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带血管腓骨移植是否能提高儿童恶性骨肿瘤骨干节段切除后大段骨移植的疗效?

Does the Addition of a Vascularized Fibula Improve the Results of a Massive Bone Allograft Alone for Intercalary Femur Reconstruction of Malignant Bone Tumors in Children?

机构信息

C. Errani, M. Colangeli, D. M. Donati, M. Manfrini, Orthopaedic Service, Musculoskeletal Oncology Department, Istituto di Ricerca e Cura a Carattere Scientifico, Istituto Ortopedico Rizzoli, Bologna, Italy.

P. A. Alfaro, Hospital Traumatologico de Concepción, Faculty of Medicine, University of Concepcion, Concepcion, Chile.

出版信息

Clin Orthop Relat Res. 2021 Jun 1;479(6):1296-1308. doi: 10.1097/CORR.0000000000001639.

Abstract

BACKGROUND

Massive bone allograft with or without a vascularized fibula is a potentially useful approach for femoral intercalary reconstruction after resection of bone sarcomas in children. However, inadequate data exist regarding whether it is preferable to use a massive bone allograft alone or a massive bone allograft combined with a vascularized free fibula for intercalary reconstructions of the femur after intercalary femur resections in children. Because the addition of a vascularized fibula adds to the time and complexity of the procedure, understanding more about whether it reduces complications and improves the function of patients who undergo these resections and reconstructions would be valuable for patients and treating physicians.

QUESTIONS/PURPOSES: In an analysis of children with bone sarcomas of the femur who underwent an intercalary resection and reconstruction with massive bone allograft with or without a vascularized free fibula, we asked: (1) What was the difference in the surgical time of these two different surgical techniques? (2) What are the complications and number of reoperations associated with each procedure? (3) What were the Musculoskeletal Tumor Society scores after these reconstructions? (4) What was the survival rate of these two different reconstructions?

METHODS

Between 1994 and 2016, we treated 285 patients younger than 16 years with a diagnosis of osteosarcoma or Ewing sarcoma of the femur. In all, 179 underwent resection and reconstruction of the distal femur and 36 patients underwent resection and reconstruction of the proximal femur. Additionally, in 70 patients with diaphyseal tumors, we performed total femur reconstruction in four patients, amputation in five, and a rotationplasty in one. The remaining 60 patients with diaphyseal tumors underwent intercalary resection and reconstruction with massive bone allograft with or without vascularized free fibula. The decision to use a massive bone allograft with or without a vascularized free fibula was probably influenced by tumor size, with the indication to use the vascularized free fibula in longer reconstructions. Twenty-seven patients underwent a femur reconstruction with massive bone allograft and vascularized free fibula, and 33 patients received massive bone allograft alone. In the group with massive bone allograft and vascularized fibula, two patients were excluded because they did not have the minimum data for the analysis. In the group with massive bone allograft alone, 12 patients were excluded: one patient was lost to follow-up before 2 years, five patients died before 2 years of follow-up, and six patients did not have the minimum data for the analysis. We analyzed the remaining 46 children with sarcoma of the femur treated with intercalary resection and biological reconstruction. Twenty-five patients underwent femur reconstruction with a massive bone allograft and vascularized free fibula, and 21 patients had reconstruction with a massive bone allograft alone. In the group of children treated with massive bone allograft and vascularized free fibula, there were 17 boys and eight girls, with a mean ± SD age of 11 ± 3 years. The diagnosis was osteosarcoma in 14 patients and Ewing sarcoma in 11. The mean length of resection was 18 ± 5 cm. The mean follow-up was 117 ± 61 months. In the group of children treated with massive bone allograft alone, there were 13 boys and eight girls, with a mean ± SD age of 12 ± 2 years. The diagnosis was osteosarcoma in 17 patients and Ewing sarcoma in four. The mean length of resection was 15 ± 4 cm. The mean follow-up was 130 ± 56 months. Some patients finished clinical and radiological checks as the follow-up exceeded 10 years. In the group with massive bone allograft and vascularized free fibula, four patients had a follow-up of 10, 12, 13, and 18 years, respectively, while in the group with massive bone allograft alone, five patients had a follow-up of 10 years, one patient had a follow-up of 11 years, and another had 13 years of follow-up. In general, there were no important differences between the groups in terms of age (mean difference 0.88 [95% CI -0.6 to 2.3]; p = 0.26), gender (p = 0.66), diagnosis (p = 0.11), and follow up (mean difference 12.9 [95% CI-22.7 to 48.62]; p = 0.46). There was a difference between groups regarding the length of the resection, which was greater in patients treated with a massive bone allograft and vascularized free fibula (18 ± 5 cm) than in those treated with a massive bone allograft alone (15 ± 4 cm) (mean difference -3.09 [95% CI -5.7 to -0.4]; p = 0.02). Complications related to the procedure like infection, neurovascular compromise, and graft-related complication, such as fracture and nonunion of massive bone allograft or vascularized free fibula and implant breakage, were analyzed by chart review of these patients by an orthopaedic surgeon with experience in musculoskeletal oncology. Survival of the reconstructions that had no graft or implant replacement was the endpoint. The Kaplan-Meier test was performed for a survival analysis of the reconstruction. A p value less than 0.05 was considered significant.

RESULTS

The surgery was longer in patients treated with a massive bone allograft and vascularized free fibula than in patients treated with a massive bone allograft alone (10 ± 0.09 and 4 ± 0.77 hours, respectively; mean difference -6.8 [95% CI -7.1 to -6.4]; p = 0.001). Twelve of 25 patients treated with massive bone allograft and vascularized free fibula had one or more complication: allograft fracture (seven), nonunion (four), and infection (four). Twelve of 21 patients treated with massive bone allograft alone had the following complications: allograft fracture (five), nonunion (six), and infection (one). The mean functional results were 26 ± 4 in patients with a massive bone allograft and vascularized free fibula and 27 ± 2 in patients with a massive bone allograft alone (mean difference 0.75 [95% CI -10.6 to 2.57]; p = 0.39). With the numbers we had, we could not detect a difference in survival of the reconstruction between patients with a massive bone allograft and free vascularized fibula and those with a massive bone allograft alone (84% [95% CI 75% to 93%] and 87% [95% CI 80% to 94%], respectively; p = 0.89).

CONCLUSION

We found no difference in the survival of reconstructions between patients treated with a massive bone allograft and vascularized free fibula and patients who underwent reconstruction with a massive bone allograft alone. Based on this experience, our belief is that we should reconstruct these femoral intercalary defects with an allograft alone and use a vascularized fibula to salvage the allograft only if a fracture or nonunion occurs. This approach would have resulted in about half of the patients we treated not undergoing the more invasive, difficult, and risky vascularized procedure.Level of Evidence Level III, therapeutic study.

摘要

背景

在儿童骨肉瘤切除术后进行股骨节段性切除重建时,使用带或不带血管化腓骨的大段同种异体骨是一种潜在有效的方法。然而,关于在儿童股骨节段性切除后,使用单纯大段同种异体骨与使用大段同种异体骨结合血管化游离腓骨进行节段性重建,哪种方法更优,目前数据不足。因为添加血管化腓骨会增加手术时间和复杂性,所以了解它是否可以减少并发症并改善接受这些切除和重建手术的患者的功能,对于患者和治疗医生来说都是有价值的。

问题/目的:在分析了 285 例股骨骨肉瘤患儿中,采用带或不带血管化游离腓骨的大段同种异体骨进行节段性切除和重建后,我们提出以下问题:(1)两种不同手术技术的手术时间有何差异?(2)每种手术的并发症和再手术次数是多少?(3)重建后肌肉骨骼肿瘤学会评分是多少?(4)两种不同重建的存活率是多少?

方法

1994 年至 2016 年间,我们治疗了 285 例年龄小于 16 岁的骨肉瘤或尤文肉瘤患儿。共有 179 例接受了股骨远端切除术和重建,36 例接受了股骨近端切除术和重建。此外,在 70 例骨干肿瘤患者中,我们有 4 例进行了全股骨重建,5 例进行了截肢,1 例行旋转成形术。其余 60 例骨干肿瘤患儿采用大段同种异体骨带或不带血管化游离腓骨进行节段性切除和重建。是否使用大段同种异体骨带或不带血管化游离腓骨可能与肿瘤大小有关,较长的重建时需要使用血管化游离腓骨。27 例患者接受了大段同种异体骨和游离腓骨重建,33 例患者接受了单纯大段同种异体骨重建。在大段同种异体骨和血管化腓骨组中,由于两名患者缺乏分析所需的最低数据,因此被排除在外。在单纯大段同种异体骨组中,由于 12 名患者缺乏分析所需的最低数据,因此被排除在外:一名患者在 2 年随访前失访,5 名患者在 2 年随访前死亡,6 名患者缺乏分析所需的最低数据。我们分析了 46 例接受节段性切除和生物重建的股骨肉瘤患儿。25 例患者接受了大段同种异体骨和游离腓骨血管重建,21 例患者接受了单纯大段同种异体骨重建。在接受大段同种异体骨和游离腓骨血管重建的患儿中,有 17 名男孩和 8 名女孩,平均年龄±标准差为 11±3 岁。诊断为骨肉瘤 14 例,尤文肉瘤 11 例。平均切除长度为 18±5cm。平均随访时间为 117±61 个月。在接受单纯大段同种异体骨重建的患儿中,有 13 名男孩和 8 名女孩,平均年龄±标准差为 12±2 岁。诊断为骨肉瘤 17 例,尤文肉瘤 4 例。平均切除长度为 15±4cm。平均随访时间为 130±56 个月。一些患者的随访时间超过 10 年,完成了临床和影像学检查。在大段同种异体骨和血管化游离腓骨组中,分别有 4 名患者随访 10、12、13 和 18 年,而在单纯大段同种异体骨组中,有 5 名患者随访 10 年,1 名患者随访 11 年,另 1 名患者随访 13 年。一般来说,两组在年龄(平均差异 0.88[95%CI-0.6 至 2.3];p=0.26)、性别(p=0.66)、诊断(p=0.11)和随访(平均差异 12.9[95%CI-22.7 至 48.62];p=0.46)方面无显著差异。两组间的切除长度存在差异,接受大段同种异体骨和血管化游离腓骨重建的患者切除长度大于接受单纯大段同种异体骨重建的患者(18±5cm 比 15±4cm)(平均差异-3.09[95%CI-5.7 至-0.4];p=0.02)。通过对这些患者进行骨科医生的图表回顾,分析了与手术相关的并发症,如感染、神经血管损伤、移植物相关并发症,如大段同种异体骨或血管化游离腓骨骨折和不愈合以及植入物断裂等。没有移植或植入物置换的重建的存活率是终点。采用 Kaplan-Meier 生存分析对重建进行生存分析。p 值小于 0.05 被认为具有统计学意义。

结果

接受大段同种异体骨和血管化游离腓骨重建的患者手术时间长于接受单纯大段同种异体骨重建的患者(分别为 10±0.09 小时和 4±0.77 小时;平均差异-6.8[95%CI-7.1 至-6.4];p=0.001)。25 例接受大段同种异体骨和血管化游离腓骨重建的患者中有 12 例发生了 1 种或多种并发症:移植物骨折(7 例)、不愈合(4 例)和感染(4 例)。21 例接受单纯大段同种异体骨重建的患者中有 12 例发生了并发症:移植物骨折(5 例)、不愈合(6 例)和感染(1 例)。患者的平均功能结果为接受大段同种异体骨和血管化游离腓骨重建的患者为 26±4,接受单纯大段同种异体骨重建的患者为 27±2(平均差异 0.75[95%CI-10.6 至 2.57];p=0.39)。根据我们现有的数据,我们无法检测到大段同种异体骨带血管化游离腓骨重建与单纯大段同种异体骨重建的重建存活率之间的差异(84%[95%CI75%至 93%]和 87%[95%CI80%至 94%];p=0.89)。

结论

我们发现接受大段同种异体骨和血管化游离腓骨重建与接受单纯大段同种异体骨重建的患者的重建存活率没有差异。基于这一经验,我们的观点是,我们应该仅用同种异体骨重建这些股骨节段性缺损,如果发生骨折或不愈合,再使用血管化腓骨来挽救同种异体骨。这样的方法可能会使我们治疗的一半患者无需进行更具侵袭性、难度更大和风险更高的血管化手术。

证据水平

III 级,治疗性研究。

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