Kaban L B, Mulliken J B, Ezekowitz R A, Ebb D, Smith P S, Folkman J
Department of Oral and Maxillofacial Surgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
Pediatrics. 1999 Jun;103(6 Pt 1):1145-9. doi: 10.1542/peds.103.6.1145.
We report a 5-year-old girl with a large rapidly growing giant cell tumor of the mandible that recurred 2 months after the first surgical excision and 3 months after a second resection. An angiogenic protein, (bFGF), was abnormally elevated in her urine. The patient was treated with interferon alfa-2a for 1 year because this agent inhibits angiogenesis by suppressing bFGF overexpression in infantile hemangiomas and in other human tumors. During this time the bone tumor regressed and disappeared, the urinary bFGF fell to normal levels, and the mandible regenerated. She has remained tumor-free and has been off therapy for 3 years at this writing. This first successful use of interferon alfa-2a to treat a mandibular tumor in a child demonstrates: 1) low grade tumors that overexpress bFGF may respond to interferon alfa-2a, in a manner similar to life-threatening infantile hemangiomas; 2) antiangiogenic therapy, given without interruption for 1 year, was safe and effective in this patient; and 3) treatment may be continued for 1 year without the development of drug resistance.
我们报告了一名5岁女孩,患有下颌骨巨大且快速生长的巨细胞瘤,首次手术切除后2个月复发,二次切除后3个月复发。血管生成蛋白(碱性成纤维细胞生长因子,bFGF)在其尿液中异常升高。该患者接受了1年的干扰素α-2a治疗,因为这种药物通过抑制婴儿血管瘤和其他人类肿瘤中bFGF的过度表达来抑制血管生成。在此期间,骨肿瘤消退并消失,尿液中的bFGF降至正常水平,下颌骨再生。截至撰写本文时,她一直无肿瘤复发,且已停药3年。首次成功使用干扰素α-2a治疗儿童下颌骨肿瘤证明了:1)过度表达bFGF的低度肿瘤可能对干扰素α-2a有反应,方式类似于危及生命的婴儿血管瘤;2)连续1年不间断给予抗血管生成治疗对该患者安全有效;3)治疗可持续1年而不产生耐药性。