Does the addition of cement improve the rate of local recurrence after curettage of giant cell tumours in bone?

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ONCOLOGY Does the addition of cement improve the rate of local recurrence after curettage of giant cell tumours in bone? C. L. Gaston, R. Bhumbra, M. Watanuki, A. T. Abudu, S. R. Carter, L. M. Jeys, R. M. Tillman, R. J. Grimer From Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, United Kingdom C. L. Gaston, MD, A. T. Abudu, FRCS, S. R. Carter, FRCS, L. M. Jeys, FRCS, MSc, R. M. Tillman, FRCS, R. J. Grimer, FRCS, Royal Orthopaedic Hospital NHS Foundation Trust, Bristol Road South, Northfield, Birmingham B31 2AP, UK. R. Bhumbra, PhD, FRCS(Tr & Orth), Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, Middlesex HA7 4LP, UK. M. Watanuki, MD, PhD, Tohoku University Hospital, 1-1 Seiryou-Cho, Aoba-ku, Sendai 980-8574, Japan. Correspondence should be sent to Dr C. L. Gaston; e-mail: louie.gaston@nhs.net 2011 British Editorial Society of Bone and Joint Surgery doi:10.1302/0301-620x.93b12. 27663 $2.00 J Bone Joint Surg Br 2011;93-B:1665 9. Received 31 March 2011; Accepted after revision 2 September 2011 We retrospectively compared the outcome after the treatment of giant cell tumours of bone either with curettage alone or with adjuvant cementation. Between 1975 and 2008, 330 patients with a giant cell tumour were treated primarily by intralesional curettage, with 84 (25%) receiving adjuvant bone cement in the cavity. The local recurrence rate for curettage alone was 29.7% (73 of 246) compared with 14.3% (12 of 84) for curettage and cementation (p = 1). On multivariate analysis both the stage of disease and use of cement were independent significant factors associated with local recurrence. The use of cement was associated with a higher risk of the subsequent need for joint replacement. In patients without local recurrence, 18.1% (13 of 72) of those with cement needed a subsequent joint replacement compared to 2.3% (4 of 173) of those without cement (p = 1). In patients who developed local recurrence, 75.0% (9 of 12) of those with previous cementation required a joint replacement, compared with 45.2% (33 of 73) of those without cement (p = 0.044). Intralesional curettage is a standard treatment for giant cell tumours (GCT) of long bones, with or without the use of polymethylmethacrylate (PMMA). 1-5 Although wide excision with reconstruction of the joint leads to the lowest rates of recurrence, the long-term outcome is better if curettage is undertaken and the joint preserved. 6-10 The rates of local recurrence and outcomes are similar for both treatment arms of curettage although some recent large studies have shown better local control after curettage with added PMMA. 1,4,5 A randomised controlled trial of the two treatments has not been performed for ethical and logistical reasons. The results from many centres which treat GCTs do not differentiate which patients receive adjuvant PMMA and conclusions cannot be made about its effect. We previously reported, in patients treated between 1970 and 1997, that Campanacci I and II 11 GCTs could be treated with simple curettage, as the rate of local recurrence (7%) was very low. 12 However, Campanacci III and recurrent lesions had significantly higher recurrence rates (29% and 34% respectively) when treated with curettage alone, which led us to consider that an adjuvant may be required for these patients. Since 1997, we started to use adjuvant PMMA, primarily for Campanacci II and III lesions where the surgeon decided that curettage left the joint with insufficient bony support. without cementation was still undertaken when the surrounding cortex was considered to be sufficient. The proponents of adjuvant cementation believe that filling the cavity with PMMA decreases the risk of local recurrence due to its thermal and toxic effects on tumour cells. 1,4,5,13-15 Also, the cement gives immediate structural support, thereby allowing for more aggressive removal of tumour and early weightbearing. 5,14 The disadvantages of PMMA include thermal damage to articular cartilage 16 and increased stiffness of the subchondral bone leading to degenerative changes in the adjacent joint, 17 although an increased risk of osteoarthritis with cementation following the treatment of GCTs has not been reported. We undertook a retrospective study of our experience in treating GCT of bone by intralesional curettage, with or without adjuvant cementation and hypothesised that curettage with cementation would lead to lower rates of local recurrence than curettage alone. Patients and Methods We identified 470 patients from our database with a histological diagnosis of GCT treated between 1975 and 2008. Inclusion criteria included that the definitive curettage was done by our unit. Recurrent tumours treated elsewhere (n = 45) were excluded, as were those VOL. 93-B, No. 12, DECEMBER 2011 1665

1666 C. L. GASTON, R. BHUMBRA, M. WATANUKI, A. T. ABUDU, S. R. CARTER, L. M. JEYS, R. M. TILLMAN, R. J. GRIMER Table I. Univariate and multivariate analysis of variables associated with local recurrence Variable Total (n = 330) With cement With local recurrence Multivariate analysis p-value Gender (n, %) Male 171 (51.8) 48 (28.1) 41 (24.0) (p = 0.4) Female 159 (48.2) 36 (22.6) 44 (27.7) Surgery (n, %) 246 (74.5) - 73 (29.7) (p = 4) 0.01 with cement 84 (25.5) 12 (14.3) Site (n, %) Distal femur 95 (28.8) 35 (36.8) 23 (24.2) (p = 0.15) Proximal tibia 85 (25.6) 29 (34.1) 21 (24.7) Proximal humerus 22 (6.7) 4 (18.2) 3 (13.6) Distal tibia 28 (8.5) 4 (14.3) 4 (14.3) Distal radius 28 (8.5) 9 (32.1) 9 (32.1) Axial 30 (9.1) 3 (10.0) 13 (43.3) Other 42 (12.7) 0 (0) 21 (28.5) Campanacci grade 11 (n, %) I 9 (2.7) 0 (0) 0 (0) < 01 II 181 (54.8) 36 (19.9) 34 (18.8) (p < 01) III 140 (42.4) 48 (34.3) 51 (36.4) Pathological fracture (n, %) Yes 62 (18.8) 28 (45.2) 18 (29.0) (p = 0.51) No 268 (81.2) 56 (20.9) 67 (25.0) with extensive bone and soft-tissue involvement treated primarily with wide or marginal excision (n = 95). Medical records, plain radiographs, CT and MR scans were reviewed where available. Of the remaining 330 patients (171 males and 159 females with a mean age of 32.5 years (13 to 73) treated primarily with intralesional curettage, 84 (25.5%) received adjuvant PMMA (Table I). The technique of curettage was as previously documented, 12 using curettes, highspeed burrs, and a high-speed pulse lavage system when available. Since 1997, adjuvant cementation was used if the residual bone was deficient or there was an associated fracture. Bone graft was not used routinely to protect the articular cartilage from the cement as described by other authors. 18 Post-operatively, patients treated with curettage alone were kept non-weight-bearing for as few as six weeks until radiographs confirmed consolidation of the cavity. 12 Those treated with PMMA were allowed full weightbearing immediately. The patients were followed-up with radiographs every three months for two years, then every six months for five years. If they requested to be seen at their local hospitals, the above plan was coordinated with the respective physicians, with instructions to refer back if indicated radiologically or clinically. MRI studies were obtained if local recurrence was suspected. This was confirmed histologically at the time of any further surgery. Other complications, such as infection, fracture and degenerative joint disease, were recorded. Joint pain and radiological changes of arthritis were not considered complications unless they required treatment and were confirmed operatively. Statistical analysis. Univariate and multivariate analyses were used to determine which variables were associated with local recurrence. Kaplan-Meier survival analysis was undertaken to record recurrence-free survival and differences in joint survival between those patients who underwent curettage alone and those with added cementation. The log-rank test of equality of survivors was used to detect differences in survival between groups. Results The mean follow-up of the 330 patients was 76.5 months (2 to 319). The Campannaci grade was I in nine patients, II in 181 and III in 140 (Table I). Pathological fractures were noted in 62 patients (18.8%) at the time of presentation. Adjuvant cementation was used in 36 Campanacci II patients (20%) and 48 Campanacci III patients (34%). Almost half of the patients with pathological fractures received cementation (45%, n = 28). There was local recurrence in 85 patients (25.8%) at a mean of 22 months (3 to 133). The local recurrence occurred in 90% of cases by 42 months and 95% by five years after the primary operation. The local recurrence rate was 29.7% (73 of 246) for curettage alone and 14.3% (12 of 84) for curettage with cementation (p = 1) (Fig. 1). Analysis of Campanacci II and III patients revealed similar advantages of cementation over curettage alone (Stage II: 8.3% (31 of 145) for local recurrence with cement, 21.3% (3 of 36) without (p = 0.02); Stage III: 18.7% (9 of 48) with cement, 45.6% (42 of 92) without (p < 1, Fig. 2)). All Campanacci I patients were treated with curettage alone. THE JOURNAL OF BONE AND JOINT SURGERY

DOES THE ADDITION OF CEMENT IMPROVE THE RATE OF LOCAL RECURRENCE AFTER CURETTAGE OF GIANT CELL TUMOURS IN BONE? 1667 Fig. 1 Kaplan-Meier survival curve showing local recurrence-free survival for giant cell tumour in relation to treatment (curettage versus curettage with cement). Fig. 2 Stage I stage II stage III stage II stage III Kaplan-Meier survival curve showing local recurrence-free survival for giant cell tumour by treatment and Campanacci stage. The site of the tumour was not a significant independent variable in predicting local recurrence although the distal tibia and proximal humerus had a lower incidence (14.3% and 13.6% respectively) than other sites, whereas axial involvement had a higher incidence (43.3%, Table I). Complications other than local recurrence are shown in Table II. Ulnar abutment with secondary collapse of the distal radius was seen in three patients treated with curettage alone but not in the nine patients treated with adjuvant cement. Despite using cement, four patients had a postoperative fracture. Two were treated conservatively and two underwent reconstruction with an endoprosthesis because of intra-articular extension of the fracture and extensive bone loss. Two patients who had curettage alone developed a painful metaphyseal cavity. At operation, there was a fluid-filled space with no signs of local recurrence and cementation of the area relieved the pain in both cases. Three patients treated with curettage alone subsequently developed osteoarthritis with much local bone loss; they underwent total knee replacement using revision components. Table II. Complications associated with curettage and curettage with adjuvant cementation Complication Cement Deep infection 1 2 Ulnar abutment 3 0 Peri-prosthetic fracture 1 0 Osteoarthritis 3 11 Treated with Complex TKR * 3 3 Treated with EPR 0 8 Neuroma 1 1 Fracture 3 4 Painful cavity 2 0 * TKR, total knee replacement EPR, endoprosthetic replacement The use of cement was associated with a higher risk of subsequent joint replacement regardless of local control (Fig. 3). In patients without local recurrence, 18.1% (13 of 72) of those with cement needed a joint replacement, compared with 2.3% (4 of 173) of those without cement (p = 1). In patients who developed local recurrence, 75.0% (9 of 12) of those with previous cementation required a joint replacement, compared with 45.2% (33 of 73) of those without cement (p = 0.044). Multivariate analysis showed that curettage with cement and local recurrence were independently associated with joint salvage. Discussion Along with others, we found that curettage with adjuvant cementation was associated with a lower risk of local recurrence. 1,4,5 in Grade II and III GCTs. An important difference in our protocol compared with other centres is that we continue to treat some Grade II and III tumours with curettage alone. The decision to use PMMA is made at operation and herein lies a limitation to our study, as this decision is left to the surgeon s experience and has not been quantified. It could be argued that only larger tumours leaving a weak cavity after curettage were cemented. This may be a possible bias towards cement, as smaller lesions have been shown to be associated with higher local recurrence. 19 However, this highlights the importance of a detailed curettage as the primary determinant of local control, and small lesions may be underestimated with a sub-optimal curettage being done. Similarly, when considering the amount of bone remaining after curettage, the surgeon can err towards a conservative curettage to avoid subsequent fracture or damage to the articular cartilage. Suzuki et al 20 found that in GCTs located within 5 mm of the articular surface, local recurrence was likely to occur at the articular side of the lesion. They correlated this with their less aggressive curettage, which avoided a burr and electrocautery, to lessen damage to cartilage. The importance of our use of PMMA is that it allows the surgeon to do an aggressive curettage without compromising on thoroughness. This advantage of cement has also been noted by others. 5,14 The disadvantage of using cement close to the articular surface is the risk of cartilage damage VOL. 93-B, No. 12, DECEMBER 2011

1668 C. L. GASTON, R. BHUMBRA, M. WATANUKI, A. T. ABUDU, S. R. CARTER, L. M. JEYS, R. M. TILLMAN, R. J. GRIMER Fig. 3a Fig. 3b Kaplan-Meier survival curves showing joint survival for patients with giant cell tumour by treatment (curettage versus curettage with cement) and a) no local recurrence and b) local recurrence. and early onset of joint degeneration. The biomechanical deficiencies of using PMMA to replace subchondral bone are recognised. 17,21,22 with the resulting degeneration mostly documented through animal studies or post-operative radiological changes. 17,20,21 Szalay et al 17 compared GCTs treated with curettage and bone grafting or cementing and found significant acceleration of degenerative changes in the latter group. The degenerative changes were based on radiological changes alone and functional knee scores at medium-term follow-up showed no differences between the groups. We considered the need for subsequent joint replacement as the determinant of degenerative changes. As local recurrence contributes to deterioration of the joint, 19 we evaluated the rate of joint replacement for those who did not have local recurrence and found that patients treated with cementation had a significantly higher rate of joint replacement surgery (Fig. 3). In the 11 patients with cementation who subsequently underwent knee replacement for osteoarthritis (Table II) cement had migrated through the articular cartilage and was found within the joint. Whether these patients with extensive joint involvement or cavities with greater than 50% circumference would have been better treated initially with an endoprosthesis is beyond the scope of this study. The high rate of joint failure in our patients who were treated with PMMA could also be explained by the lack of support by internal fixation. Fraquet et al 13 recommend routine osteosynthesis to support large cavities filled with cement to prevent the remaining joint surface from rolling around the cement block and fracturing. 13 alone was associated with higher rates of local recurrence (30%) but this was comparable with those (18% to 51%) from other centres. 1,2,4,5 The advantage of curettage alone was the lower rate of joint replacement. We reported earlier that with curettage alone, the empty cavity gradually consolidates. 12 In a more detailed study, Hirn et al 23 found that most cavities occupying < 60 cc filled spontaneously but those > 60 cc did not do as well. In this study, we identified patients (Table II) where, although new bone formed around the cavity, its volume remained significant enough to cause structural weakness and symptoms which were relieved with subsequent cementation. The fact that joint replacements in these patients required revision implants indicates the amount of bone loss still present after ten years. Given this, structural fillers should still play a role in the treatment of GCTs with large subchondral defects. Bone allografts have been used as fillers 2,24,25 but they do not provide immediate stability and have inherent risks of infection and graft failure. A layer of bone graft between the cement and articular cartilage is an attractive solution but has yet to gain popularity or show better results. 18 Osteoconductive calcium phosphate bone graft substitutes can provide support to articular cartilage and have the capacity to be resorbed and replaced by host bone. 26 However, the quantities required to fill curetted GCT cavities (50 cc to 100 cc) are unlikely to be technically or financially feasible. Although adjuvant cement gives better local control rates for curettage of GCTs of bone, it leads to an increased risk for joint replacement, regardless of the control of the disease and discussions with patients must take this into account. No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. References 1. Becker WT, Dohle J, Bernd L, et al. Local recurrence of giant cell tumor of bone after intralesional treatment with and without adjuvant therapy. J Bone Joint Surg [Am] 2008;90-A:1060 1067. 2. Blackley HR, Wunder JS, Davis AM, et al. Treatment of giant cell tumors of long bones with curettage and bone-grafting. J Bone Joint Surg [Am] 1999;81-A:811 820. 3. Errani C, Ruggieri P, Asenzio MA, et al. Giant cell tumor of the extremity: a review of 349 cases from a single institution. Cancer Treat Rev 2010;36:1 7. 4. Kivioja AH, Blomqvist C, Hietaniemi K, et al. Cement is recommended in intralesional surgery of giant cell tumors: a Scandinavian Sarcoma Group study of 294 patients followed for a median time of 5 years. Acta Orthop 2008;79:86 93. 5. Klenke FM, Wenger DE, Inwards CY, Rose PS, Sim FH. Giant cell tumor of bone: risk factors for recurrence. Clin Orthop 2011;489:591 599. 6. Gitelis S, Mallin BA, Piasecki P, Turner F. Intralesional excision compared with en bloc resection for giant cell tumors of bone. J Bone Joint Surg [Am] 1993;75- A:1648 1655. THE JOURNAL OF BONE AND JOINT SURGERY

DOES THE ADDITION OF CEMENT IMPROVE THE RATE OF LOCAL RECURRENCE AFTER CURETTAGE OF GIANT CELL TUMOURS IN BONE? 1669 7. Labs K, Perka C, Schmidt RG. Treatment of stage 2 & 3 giant cell tumor. Arch Orthop Trauma Surg 2001;121:83 86. 8. Lackman RD, Hosalkar HS, Ogilvie CM, Torbert JB, Fox ET. Intralesional curettage for grades II and III giant cell tumors of bone. Clin Orthop 2005;438:123 127. 9. Liu HS, Wang JW. Treatment of giant cell tumor of bone: a comparison of local curettage and wide resection. Changgeng Yi Xue Za Zhi 1998;21:37 43. 10. Wang HC, Chien SH, Lin GT. Management of grade III giant cell tumors of bones. J Surg Oncol 2005;92:46 51. 11. Campanacci M, Baldini N, Boriani S, Sudanese A. Giant-cell tumor of bone. J Bone Joint Surg [Am] 1987;69-A:106 114. 12. Prosser GH, Baloch KG, Tillman RM, et al. Does curettage without adjuvant therapy provide low recurrence rates in giant-cell tumors of bone? Clin Orthop 2005;435:211 218. 13. Fraquet N, Faizon G, Rosset P, et al. Long bones giant cell tumors: treatment by curettage and cavity filling cementation. Orthop Traumatol Surg Res 2009;95:402 406. 14. Ghert MA, Rizzo M, Harrelson JM, Scully SP. Giant cell tumor of the appendicular skeleton. Clin Orthop 2002;400:201 210. 15. Leeson MC, Lippitt SB. Thermal aspects of the use of polymethylmethacrylate in large metaphyseal defects of bone: a clinical review and laboratory study. Clin Orthop 1993;295:239 245. 16. Radev BR, Kase JA, Askew MJ, Weiner SD. Potential for thermal damage to articular cartilage by PMMA reconstruction of a bone cavity following tumor excision: a finite element study. J Biomech 2009;42:1120 1126. 17. Szalay K, Antal I, Kiss J, Szendroi M. Comparison of the degenerative changes in weight-bearing joints following cementing or grafting techniques in giant cell tumour patients: medium-term results. Int Orthop 2006;30:505 509. 18. Ward WG Sr, Li G 3rd. Customized treatment algorithm for giant cell tumor of bone: report of a series. Clin Orthop 2002;397:259 270. 19. Jeys LM, Suneja R, Chami G et al. Impending fractures in giant cell tumours of the distal femur: incidence and outcome. Int Orthop 2006;30:135 138. 20. Suzuki Y, Nishida Y, Yamada Y, et al. Re-operation results in osteoarthritic change of knee joints in patients with giant cell tumor of bone. Knee 2007;14:369 374. 21. Manley PA, McKeown DB, Schatzker J, Palmer NC, Carman S. Replacement of epiphyseal bone with methylmethacrylate: its effects on articular cartilage. Arch Orthop Trauma Surg 1982;100:3 10. 22. Persson BM, Ekelund L, Lövdahl R, Gunterberg B. Favourable results of acrylic cementation for giant cell tumors. Acta Orthop Scand 1984;55:209 214. 23. Hirn M, de Silva U, Sidharthan S, et al. Bone defects following curettage do not necessarily need augmentation. Acta Orthop 2009;80:4 8. 24. Zhen W, Yaotian H, Songjian L, Ge L, Qingliang W. Giant-cell tumour of bone: the long-term results of treatment by curettage and bone graft. J Bone Joint Surg [Br] 2004;86-B:212 216. 25. Ayerza MA, Aponte-Tinao LA, Farfalli GL, Restrepo CA. Joint preservation after extensive curettage of knee giant cell tumors. Clin Orthop 2009;467:2845 2851. 26. Welch RD, Berry BH, Crawford K, et al. Subchondral defects in caprine femora augmented with in situ setting hydroxyapatite cement, polymethylmethacrylate, or autogenous bone graft: biomechanical and histomorphological analysis after twoyears. J Orthop Res 2002;20:464 472. VOL. 93-B, No. 12, DECEMBER 2011