Piccaluga Pier Paolo, Rondoni Michela, Paolini Stefania, Rosti Gianantonio, Martinelli Giovanni, Baccarani Michele
Institute of Haematology and Medical Oncology L and A Seràgnoli, S. Orsola-Malpighi Hospital, University of Bologna, Molecular Pathology Laboratory, Unit of Hematopathology, Via Massarenti, 9-40138 Bologna, Italy.
Expert Opin Biol Ther. 2007 Oct;7(10):1597-611. doi: 10.1517/14712598.7.10.1597.
The treatment of hematologic malignancies has been based for many years on chemotherapy and possibly, for the more aggressive forms, stem cell transplantation. In 2001, the signal transduction inhibitor 571 (STI571, imatinib mesylate) was reported to have striking effects in chronic myeloid leukaemia patients. Since then, imatinib became the first molecular-targeted agent approved for the treatment of human cancer and was later on demonstrated to be effective in other malignancies, such as Philadelphia positive acute lymphoid leukemia, hypereosinophilic syndromes, gastrointestinal stromal tumours and more recently, systemic mastocytosis and other myeloprolipherative disease-carrying platelet-derived growth factor receptor abnormalities. In this article, the authors review the evidence which led to imatinib approval in the treatment of several of the above mentioned diseases.
多年来,血液系统恶性肿瘤的治疗一直基于化疗,对于侵袭性更强的类型,可能还会采用干细胞移植。2001年,有报道称信号转导抑制剂571(STI571,甲磺酸伊马替尼)对慢性髓性白血病患者有显著疗效。从那时起,伊马替尼成为首个被批准用于治疗人类癌症的分子靶向药物,后来还被证明对其他恶性肿瘤有效,如费城染色体阳性的急性淋巴细胞白血病、高嗜酸性粒细胞综合征、胃肠道间质瘤,以及最近的系统性肥大细胞增多症和其他携带血小板衍生生长因子受体异常的骨髓增殖性疾病。在本文中,作者回顾了使伊马替尼被批准用于治疗上述几种疾病的证据。