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初发寡转移去势敏感性前列腺癌的流行病学、治疗模式和临床结局。

Epidemiology, treatment patterns, and clinical outcomes in de novo oligometastatic hormone-sensitive prostate cancer.

机构信息

Division of Urology, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.

出版信息

Cancer. 2024 Nov 15;130(22):3815-3825. doi: 10.1002/cncr.35466. Epub 2024 Jul 1.

Abstract

BACKGROUND

This study was conducted to better characterize the epidemiology, clinical outcomes, and current treatment patterns of de novo oligometastatic hormone-sensitive prostate cancer (omHSPC) in the United States Veterans Affairs Health Care System.

METHODS

In this observational retrospective cohort study, 400 de novo metastatic hormone-sensitive PC (mHSPC) patients diagnosed from January 2015 to December 2020 (follow-up through December 2021) were randomly selected. omHSPC was defined as five or less total metastases (excluding liver) by conventional imaging. Kaplan-Meier methods estimated overall survival (OS) and castration-resistant prostate cancer (CRPC)-free survival from mHSPC diagnosis date and a log-rank test compared these outcomes by oligometastatic status.

RESULTS

Twenty percent (79 of 400) of de novo mHSPC patients were oligometastatic. Most baseline characteristics were similar by oligometastatic status; however, men with non-omHSPC had higher median prostate-specific antigen at diagnosis (151.7) than omHSPC (44.1). First-line (1L) novel hormonal therapy was similar between groups (20%); 1L chemotherapy was lower in omHSPC (5%) versus non-omHSPC (14%). More omHSPC patients received metastasis-directed therapy/prostate radiation therapy (14%) versus non-omHSPC (2%). Median OS and CRPC-free survival (in months) were higher in omHSPC versus non-omHSPC (44.4; 95% confidence interval [CI], 33.9-not estimated vs. 26.2; 95% CI, 20.5-32.5, p = .0089 and 27.6; 95% CI, 22.1-37.2 vs. 15.3; 95% CI, 12.8-17.9, p = .0049), respectively.

CONCLUSIONS

Approximately 20% of de novo mHSPC were oligometastatic, and OS was significantly longer in omHSPC versus non-omHSPC. Although potentially "curative" therapy use was higher in omHSPC versus non-omHSPC, the percentages were still relatively low. Future studies are warranted given potential for prolonged responses with multimodal therapy inclusive of systemic and local therapies.

摘要

背景

本研究旨在更好地描述美国退伍军人事务医疗保健系统中初发寡转移性激素敏感前列腺癌(omHSPC)的流行病学、临床结局和当前治疗模式。

方法

在这项观察性回顾性队列研究中,随机选择了 400 名初诊转移性激素敏感前列腺癌(mHSPC)患者(随访至 2021 年 12 月),这些患者于 2015 年 1 月至 2020 年 12 月确诊(随访至 2021 年 12 月)。通过常规影像学检查,将 omHSPC 定义为转移灶总数(不包括肝脏)不超过 5 个。采用 Kaplan-Meier 方法估计 mHSPC 诊断日期的总生存期(OS)和去势抵抗性前列腺癌(CRPC)无进展生存期,并采用对数秩检验比较寡转移状态的这些结果。

结果

初发 mHSPC 患者中有 20%(79/400)为寡转移。根据寡转移状态,大多数基线特征相似;然而,非寡转移患者的前列腺特异性抗原中位值更高(151.7),而寡转移患者的前列腺特异性抗原中位值为 44.1。两组一线(1L)新型激素治疗相似(20%);寡转移患者的 1L 化疗率(5%)低于非寡转移患者(14%)。更多的寡转移患者接受了转移灶定向治疗/前列腺放疗(14%),而非寡转移患者(2%)。寡转移患者的中位 OS 和 CRPC 无进展生存期(月)均高于非寡转移患者(44.4;95%置信区间[CI],33.9-未估计 vs. 26.2;95% CI,20.5-32.5,p=0.0089 和 27.6;95% CI,22.1-37.2 vs. 15.3;95% CI,12.8-17.9,p=0.0049)。

结论

约 20%的初发 mHSPC 为寡转移,寡转移患者的 OS 明显长于非寡转移患者。尽管寡转移患者中使用潜在的“治愈性”治疗的比例高于非寡转移患者,但这一比例仍然相对较低。鉴于系统和局部治疗相结合的多模式治疗可能会带来更长的缓解期,因此有必要开展进一步的研究。

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