Department of Orthopaedic Surgery, Nara Medical University, 840, Shijo-cho, Kashihara-city, Nara, 634-8521, Japan.
Department of Orthopaedic Oncology, IRCCS Istituto Ortopedico Rizzoli, Via Pupilli 1, 40136, Bologna, Italy.
BMC Musculoskelet Disord. 2021 Dec 6;22(1):1023. doi: 10.1186/s12891-021-04907-0.
There is no standard treatment for giant cell tumors of the sacrum. We compared the outcomes and complications in patients with sacral giant cell tumors who underwent intralesional nerve-sparing surgery with or without (neo-) adjuvant therapies versus those who underwent non-surgical treatment (denosumab therapy and/or embolization).
We retrospectively investigated 15 cases of sacral giant cell tumors treated at two institutions between 2005 and 2020. Nine patients underwent intralesional nerve-sparing surgery with or without (neo-) adjuvant therapies, and six patients received non-surgical treatment. The mean follow-up period was 85 months for the surgical group (range, 25-154 months) and 59 months (range, 17-94 months) for the non-surgical group.
The local recurrence rate was 44% in the surgical group, and the tumor progression rate was 0% in the non-surgical group. There were two surgery-related complications (infection and bladder laceration) and three denosumab-related complications (apical granuloma of the tooth, stress fracture of the sacroiliac joint, and osteonecrosis of the jaw). In the surgical group, the mean modified Biagini score (bowel, bladder, and motor function) was 0.9; in the non-surgical group, it was 0.5. None of the 11 female patients became pregnant or delivered a baby after developing a sacral giant cell tumor.
The cure rate of intralesional nerve-sparing surgery is over 50%. Non-surgical treatment has a similar risk of complications to intralesional nerve-sparing surgery and has better functional outcomes than intralesional nerve-sparing surgery, but patients must remain on therapy over time. Based on our results, the decision on the choice of treatment for sacral giant cell tumors could be discussed between the surgeon and the patient based on the tumor size and location.
目前对于骶骨巨细胞瘤尚无标准的治疗方法。我们比较了行保留神经的病灶内切除术(辅以或不辅以(新)辅助治疗)与非手术治疗(地舒单抗治疗和/或栓塞)的骶骨巨细胞瘤患者的疗效和并发症。
我们回顾性研究了 2005 年至 2020 年在两个机构治疗的 15 例骶骨巨细胞瘤患者。9 例行保留神经的病灶内切除术(辅以或不辅以(新)辅助治疗),6 例行非手术治疗。手术组的平均随访时间为 85 个月(范围,25-154 个月),非手术组为 59 个月(范围,17-94 个月)。
手术组的局部复发率为 44%,非手术组的肿瘤进展率为 0%。手术组有 2 例手术相关并发症(感染和膀胱裂伤),3 例地舒单抗相关并发症(牙冠部肉芽肿、骶髂关节应力性骨折和下颌骨坏死)。手术组改良 Biagini 评分(肠道、膀胱和运动功能)平均为 0.9,非手术组为 0.5。11 例女性患者在发生骶骨巨细胞瘤后均未怀孕或分娩。
保留神经的病灶内切除术的治愈率超过 50%。非手术治疗与保留神经的病灶内切除术有相似的并发症风险,且功能结局优于保留神经的病灶内切除术,但患者需要长期接受治疗。基于我们的结果,可根据肿瘤的大小和位置,由外科医生和患者共同讨论骶骨巨细胞瘤的治疗选择。