Fujiwara Motohiro, Yuasa Takeshi, Komai Yoshinobu, Fujiwara Ryo, Oguchi Tomohiko, Numao Noboru, Yamamoto Shinya, Yonese Junji
Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Cancer Diagn Progn. 2021 Mar 3;1(1):1-5. doi: 10.21873/cdp.10000. eCollection 2021 Mar-Apr.
To reduce the frequency of the need for hospital visits for patients with prostate cancer (PCa) taking androgen-deprivation therapy during the SARS-CoV-2 (COVID-19) pandemic, we switched them from gonadotropin-releasing hormone (GnRH) antagonist to a long-acting luteinizing hormone-releasing hormone (LH-RH) agonist. Here, we confirmed the efficacy and safety profile of this switching.
We analyzed the medical records of 32 patients with PCa who received ADT and switched from GnRH antagonist to a long-acting LH-RH agonist during the COVID-19 pandemic, evaluating hematological and serological variables, including serum testosterone and prostate-specific antigen.
Before and after the switching from GnRH antagonist to LH-RH agonist, the median serum testosterone levels were 0.22 and 0.18 ng/ml, respectively, and the median serum prostate-specific antigen levels were 0.18 and 0.11 ng/ml, respectively. No changes in the rates of flare-ups of conditions or adverse events were observed.
Switching from GnRH antagonist to a long-acting LH-RH agonist appears to be a reasonable option that does not diminish efficacy or exacerbate adverse events.
为了减少在严重急性呼吸综合征冠状病毒2(COVID-19)大流行期间接受雄激素剥夺治疗的前列腺癌(PCa)患者的医院就诊频率,我们将他们从促性腺激素释放激素(GnRH)拮抗剂转换为长效促黄体生成素释放激素(LH-RH)激动剂。在此,我们证实了这种转换的疗效和安全性。
我们分析了32例在COVID-19大流行期间接受雄激素剥夺治疗并从GnRH拮抗剂转换为长效LH-RH激动剂的PCa患者的病历,评估血液学和血清学变量,包括血清睾酮和前列腺特异性抗原。
从GnRH拮抗剂转换为LH-RH激动剂前后,血清睾酮中位数水平分别为0.22和0.18 ng/ml,血清前列腺特异性抗原中位数水平分别为0.18和0.11 ng/ml。未观察到病情发作率或不良事件的变化。
从GnRH拮抗剂转换为长效LH-RH激动剂似乎是一种合理的选择,不会降低疗效或加剧不良事件。