Department of Pediatrics, Texas Children's Cancer and Hematology Centers, Baylor College of Medicine, Houston, Texas.
Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.
Curr Probl Cancer. 2021 Aug;45(4):100768. doi: 10.1016/j.currproblcancer.2021.100768. Epub 2021 Jul 1.
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumor of intermediate malignant potential that predominantly affects children, adolescents and young adults. IMT has a predilection for the lung, abdomen, pelvis, and retroperitoneum, however, can affect any part of the body. IMT is typically localized, and multifocal or metastatic disease is uncommon. Complete surgical resection is the treatment of choice when feasible. There is no established standard of care for unresectable and advanced IMT. Approximately half of IMTs harbor anaplastic lymphoma kinase (ALK) gene rearrangements, and fusions involving ROS1, PDGFRβ, RET and NTRK have also been described. Given the molecular landscape of IMT, management of these tumors has evolved to include tyrosine kinase inhibitors and novel targeted therapeutics. This review highlights the molecular characteristics, evolution of targeted therapies and the remaining challenges in the management of IMT.
炎性肌纤维母细胞瘤(IMT)是一种罕见的具有中等恶性潜能的间叶性肿瘤,主要影响儿童、青少年和年轻成年人。IMT 偏爱肺、腹部、骨盆和腹膜后,但也可影响身体的任何部位。IMT 通常为局限性,多灶性或转移性疾病不常见。当可行时,完全手术切除是首选治疗方法。对于无法切除和晚期的 IMT,尚无既定的治疗标准。大约一半的 IMT 存在间变性淋巴瘤激酶(ALK)基因重排,并且还描述了涉及 ROS1、PDGFRβ、RET 和 NTRK 的融合。鉴于 IMT 的分子特征,这些肿瘤的管理已发展为包括酪氨酸激酶抑制剂和新型靶向治疗药物。本综述重点介绍了 IMT 的分子特征、靶向治疗的演变以及管理中仍然存在的挑战。