Clinical Treatment Score Post-5 Years as a Tool for Risk Estimation of Late Recurrence in Thai Patients With Estrogen-Receptor-Positive, Early Breast Cancer: A Validation Study.
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引用次数: 0
Abstract
Background: The risk of late distant recurrence (LDR) of estrogen receptor (ER)-positive breast cancer continues even after 5 years of endocrine treatment. Clinical Treatment Score after 5 years (CTS5) was developed and validated as a tool to assess the risk of LDR using data from Tamoxifen, Arimidex Alone or in Combinations (ATAC) and Breast International Group 1-98 (BIG1-98) trials. This study aimed to externally validate CTS5 in a real-world cohort of patients treated at an academic center in Thailand.
Methods: The study was a retrospective analytical research study of early-stage, ER-positive breast cancer patients. The primary endpoint was LDR. The risk of LDR was determined using the CTS5 calculator. Cox regression model and Kaplan-Meier survival analysis were applied for prognostic validation of CTS5. Calibration was performed by comparing observed LDR to expected LDR using the Hosmer-Lemeshow (H-L) test.
Results: A total of 323 women were included with a median follow-up period of 11.6 years. The rate of LDR was 10.8%. The CTS5 was prognostic for LDR. C-index of the area under the ROC curve was 0.672. There was no significant difference between actual and expected numbers of LDR with an observed (O) LDR events to expected (E) number of LDR events ratio of 0.99 (0.86-1.12) (H-L P = .79) indicating a proper calibration in this cohort.
Conclusions: Our study validated that CTS5 is accurate in predicting the risk of LDR in ER-positive breast cancer cases in Thai patients. Its performance seemed to be better in postmenopausal patients. CTS5 could be applied in routine clinical practice to improve decisions regarding prolonged endocrine therapy, particularly in resource-limited countries where molecular profiling are inaccessible.
背景:雌激素受体(ER)阳性乳腺癌在接受内分泌治疗5年后晚期远处复发(LDR)的风险仍在继续。5年后临床治疗评分(CTS5)被开发并验证为评估LDR风险的工具,使用的数据来自他莫昔芬、阿里米得昔单独或联合(ATAC)和Breast International Group 1-98 (BIG1-98)试验。本研究旨在外部验证CTS5在泰国一个学术中心接受治疗的真实世界患者队列。方法:对早期er阳性乳腺癌患者进行回顾性分析研究。主要终点为LDR。使用CTS5计算器确定LDR的风险。采用Cox回归模型和Kaplan-Meier生存分析对CTS5的预后进行验证。采用Hosmer-Lemeshow (H-L)检验比较观察到的LDR与预期的LDR进行校准。结果:共纳入323名女性,中位随访期为11.6年。LDR率为10.8%。CTS5是LDR的预后指标。ROC曲线下面积c指数为0.672。实际LDR数与预期LDR数之间无显著差异,观察到的(O) LDR事件数与预期(E) LDR事件数之比为0.99 (0.86-1.12)(H-L P = 0.79),表明该队列的校准是正确的。结论:我们的研究证实了CTS5在预测泰国er阳性乳腺癌患者LDR风险方面是准确的。它在绝经后患者中的表现似乎更好。CTS5可用于常规临床实践,以改善长期内分泌治疗的决策,特别是在无法获得分子谱分析的资源有限的国家。
期刊介绍:
Breast Cancer: Basic and Clinical Research is an international, open access, peer-reviewed, journal which considers manuscripts on all areas of breast cancer research and treatment. We welcome original research, short notes, case studies and review articles related to breast cancer-related research. Specific areas of interest include, but are not limited to, breast cancer sub types, pathobiology, metastasis, genetics and epigenetics, mammary gland biology, breast cancer models, prevention, detection, therapy and clinical interventions, and epidemiology and population genetics.