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在一组去势敏感性转移性前列腺癌亚组中, upfront 治疗强化的缺失不会对肿瘤学结果产生不利影响。

The Omission of Upfront Treatment Intensification Does Not Adversely Affect Oncological Outcomes in a Subset of Castration-Highly Sensitive Metastatic Prostate Cancer.

机构信息

Department of Urology, Local Incorporated Administrative Agency Kurate Hospital, Kurate, Japan;

Department of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

In Vivo. 2024 Sep-Oct;38(5):2328-2334. doi: 10.21873/invivo.13698.

Abstract

BACKGROUND/AIM: In patients with metastatic castration-sensitive prostate cancer (mCSPC), upfront treatment intensification with the addition of new hormonal agents and/or docetaxel to androgen deprivation therapy (ADT) is recommended. However, this modality is potentially excessive in a subset of these patients. This study aimed to identify patients who may be eligible to omit upfront treatment intensification.

PATIENTS AND METHODS

Patients with mCSPC who underwent ADT were enrolled. The association between undetectable prostate-specific antigen (PSA) (<0.2 ng/ml) after ADT initiation and overall or castration-resistance-free survival was evaluated.

RESULTS

Ninety-seven out of the 242 enrolled patients had low-risk and/or low-volume cancer and were further analyzed. Of these, 45 (46.4%) patients achieved undetectable PSA. The median follow-up period after ADT initiation was 70 months. The median overall survival among patients with undetectable PSA was quite long, reaching 226 months and significantly longer than that among patients with detectable PSA [71 months, hazard ratio (HR)=0.27, 95% confidence interval (CI)=0.15-0.49, p<0.001]. Time to development of castration-resistance was also long and significantly longer in the undetectable PSA group than that in the detectable PSA group (median: 124 vs. 17 months, HR=0.20, 95% CI=0.12-0.34, p<0.001).

CONCLUSION

Patients with low-risk and/or low-volume mCSPC showed long-term survival when undetectable PSA was achieved during conventional ADT. In these patients, skipping upfront treatment intensification does not seem to negatively impact survival.

摘要

背景/目的:在转移性去势敏感型前列腺癌(mCSPC)患者中,建议在雄激素剥夺治疗(ADT)的基础上强化治疗,增加新的激素药物和/或多西他赛。然而,对于这些患者中的一部分亚组,这种治疗方法可能是过度的。本研究旨在确定可能有资格省略强化治疗的患者。

方法

招募了接受 ADT 的 mCSPC 患者。评估 ADT 起始后前列腺特异性抗原(PSA)不可检测(<0.2ng/ml)与总生存或去势抵抗生存之间的关系。

结果

在 242 名入组患者中,有 97 名患有低危和/或低体积癌症,进一步进行了分析。其中,45 名(46.4%)患者达到了 PSA 不可检测。ADT 起始后中位随访时间为 70 个月。PSA 不可检测的患者中位总生存时间相当长,达到 226 个月,明显长于 PSA 可检测的患者[71 个月,风险比(HR)=0.27,95%置信区间(CI)=0.15-0.49,p<0.001]。不可检测 PSA 组比可检测 PSA 组发生去势抵抗的时间也更长(中位:124 与 17 个月,HR=0.20,95%CI=0.12-0.34,p<0.001)。

结论

在接受常规 ADT 时达到 PSA 不可检测的低危和/或低体积 mCSPC 患者具有长期生存。在这些患者中,跳过强化治疗似乎不会对生存产生负面影响。

相似文献

本文引用的文献

1
Updates to Advanced Prostate Cancer: AUA/SUO Guideline (2023).《晚期前列腺癌更新:AUA/SUO 指南(2023)》。
J Urol. 2023 Jun;209(6):1082-1090. doi: 10.1097/JU.0000000000003452. Epub 2023 Apr 25.

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