Acessibilidade / Reportar erro

Isolated cauterization as an adjuvant in the treatment of benign bone tumors

Abstracts

OBJECTIVES: To evaluate the efficacy of cauterization as a sole adjuvant method inintralesional resection of benign bone tumors, taking into account associated factors that could influence local recurrence. METHODS: 47 patients diagnosed with different benign bone tumors were included in this study, all of whom had been treated with curettage associated with cauterization as an adjuvant method. The medium follow-up was 32.7 ± 19.4 months. The recurrence rate was then evaluated in relation to age, sex, location of the tumor, histologic type, tumor grade ( B1, B2 or B3 ), and size and type of material used to fill the tumor cavity ( PMMA or autologus bone). The type and percentage of complications were also included in the analysis. RESULTS: Global recurrence was 19.1%. There was statistic significance relating tumor grade to time to recurrence (p=0,028). No other factors were found that directly correlated with global recurrence of the tumors. CONCLUSION: Cauterization proved to be a simple, inexpensive and effective adjuvant method for the treatment of benign bone tumors. Level of Evidence: Level IV, case series.

Bone neoplasms; Bone and bones; Recurrence


OBJETIVOS: Avaliar o papel da eletrocauterização como método adjuvante isolado na ressecção intralesional dos tumores ósseos benignos, levando em conta fatores associados à recorrência dessas lesões. MÉTODOS: Foram incluídos 47 pacientes com diagnóstico de tumores ósseos benignos que foram tratados com curetagem associada a eletrocauterização como método adjuvante. Os pacientes foram acompanhados por um tempo médio de 32,7± 19,4 meses e foi avaliada a taxa de recidiva em relação às seguintes variáveis: idade, sexo, localização do tumor, tipo histológico, estadiamento (B1, B2, B3), tamanho, tipo de material utilizado como preenchimento (PMMA ou enxerto ósseo). A taxa e o tipo de complicação pós-operatória também foram analisadas. RESULTADOS: A recidiva global foi de 19,1%, havendo correlação significante do grau do tumor em relação ao tempo de recidiva (p=0,028). Não foram observados outros fatores diretamente relacionados à recidiva local. CONCLUSÃO: A eletrocauterização mostrou-se um método simples, barato e eficaz no tratamento adjuvante dos tumores ósseos benignos. Nivel de Evidência IV, serie de casos.

Neoplasias ósseas; Osso e ossos; Recidiva


ORIGINAL ARTICLE

IOrthopedic Oncology Service of Hospital das Clínicas da Universidade Federal de Minas Gerais, Brazil

IIOrthopedic Oncology Service of Santa Casa de Belo Horizonte, MG, Brazil

Mailing address

ABSTRACT

OBJECTIVES: To evaluate the efficacy of cauterization as a sole adjuvant method in intralesional resection of benign bone tumors, taking into account associated factors that could influence local recurrence.

METHODS: 47 patients diagnosed with different benign bone tumors were included in this study, all of whom had been treated with curettage associated with cauterization as an adjuvant method. The medium follow-up was 32.7 ± 19.4 months. The recurrence rate was then evaluated in relation to age, sex, location of the tumor, histologic type, tumor grade ( B1, B2 or B3), and size and type of material used to fill the tumor cavity (PMMA or autologus bone). The type and percentage of complications were also included in the analysis.

RESULTS: Global recurrence was 19.1%. There was statistic significance relating tumor grade to time to recurrence (p=0.028). No other factors were found that directly correlated with global recurrence of the tumors.

CONCLUSION: Cauterization proved to be a simple, inexpensive and effective adjuvant method for the treatment of benign bone tumors. Level of Evidence: Level IV, case series.

Keywords: Bone neoplasms. Bone and bones. Recurrence.

INTRODUCTION

Benign bone tumors represent a heterogeneous group of bone lesions with variable histological characteristics and biological behavior. Although rarely lethal, they can result in important alterations of the bone architecture, causing not only mechanical fragility but also destruction of the adjacent joints.1

These tumors are classified by the histological aspect or by their behavior and aggressiveness, where the staging system proposed by Enneking et al.2 that divides tumors into latent (B1), active (B2) and aggressive (B3) is used the most often.

The treatment of these lesions ranges from simple curettage to ample resection. Although simple curettage presents a greater risk of recurrence, ample resection increases morbidity and usually presents precarious functional results.3 Treatment should then be individualized, aiming to reduce recurrence and to preserve function.

Initial studies showed that simple curettage presented high local recurrence,4 especially in aggressive tumors. To reduce recurrence, various adjuvant methods were described, such as cryosurgery and intralesional application of phenol or ethanol.3 The use of these adjuvants reduces recurrence, but can increase complications such as pathological fractures and injury of adjacent soft tissues. Cauterization is a simple, low-cost method of easy access, but few studies describe its isolated use as a method adjuvant to intralesional resection of benign bone tumors.

The aim of this study is to evaluate the results of isolated cauterization as a method adjuvant to the intralesional resection of benign bone tumors and the factors associated with the recurrence of these lesions, comparing its results with other methods described in literature.

PATIENTS AND METHOD

The study was approved by the ethics committee of the Orthopedics and Traumatology Service of Hospital das Clínicas da Universidade Federal de Minas Gerais (HC - UFMG) and of Santa Casa de Belo Horizonte.

During the period from January 2002 to March 2008, 71 patients diagnosed with benign bone tumors were submitted to surgical treatment in the Orthopedic Oncology Service of HC - UFMG and of Santa Casa de Belo Horizonte. Forty-seven patients were included in the study, in which the treatment consisted of curettage and isolated cauterization with as an adjuvant method. Patients that were submitted to simple segmental resection (n=5), to reconstruction with conventional prostheses (n=2), reconstruction with non-conventional prostheses (n=8), reconstructions with arthrodesis (n=1) and patients with follow-up of less than six months (n=9) were excluded from the study.

The average age of the patients was 27.0±12.8 years, with 32 (68.1%) males and 15 (31.9%) females. Follow-up time was 32.7±19.4 (ranging from seven to 79 months). The patients were staged as proposed by Enneking et al.2 and two (4.3%) patients were classified as B1, 27 (57.4%) as B2 and 18 (38.3%) as B3. All the cases, except for two patients (clinical diagnosis of non-ossifying fibroma) were confirmed by incisional biopsy using a trephine needle, and the histological types are listed in Table 1.

The average size of the tumors was 8.4±3.8 cm (minimum of 1.5 cm and maximum of 18 cm). The femur was the most common location, affected in 14 (29.8%) patients. (Table 2)

Surgical treatment consisted of lesion opening through a wide bone window, which provided a view of the entire tumor cavity, allowing curettage with curettes in a series of sizes, until complete removal of the whole macroscopic tumor. The cavity was washed with margin expansion through abrasion boring. Cauterization was performed all over the cavity, under direct visualization until the whole surface takes on a darkened appearance due to debris carbonized for 5 minutes. (Figure 1) After a further pulsatile washing with 0.9% saline solution, the cavity was filled by autograft, bioceramics or polymethylmethacrylate (PMMA).


The cavity defect was filled with autologous bone graft in 28 (59.6%) patients and with PMMA in 19 (40.4%) cases. The autogenous cortico-cancellous graft was simple in 22 (46.8%) patients, structured in one (2.1%) case and combined in two (4.3%) and associated with bioceramics in three (6.9%) patients.

The patients were monitored weekly until complete healing of the surgical site, then had monthly follow-up until the sixth postoperative month. From then on, they had clinical and radiographic follow-up every three months and follow-up through computed tomography or magnetic nuclear resonance of the surgical site. Simple chest x-rays were taken annually. In case of recurrence, the patients underwent further staging and a new local surgical procedure, including further curettage or resection with broad margins and reconstructions using prostheses or autografts.

Global recurrence was assessed and correlated with the following variables: age (above or below 20 years), gender, location (upper or lower limbs), histological type, staging (B1, B2, B3), size (larger or smaller than 10 cm), type of material used as filling (PMMA or bone graft). The rate and the type of postoperative complication were also analyzed.

The data were evaluated through simple descriptive analysis and based on survival curves by the Kaplan-Meier method. The univariate analysis was conducted through the survival curves with the log rank method and the multivariate analysis was conducted through the Cox model, considering p values <0.05 significant. The statistical study was carried out with the help of version 12.0 SPSS® software (Chicago, USA).

RESULTS

Relapse occurred in nine (19.1%) patients, with mean time of 14.0±14.6 months. As regards the histological type, recurrence was observed in five (20.8%) cases of giant cell tumor (GCT), two (18.0%) of aneurysmal bone cyst (ABC), one (20%) of chondroblastoma and one (33.3%) of chondromyxoid fibroma (CMF).

In the univariate analysis, age (p=0.524), gender (p = 0. 217), location (p=0.581) and bone with tumor (p=0.928) did not present significant correlation with local recurrence. In the comparison among histological types no greater occurrence was observed in a specific type of tumor either (p=0.246). As regards lesion size, there was no significant correlation with recurrence (p=0.642).

Staging was not a variable that presented correlation with recurrence (p=0.245); however, the recurrence of B3 tumors occurred at an average 6.4±2.0 months; while the B2 tumors recurred at 23.5 ± 18.7 months, considered a statistically significant difference (p=0.028). (Figure 2)


Regarding the type of surgery performed, relapses occurred in six (30%) patients submitted to filling with autograft and in three (18%) of the patients submitted to reconstruction with PMMA; however, this difference was not significant in the univariate analysis (p=0.345).

In evaluating complications, we observed four patients that presented postoperative complications with two (4.4%) cases of fracture and one (2.2%) of infection.

The multivariate analysis conducted through the Cox model did not show significance among the studied variables either.

DISCUSSION

The treatment of benign bone tumors is based on histological type, location, size and the biological behavior of these lesions. The main challenge in the treatment of these tumors is to balance low surgical morbidity with acceptable rates of local recurrence.

Initial reports of simple curettage, especially of giant cell tumors, showed recurrence rates of up to 60%, suggesting more aggressive methods for local control of these lesions.5 Capanna et al.6 obtained recurrence of 45% in 280 patients treated with curettage compared to 18% in 387 in which some adjuvant method was added. The use of ample curettage, in association with local boring and chemical adjuvants, reduced recurrence especially in more aggressive tumors (B3); yet the choice of the ideal adjuvant method is still controversial.3-5

Several methods have been described in literature and have resulted in different recurrence rates.3-18 (Table 3) The most frequently used include application of phenol, cryotherapy and cavity filling with PMMA.

Phenol is used extensively as an adjuvant. After curettage, the phenol is sprayed inside the lesion or applied with the help of a swab, causing tissue necrosis at a depth of around 1 to 2mm.19 As it is extremely caustic, it must be handled with care, protecting the adjacent soft tissues. Moreover, it can be absorbed and result in undesirable effects in other organs such as the heart, lungs and liver.

Another method is cryotherapy, performed through the application of liquid nitrogen in the cavity with protection of the adjacent tissues using heated saline solution. The nitrogen acts by creating intracellular ice crystals, which will injure the cell membrane and cause necrosis of the exposed tissue, reaching a depth of about eight to 10mm.20 It has a higher cost and its main complication is fracture resulting from persistent bone lesion.17

In our study, we used cauterization on its own as an adjuvant method. Some studies report its use, but in association with other methods such as phenol application.15 We observed that it is a simple, easily applicable method that resulted in recurrence in 19.1% of the cases, compatible with most studies from literature that used other adjuvants.5-17 We also observed that the rate of complications is low, with little repercussion in the adjacent tissues and with a low cost of use.

A controversial point is the use of PMMA as an adjuvant. Some studies suggest that PMMA would increase the tumor resection margin due to thermal and cytotoxic effects; however, other studies showed similar rates of recurrence with or without filling with PMMA after GCT curettage21. In this study, we observed that, although not significant, in tumors completed with PMMA recurrence was 18%, while those filled with autograft had recurrence of 30%, suggesting that the use of cement can help in the local control of benign bone tumors, which is consistent with the findings of Camargo et al.22, who suggests adjuvant action of the bone cement. PMMA also presents the advantages of immediate mechanical stabilization and ease in recurrence identification.2

Our study also observed that tumors considered aggressive (B3) recur earlier than active tumors (B2), suggesting that less aggressive benign tumors should also be monitored for longer periods of time.

We also observed a low incidence of complications that occurred in 6.7% of the cases. The risk of pathological fracture was also lower than other methods, especially in the treatment with cryotherapy that presents an incidence of complications above 10%.11

CONCLUSION

Cauterization proved efficacious as an adjuvant in the treatment of bone tumors, with results similar to the other methods described in literature and with low incidence of complications.

REFERENCES

  • 1. Buecker PJ, Gebhardt MC. Are fibula strut allografts a reliable alternative for periarticular reconstruction after curettage for bone tumors? Clin Orthop Relat Res. 2007;461:170-4.
  • 2. Enneking WF, Spanier SS, Goodman MA. A system for the surgical staging of musculoskeletal sarcoma. Clin Orthop Relat Res. 1980;(153):106-20.
  • 3. Jones KB, DeYoung BR, Morcuende JA, Buckwalter JA. Ethanol as a local adjuvant for giant cell tumor of bone. Iowa Orthop J. 2006;26:69-76.
  • 4. Campanacci M, Baldini N, Boriani S, Sudanese A. Giant-cell tumor of bone. J Bone Joint Surg Am. 1987;69:106-14.
  • 5. McDonald DJ, Sim FH, McLeod RA, Dahlin DC. Giant-cell tumor of bone. J Bone Joint Surg Am. 1986;68:235-42.
  • 6. Capanna R, Fabbri N, Bettelli G. Curettage of giant cell tumor of bone. The effect of surgical technique and adjuvants on local recurrence rate. Chir Organi Mov. 1990;75(Suppl 1):206.
  • 7. Saglik Y, Yildiz Y, Karakas A, Ogüt H, Erekul S. Giant cell tumor of bone. Bull Hosp Jt Dis. 1999;58:98-104.
  • 8. O'Donnell RJ, Springfield DS, Motwani HK, Ready JE, Gebhardt MC, Mankin HJ. Recurrence of giant-cell tumors of the long bones after curettage and packing with cement. J Bone Joint Surg Am. 1994;76:1827-33.
  • 9. Turcotte RE, Wunder JS, Isler MH, Bell RS, Schachar N, Masri BA et al. Giant cell tumor of long bone: a Canadian Sarcoma Group study. Clin Orthop Relat Res. 2002;(397):248-58.
  • 10. Su YP, Chen WM, Chen TH. Giant-cell tumors of bone: an analysis of 87 cases. Int Orthop. 2004;28:239-43.
  • 11. Malawer MM, Bickels J, Meller I, Buch RG, Henshaw RM, Kollender Y. Cryosurgery in the treatment of giant cell tumor. A long-term followup study. Clin Orthop Relat Res. 1999;(359):176-88.
  • 12. 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;86:212-6.
  • 13. Ghert MA, Rizzo M, Harrelson JM, Scully SP. Giant-cell tumor of the appendicular skeleton. Clin Orthop Relat Res. 2002;(400):201-10.
  • 14. Ward WG Sr, Li G 3rd. Customized treatment algorithm for giant cell tumor of bone: report of a series. Clin Orthop Relat Res. 2002;(397):259-70.
  • 15. Ramírez AR, Stanton RP. Aneurysmal bone cyst in 29 children. J Pediatr Orthop. 2002;22:533-9.
  • 16. Ozaki T, Hillmann A, Lindner N, Winkelmann W. Cementation of primary aneurysmal bone cysts. Clin Orthop Relat Res. 1997;(337):240-8.
  • 17. Marcove RC, Sheth DS, Takemoto S, Healey JH. The treatment of aneurysmal bone cyst. Clin Orthop Relat Res. 1995;(311):157-63.
  • 18. Garin IE, Wang EH. Chondroblastoma. J Orthop Surg (Hong Kong). 2008;16:84-7.
  • 19. Quint U, Müller RT, Müller G. Characteristics of phenol. Instillation in intralesional tumor excision of chondroblastoma, osteoclastoma and enchondroma. Arch Orthop Trauma Surg. 1998;117:43-6.
  • 20. Capanna R, Sudanese A, Baldini N, Campanacci M. Phenol as an adjuvant in the control of local recurrence of benign neoplasms of bone treated by curettage. Ital J Orthop Traumatol. 1985;11:381-8.
  • 21. Blackley HR, Wunder JS, Davis AM, White LM, Kandel R, Bell RS. Treatment of giant-cell tumors of long bones with curettage and bone-grafting. J Bone Joint Surg Am. 1999;81:811-20.
  • 22. Camargo OP, Croci AT, Oliveira CR, Baptista AM, Caiero MT. Functional and radiographic evaluation of 214 aggressive benign bone lesions treated with curettage, cauterization, and cementation: 24 years of follow-up. Clinics (Sao Paulo). 2005;60:439-44.
  • Isolated cauterization as an adjuvant in the treatment of benign bone tumors

    Luiz Eduardo Moreira TeixeiraI; Ricardo Horta MirandaII; Otavio de Luca DrudaI; João Garcia de Azevedo NetoII; Graziane Diego Santos RajãoII
  • Publication Dates

    • Publication in this collection
      18 Oct 2011
    • Date of issue
      2011

    History

    • Received
      02 Dec 2009
    • Accepted
      18 Feb 2010
    ATHA EDITORA Rua: Machado Bittencourt, 190, 4º andar - Vila Mariana - São Paulo Capital - CEP 04044-000, Telefone: 55-11-5087-9502 - São Paulo - SP - Brazil
    E-mail: actaortopedicabrasileira@uol.com.br