Table · dataset · 2026
Table 5_Prognostic performance of baseline serum immunoglobulin G in patients with metastatic renal cell carcinoma receiving first-line ICI–TKI therapy.xlsx
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Background<p>In the era of immune checkpoint inhibitor–tyrosine kinase inhibitor (ICI–TKI) combination therapy for metastatic renal cell carcinoma (mRCC), reliable biomarkers for prognostic stratification and long-term prognosis remain clinically unmet needs.
Description
This study aimed to investigate the prognostic significance of baseline serum IgG in patients with mRCC receiving first-line systemic therapy and to evaluate its potential in complementing current risk stratification models.</p>Methods<p>We retrospectively analyzed 153 patients with mRCC receiving first-line ICI-TKI therapy between May 2019 and April 2026.
Baseline serum IgG levels were categorized as elevated (>17.4 g/L) or normal based on the institutional reference limit. Survival outcomes were assessed using Kaplan–Meier analysis and Cox proportional hazards models. A prognostic nomogram was developed for individualized survival prediction.</p>Results<p>The median follow-up was 29.0 months.
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Elevated baseline IgG was associated with higher IMDC risk (P = 0.022). Kaplan–Meier analysis showed significantly worse overall survival (OS; P < 0.001) and progression-free survival (PFS; P = 0.049) in patients with elevated IgG. In multivariable analysis, elevated IgG was not associated with PFS but remained an independent predictor of inferior OS (HR = 2.55; 95% CI, 1.30–5.00; P = 0.006).
Incorporating IgG into the IMDC model improved the C-index from 0.645 to 0.689, with the greatest incremental benefit observed for 3-year OS prediction. The exploratory nomogram demonstrated acceptable calibration, particularly for 3-year OS prediction.</p>Conclusions<p>Baseline serum IgG is an independent prognostic biomarker for OS in mRCC patients treated with first-line ICI–TKI therapy. Its integration into the IMDC model improves survival prediction and provides additional prognostic information in the immunotherapy era.</p>
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- DOI doi.org/10.3389/fonc.2026.1928984.s011 ↗
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