Ioannou Markos, Demertzis Nikolaos, Iakovidou Ioanna, Kottakis Stamatios
Department of Orthopaedic Surgery, "METAXA" Cancer Hospital, Piraeus, Greece.
Anticancer Res. 2007 Mar-Apr;27(2):1143-7.
Extra-abdominal desmoid tumors are rare neoplasms with variable biological behavior. The mainstay of treatment is surgery. Complementary treatment with tyrosine-kinase receptor inhibitor drugs, particularly imatinib mesylate, has been reported in the literature. The purpose of this study was to determine the possible presence of tyrosine-kinase receptors in extra-abdominal desmoid tumors as a marker for imatinib mesylate therapy.
From 1999 to 2004, immunohistochemical methods were carried-out in 14 patients with histologically confirmed extra-abdominal desmoid tumors to determine c-KIT positivity (existence of tyrosine-kinase receptors and PDGFRA and PDGFRB).
All desmoid tumors were c-KIT negative, which demonstrates absence of tyrosine-kinase receptors.
The histological c-KIT markup is an easy and reliable method that can detect whether a desmoid tumor is sensitive to additional treatment with a tyrosine-kinase receptor inhibitor. Molecular biological analysis for the identification of KIT and PDGFR mutation should be performed before imatinib mesylate is included in any treatment protocol.
腹外硬纤维瘤是一种生物学行为多样的罕见肿瘤。治疗的主要方法是手术。文献报道了酪氨酸激酶受体抑制剂药物,特别是甲磺酸伊马替尼的辅助治疗。本研究的目的是确定腹外硬纤维瘤中酪氨酸激酶受体的可能存在情况,作为甲磺酸伊马替尼治疗的标志物。
1999年至2004年,对14例经组织学确诊的腹外硬纤维瘤患者进行免疫组化方法检测,以确定c-KIT阳性(酪氨酸激酶受体以及血小板衍生生长因子受体α和β的存在情况)。
所有硬纤维瘤均为c-KIT阴性,表明不存在酪氨酸激酶受体。
组织学c-KIT标记是一种简单可靠的方法,可检测硬纤维瘤是否对酪氨酸激酶受体抑制剂的额外治疗敏感。在将甲磺酸伊马替尼纳入任何治疗方案之前,应进行KIT和血小板衍生生长因子受体突变鉴定的分子生物学分析。