Integration of circulating tumor cell and neutrophil-lymphocyte ratio to identify high-risk metastatic castration-resistant prostate cancer patients

被引:19
作者
Chong, Weelic [1 ]
Zhang, Zhenchao [1 ]
Luo, Rui [1 ]
Gu, Jian [2 ]
Lin, Jianqing [3 ]
Wei, Qiang [4 ]
Li, Bingshan [4 ]
Myers, Ronald [1 ]
Lu-Yao, Grace [1 ]
Kelly, William Kevin [1 ]
Wang, Chun [1 ]
Yang, Hushan [1 ]
机构
[1] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Med Oncol, Philadelphia, PA 19107 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
[3] George Washington Univ, GW Canc Ctr, Dept Med, Washington, DC 20037 USA
[4] Vanderbilt Univ, Dept Mol Physiol & Biophys, 221 Kirkland Hall, Nashville, TN 37235 USA
基金
美国国家卫生研究院;
关键词
Circulating tumor cell; Neutrophil-lymphocyte ratio; Platelet-lymphocyte ratio; Metastatic castration-resistant prostate cancer; Prognosis; CLINICAL-TRIALS; END-POINTS; SURVIVAL; MEN; ABIRATERONE; BIOMARKERS; ANTIGEN;
D O I
10.1186/s12885-021-08405-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), and circulating tumor cells (CTCs) have been associated with survival in castration-resistant prostate cancer (CRPC). However, no study has examined the prognostic value of NLR and PLR in the context of CTCs.MethodsBaseline CTCs from mCRPC patients were enumerated using the CellSearch System. Baseline NLR and PLR values were calculated using the data from routine complete blood counts. The associations of CTC, NLR, and PLR values, individually and jointly, with progression-free survival (PFS) and overall survival (OS), were evaluated using Kaplan-Meier analysis, as well as univariate and multivariate Cox models.ResultsCTCs were detected in 37 (58.7%) of 63 mCRPC patients, and among them, 16 (25.4%) had >= 5 CTCs. The presence of CTCs was significantly associated with a 4.02-fold increased risk for progression and a 3.72-fold increased risk of death during a median follow-up of 17.6months. OS was shorter among patients with high levels of NLR or PLR than those with low levels (log-rank P=0.023 and 0.077). Neither NLR nor PLR was individually associated with PFS. Among the 37 patients with detectable CTCs, those with a high NLR had significantly shorter OS (log-rank P=0.024); however, among the 26 patients without CTCs, the OS difference between high- and low-NLR groups was not statistically significant. Compared to the patients with CTCs and low NLR, those with CTCs and high levels of NLR had a 3.79-fold risk of death (P=0.036). This association remained significant after adjusting for covariates (P=0.031). Combination analyses of CTC and PLR did not yield significant results.ConclusionAmong patients with detectable CTCs, the use of NLR could further classify patients into different risk groups, suggesting a complementary role for NLR in CTC-based prognostic stratification in mCRPC.
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页数:11
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