Department of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, CA, USA .
Immunopharmacol Immunotoxicol. 2014 Apr;36(2):182-6. doi: 10.3109/08923973.2013.864671. Epub 2014 Feb 5.
Talactoferrin alfa (TLF) is a unique recombinant form of human lactoferrin. The hypothesized mechanism of action involves TLF binding to the intestinal endothelium inducing dendritic cell maturation and cytokine release leading to infiltration of tumor with monocytes and T-lymphocytes and inhibition of tumor growth.
Based on promising phase II trial results, this correlative study was undertaken to examine immune mechanism of action of TLF in metastatic non-small cell lung cancer (NSCLC) patients.
Talactoferrin was administered orally at 1.5 g bid weeks 1-12 with 2 weeks off on a 14-week cycle. Enrolled patients had a pathologic diagnosis of NSCLC previously treated with at least two lines of systemic treatment. Patients had core biopsy of tumor before initiation of talactoferrin and at week 7 on TLF. Flow cytometry and quantitative immunohistochemistry for immune correlates were performed on the biopsied specimens.
Four patients with metastatic NSCLC were enrolled. The trial was halted pre-maturely in light of negative phase III trial results. For the two patients who had repeat on-treatment tumor biopsies, a consistent increase in monocytes as a percentage of total immune cells was observed. Otherwise, no clear trend of increase or decrease was observed in any other immune cell parameters compared to matched patient pre-treatment biopsies.
Repeat biopsies for immune correlates by flow cytometry and quantitative immunohistochemistry in NSCLC patients are feasible. In the few patients sampled before trial closure, increased monocytes as a total percentage of the immune cell population within tumor was observed in response to TLF.
乳铁蛋白 alpha(TLF)是一种独特的重组人乳铁蛋白形式。其作用机制假设涉及 TLF 与肠道内皮结合,诱导树突状细胞成熟和细胞因子释放,导致单核细胞和 T 淋巴细胞浸润肿瘤,并抑制肿瘤生长。
基于有前景的 II 期试验结果,进行了这项相关性研究,以检查 TLF 在转移性非小细胞肺癌(NSCLC)患者中的免疫作用机制。
TLF 口服给药,剂量为 1.5g bid,每周 1-12 天,每 14 天停药 2 天。入组患者均经病理诊断为 NSCLC,既往接受过至少两种系统治疗。患者在开始使用 TLF 前和第 7 周进行肿瘤核心活检。对活检标本进行流式细胞术和免疫组织化学定量检测以评估免疫相关性。
共入组 4 例转移性 NSCLC 患者。鉴于 III 期试验的阴性结果,该试验提前终止。对于 2 例接受重复治疗后肿瘤活检的患者,观察到单核细胞作为总免疫细胞的百分比持续增加。否则,与患者治疗前活检相比,任何其他免疫细胞参数均未观察到明显的增加或减少趋势。
对 NSCLC 患者进行流式细胞术和免疫组织化学定量检测以评估免疫相关性是可行的。在试验关闭前采样的少数患者中,观察到肿瘤内单核细胞作为总免疫细胞百分比增加。