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依维莫司和奥曲肽长效释放剂治疗无功能性胃肠神经内分泌肿瘤的 II 期研究:GETNE1003_EVERLAR 研究。

Phase II Study of Everolimus and Octreotide LAR in Patients with Nonfunctioning Gastrointestinal Neuroendocrine Tumors: The GETNE1003_EVERLAR Study.

机构信息

Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, Barcelona, Spain

Catalan Institute of Oncology (ICO), Bellvitge, Barcelona, Spain.

出版信息

Oncologist. 2019 Jan;24(1):38-46. doi: 10.1634/theoncologist.2017-0622. Epub 2018 May 23.

Abstract

BACKGROUND

Antitumor activity of the combination of somatostatin analogues (SSAs) and the mammalian target of rapamycin (mTOR) inhibitor everolimus in patients with neuroendocrine tumors (NETs) has been reported but not confirmed in prospective trials.

MATERIALS AND METHODS

This prospective, multicenter, single-arm phase II EVERLAR study evaluated everolimus 10 mg/day and the SSA octreotide 30 mg every 28 days in patients with advanced nonfunctioning well-differentiated gastrointestinal NETs (GI-NETs) that progressed in the last 12 months (ClinicalTrials.gov NCT01567488). Prior treatment with SSAs and any systemic or locoregional therapy was allowed except for mTOR inhibitors. Patients continued treatment until disease progression or unacceptable adverse events (AEs). The primary endpoint was progression-free survival (PFS) at 12 months; secondary endpoints included early biochemical response, objective response rate (ORR) by RECIST v1.0, overall survival (OS), AEs, activation of mTOR pathway (insulin-like growth factor 1 receptor [IGF1R] and phosphoS6 [pS6] expression).

RESULTS

Forty-three patients were included in the intent-to-treat analyses. After 12 months of treatment, 62.3% (95% confidence interval [CI] 48%-77%) of patients had not progressed or died. The 24-month PFS rate was 43.6% (95% CI 29%-58%). The confirmed ORR was 2.3%, and stable disease was 58.1%. Median OS was not reached after 24 months of median follow-up. Dose reductions and temporary interruptions due to AEs were required in 14 (33%) and 33 (77%) patients, respectively. The most frequent AEs were diarrhea, asthenia, mucositis, rash, and hyperglycemia. No correlation was observed between IGFR1 and pS6 expression and PFS/OS.

CONCLUSION

The everolimus-octreotide combination provided clinically relevant efficacy in nonfunctioning GI-NETs, similar to the results of RADIANT-2 in functioning setting.

IMPLICATIONS FOR PRACTICE

The EVERLAR study reports prospective data of somatostatin analogue in combination with everolimus in nonfunctioning gastrointestinal neuroendocrine tumors suggesting meaningful activity and favorable toxicity profile that supports drug combination in this setting.

摘要

背景

已有报道称,生长抑素类似物(SSA)与哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂依维莫司联合应用于神经内分泌肿瘤(NET)患者具有抗肿瘤活性,但尚未在前瞻性试验中得到证实。

材料与方法

本研究为前瞻性、多中心、单臂 II 期 EVERLAR 研究,评估了依维莫司 10 mg/天联合奥曲肽 30 mg/28 天治疗在过去 12 个月内进展的晚期非功能性分化良好的胃肠神经内分泌肿瘤(GI-NET)患者中的疗效(ClinicalTrials.gov NCT01567488)。允许患者在使用 SSA 治疗的基础上接受任何全身性或局部治疗,但不包括 mTOR 抑制剂。患者继续接受治疗,直至疾病进展或出现不可接受的不良事件(AE)。主要终点为 12 个月时的无进展生存期(PFS);次要终点包括早期生化缓解、根据 RECIST v1.0 评估的客观缓解率(ORR)、总生存期(OS)、AE、mTOR 通路的激活(胰岛素样生长因子 1 受体 [IGF1R] 和磷酸化 S6 [pS6] 表达)。

结果

43 例患者纳入意向治疗分析。治疗 12 个月后,62.3%(95%置信区间 [CI] 48%-77%)的患者未进展或死亡。24 个月 PFS 率为 43.6%(95%CI 29%-58%)。确认的 ORR 为 2.3%,疾病稳定率为 58.1%。中位随访 24 个月后,中位 OS 尚未达到。分别有 14 例(33%)和 33 例(77%)患者因 AE 而需要减少剂量和暂时中断治疗。最常见的 AE 为腹泻、乏力、黏膜炎、皮疹和高血糖。IGF1R 和 pS6 表达与 PFS/OS 之间未观察到相关性。

结论

依维莫司-奥曲肽联合方案在非功能性 GI-NET 中提供了具有临床意义的疗效,与在功能性 NET 中 RADIANT-2 研究的结果相似。

临床意义

EVERLAR 研究报告了生长抑素类似物联合依维莫司在非功能性胃肠神经内分泌肿瘤中的前瞻性数据,提示该联合方案具有显著的活性和良好的毒性特征,支持在该治疗环境下使用药物联合治疗。

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