Published online Apr 18, 2023. doi: 10.5312/wjo.v14.i4.218
Peer-review started: January 13, 2023
First decision: February 2, 2023
Revised: February 10, 2023
Accepted: April 4, 2023
Article in press: April 4, 2023
Published online: April 18, 2023
Processing time: 95 Days and 8.1 Hours
Future prospective studies with larger sample sizes and longer term followup are necessary to determine the optimal construct for oncologic distal femoral replacement (DFR). Comparative studies investigating the differences in clinical, functional, and patient-reported outcomes between the use of metal-backed vs all-polyethylene tibial components and cemented vs cementless fixation will provide further insight into the specific failure mechanisms associated with each construct.
This study proposes that DFR with all-polyethylene tibial (APT) is a reliable reconstruction option for oncologic defects of the distal femur.
DFR with APT implantation was performed as a primary procedure in 29 patients (52.7%) and a revision procedure in 26 patients (47.3%). Overall, twenty patients (36.4%) experienced a postoperative complication requiring reoperation. In total, 12 patients (21.8%) required a revision while 20 patients (36.4%) required a reoperation, resulting in three-year cumulative incidences of 24.0% (95%CI 9.9%-41.4%) and 47.2% (95%CI 27.5%-64.5%), respectively.
A retrospective review of consecutive patients who underwent DFR with a GMRS® (Global Modular Replacement System, Stryker, Kalamazoo, MI, United States) cemented distal femoral endoprosthesis and APT component for an oncologic indication was performed using a single-institutional database. Univariate analyses were performed to compare differences between those who had a DFR performed either as the primary treatment for the disease in question vs those who had a DFR as a revision of a previous failed surgery (indications included recurrence, fracture, etc.). Competing risk analyses were performed to evaluate the cumulative incidence of all-cause reoperation, need for revision surgery, and patient death.
This study was designed to answer the following research questions: (1) What are the most common modes of implant failure for patients undergoing cemented DFR with APT for oncologic indications? (2) What is the survivorship, rate of all-cause reoperation, and rate of revision for aseptic loosening of these implants? and (3) Is there a difference in implant survivorship or patient demographics between cemented DFRs with APT performed as a primary reconstruction vs those performed as a revision procedure?
Prior studies investigating the outcomes of endoprosthetic distal femoral replacement have largely failed to describe the type of tibial component or fixation used. Unlike the femoral component, tibial components are available in both metal-backed and all-polyethylene designs, and fixation may be achieved via cemented, cementless, or hybrid fixation. Future research investigating the effect of tibial component design and fixation on clinical outcomes is critical to determining the optimal construct for oncologic DFR.
Endoprosthetic reconstruction of the distal femur has been used as a limb-salvage procedure to treat oncologic processes of the distal femur for nearly five decades, and is currently considered standard of practice for this indication. However, there is a paucity of literature examining the survivorship of DFRs with respect to the type of tibial component utilized. The purpose of this study was to report on the clinical outcomes of patients undergoing cemented DFR with all-polyethylene tibial components for oncologic indications.