Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Terasaki Research Institute, Los Angeles, CA, USA.
Clin Ther. 2018 Dec;40(12):2006-2020.e2. doi: 10.1016/j.clinthera.2018.10.008. Epub 2018 Nov 24.
Patients with metastatic neuroendocrine tumors and carcinoid syndrome (CS) may experience chronic, recurring symptoms despite somatostatin analogue therapy. Little is known about the relationship between bowel movement (BM) frequency, patient-reported symptoms and health-related quality of life (QoL). Data from the TELESTAR study were used in exploratory, post hoc analyses to understand the relationship between durable reductions in BM frequency, symptom relief, and health-related QoL.
Patients with metastatic neuroendocrine tumors and CS in the Phase III TELESTAR study were randomized (1:1:1) to receive telotristat ethyl (TE) 250 mg, TE 500 mg, or placebo three times daily (TID) during a 12-week double-blind treatment period (DBTP). All patients received TE 500 mg TID in an open-label extension (OLE) to Week 48. Durable response was predefined. Analyses compared durable responders (DRs) and non-durable responders (NDRs), irrespective of treatment group, at Weeks 12, 24, and 48.
At the start of the DBTP, 135 patients were randomized, 45 patients each to TE 250 mg, TE 500 mg, and placebo. After the 12-week DBTP, 48 of 135 patients were DRs (TE 250 mg, n = 20; TE 500 mg, n = 19; placebo, n = 9). Of the 115 patients who entered the OLE, 35 were DRs initially randomized to TE 250 mg (n = 18) or 500 mg (n = 17), 29 of whom maintained a durable response throughout the OLE. Of the 71 DBTP-NDRs (inclusive of patients initially randomized to placebo), 28 became OLE-DRs. There were 29 NDRs initially randomized to placebo who entered the OLE, 16 of whom became DRs when switched to TE 500 mg. DRs during the DBTP had greater symptom improvements in the DBTP; these improvements continued over the OLE. DBTP-DRs also maintained more meaningful QoL improvements in EORTC QLQ-C30 global health status, nausea and vomiting, pain, diarrhea, and EORTC QLQ-GINET21 gastrointestinal symptoms over the DBTP and OLE periods than DBTP-NDRs.
These results suggest that sustained improvements in BM frequency in patients with CS may have multifaceted, long-term effects on a patient's well-being. ClinicalTrials.gov identifiers: NCT01677910.
尽管使用了生长抑素类似物治疗,但转移性神经内分泌肿瘤和类癌综合征(CS)患者仍可能出现慢性、反复发作的症状。对于排便频率、患者报告的症状和健康相关生活质量(QoL)之间的关系,人们知之甚少。TELESTAR 研究的数据被用于探索性的事后分析,以了解BM 频率持久降低、症状缓解和健康相关 QoL 之间的关系。
在 III 期 TELESTAR 研究中,转移性神经内分泌肿瘤和 CS 患者被随机(1:1:1)接受替曲唑特乙基(TE)250mg、TE 500mg 或安慰剂,每日 3 次(TID),持续 12 周双盲治疗期(DBTP)。所有患者在开放标签扩展(OLE)中均接受 TE 500mg TID,持续至第 48 周。持久反应是预先定义的。分析比较了第 12、24 和 48 周时的持久应答者(DR)和非持久应答者(NDR),无论治疗组如何。
在 DBTP 开始时,135 名患者被随机分组,每组 45 名患者,分别接受 TE 250mg、TE 500mg 和安慰剂。在 12 周的 DBTP 后,135 名患者中有 48 名是 DR(TE 250mg,n=20;TE 500mg,n=19;安慰剂,n=9)。在 115 名进入 OLE 的患者中,最初随机分配至 TE 250mg(n=18)或 500mg(n=17)的 35 名患者为 DR,其中 29 名在整个 OLE 期间保持持久应答。在 71 名 DBTP-NDR 中(包括最初随机分配至安慰剂的患者),有 28 名成为 OLE-DR。最初随机分配至安慰剂的 29 名 NDR 进入 OLE,其中 16 名在转换为 TE 500mg 后成为 DR。DBTP-DR 在 DBTP 期间的症状改善更大;这些改善在 OLE 期间持续。DBTP-DR 在 DBTP 和 OLE 期间还保持了 EORTC QLQ-C30 整体健康状况、恶心和呕吐、疼痛、腹泻和 EORTC QLQ-GINET21 胃肠道症状的更有意义的 QoL 改善,优于 DBTP-NDR。
这些结果表明,CS 患者 BM 频率的持续改善可能对患者的幸福感产生多方面的长期影响。临床试验注册号:NCT01677910。