| Clinical Orthopaedics and Related Research |
| © The Association of Bone and Joint Surgeons 2008 |
| 10.1007/s11999-008-0374-5 |
Kwok Chuen Wong1
, Shekhar Madhuker Kumta1, Gregory Ernest Antonio2 and Lung Fung Tse1
| (1) | Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong |
| (2) | Department of Diagnostic Radiology and Organ Imaging, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong |
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Kwok Chuen Wong Email: skcwong@ort.cuhk.edu.hk |
Received: 21 January 2008 Accepted: 20 June 2008 Published online: 22 July 2008
Computer-assisted intraoperative navigation has been used effectively in orthopaedic trauma, spinal, and joint replacement surgery [1, 3, 4, 8, 16], but has not been used extensively in musculoskeletal bone tumor surgery [6, 7]. Computed tomography (CT)-based navigation for pelvic tumor resection and reconstruction with a custom pelvic prosthesis was reported to be successful [18].
Computed tomography and MRI are essential preoperative studies before complex bone tumor surgery. Computed tomography scans show intricate bony details well, whereas MRI is superior in delineating the intraosseous and extraosseous extensions of tumor, particularly in soft tissues and in relation to regional anatomy. Fusion of CT and MRI yields hybrid images that combine the key characteristics of each technique, thus enabling better interpretation of each and accurate localization of the lesion. This image processing technique has been used in navigation-assisted neurosurgical and otorhinolaryngeal procedures [9, 12], but has not been widely used in musculoskeletal tumor surgery [17].
We investigated the possibility of fusing multimodal preoperative imaging studies, using a proprietary surgical navigation software for three-dimensional (3-D) surgical planning for resection of musculoskeletal bone tumors. We also examined whether the image-fusion technique allowed us to reproduce the surgical plan reliably and accurately by evaluating the: (1) accuracy of the image fusion and preoperative time to achieve it; (2) accuracy as determined by comparing the resection with the preoperative surgical plan, assessing the margins of the resected tumor specimens, and assessing the fit of the custom tumor prostheses to the remaining bone; (3) additional time needed for navigation procedures at the time of surgery and complications of the procedures; and (4) accuracy of the image-to-patient registration.
|
Patient number |
Age (years) |
Gender |
Diagnosis |
Location |
Surgery |
Bone reconstruction |
Preoperative fusion imaging data sets |
Fusion time (minutes) |
Navigation planning time (hours) |
Navigation time (minutes) |
Function (MSTS score*) |
Followup (months) |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 |
46 |
F |
Parosteal osteosarcoma |
Left proximal tibia (posterior aspect) |
Joint-saving resection |
Vascularized fibular graft |
CT angiogram and MRI of proximal tibia |
60 |
2 |
40 |
28 |
19 |
|
2 |
42 |
F |
Metastatic uterine carcinoma |
Left ischial tuberosity |
Local resection |
No |
CT and MRI of pelvis |
40 |
0.75 |
13 |
— |
18 |
|
3 |
24 |
F |
Undifferentiated bone sarcoma |
Right proximal femur |
Local resection after neoadjuvant chemotherapy |
Modular tumor prosthesis |
CT and MRI of proximal femur |
60 |
1.5 |
18 |
29 |
17 |
|
4 |
53 |
F |
Schwannoma |
Right S2 nerve root |
Excision through posterior approach |
No |
CT of pelvis and MRI of sacrum |
30 |
1.0 |
15 |
— |
13 |
|
5 |
14 |
M |
Conventional osteosarcoma |
Right femur (from sub-trochanteric region to distal physis) |
Joint-saving resection after neoadjuvant chemotherapy |
Custom tumor prosthesis† |
CT of femur and MRI of proximal femur; CT of femur and MRI of distal femur§ |
80 |
2.5 |
30 |
29 |
12 |
|
6 |
80 |
F |
Chordoma |
Sacrum (below and including S2) |
Resection |
No |
CT of pelvis and MRI of sacrum |
40 |
1.5 |
35 |
— |
11 |
|
7 |
6 |
M |
Conventional osteosarcoma |
Right distal femur |
Joint-saving resection after neoadjuvant chemotherapy |
Custom tumor prosthesis† |
CT of femur and MRI of distal femur |
30 |
2.0 |
20 |
26 |
7 |
|
8 |
54 |
M |
Giant cell tumor |
Sacrum (from S1 to S4) |
Intralesional curettage through posterior approach |
No |
CT angiogram and MRI of pelvis |
40 |
1.5 |
25 |
— |
6 |
|
9 |
8 |
M |
Conventional osteosarcoma |
Left distal femur |
Joint-saving resection after neoadjuvant chemotherapy |
Custom tumor prosthesis† |
CT and MRI of distal femur |
10 |
1.0 |
15 |
29 |
5 |
|
10 |
50 |
M |
Recurrent chordoma |
Left pelvic metastases |
Resection (PII) |
Custom tumor prosthesis† |
CT angiogram, MRI, and PET of pelvis |
20 |
1.5 |
15 |
25 |
4 |
|
11 |
18 |
M |
Conventional osteosarcoma |
Sacrum (from S1 to S5) |
Total sacrectomy |
No |
CT and MRI of pelvis |
8 |
1.0 |
15 |
— |
4 |
|
12 |
54 |
F |
Recurrent chondrosarcoma |
Sacrum (from S1 to S5) |
Total sacrectomy |
No |
CT angiogram and MRI of pelvis |
10 |
1.0 |
25 |
— |
4 |
|
13 |
17 |
M |
Recurrent malignant nerve sheath tumor |
Left sciatic nerve and involving ilium and sacrum |
Left extended hemipelvectomy (resection through sacral alar and neural formina) |
No |
CT angiogram, MRI, and PET of pelvis |
20 |
1.5 |
30 |
— |
3 |
Axial CT images of the lesion and surrounding area were acquired using a 16-detector scanner (General Electric Light Speed, Milwaukee, WI). Slices with 0.625-mm or 1.25-mm thickness were obtained using a soft tissue algorithm. Magnetic resonance images of the corresponding region were acquired using a 1.5-T unit (Siemens Sonata, Erlangen, Germany). For Patients 1 through 8, postcontrast T1-weighted axial images (TR 512 ms, TE 13 ms, 2-mm thick slices) were used for fusion with CT images because of better bone-soft tissue contrast. For Patients 1 through 8, image data sets were imported into a navigation system (Stryker Navigation, Freiburg, Germany; CT spine, version 1.6) for image fusion. For Patients 9 through 13, an upgraded version of the software for cranial navigation (Stryker Navigation; iNtellect Cranial, version 1.1) allowed us to use MR image sequences regardless of scan orientation.
For the CT spine navigation software, image fusion involved cross-sectional matching of the anatomic structures on the CT with those on the MR image—a process called “coregistration.” The system allowed CT and MR images to be fused by matching the manually segmented known structures in corresponding CT and MRI data sets.
We recorded the following variables: (1) accuracy and time required for image fusion and navigation planning; (2) intraoperative error of image-to-patient registration; (3) histologic evaluation of resection margins in all tumor specimens (except those of Patient 4 with a sacral schwannoma and Patient 8 with a sacral giant cell tumor as both underwent marginal or intralesional excisions of their tumors); and (4) matching between residual bone and custom prosthesis junction at the surgery. To validate whether the resection achieved was the same as planned, CT images of the resected specimen for Patient 3 and postoperative CT images of the pelvis for Patients 2 and 6 were obtained and fused with preoperative CT images. The cross sections at the resection plane of the resected specimens for Patient 5, 7, 8, 10 were measured and compared with their preoperative navigation plans. The resection achieved was considered the same as planned if the matching was within 1 mm difference. We did not validate the resections for Patients 4 and 8 with benign tumors (marginal/intralesional excision) and Patients 1, 11, 12, and 13 as their resection planes were irregular and curved. Functional assessment was performed using the Musculoskeletal Tumor Society (MSTS) score [2] in patients with limb salvage surgery.
The resection achieved, in terms of dimensions and orientation, was as planned in the seven patients whose resections were validated either by fusing postoperative with preoperative CT images or comparing the resection plane of resected specimens with that in surgical navigation planning. Histologic examinations of all specimens showed a clear tumor margin in patients with malignant bone tumors. We found a match between residual bone and custom prosthesis junction in four patients at surgery.
With the CT spine navigation software (Patients 1 through 8), the mean time for image fusion was 47.5 minutes (range, 30–80 minutes), whereas it was 13.6 minutes (range, 8–20 minutes) when the newer cranial navigation software was used (Patients 9 through 13). The mean time for preoperative navigation planning after image fusion in CT spine navigation software was 1.4 hours (range, 0.75–2.5 hours). The planning time depended on case complexity.
The mean intraoperative accuracy of image-to-patient registration was 0.46 mm (range, 0.35–0.68 mm). The virtual preoperative CT images correlated well with the patients’ anatomy after registration. All surgeries were performed as planned under navigation guidance after registration. The mean time for navigation procedures during surgery was 24.3 minutes (range, 13–40 minutes).
A postoperative superficial wound infection developed in one patient (Patient 6 with a sacral chordoma) that resolved with administration of an intravenous antibiotic, whereas a wound infection in another patient (Patient 11 with a sacral osteosarcoma) required surgical debridement and antibiotics. No patients experienced local recurrence at a minimum followup of 3 months (mean, 9.5 months; range, 3–19 months). The mean functional MSTS score for patients with limb salvage surgery was 27.7 of 30 (range, 25–29).
To achieve safe tumor resections, one must observe the extent of the tumor in the bone and soft tissues. Computed tomography and MRI are preoperative investigations necessary for planning complex musculoskeletal bone tumor resections and reconstructions. Computed tomography and MRI provide information that is represented in a 2-D imaging format. Tumor surgeons must mentally integrate this 2-D information into a 3-D model for surgical planning. The difficulty of this mental integration increases with the complexity of the regional anatomy. We evaluated the (1) accuracy of image fusion and preoperative time to achieve it; (2) accuracy as determined by comparing the resection with the preoperative surgical plan, assessing the margins of the resected tumor specimens, and assessing the fit of the custom tumor prostheses to the remaining bone; (3) additional time needed for navigation procedures at the time of surgery and complications of the procedures; and (4) accuracy of the image-to-patient registration.
Our study has important limitations. Although histologic examination of all specimens with bone sarcoma showed a clear tumor margin, margins alone are not the only determinants of good clinical results in terms of better survival or reduced local recurrence; further, a judgment of clear margins is based upon a small sampling of the entire margin. Our series is heterogeneous in diagnosis and lacks a control group; therefore, it is not possible to make a comparative assessment of clinical results. Long-term followup in a larger series is needed to evaluate the clinical importance of the technique. However, we presume if surgical planning can be reproduced accurately and reliably, the chances of a good clinical result are likely to be greater. The technique requires surgeons who have prior experience in navigation surgery and additional resources for navigation facilities. Therefore, we used navigation only for patients in whom tumor resection was expected to be complicated owing to anatomic reasons or scarring, or for patients in whom the complexity of resection demanded customized prostheses that could be fitted into the defect only if the precise amount of bone was resected.
Image fusion technology has been used successfully in complex lesions at the head and neck regions [9, 12]. Incorporation of this technology has enhanced the capacity of surgical navigation, especially for skull base surgery. Our experience shows fusion images could be feasible and accurate in other complex regions such as the pelvis and sacrum. Navigation software allowed us to scrutinize all fused image data sets in three spatial dimensions in a short time. An additional fourth dimension of image analysis was possible by continuous blending of CT and MRI data, thus providing an excellent mental picture of anatomic tumor location and extent of infiltration into surrounding tissues. Image fusion might not be restricted to plain CT or MRI data sets. The CT angiogram and MRI fusion (Patients 1, 8, 10, 12, 13) provided key additional information regarding regional vascular anatomy that facilitated preoperative planning. Functional imaging such as F-18 fluorodeoxyglucose PET scans also could be incorporated into the navigation software. As PET images have low spatial resolution, they should be combined with anatomic CT or MRI data sets for interpretation. We found this metabolic information of the tumor was particularly useful in patients with previous surgery and radiotherapy because it helped us differentiate tumor from scar tissue or postradiotherapy changes on anatomic imaging data sets (Patients 10 and 13) [14, 19]. This detailed and interactive image analysis was particularly helpful in difficult pelvic, sacral, or joint-saving bone tumor resections; the spatial relation of the tumor to nearby neural and vascular structures was seen better with the 3-D bone-tumor model. Surgical planning on the fused images could be transferred and performed under navigation guidance if the image preparation was performed with the same navigation system. We found the fusion images valuable for surgical planning in all our patients as they provided better intraosseous and extraosseous extent of the tumors.
We are unaware of any reports asking whether surgeons could reproduce an intended resection of musculoskeletal bone tumors. Merging of postoperative with preoperative images and precise fitting of custom tumor prostheses might allow validation of the accuracy of a resection as planned. Our results suggest surgeons should be able to reproduce an intended resection reliably using a surgical navigation system. For Patients 5, 7, and 9 who had joint-saving intercalated resection after neoadjuvant chemotherapy, only 1.5 to 2 cm of the distal femoral epiphyses could be retained. Thus, even a small deviation from the planned resection would have compromised the precise fit and distal fixation of the custom joint-saving prostheses used in the reconstructions. Surgical navigation after image fusion made it possible for us to resect the bone exactly as planned in length and orientation, yielding a perfect match between the residual bone and the custom prostheses junctions. Studies have described using anatomic landmarks and correlating with measurements on preoperative MR images to define bone resection [5, 11]. However, that technique relies on 2-D measurements and may result in errors between the perceived anatomy and that seen during actual surgery.
In Patients 4 and 8 with an S2 schwannoma and a sacrum giant cell tumor (S2 and below) respectively, the tumors involved mainly the anterior bony structure of the sacrum rather than posterior structure. Image fusion when combined with surgical navigation allowed us to precisely mark the extent of the posterior bone window just enough to remove the tumor via one posterior approach. Thus we avoided unnecessary bony resection in a critical area without compromising oncologic principles.
Although the CT-based navigation system in this study originally was designed for spine surgery, accurate image-to-patient registration could be achieved in our patients with tumors involving pelvis and long bones. In image-guided craniomaxillofacial surgery, accurate and direct image-to-patient registration on MRI data sets can be achieved using the laser surface scanning technique [10, 13]. This technique, however, cannot be used in musculoskeletal tumor surgery. Thin 1- to 2-mm thick MR slices, which are necessary for accurate registration, are difficult to obtain in musculoskeletal bone tumors because the tumor dimensions often are quite large and there can be movement artifacts generated during the long scanning times. Magnetic resonance imaging data sets thus are not used routinely in computer-assisted orthopaedic surgery. The overall accuracy of computer navigation-assisted bone tumor surgery depends on the quality of the image fusion and accuracy of image-to-patient registration [15]. The accuracy of image fusion in turn depends on the quality of raw data images and is not able to outreach the resolution of primary data sets. The navigation system is only as good as the raw data. Therefore, the time between imaging and surgery must be short to avoid a discrepancy resulting from changes in tumor size. We anticipate with the advent of a newer generation of CT and MRI scanners, image resolution will increase and will enable more accurate anatomic visualization.
Our study suggests it is technically feasible to integrate all anatomic and functional data to facilitate 3-D surgical planning in musculoskeletal bone tumors. This integrated image data set, when combined with surgical navigation, enabled us to reliably perform planned tumor resections, and it may offer clinical benefits. As technology is evolving, more precise and faster navigation software will be available for this new image processing technique in computer navigation-assisted tumor surgery.