Nomogram Analysis for Predicting Response to Androgen-Receptor-Axis-Targeted Therapies in Patients With Metastatic Castration-Resistant Prostate Cancer

IF 2.9 2区 医学 Q2 ONCOLOGY Cancer Medicine Pub Date : 2024-11-08 DOI:10.1002/cam4.70319
I-Hung Shao, Hsiang-Shen Wang, Chin-Hsuan Hsieh, Tsung-Lin Lee, Ying-Hsu Chang, Liang-Kang Huang, Yuan-Cheng Chu, Hung-Chen Kan, Po-Hung Lin, Kai-Jie Yu, Chun-Te Wu, Cheng-Keng Chuang, See-Tong Pang
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Abstract

Background

This study aimed to identify the clinical predictors for the response of patients with mCRPC to ARATs.

Materials and Methods

We retrospectively collected data on consecutive patients who were diagnosed with mCRPC and underwent ARAT treatment during this stage of the disease. Clinical parameters were obtained through medical chart reviews. ARAT failure was defined as a continuous increase in the serum prostate-specific antigen (PSA) level above nadir to > 2 ng/mL, accompanied by radiographic progression. ARAT failure-free survival and overall survival were assessed through Kaplan–Meier survival analysis and Cox regression survival analysis. Nomogram analysis based on significant predictors of ARAT failure-free survival was performed.

Results

In total, 319 patients with mCRPC who underwent ARAT were included. Multivariate analysis revealed that age, International Society of Urological Pathology (ISUP) grading, and chemotherapy-naïve status were significant predictors of ARAT failure-free survival. For overall survival, age, ISUP grading, and nadir PSA level during androgen deprivation therapy (ADT) were significant predictors. Through nomogram analysis based on age, ISUP grading, and chemotherapy-naïve status, the likelihood of ARAT duration being more or less than 1 year could be predicted.

Conclusion

For mCRPC patients, being older, having ISUP Grade 5 cancer, and having a history of chemotherapy were associated with a shorter duration of response to next-line ARATs. Therefore, other therapeutic agents should be prioritized for such patients. Notably, among the included patients, those who were older, had a higher ISUP grade and a higher nadir PSA level during ADT exhibited worse overall survival.

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预测转移性阉割抗性前列腺癌患者对雄激素受体轴靶向治疗反应的提名图分析法
背景:本研究旨在确定mCRPC患者对ARATs反应的临床预测因素:本研究旨在确定mCRPC患者对ARATs反应的临床预测因素:我们回顾性地收集了被诊断为mCRPC并在这一疾病阶段接受ARAT治疗的连续患者的数据。临床参数通过病历审查获得。ARAT治疗失败的定义是血清前列腺特异性抗原(PSA)水平持续上升,超过纳迪值,达到> 2纳克/毫升,并伴有放射学进展。通过 Kaplan-Meier 生存分析和 Cox 回归生存分析评估了无 ARAT 失败生存率和总生存率。根据ARAT无失败生存率的重要预测因素进行了提名图分析:结果:共纳入了319名接受ARAT治疗的mCRPC患者。多变量分析显示,年龄、国际泌尿病理学会(ISUP)分级和化疗无效状态是ARAT无失败生存率的重要预测因素。就总生存率而言,年龄、ISUP分级和雄激素剥夺疗法(ADT)期间的PSA最低水平是重要的预测因素。通过基于年龄、ISUP分级和化疗无效状态的提名图分析,可以预测ARAT持续时间大于或小于1年的可能性:结论:对于mCRPC患者来说,年龄较大、患有ISUP 5级癌症和有化疗史与下线ARATs反应持续时间较短有关。因此,这类患者应优先考虑其他治疗药物。值得注意的是,在纳入的患者中,年龄较大、ISUP分级较高和ADT期间PSA最低水平较高的患者总生存期较短。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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