# The C-Reactive Protein–Albumin–Lymphocyte (CALLY) Index as an Independent Predictor of Progression and Survival in Metastatic Renal Cell Carcinoma

**Authors:** Beril Balci Topuz, Ahmet Tufekci, Sibel Cangi, Omer Aydin Yildirim, Mustafa Yildirim

PMC · DOI: 10.3390/jcm15041475 · Journal of Clinical Medicine · 2026-02-13

## TL;DR

The study shows that the CALLY index, which combines inflammation, nutrition, and immune markers, can predict progression and survival in metastatic kidney cancer patients.

## Contribution

The CALLY index is introduced as a novel composite biomarker for predicting outcomes in metastatic renal cell carcinoma.

## Key findings

- Low CALLY index was significantly associated with shorter progression-free and overall survival in mRCC patients.
- The CALLY index independently predicted progression and survival outcomes in multivariate analysis.
- CALLY demonstrated strong discriminative power and associations with IMDC risk classification and peritoneal metastasis.

## Abstract

Background/Objectives: Systemic inflammation, nutritional status, and immune competence have emerged as important prognostic determinants in metastatic renal cell carcinoma (mRCC). The C-reactive protein–albumin–lymphocyte (CALLY) index integrates these parameters into a single composite biomarker, yet its utility in mRCC remains insufficiently explored. This study aimed to evaluate the prognostic significance of the CALLY index in mRCC and its associations with clinicopathological features and survival outcomes. Methods: A total of 68 patients with mRCC treated between 2017 and 2024 were retrospectively analyzed. All patients received first-line VEGF–TKI therapy, and 73.5% subsequently received second-line treatment, predominantly nivolumab. The CALLY index was calculated as (albumin × lymphocyte count)/(CRP × 104), and patients were stratified using the median cut-off (0.16). Survival outcomes were assessed with Kaplan–Meier and Cox regression analyses. Discriminative performance was evaluated using Harrell’s C-index and time-dependent ROC curves at 6, 12, and 24 months. Results: Low CALLY (≤0.16) was significantly associated with shorter PFS (4 vs. 8 months, p < 0.001) and OS (9 vs. 26 months, p < 0.001). In multivariate analysis, the CALLY index independently predicted both PFS (HR = 1.91, p = 0.045) and OS (HR = 2.89, p = 0.005). Time-dependent ROC analysis demonstrated increasing discriminative strength for PFS (AUC: 0.70 → 0.95) and modest decline for OS over time (AUC: 0.83 → 0.72). CALLY also showed strong associations with IMDC risk classification and peritoneal metastasis. Conclusions: The CALLY index is a simple, cost-effective, and objective prognostic biomarker that may independently predict progression and survival in mRCC. Its complementary value to the IMDC model supports its integration into routine risk stratification and real-world clinical decision-making.

## Linked entities

- **Proteins:** LOC100189571 (uncharacterized LOC100189571)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, VHL (von Hippel-Lindau tumor suppressor) [NCBI Gene 7428] {aka HRCA1, RCA1, VHL1, pVHL}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** infections (MESH:D007239), lung, bone, and peritoneal (MESH:D010538), Solid Tumors (MESH:D009369), inflammation (MESH:D007249), injury to (MESH:D014947), bone and lung metastases (MESH:D009362), genitourinary cancers (MESH:D014565), death (MESH:D003643), pain (MESH:D010146), hepatocellular carcinoma (MESH:D006528), RCC (MESH:D002292), Hypoxia (MESH:D000860), LVI (MESH:D009361), I disease (MESH:D009081), liver and brain metastases (MESH:D001932), gastrointestinal, lung, and breast cancers (MESH:D001943), lymph node metastasis (MESH:D008207), liver (MESH:D017093), hypoalbuminemia (MESH:D034141), systemic (MESH:D015619), IMDC (MESH:C538445)
- **Chemicals:** pazopanib (MESH:C516667), CheckMate (-), ipilimumab (MESH:D000074324), nivolumab (MESH:D000077594), calcium (MESH:D002118), sunitinib (MESH:D000077210)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942612/full.md

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Source: https://tomesphere.com/paper/PMC12942612