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黄体生成素释放激素激动剂给药时间对前列腺癌患者睾酮抑制的影响:美国临床数据分析。

The Impact of Late Luteinizing Hormone-Releasing Hormone Agonist Dosing on Testosterone Suppression in Patients with Prostate Cancer: An Analysis of United States Clinical Data.

机构信息

University of California-San Diego, San Diego, California.

John Wayne Cancer Institute, Santa Monica, California.

出版信息

J Urol. 2020 Apr;203(4):743-750. doi: 10.1097/JU.0000000000000577. Epub 2019 Oct 3.

Abstract

PURPOSE

We evaluated the timeliness of androgen deprivation therapy dosing, the impact of dosing nonadherence on testosterone, and the frequency of testosterone and prostate specific antigen testing in patients with prostate cancer.

MATERIALS AND METHODS

We retrospectively analyzed the records of 22,860 patients with prostate cancer treated with luteinizing hormone-releasing hormone agonists. Analyses were done using 2 definitions of month, including a 28-day month (late dosing after day 28, 84, 112 or 168) and an extended month (late after day 32, 97, 128 or 194) for 1, 3, 4 and 6-month formulations, respectively. The prevalence of late dosing, associated testosterone values, and the frequency of testosterone and prostate specific antigen testing were assessed. Statistical significance was assessed with the unpaired t-test.

RESULTS

Of the injections 84% and 27% were late for the 28-day and extended month analyses, respectively. For the 28-day month 60% and 29% of injections were late by more than 1 and more than 2 weeks, respectively. Of testosterone values 4% were greater than 50 ng/dl for early/on time injections using both definitions, and 15% and 27% were greater than 50 ng/dl when late, and for the 28-day month and the extended month, respectively. For early/on time vs late injections 22% vs 31% of testosterone values were greater than 20 ng/dl for the 28-day month and 21% vs 43% for the extended month. Mean testosterone was higher when late 49 ng/dl for 28-day month, 79 ng/dl for extended month) vs early/on time (both 21 ng/dl). Of the injections prostate specific antigen measurements were performed in 83% and testosterone assessment was done in only 13%.

CONCLUSIONS

Luteinizing hormone-releasing hormone agonists were frequently (84%) administered later than the schedules used in pivotal trials. Nearly half of the late testosterone values for the extended month were greater than 20 ng/dl and mean testosterone was almost double the castration level. Elevated testosterone remained unidentified with infrequent testing.

摘要

目的

我们评估了去势治疗剂量的及时性、剂量不依从对睾酮的影响,以及前列腺癌患者的睾酮和前列腺特异性抗原检测的频率。

材料和方法

我们回顾性分析了 22860 例接受黄体生成素释放激素激动剂治疗的前列腺癌患者的记录。分析采用 2 种月份定义,包括 28 天(第 28 天、84、112 或 168 天后的晚期剂量)和扩展月份(第 32 天、97、128 或 194 天后的晚期剂量),分别用于 1、3、4 和 6 个月的配方。评估了晚期剂量的发生率、相关的睾酮值,以及睾酮和前列腺特异性抗原检测的频率。使用未配对的 t 检验评估统计学意义。

结果

在 28 天和扩展月份分析中,84%和 27%的注射剂是晚期的。对于 28 天的月份,60%和 29%的注射剂分别延迟超过 1 周和 2 周。使用这两种定义,4%的睾酮值对于早期/按时注射是大于 50ng/dl 的,而晚期时,15%和 27%的睾酮值大于 50ng/dl,分别用于 28 天的月份和扩展月份。对于早期/按时注射和晚期注射,28 天的月份和扩展月份的睾酮值分别有 22%和 31%大于 20ng/dl,21%和 43%大于 50ng/dl。晚期时的平均睾酮值更高,28 天的月份为 49ng/dl,扩展月份为 79ng/dl(两者均为 21ng/dl)。在注射剂中,83%进行了前列腺特异性抗原检测,而仅进行了 13%的睾酮评估。

结论

黄体生成素释放激素激动剂经常(84%)延迟于关键试验中使用的方案进行给药。扩展月份近一半的晚期睾酮值大于 20ng/dl,平均睾酮值几乎是去势水平的两倍。由于检测不频繁,升高的睾酮仍然未被发现。

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