Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-Machi, Abeno-Ku, Osaka 545-8585, Japan.
Curr Oncol. 2022 Jan 31;29(2):758-765. doi: 10.3390/curroncol29020064.
Giant cell tumor of soft tissue (GCT-ST), histologically resembling the GCT of the bone, is a rare tumor. The tumor has been categorized to have low malignancy. Few reports of local recurrence or distant metastasis and the use of chemotherapeutic agents for metastatic GCT-ST exist. Herein, we report the efficacy of pazopanib in a 78-year-old Japanese woman with GCT in the intrinsic back musculature with both post-operative local recurrence and lung metastasis. The patient visited the hospital with a three-month history of a palpable mass in the intrinsic back musculature. Following magnetic resonance imaging, the tumor predominantly exhibited slight hyperintensity on T2-weighted images and intense heterogeneous enhancement on contrast-enhanced T1-weighted images. A percutaneous needle biopsy was performed, and the pathological diagnosis was GCT-ST. The patient underwent surgery, and three months later she presented with not only local recurrence but also multiple lung metastases. The patient was immediately treated with pazopanib 400 mg once daily. One month after initiating treatment, a partial response in the pulmonary lesions was observed, and stable disease (SD) effects lasted for 11 months without severe adverse effects. Therefore, pazopanib treatment for metastatic malignant giant cell tumor of soft tissue achieved reasonable success.
软组织巨细胞瘤(GCT-ST)在组织学上类似于骨巨细胞瘤,是一种罕见的肿瘤。该肿瘤被归类为低度恶性。关于局部复发或远处转移的报道较少,也很少使用化疗药物治疗转移性 GCT-ST。本文报告了帕唑帕尼治疗一名 78 岁日本女性内在背部肌肉内 GCT 的疗效,该患者既有术后局部复发又有肺部转移。该患者因背部内在肌肉可触及肿块就诊,病史为 3 个月。磁共振成像(MRI)检查后,肿瘤在 T2 加权图像上主要表现为轻度高信号,在对比增强 T1 加权图像上呈不均匀强化。进行了经皮针活检,病理诊断为 GCT-ST。患者接受了手术,术后 3 个月不仅出现局部复发,还出现了多个肺部转移。患者立即接受了帕唑帕尼 400 mg 每日一次治疗。治疗开始后 1 个月,肺部病变出现部分缓解,疾病稳定(SD)效应持续了 11 个月,无严重不良反应。因此,帕唑帕尼治疗转移性软组织恶性巨细胞瘤取得了合理的疗效。