Hellenic Oncology Research Group (HORG), 55 Lombardou St, 11474, Athens, Greece.
Target Oncol. 2019 Jun;14(3):285-293. doi: 10.1007/s11523-019-00647-3.
FOLFIRI/aflibercept is approved as a second-line treatment in metastatic colorectal cancer (mCRC) but there are limited data for its use as a first-line treatment.
To investigate the activity and safety of first-line FOLFIRI/aflibercept in mCRC, as well as to prospectively evaluate biomarkers of early response to treatment.
MINOAS was a phase II trial that aimed to evaluate the activity and toxicity of first-line FOLFIRI/aflibercept in mCRC. The primary endpoint was objective response rate (ORR). The secondary endpoints were toxicity, progression-free survival (PFS), overall survival (OS), and the evaluation of CEACAM-positive circulating tumor cells (CTC) and diffusion-weighted (DW)-MRI as biomarkers.
Thirty-one patients were enrolled and 259 chemotherapy cycles were administered. At the time of the preplanned interim analysis, all patients had discontinued treatment and the ORR was 61.3%, crossing the activity threshold for trial discontinuation. Median PFS was 8.4 months (95% CI 7.8-9.0). Median OS had not been reached. There was one toxic death due to sepsis; grade 3/4 adverse events included neutropenia (n = 5), diarrhea (n = 6), hypertension (n = 4), asthenia (n = 3), proteinuria (n = 1), and bowel perforation (n = 1). Retaining CTC-negative status predicted better OS compared to continuous detection of CTCs (p = 0.015). Early decrease of the apparent diffusion coefficient (ADC) in DW-MRI was associated with an objective response.
The activity and safety of first-line FOLFIRI/aflibercept merit further evaluation in randomized studies. CLINICALTRIALS.
NCT02624726.
FOLFIRI/aflibercept 已被批准作为转移性结直肠癌(mCRC)的二线治疗药物,但作为一线治疗药物的数据有限。
研究 FOLFIRI/aflibercept 作为一线治疗药物在 mCRC 中的疗效和安全性,并前瞻性评估早期治疗反应的生物标志物。
MINOAS 是一项 II 期临床试验,旨在评估 FOLFIRI/aflibercept 作为一线治疗药物在 mCRC 中的疗效和毒性。主要终点是客观缓解率(ORR)。次要终点包括毒性、无进展生存期(PFS)、总生存期(OS),以及 CEACAM 阳性循环肿瘤细胞(CTC)和弥散加权磁共振成像(DW-MRI)的评估。
共纳入 31 例患者,共接受 259 个化疗周期。在计划的中期分析时,所有患者均已停止治疗,ORR 为 61.3%,超过了试验停药的疗效阈值。中位 PFS 为 8.4 个月(95%CI 7.8-9.0)。中位 OS 尚未达到。有 1 例因败血症导致毒性死亡;3/4 级不良事件包括中性粒细胞减少症(n=5)、腹泻(n=6)、高血压(n=4)、乏力(n=3)、蛋白尿(n=1)和肠穿孔(n=1)。与持续检测 CTC 相比,持续阴性的 CTC 状态预测了更好的 OS(p=0.015)。DW-MRI 中表观扩散系数(ADC)的早期下降与客观缓解相关。
FOLFIRI/aflibercept 作为一线治疗药物的疗效和安全性值得在随机研究中进一步评估。临床试验.gov 注册号:NCT02624726。