Division of Medical Oncology, Department of Internal Medicine, Huntsman Cancer Institute, University of Utah, Salt Lake City.
Department of Internal Medicine, Detroit Medical Center Sinai Grace Hospital, Detroit, Michigan.
JAMA Netw Open. 2024 May 1;7(5):e249417. doi: 10.1001/jamanetworkopen.2024.9417.
The treatment paradigm for advanced urothelial carcinoma (aUC) has undergone substantial transformation due to the introduction of effective, novel therapeutic agents. However, outcomes remain poor, and little is known about current treatment approaches and attrition rates for patients with aUC.
To delineate evolving treatment patterns and attrition rates in patients with aUC using a US-based patient-level sample.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study used patient-level data from the nationwide deidentified electronic health record database Flatiron Health, originating from approximately 280 oncology clinics across the US. Patients included in the analysis received treatment for metastatic or local aUC at a participating site from January 1, 2011, to January 31, 2023. Patients receiving treatment for 2 or more different types of cancer or participating in clinical trials were excluded from the analysis.
Frequencies and percentages were used to summarize the (1) treatment received in each line (cisplatin-based regimens, carboplatin-based regimens, programmed cell death 1 and/or programmed cell death ligand 1 [PD-1/PD-L1] inhibitors, single-agent nonplatinum chemotherapy, enfortumab vedotin, erdafitinib, sacituzumab govitecan, or others) and (2) attrition of patients with each line of therapy, defined as the percentage of patients not progressing to the next line.
Of the 12 157 patients within the dataset, 7260 met the eligibility criteria and were included in the analysis (5364 [73.9%] men; median age at the start of first-line treatment, 73 [IQR, 66-80] years). All patients commenced first-line treatment; of these, only 2714 (37.4%) progressed to receive second-line treatment, and 857 (11.8%) advanced to third-line treatment. The primary regimens used as first-line treatment contained carboplatin (2241 [30.9%]), followed by PD-1/PD-L1 inhibitors (2174 [29.9%]). The PD-1/PD-L1 inhibitors emerged as the predominant choice in the second- and third-line (1412 of 2714 [52.0%] and 258 of 857 [30.1%], respectively) treatments. From 2019 onward, novel therapeutic agents were increasingly used in second- and third-line treatments, including enfortumab vedotin (219 of 2714 [8.1%] and 159 of 857 [18.6%], respectively), erdafitinib (39 of 2714 [1.4%] and 28 of 857 [3.3%], respectively), and sacituzumab govitecan (14 of 2714 [0.5%] and 34 of 857 [4.0%], respectively).
The findings of this cohort study suggest that approximately two-thirds of patients with aUC did not receive second-line treatment. Most first-line treatments do not include cisplatin-based regimens and instead incorporate carboplatin- or PD-1/PD-L1 inhibitor-based therapies. These data warrant the provision of more effective and tolerable first-line treatments for patients with aUC.
由于有效、新型治疗药物的引入,晚期尿路上皮癌 (aUC) 的治疗模式发生了重大转变。然而,治疗效果仍然不佳,对于接受 aUC 治疗的患者目前的治疗方法和淘汰率知之甚少。
使用基于美国的患者水平样本描绘 aUC 患者不断变化的治疗模式和淘汰率。
设计、设置和参与者:本回顾性队列研究使用来自美国全国性匿名电子健康记录数据库 Flatiron Health 的患者水平数据,该数据库来自美国约 280 个肿瘤诊所。分析中纳入的患者在参与地点接受转移性或局部 aUC 的治疗,从 2011 年 1 月 1 日至 2023 年 1 月 31 日。排除接受 2 种或多种不同类型癌症治疗或参加临床试验的患者。
使用频率和百分比总结 (1) 每种治疗线接受的治疗 (顺铂类方案、卡铂类方案、程序性细胞死亡 1 和/或程序性细胞死亡配体 1 [PD-1/PD-L1] 抑制剂、单药非铂类化疗、enfortumab vedotin、erdafitinib、sacituzumab govitecan 或其他) 和 (2) 每种治疗线的患者淘汰情况,定义为未进展至下一线的患者百分比。
在数据集内的 12157 名患者中,符合入选标准并纳入分析的有 7260 名患者(73.9%为男性;一线治疗开始时的中位年龄为 73[IQR,66-80]岁)。所有患者均开始一线治疗;其中,仅有 2714 名(37.4%)进展接受二线治疗,857 名(11.8%)进展接受三线治疗。作为一线治疗使用的主要方案包括卡铂(2241[30.9%]),其次是 PD-1/PD-L1 抑制剂(2174[29.9%])。PD-1/PD-L1 抑制剂成为二线(52.0%,1412/2714)和三线(30.1%,258/857)治疗的主要选择。自 2019 年以来,新型治疗药物越来越多地用于二线和三线治疗,包括 enfortumab vedotin(8.1%,219/2714 和 18.6%,159/857)、erdafitinib(1.4%,39/2714 和 3.3%,28/857)和 sacituzumab govitecan(0.5%,14/2714 和 4.0%,34/857)。
本队列研究的结果表明,大约三分之二的 aUC 患者未接受二线治疗。大多数一线治疗不包括顺铂类方案,而是包含卡铂或 PD-1/PD-L1 抑制剂为基础的治疗。这些数据需要为 aUC 患者提供更有效和更耐受的一线治疗。