Zucker School of Medicine at Hofstra, Hempstead, NY, USA.
Dana Farber Cancer Institute - ECOG-ACRIN Biostatistics Center, Boston, MA, USA.
Invest New Drugs. 2022 Dec;40(6):1306-1314. doi: 10.1007/s10637-022-01311-w. Epub 2022 Oct 20.
This was a two-stage phase II trial of a mTORC1/2 inhibitor (mTORC: mammalian target of rapamycin complex) Sapanisertib (TAK228) in patients with rapalog-resistant pancreatic neuroendocrine tumors (PNETs) (NCT02893930). Approved rapalogs such as everolimus inhibit mTORC1 and have limited clinical activity, possibly due to compensatory feedback loops. Sapanisertib addresses the potential for incomplete inhibition of the mTOR pathway through targeting of both mTORC1 and mTORC2, and thus to reverse resistance to earlier rapamycin analogues. In stage 1, patients received sapanisertib 3 mg by mouth once daily on a continuous dosing schedule in 28-day cycle. This trial adopted a two-stage design with the primary objective of evaluating objective tumor response. The first stage would recruit 13 patients in order to accrue 12 eligible and treated patients. If among the 12 eligible patients at least 1 patient had an objective response to therapy, the study would move to the second stage of accrual where 25 eligible and treated patients would be enrolled. This study activated on February 1, 2017, the required pre-determined number of patients (n = 13) had entered by November 5, 2018 for the first stage response evaluation. The accrual of this trial was formally terminated on December 27, 2019 as no response had been observed after the first stage accrual. Treatment-related grade 3 adverse events were reported in eight (61%) patients with hyperglycemia being the most frequent, in three patients (23%). Other toxicities noted in the trial included fatigue, rash diarrhea, nausea, and vomiting. The median PFS was 5.19 months (95% CI [3.84, 9.30]) and the median OS was 20.44 months (95% CI [5.65, 22.54]). Due to the lack of responses in Stage 1 of the study, the study did not proceed to stage 2. Thus the potential to reverse resistance was not evident.
这是一项关于 mTORC1/2 抑制剂(mTOR:哺乳动物雷帕霉素靶蛋白复合物) Sapanisertib(TAK228)在对 rapalog 耐药的胰腺神经内分泌肿瘤(PNETs)患者中的 2 期临床试验(NCT02893930)。已批准的 rapalog 类药物(如依维莫司)抑制 mTORC1,且临床活性有限,这可能是由于补偿性反馈环所致。Sapanisertib 通过靶向 mTORC1 和 mTORC2 解决了 mTOR 通路不完全抑制的可能性,从而逆转了对早期雷帕霉素类似物的耐药性。在第 1 阶段,患者接受口服 Sapanisertib,每日一次,连续 28 天为一个周期,剂量为 3mg。本试验采用两阶段设计,主要目的是评估客观肿瘤反应。第 1 阶段招募 13 名患者,以入组 12 名符合条件且接受治疗的患者。如果在 12 名符合条件的患者中至少有 1 名对治疗有客观反应,则研究将进入第 2 阶段入组,共入组 25 名符合条件且接受治疗的患者。本研究于 2017 年 2 月 1 日启动,至 2018 年 11 月 5 日已入组所需的预定患者数量(n=13),用于第 1 阶段反应评估。由于第 1 阶段入组后未观察到反应,本试验于 2019 年 12 月 27 日正式终止入组。有 8 名(61%)患者发生了与治疗相关的 3 级不良事件,以高血糖最为常见,发生于 3 名患者(23%)。试验中还观察到其他毒性包括疲劳、皮疹、腹泻、恶心和呕吐。中位无进展生存期(PFS)为 5.19 个月(95%CI [3.84,9.30]),中位总生存期(OS)为 20.44 个月(95%CI [5.65,22.54])。由于第 1 阶段研究无应答,故未进入第 2 阶段。因此,逆转耐药的潜力并不明显。