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Megaprosthesis versus Condyle-sparing Intercalary Allograft: Distal Femoral Sarcoma
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Symposium: Selected Papers Presented at the 2008 Meeting of the Musculoskeletal Tumor Society
Megaprosthesis versus Condyle-sparing Intercalary Allograft: Distal Femoral Sarcoma
Melissa N. Zimel1, Amy M. Cizik2 , Timothy B. Rapp3, Jason S. Weisstein2 and Ernest U. Conrad III2
| (1) |
William Beaumont Hospital, Royal Oak, MI, USA |
| (2) |
Department of Orthopaedics and Sports Medicine, University of Washington Medical Center, Box 356500, 959 NE Pacific Street, Seattle, WA 98195-6500, USA |
| (3) |
Department of Orthopaedics, Loyola University Medical Center, Chicago, IL, USA |
Received: 6 January 2009 Accepted: 22 July 2009 Published online: 7 August 2009
Abstract Although functionally appealing in preserving the native knee, the condyle-sparing intercalary allograft of the distal femur
may be associated with a higher risk of tumor recurrence and endoprosthetic replacement for malignant distal femoral bone
tumors. We therefore compared the risk of local tumor recurrence between patients in these two types of reconstruction groups.
We retrospectively reviewed 85 patients (mean age, 22 years; range, 4–82 years), 38 (45%) of whom had a condyle-sparing allograft
and 47 (55%) of whom had endoprostheses. The minimum followup for both groups was 2 years (mean, 7 years; range, 2–19 years).
Local recurrences occurred in 11% (five of 47) of the patients having implants versus 18% (seven of 38) of the patients having
allografts. Using time to local recurrence as an end point, the Kaplan-Meier survivorship of the implant group was similar
to that of the condyle-sparing allograft group at 2, 5, and 10 years (93% versus 87% at 2 years, 87% versus 81% at 5 years,
and 87% versus 81% at 10 years, respectively). The condyle-sparing allograft procedure offers the potential advantage of retaining
the native knee in a young patient population while incurring no greater risk of local recurrence as those offered the endoprosthetic
procedure.
Level of Evidence: Level IV, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence.
One of the authors (EUC) has received funding from Stryker Orthopaedics (Mahwah, NJ).
Each author certifies that his or her institution has approved the human protocol for this investigation, that all investigations
were conducted in conformity with ethical principles of research, and that informed consent for participation in the study
was obtained.
This work was performed at the University of Washington Medical Center, Seattle, WA.
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