Hutajulu Susanna Hilda, Astari Yufi Kartika, Ucche Meita, Kertia Nyoman, Subronto Yanri Wijayanti, Paramita Dewi Kartikawati, Choridah Lina, Ekaputra Ericko, Widodo Irianiwati, Suwardjo Suwardjo, Hardianti Mardiah Suci, Taroeno-Hariadi Kartika Widayati, Purwanto Ibnu, Kurnianda Johan
Division of Hematology and Medical Oncology, Department of Internal Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/Dr. Sardjito General Hospital, Sleman, Yogyakarta Special Region, Indonesia.
Division of Hematology and Medical Oncology, Department of Internal Medicine, Dr. Sardjito General Hospital, Sleman, Yogyakarta Special Region, Indonesia.
PeerJ. 2025 May 21;13:e19319. doi: 10.7717/peerj.19319. eCollection 2025.
Breast cancer patients with similar clinicopathologic characteristics may experience varied outcomes. This urges an increased effort to investigate other prognostic factors. C-reactive protein (CRP)-to-albumin ratio (CAR) is an inflammatory and nutritional biomarker that has been well studied and reported to have an impact on the survival of patients with diverse types of cancer, but limitedly in breast cancer. Therefore, this study aimed to investigate the prognostic significance of CAR in local patients with breast cancer.
This study included 202 stage I-IV breast cancer patients receiving first-line chemotherapy. We calculated inflammatory and nutritional biomarkers including CAR, neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), systemic immune-inflammation index (SII), systemic inflammation response index (SIRI), pan-immune-inflammation value (PIV), and prognostic nutrition index (PNI) before treatment. The Kaplan-Meier with log-rank test and Cox proportional hazard regression were used to analyze the prognostic role of clinicopathologic factors and biomarkers on disease-free survival (DFS), progression-free survival (PFS), and overall survival (OS).
The median follow-up period was 46 months (1-77 months). The 3-year DFS and 3-year OS in patients with high CAR (CAR > 1.5) were significantly lower than those with low CAR (CAR ≤ 1.5) (47.0% 68.9%, = 0.022 and 59.5% 78.6%, = 0.009, respectively). Multivariate analysis showed high CAR as prognostic factors for poor DFS (HR 2.10, 95% confidence interval/CI [1.10-3.99], = 0.023) and OS (HR 2.16, 95% CI [1.27-3.68], = 0.005), but not for PFS (HR 1.43, 95% CI [0.73-2.80], = 0.293). In addition, more advanced stage and HER2 positive were correlated with unfavorable DFS and OS, older age predicted poor DFS, and stage was the only prognostic factor of PFS (all values < 0.05).
Besides age, stage, and molecular subtypes that have been widely observed to have impact on the survival of breast cancer patients, CAR was demonstrated as a promising prognostic marker in our local patients. A high CAR at diagnosis was associated with unfavorable DFS and OS, which can aid in identifying patients at risk and guide personalized treatment planning.
具有相似临床病理特征的乳腺癌患者可能会有不同的预后结果。这促使人们加大力度研究其他预后因素。C反应蛋白(CRP)与白蛋白比值(CAR)是一种炎症和营养生物标志物,已得到充分研究,据报道对多种癌症患者的生存有影响,但在乳腺癌方面的研究有限。因此,本研究旨在探讨CAR在本地乳腺癌患者中的预后意义。
本研究纳入了202例接受一线化疗的I-IV期乳腺癌患者。我们在治疗前计算了包括CAR、中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)、淋巴细胞与单核细胞比值(LMR)、全身免疫炎症指数(SII)、全身炎症反应指数(SIRI)、泛免疫炎症值(PIV)和预后营养指数(PNI)在内的炎症和营养生物标志物。采用Kaplan-Meier对数秩检验和Cox比例风险回归分析临床病理因素和生物标志物对无病生存期(DFS)、无进展生存期(PFS)和总生存期(OS)的预后作用。
中位随访期为46个月(1-77个月)。高CAR(CAR>1.5)患者的3年DFS和3年OS显著低于低CAR(CAR≤1.5)患者(分别为47.0%对68.9%,P=0.022;59.5%对78.6%,P=0.009)。多因素分析显示,高CAR是DFS不良(风险比[HR]2.10,95%置信区间[CI][1.10-3.99],P=0.023)和OS不良(HR 2.16,95%CI[1.27-3.68],P=0.005)的预后因素,但不是PFS的预后因素(HR 1.43,95%CI[0.73-2.80],P=0.293)。此外,更晚期和HER2阳性与不良的DFS和OS相关,年龄较大预示着不良的DFS,而分期是PFS的唯一预后因素(所有P值<0.05)。
除了已广泛观察到对乳腺癌患者生存有影响的年龄、分期和分子亚型外,CAR在我们本地患者中被证明是一个有前景的预后标志物。诊断时高CAR与不良的DFS和OS相关,这有助于识别有风险的患者并指导个性化治疗计划。