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HALP评分在转移性去势抵抗性前列腺癌中的预后价值:结合去势抵抗时间的分析

Prognostic value of the HALP score in metastatic castration-resistant prostate cancer: an analysis combined with time to castration resistance.

作者信息

Gökmen İvo, Demir Nazan, Peker Pınar, Özcan Erkan, Akgül Fahri, Bayrakçı İsmail, Divriklioğlu Didem, Erdoğan Bülent, Topaloğlu Sernaz, Hacıoğlu Muhammet Bekir

机构信息

Division of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Türkiye.

Department of Medical Oncology, Sultan I. Murat Public Hospital, Edirne, Türkiye.

出版信息

Front Oncol. 2024 Dec 5;14:1431629. doi: 10.3389/fonc.2024.1431629. eCollection 2024.

Abstract

OBJECTIVE

The aim of our study was to assess the impact of the combination of HALP score with TTCR score on OS and PFS in PC patients who developed castration resistance.

PATIENTS AND METHODS

The study enrolled 152 patients with metastatic disease who had received either ARTAs or docetaxel as first-line treatment. The median cut-off was 30.83 months for the HALP score and 16.1 months for TTCR determined by ROC analysis. Based on these cut-off values, patients were categorized into low-high HALP score and TTCR <16.1 months-TTCR ≥16.1 months groups. The combination of HALP score and TTCR was then stratified by risk into three new groups: Factor 0, Factor 1, and Factor 2.

RESULTS

PFS was significantly shorter in the TTCR <16.1 months group compared to the TTCR ≥16.1 months group, as well as in the low-HALP score group compared to the high-HALP score group. Furthermore, as the number of factors increased, a significant increase in OS and PFS was observed in the groups formed by the combination of HALP score and TTCR.

CONCLUSION

We have validated the predictive capability of combining low HALP score (<30.38) and short TTCR (<16.1 months) parameters in estimating the OS and PFS durations of mCRPC patients, both recognized as unfavorable prognostic indicators.

摘要

目的

我们研究的目的是评估HALP评分与TTCR评分相结合对去势抵抗性前列腺癌(PC)患者总生存期(OS)和无进展生存期(PFS)的影响。

患者与方法

本研究纳入了152例转移性疾病患者,这些患者接受了雄激素受体靶向药物(ARTAs)或多西他赛作为一线治疗。通过ROC分析确定,HALP评分的中位数截断值为30.83个月,TTCR的中位数截断值为16.1个月。基于这些截断值,患者被分为HALP评分低-高组以及TTCR<16.1个月-TTCR≥16.1个月组。然后将HALP评分和TTCR的组合按风险分层为三个新组:因素0、因素1和因素2。

结果

与TTCR≥16.1个月组相比,TTCR<16.1个月组的PFS显著缩短,与高HALP评分组相比,低HALP评分组的PFS也显著缩短。此外,随着因素数量的增加,HALP评分与TTCR组合形成的组中OS和PFS显著增加。

结论

我们已经验证了低HALP评分(<30.38)和短TTCR(<16.1个月)参数相结合在估计mCRPC患者OS和PFS持续时间方面的预测能力,这两个参数均被认为是不良预后指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98a5/11655342/c656913bd16d/fonc-14-1431629-g001.jpg

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