- Open Access
Ki-67 immuno-histochemistry index in stage III giant cell tumor of the bone
© Ismail et al; licensee BioMed Central Ltd. 2010
- Received: 21 December 2009
- Accepted: 12 March 2010
- Published: 12 March 2010
Giant cell tumor is an infrequent and unpredictable bony lesion. Although numerous attempts have been made to predict the behaviour of GCT, there are no definite biological or histological parameters to determine the prognosis or aggressiveness of this lesion
Materials and methods
We analyzed Ki 67 immuno-histochemistry of 31 consecutive cases staged III giant cell tumor to determine the clinico-pathological correlation. There were 19 male patients compare to 12 females. The mean age was 33.8 years ranged from 18 to 59 years. Five cases presented with local recurrence prior to wide resection and one case had multiple recurrences there after. Six cases had pulmonary metastases. Expression of Ki 67 antigen was evaluated by immuno-histochemical staining techniques using the avidin-biotin perioxidase complex method using an LSAB2 kit (Dako, Glostrup, Denmark). The primary antibody used in this study was Ki-67 (MIB-I clone, dilution 1:25; Dako).
The mean value of Ki-67 index obtained as a percentage of 1000 background cells was 8.15 (ranged 1.00 - 20.0). The median Ki 67 index was 7.5 with standard deviation of 5.12. The Ki 67 index of recurrence tumor was 4.323 compared to 6.05 without recurrence and was not statistically significant (mean difference of 0.865 with p value in independent t test of 0.736). The Ki 67 index was also not statistically significant in the presence of pulmonary metastases with the mean value of metastases group of 6.681 compared to 2.890 without metastases (mean difference of 1.895 with p value in independent t test of 0.424).
Ki 67 index is not use-full prognostic marker for aggressive type of giant cell tumor of the bone.
- Pulmonary Metastasis
- Giant Cell Tumor
- Giant Cell Tumor
- Wide Resection
- Wide Resection Margin
Giant cell tumor (GCT) of the bone is an infrequent and unpredictable bony lesion . Although numerous attempts have been made to predict the behaviour of GCT, there are no definite biological or histological parameters to determine the prognosis or aggressiveness of this lesion . Aggressive lesions (stage III Campanacci) are common in oriental population, and they have been shown to have higher risk of recurrence and pulmonary metastases [3–5].
Ki-67 represents a nuclear protein forming part of DNA replicase complex that provides a simple, rapid and reliable means of evaluating the growth fraction of neoplastic cell populations . Ki-67 was shown to correlate with the biological behaviour and risk of pulmonary metastases in a few reported cases of GCT of the bone . However; there are no reported studies to identify the effectiveness of this marker to correlate with the aggressiveness and prognosis of the disease.
The aim of this study is to identify the effectiveness of Ki-67 as prognostic marker and in predicting the risk of local recurrence and pulmonary metastases for aggressive (stage III) GCT of the bone.
Thirty-one consecutive patients with histologically proven giant cell tumor, seen at our institution between January 1999 and December 2006, were included. The clinical and radiological records of all the patients were reviewed. Tissue diagnosis and immuno-histopathological study was obtained in all cases from the surgical specimen. Stage III or aggressive GCT in this study is defined as symptomatic, rapidly growing lesion. Bone scans showed intense activity that often extended beyond the lytic area on radiograph and magnetic resonance imaging showed infiltration of the surrounding soft tissue, which was confirmed histologically by tumor that has breached the cortex and extended into the surrounding soft tissue.
There were 19 males and 12 females patents. The mean age was 33.8 years with range from 18 to 59 years. Eleven GCT were located at the proximal tibia followed by 9, involving distal femur, 4 distal radius, 2 distal ulna and one each at the proximal femur, sacrum, metacarpal, distal tibia and proximal humerus. All cases were stage III based on Campanacci staging system3. All cases were treated with wide resection margin. The surgical specimens were evaluated for microscopic extent of tumor at the margins and intramedullary marrow extension, and all were found clear of extension. Five cases presented with local recurrence prior to wide resection and one case had multiple recurrences thereafter. Six cases had pulmonary metastases during follow up, two of which underwent surgical resection and four had chemotherapy.
Evaluation of Ki-67 immuno-histochemical expression
Expression of Ki-67 antigen was evaluated by immuno-histochemical staining in all representative sections from each patient. Serial sections, 5 μm thick, were cut and immuno-histochemical techniques were carried out using the avidin-biotin perioxidase complex method using an LSAB2 kit (Dako, Glostrup, Denmark). The primary antibody used in this study was Ki-67 (MIB-I clone, dilution 1:25; Dako). Expression of proliferation index marker Ki-67 in the nuclear area of the tumor cells were examined using immuno-histochemistry. The labeled-cell count (Ki-67 proliferation index) was determined in ten high-power fields by two blinded observers. Ki-67 proliferation index was defined as the ratio of labeled cells to total cells.
All data obtained were analysed by using SPSS 12.0.1 software. Statistical analysis between different group were determined using independent t-test and considered statistically significant when the p values were less than 0.05.
The staining was confined to the nuclei of the stromal cells in all cases. The mean value of Ki-67 index obtained as a percentage of 1000 background cells was 8.15 (range 1.00 - 20.0). The median Ki-67 index was 7.5 with standard deviation of 5.12. The Ki-67 index of recurrent tumor was 4.323 as compared to 6.05 without recurrence and was not statistically significant (mean difference of 0.865 with 0.736 of p value in independent t test). The Ki-67 index was also not statistically significant in those with pulmonary metastases with the mean value of 6.68 with metastatic group as compared to 2.89 of those without metastases (mean difference of 1.895 with 0.424 of p value in independent t test).
In the recurrent tumors with pulmonary metastasis, Ki-67 index was 6.40 when compared with 2.20 in disease free cases. The mean difference was 2.099 with p value of 0.326 and was not statistically significant.
Stage III or aggressive giant cell tumor is defined as symptomatic, rapidly growing lesion that is often associated with spontaneous fracture [2, 3]. GCT is an infrequent and unpredictable bony lesion, and in our series it was not only presented with locally aggressive behaviour, but it also had higher incidence of local recurrent and pulmonary metastasis [4, 5].
Various proliferation markers had been studied to correlate with the aggressive behaviour of GCT and surgical outcome. These included the expression of Ki 67, proliferating cell nuclear antigen, p 53 tumor suppressor gene, matrix metalloproteinase (MMP)-1/9, parathyroid hormone-like protein (PTH-LP) in the mononuclear histiocytic stromal cell. The observations may suggest that mononuclear histiocytic stromal cells are induced by several cytokines acting in an autocrine or paracrine fashion, which are closely related to the biologic aggressiveness of GCT [8–10]. However, most of the studies compared the overall stage of GCT, which were variable in their clinical behaviour. There was no study to quantify the value of proliferative markers in stage III GCT and correlate statistically with the risk of pulmonary metastases. Our series suggest that the Ki-67 index in aggressive type of GCT varies significantly with range between 1.00 to 20.00.
Ki-67 immuno-pathological marker was not a useful marker to predict the risk of recurrence and pulmonary metastases in aggressive giant cell tumor.
The study was funded by short term grant Universiti Sains Malaysia 304/PPSP/6131385
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