Freedland Stephen J, De Hoedt Amanda M, DerSarkissian Maral, Chang Rose, Satija Ambika, Nguyen Catherine, Park Suna, Aillaud Aurore, Drea Edward, Duh Mei S, Polascik Thomas J, Szatrowski Ted
Division of Urology, Cedars-Sinai Medical Center, Los Angeles, California.
Section of Urology, Durham Veterans Affairs Health Care System, Durham, North Carolina.
Urol Pract. 2021 Jan;8(1):112-118. doi: 10.1097/UPJ.0000000000000166. Epub 2020 May 29.
Limited real-world data are available on treatment sequences for patients with metastatic hormone-sensitive prostate cancer treated with androgen deprivation therapy plus docetaxel or abiraterone who progress to castrate resistance.
Veterans Health Affairs electronic medical records were used to analyze 240 men treated for metastatic hormone-sensitive prostate cancer with androgen deprivation therapy plus either docetaxel ("docetaxel cohort," 208 patients, selected to be overrepresented, July 2014 to August 2018) or abiraterone ("abiraterone cohort," 32 patients, December 2016 to September 2018) who received at least 1 treatment after progressing to castrate resistance.
For docetaxel and abiraterone cohorts, respectively, mean age at androgen deprivation therapy initiation was 65 and 72 years, and median followup was 2.2 and 1.4 years. Overall, the maximum number of metastatic castrate resistant prostate cancer treatment lines was 6; 106 patients (44%) had 1, 71 (30%) had 2, and 63 (26%) had 3 or more lines. Most patients received an androgen receptor targeted agent for initial metastatic castrate resistant prostate cancer treatment (94% vs 78% in docetaxel vs abiraterone cohort). Androgen receptor targeted agents were given consecutively to 62% of the docetaxel cohort receiving second line therapy, and to 78% of the abiraterone cohort. Across all metastatic castrate resistant prostate cancer treatment lines 72 (30%) received a taxane (47 docetaxel and 41 cabazitaxel).
Most patients received androgen receptor targeted agents as first metastatic castrate resistant prostate cancer treatment regardless of initial metastatic hormone-sensitive treatment. Moreover, a large proportion were treated with consecutive androgen receptor targeted agents. Given recent evidence suggesting poorer outcomes with this treatment in some patients, longer followup is needed to assess the association between treatment sequence and optimal outcomes.
关于接受雄激素剥夺疗法联合多西他赛或阿比特龙治疗后进展为去势抵抗性的转移性激素敏感性前列腺癌患者的治疗顺序,现有的真实世界数据有限。
利用退伍军人健康管理局的电子病历分析240例接受雄激素剥夺疗法联合多西他赛(“多西他赛队列”,208例患者,选择该队列以使其占比过高,2014年7月至2018年8月)或阿比特龙(“阿比特龙队列”,32例患者,2016年12月至2018年9月)治疗转移性激素敏感性前列腺癌且在进展为去势抵抗后接受至少1次治疗的男性患者。
对于多西他赛和阿比特龙队列,雄激素剥夺疗法开始时的平均年龄分别为65岁和72岁,中位随访时间分别为2.2年和1.4年。总体而言,转移性去势抵抗性前列腺癌治疗线的最大数量为6条;106例患者(44%)有1条治疗线,71例(30%)有2条,63例(26%)有3条或更多治疗线。大多数患者接受雄激素受体靶向药物作为初始转移性去势抵抗性前列腺癌治疗(多西他赛队列中为94%,阿比特龙队列中为78%)。接受二线治疗的多西他赛队列中62%的患者连续给予雄激素受体靶向药物,阿比特龙队列中这一比例为78%。在所有转移性去势抵抗性前列腺癌治疗线中,72例(30%)接受了紫杉烷类药物(47例多西他赛和41例卡巴他赛)。
大多数患者无论初始转移性激素敏感性治疗如何,均接受雄激素受体靶向药物作为首次转移性去势抵抗性前列腺癌治疗。此外,很大一部分患者接受了连续的雄激素受体靶向药物治疗。鉴于最近有证据表明部分患者接受这种治疗的预后较差,需要更长时间的随访来评估治疗顺序与最佳预后之间的关联。