P. Piakong, D. Joyce, D. Letson, O. Binitie, Sarcoma Department, H. Lee Moffitt Cancer and Research Institute, Tampa, Florida, USA.
P. Piakong, P. Kiatisevi, Institute of Orthopaedics, Lerdsin Hospital, Bangkok, Thailand.
Clin Orthop Relat Res. 2020 Nov;478(11):2573-2581. doi: 10.1097/CORR.0000000000001336.
Aseptic loosening is one of the most common causes of revision of distal femoral endoprostheses and is considered a mid- to long-term complication. There are not many reports of 10-year survivorship free from aseptic loosening and all-cause survivorship in cemented stems. To our knowledge, there are no reports on radiographic features that are associated with aseptic loosening of these implants.
QUESTIONS/PURPOSES: (1) What is the 5- and 10-year survivorship free from aseptic loosening in patients undergoing reconstruction with a cemented distal femoral endoprosthesis after a tumor resection? (2) What is the all-cause 5- and 10-year survivorship at in these patients? (3) What radiographic features are associated with aseptic loosening at long-term follow-up?
We performed a multicenter retrospective study reviewing aseptic loosening in cemented prostheses to determine radiographic features associated with long-term implant survivorship. Patients who underwent a cemented distal femoral reconstruction with a modular endoprosthesis after resection of a musculoskeletal tumor between 1997 and 2017 were reviewed. A total of 246 patients were identified from five institutions and met initial inclusion criteria. Of those, 21% (51) were lost to follow-up before 2 years, leaving 195 patients available for us to evaluate and analyze the survivorship and radiologic features associated with long-term implant survival. The mean (range) follow-up was 78 months (22 to 257). At the time of this analysis, 69% (135 of 195) of the patients were alive. Osteosarcoma was the most common diagnosis in 43% of patients (83 of 195), followed by metastatic carcinoma 13% (25 of 195). Fifty-six percent (110 of 195) of patients received chemotherapy; 15% (30 of 195) had radiation therapy. Aseptic loosening was diagnosed radiographically and was defined as a circumferential radiolucent line on all views, or subsidence around the stem in the absence of infection. We present 5- and 10-year Kaplan-Meier survivorship free from aseptic loosening, 5- and 10-year all-cause survivorship, and a qualitative assessment of radiographic features potentially associated with aseptic loosening (including the junctional radiolucent area, and cortical expansion remodeling). The junctional radiolucent area was defined as a radiolucent area of the bone starting at the bone-endoprosthesis junction to the tip of the femoral stem, and cortical expansion remodeling was defined as an increased cortical thickness at the stem tip. Although we wished to statistically analyze radiographic factors potentially associated with aseptic loosening, we did not have enough clinical material to do so (only nine patients developed loosening). Instead, we will report a few preliminary qualitative observations, which necessarily are preliminary, and which will need to be confirmed or refuted by future studies. We urge caution in interpreting these findings because of the very small numbers involved.
Kaplan-Meier survivorship free from aseptic loosening of the femoral component at 5 and 10 years were 95% (95% CI 89 to 98) and 93% (95% CI 86 to 97), respectively. Kaplan-Meier survivorship free from revision for any cause at 5 and 10 years were 74% (95% CI 65 to 79) and 64% (95% CI 49 to 70), respectively. Although the numbers were too small to analyze statistically, all patients with aseptic loosening had a junctional radiolucent area more than 20% of the total length of the stem without cortical expansion remodeling at the stem tip. No aseptic loosening was observed if there was cortical ex remodeling, a junctional radiolucent area less than 20%, or curved stems that were 13 mm or greater in diameter. The numbers of patients with aseptic loosening in this series were too small to analyze statistically.
Cemented distal femoral endoprostheses have a relatively low rate of aseptic loosening and acceptable projected first-decade survivorship. The presence of a radiolucent area more than 20% without cortical expansion remodeling at the stem tip may lead to aseptic loosening in patients with these implants. Close radiographic surveillance and revision surgery may be considered for progressive lucencies and clinical symptoms of pain. If revision is contemplated, we recommend using larger diameter curved cemented stems. These are preliminary and provisional observations based on a low number of patients with aseptic loosening; future studies with greater numbers of patients are needed to validate or refute these findings.
Level III, therapeutic study.
无菌性松动是导致远端股骨假体翻修的最常见原因之一,被认为是中期至长期并发症。关于骨水泥固定柄的无菌性松动和全因生存率 10 年无丢失的报道并不多。据我们所知,关于这些植入物无菌性松动相关的放射学特征的报告也很少。
问题/目的:(1)在肿瘤切除后接受骨水泥固定远端股骨假体重建的患者中,无菌性松动的 5 年和 10 年生存率是多少?(2)这些患者的全因 5 年和 10 年生存率是多少?(3)在长期随访中,哪些放射学特征与无菌性松动有关?
我们进行了一项多中心回顾性研究,以确定与长期植入物存活率相关的骨水泥假体的无菌性松动的放射学特征。我们回顾了 1997 年至 2017 年间因肌肉骨骼肿瘤切除而接受模块化假体骨水泥固定远端股骨重建的患者。从五个机构中确定了 246 名患者,其中 21%(51 名)在 2 年前失访,留下 195 名患者可供我们评估和分析与长期植入物生存相关的生存率和放射学特征。平均(范围)随访时间为 78 个月(22 至 257)。在本次分析时,69%(135/195)的患者仍然存活。骨肉瘤是最常见的诊断,占 43%(83/195),其次是转移性癌 13%(25/195)。56%(110/195)的患者接受了化疗;15%(30/195)接受了放疗。无菌性松动是通过放射学诊断的,定义为所有视图上的环形透亮线,或在没有感染的情况下柄周围的下沉。我们提出了 5 年和 10 年无无菌性松动生存率、5 年和 10 年全因生存率,以及与无菌性松动相关的放射学特征的定性评估(包括交界区透亮区和皮质扩张重塑)。交界区透亮区定义为从骨-假体交界区开始到股骨柄尖端的骨透亮区,皮质扩张重塑定义为柄尖端的皮质厚度增加。尽管我们希望对可能与无菌性松动相关的放射学因素进行统计学分析,但我们没有足够的临床资料来进行分析(只有 9 名患者发生松动)。相反,我们将报告一些初步的定性观察结果,这些结果必然是初步的,需要通过未来的研究来证实或反驳。由于涉及的数量非常少,我们在解释这些发现时应谨慎。
股骨组件 5 年和 10 年无无菌性松动生存率分别为 95%(95%可信区间 89 至 98)和 93%(95%可信区间 86 至 97)。5 年和 10 年全因无翻修生存率分别为 74%(95%可信区间 65 至 79)和 64%(95%可信区间 49 至 70)。尽管数量太少无法进行统计学分析,但所有无菌性松动患者的柄尖端都有一个大于 20%总柄长度的交界区透亮区,没有皮质扩张重塑。如果存在皮质外重塑、交界区透亮区小于 20%或直径为 13 毫米或更大的弯曲柄,则不会发生无菌性松动。本系列中无菌性松动患者的数量太少,无法进行统计学分析。
骨水泥固定远端股骨假体的无菌性松动率相对较低,预期 10 年生存率可接受。在柄尖端没有皮质扩张重塑的情况下,如果交界区透亮区大于 20%,可能会导致这些植入物发生无菌性松动。对于有进展性透亮线和疼痛的临床症状的患者,可能需要进行密切的放射学监测和翻修手术。如果考虑翻修,我们建议使用更大直径的弯曲骨水泥固定柄。这些是基于少数无菌性松动患者的初步和临时观察结果;需要更多患者的未来研究来验证或反驳这些发现。
III 级,治疗性研究。