地诺单抗在脊柱巨细胞瘤综合治疗中的作用:减少局部复发率、手术时间和出血量

A. Tararykova, A. A. Fedenko, E. Musaev, A. Valiev, R. M. Kabardaev, K. A. Borzov, Valeria Igorevna Melnikova
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摘要

目标。目的:评价包括术前地诺单抗治疗在内的联合治疗方法对脊柱巨细胞瘤患者治疗效果的影响。材料和方法。对15例椎骨巨细胞瘤患者进行了单中心回顾性前瞻性研究。平均随访时间为56个月。共有11例患者接受denosumab治疗,治疗方案为:在第一个月的第1、8、15、28天皮下注射120 mg,然后每28天注射1次。手术选择包括边缘切除、节段性切除或整体切除,伴或不伴脊柱重建/稳定。对于局部晚期和不能手术的疾病,长期使用denosumab治疗,直到疾病进展或出现严重不良事件。15例中累及胸椎7例(46.6%),腰椎4例(26.7%),颈椎4例(26.7%)。单纯术后局部复发率为40%(2/5),平均复发时间为4.5个月。4例患者经综合治疗后均无复发。在长期denosumab治疗无法手术的疾病复发期间,没有记录疾病进展(0/7)。术前和长期治疗期间,denosumab的平均注射次数分别为15次和24次。Denosumab治疗可以减少手术时间和出血量。巨细胞椎体肿瘤的联合治疗可以降低疾病复发的风险,同时减少手术时间和出血量。对于不能手术的病例,长期持续的治疗可以达到长期稳定的效果。由于脊柱巨细胞瘤的罕见性,需要进一步的前瞻性招募患者来研究联合治疗的有效性和安全性。
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The role of denosumab in the complex treatment of giant cell tumor of the spine: reducing of local recurrence rate, surgery time and blood loss
Objective. To assess the effect of the combined treatment method including preoperative denosumab therapy on the results of treatment of patients with giant cell tumors of the spine.Material and Methods. A single-center retrospective-prospective study of a series of clinical cases included 15 patients with giant cell tumors of vertebrae. The average follow-up period was 56 months. A total of 11 patients received denosumab therapy according to the following scheme: 120 mg subcutaneously on the 1st, 8th, 15th and 28th days of the first month and then once every 28 days. Surgical options included marginal resection, segmental resection, or en-bloc resection with or without spinal reconstruction/stabilization. In the case of locally advanced and inoperable disease, long-term therapy with denosumab was carried out until the disease progressed or serious adverse events appeared.Results. Thoracic vertebrae were involved in 7 (46.6 %) of 15 cases, lumbar in 4 (26.7 %) and cervical in 4 (26.7 %). Local recurrence rate after surgery alone was 40 % (2/5), average time to recurrence onset was 4.5 months. No relapses were observed after combined treatment performed in four patients. Disease progression during long-term denosumab therapy for inoperable disease recurrence was not recorded (0/7). The average number of denosumab injections before surgery and during long-term therapy was 15 and 24 injections, respectively. Denosumab therapy allows reducing the duration of surgery and the volume of blood loss.Conclusion. Combined therapy of giant cell vertebral tumor allows to reduce the risk of recurrence of the disease, as well as to reduce surgery duration and blood loss. Long-term continuous therapy for inoperable cases allows achieving long-term stabilization of the effect. Due to the rarity of giant cell tumors of the spine, a further prospective recruitment of patients is required to study the efficacy and safety of combined therapies.
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