INSERM U618, Université François Rabelais de Tours, Tours, France.
Pharm Res. 2011 Sep;28(9):2147-56. doi: 10.1007/s11095-011-0442-5. Epub 2011 Apr 14.
Lung cancer is the leading cause of cancer-related death worldwide. The efficacy of current systemic treatments is limited, with major side effects and only modest survival improvements. Aerosols routinely used to deliver drugs into the lung for treating infectious and inflammatory lung diseases have never been used to deliver monoclonal antibodies to treat lung cancer. We have shown that cetuximab, a chimeric anticancer anti-EGFR mAb, is suitable for airway delivery as it resists the physical constraints of aerosolization, and have evaluated the aerosol delivery of cetuximab in vivo.
We developed an animal model of lung tumor sensitive to cetuximab by injecting Balb/c Nude mice intratracheally with A431 cells plus 10 mM EDTA and analyzed the distribution, pharmacokinetics and antitumor efficacy of cetuximab aerosolized into the respiratory tract.
Aerosolized IgG accumulated durably in the lungs and the tumor, but passed poorly and slowly into the systemic circulation. Aerosolized cetuximab also limited the growth of the mouse tumor. Thus, administering anticancer mAbs via the airways is effective and may limit systemic side effects.
Delivery of aerosolized-mAbs via the airways deserves further evaluation for treating lung cancers.
肺癌是全球癌症相关死亡的主要原因。目前的系统治疗方法疗效有限,且存在严重的副作用,仅能适度提高生存率。用于治疗感染性和炎症性肺部疾病的气溶胶,已被常规用于将药物递送至肺部,但从未用于输送单克隆抗体来治疗肺癌。我们已经证明,西妥昔单抗(一种嵌合抗癌抗 EGFR mAb)适合气道输送,因为它能抵抗气溶胶化的物理限制,并且已经在体内评估了西妥昔单抗的气溶胶输送。
我们通过将 A431 细胞和 10mM EDTA 气管内注射到 Balb/c Nude 小鼠中来建立对西妥昔单抗敏感的肺部肿瘤动物模型,并分析了吸入呼吸道的西妥昔单抗的分布、药代动力学和抗肿瘤疗效。
吸入的 IgG 可持久地在肺部和肿瘤中蓄积,但进入全身循环的速度较慢且较差。吸入的西妥昔单抗也限制了小鼠肿瘤的生长。因此,通过气道给予抗癌 mAbs 是有效的,并且可能限制全身副作用。
通过气道输送雾化 mAbs 治疗肺癌值得进一步评估。