Department of Orthopaedics, Semmelweis University, Budapest, Hungary.
Department of Oncology, Hungarian Defence Forces Medical Center, Budapest, Hungary.
Pathol Oncol Res. 2022 Aug 24;28:1610633. doi: 10.3389/pore.2022.1610633. eCollection 2022.
Due to the relatively high recurrence rate and the destructive nature of the tumor, the treatment of giant cell tumor is still a challenge. Denosumab appeared to be a promising candidate as a therapeutic drug. However, several studies have reported that tumors can recur during/after treatment with denosumab. Based on activated receptor tyrosine kinase signaling pattern of the stromal/tumor cells, a combination treatment with denosumab and sunitinib has recently been proposed to inhibit recurrences. This prompted us to investigate the PDGFRβ expression of five denosumab treated cases using both primary and recurrent tumors during and after denosumab treatment. In addition, to recognise morphological changes, immunohistochemical analysis of H3F3A and PDGFRβ was also performed. As an effect of denosumab treatment, the permanent absence of giant cells associated with severe to mild fibrosis was the most consistent morphological change, but H3F3A positive stromal/tumor cells were observed in all cases. Furthermore, an increased immunopositivity of PDGFRβ in stromal/tumor cells was evident in all recurrent cases during denosumab treatment. Upon tumor recurrence (after the discontinuation of denosumab treatment) the intensity of PDGFRβ immunostaining in stromal/tumor cells was restored/decreased. Our results confirm (for the first time) the activation of PDGFRβ on mononuclear stromal/tumor cells at protein level as an effect of denosumab treatment, which has so far only been demonstrated by phosphoprotein array analysis (protein lysates). The decreased PDGFRβ activity after the discontinuation of denosumab treatmeant and the increased PDGFRβ activity during denosumab treatment underlines the need for denosumab and sunitinib combination therapy.
由于肿瘤的复发率相对较高且具有破坏性,因此治疗巨细胞瘤仍然是一个挑战。地舒单抗似乎是一种很有前途的治疗药物候选物。然而,有几项研究报告称,在使用地舒单抗治疗期间/之后,肿瘤可能会复发。基于基质/肿瘤细胞中激活的受体酪氨酸激酶信号模式,最近提出了地舒单抗和舒尼替尼联合治疗以抑制复发。这促使我们使用原发性和复发性肿瘤,在使用地舒单抗治疗期间和之后,研究五例接受地舒单抗治疗的病例中 PDGFRβ 的表达。此外,为了识别形态变化,还对地舒单抗治疗的五例病例的 H3F3A 和 PDGFRβ 进行了免疫组织化学分析。作为地舒单抗治疗的一种效果,与严重至轻度纤维化相关的巨细胞永久性缺失是最一致的形态变化,但在所有病例中都观察到 H3F3A 阳性的基质/肿瘤细胞。此外,在所有接受地舒单抗治疗的复发性病例中,均可见基质/肿瘤细胞中 PDGFRβ 的免疫阳性表达增加。在肿瘤复发(停止地舒单抗治疗后)时,基质/肿瘤细胞中 PDGFRβ 免疫染色的强度恢复/降低。我们的研究结果首次证实(在蛋白水平上)地舒单抗治疗会导致单核基质/肿瘤细胞中 PDGFRβ 的激活,这迄今为止仅通过磷酸化蛋白阵列分析(蛋白裂解物)得到证明。地舒单抗停药后 PDGFRβ 活性降低,以及地舒单抗治疗期间 PDGFRβ 活性增加,强调了地舒单抗和舒尼替尼联合治疗的必要性。