Taylor Kathryn L, Luta George, Zotou Vasiliki, Lobo Tania, Hoffman Richard M, Davis Kimberly M, Potosky Arnold L, Li Tengfei, Aaronson David, Van Den Eeden Stephen K
Cancer Prevention and Control Program, Lombardi Comprehensive Cancer Center Georgetown University Washington District of Columbia USA.
Department of Biostatistics, Bioinformatics, and Biomathematics, Lombardi Comprehensive Cancer Center Georgetown University Washington District of Columbia USA.
BJUI Compass. 2021 Dec 14;3(3):226-237. doi: 10.1002/bco2.124. eCollection 2022 May.
In a prospective, comparative effectiveness study, we assessed clinical and psychological factors associated with switching from active surveillance (AS) to active treatment (AT) among low-risk prostate cancer (PCa) patients.
Using ultra-rapid case identification, we conducted pretreatment telephone interviews ( = 1139) with low-risk patients (PSA ≤ 10, Gleason≤6) and follow-up interviews 6-10 months post-diagnosis ( = 1057). Among men remaining on AS for at least 12 months ( = 601), we compared those who continued on AS ( = 515) versus men who underwent delayed AT ( = 86) between 13 and 24 months, using Cox proportional hazards models.
Delayed AT was predicted by time dependent PSA levels (≥10 vs. <10; HR = 5.6, 95% CI 2.4-13.1) and Gleason scores (≥7 vs. ≤6; adjusted HR = 20.2, 95% CI 12.2-33.4). Further, delayed AT was more likely among men whose urologist initially recommended AT (HR = 2.13, 95% CI 1.07-4.22), for whom tumour removal was very important (HR = 2.18, 95% CI 1.35-3.52), and who reported greater worry about not detecting disease progression early (HR = 1.67, 1.05-2.65). In exploratory analyses, 31% (27/86) switched to AT without evidence of progression, while 4.7% (24/515) remained on AS with evidence of progression.
After adjusting for clinical evidence of disease progression over the first year post-diagnosis, we found that urologists' initial treatment recommendation and patients' early treatment preferences and concerns about AS each independently predicted undergoing delayed AT during the second year post-diagnosis. These findings, along with almost one-half undergoing delayed AT without evidence of progression, suggest the need for greater decision support to remain on AS when it is clinically indicated.
在一项前瞻性、比较有效性研究中,我们评估了低风险前列腺癌(PCa)患者从主动监测(AS)转为积极治疗(AT)相关的临床和心理因素。
通过超快速病例识别,我们对低风险患者(前列腺特异抗原[PSA]≤10, Gleason评分≤6)进行了诊断前电话访谈(n = 1139),并在诊断后6 - 10个月进行了随访访谈(n = 1057)。在至少接受12个月AS的男性(n = 601)中,我们使用Cox比例风险模型比较了继续接受AS的患者(n = 515)与在13至24个月之间接受延迟AT的患者(n = 86)。
延迟AT可由随时间变化的PSA水平(≥10 vs. <10;风险比[HR] = 5.6,95%置信区间[CI] 2.4 - 13.1)和Gleason评分(≥7 vs. ≤6;调整后HR = 20.2,95% CI 12.2 - 33.4)预测。此外,泌尿科医生最初建议AT的男性(HR = 2.13,95% CI 1.07 - 4.22)、认为肿瘤切除非常重要的男性(HR = 2.18,95% CI 1.35 - 3.52)以及报告更担心未早期发现疾病进展的男性(HR = 1.67,1.05 - 2.65)更有可能接受延迟AT。在探索性分析中,31%(27/86)在无进展证据的情况下转为AT,而4.7%(24/515)在有进展证据的情况下仍接受AS。
在调整诊断后第一年疾病进展的临床证据后,我们发现泌尿科医生的初始治疗建议、患者的早期治疗偏好以及对AS的担忧各自独立预测了诊断后第二年接受延迟AT的情况。这些发现,以及近一半患者在无进展证据的情况下接受延迟AT表明,在临床指征允许时,需要更多的决策支持以继续接受AS。