethics Committee (date:11/09/2024, approval number I09-701–24) and it was carried out in accordance with the Code of Ethics of the World Medical Association also known as a declaration of Helsinki. Due to the retrospective nature of the study the use of anonymized data, no informed consent was required as per the ethics committee approval. Consent for publication: Not applicable. Competing interests: Yüksel Ürün: Advisory work —Abdi-İbrahim, Astellas, AstraZeneca, Bristol Myers-Squibb, Deva, Eczacıbaşı, Gen ilaç, Gilead, GSK, Janssen, Merck, MSD, Novartis, Pfizer, Roche; travel, honoraria and consultation fees—Abdi-İbrahim, Astellas, Bristol Myers-Squibb, Deva, Eczacıbaşı, Gen ilaç, Gilead, GSK, Janssen, Merck, Novartis, Pfizer, Roche. All remaining authors have declared no conflicts of interest.

Figures

Fig. 1
Fig. 1
Kaplan–Meier curve for time to treatment failure
Fig. 2
Fig. 2
Kaplan–Meier curve for overall survival-2
Fig. 3
Fig. 3
Kaplan–Meier curve for overall survival-1
Fig. 4
Fig. 4
Kaplan–Meier curves for time to treatment failure and overall survival for patients without sarcomatoid features (A and C) and patients with sarcomatoid features (B and D)

References

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