Preoperative C-reactive protein to albumin ratio as a novel prognostic biomarker for the oncological outcomes of radical nephroureterectomy

Upper urinary tract urothelial carcinoma (UTUC), which arises from the urothelium of the renal calyx to the ureter, accounts for 10% of all urothelial carcinoma [1]. The current gold standard therapy for UTUC is radical nephroureterectomy (RNU) with bladder cuff excision [2,3]. In advanced stages, the 5-year cancer-specific survival is low; <50% for pT2 and pT3 tumors and <10% for pT4 tumors [4], [5], [6]. Approximately 60% of patients are diagnosed with muscle invasion (pT2 or higher) at the initial presentation, which may be advantageous for perioperative treatment [2,7]. Therefore, identifying prognostic factors that accurately predict outcomes is crucial for determining the appropriate treatment for patients with UTUC.

Cancer progression and cancer-related mortality result from a complex interplay between tumor pathogenesis and the host immune response [8,9]. Although several clinicopathologic factors have been utilized for prognostic assessment of UTUC following RNU, they predominantly reflect tumor-related conditions rather than host-related factors [10], [11], [12]. Systemic inflammatory reactions and chronic nutritional status are well-established host-related mechanisms associated with cancer development and progression [13,14]. Due to the importance of blood-based calculation of inflammatory signatures from routine pre-operative laboratory tests, several attempts have been made to assess the prognostic role of biomarkers such as the neutrophil-to-lymphocyte ratio, platelet-to-lymphocyte ratio, and C-reactive protein (CRP) in various malignancies [15]. CRP, in particular, offers advantages in terms of standardized measurement and reliability, as it reflects acute phase inflammation [16]. Hypoalbuminemia is recognized as a reflection of both chronic systemic inflammatory response and nutritional status [17]. Therefore, the CRP to albumin ratio (CAR) has the potential to capture both acute and chronic systemic inflammatory responses and cancer-related cachexia. Consequently, the prognostic role of CAR has been actively investigated in the pre-treatment setting of several malignancies [18,19]. However, few studies have examined the prognostic significance of CAR in UTUC.

Herein, we aimed to examine the prognostic value of CAR on progression-free survival (PFS) and cancer-specific survival (CSS) in patients with UTUC after RNU.

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