Outcome of lung metastases due to bone giant cell tumor initially managed with observation
Journal of Orthopaedic Surgery and Research volume 15, Article number: 510 (2020)
The outcomes of patients with lung metastases from giant cell tumor of bone (GCTB) vary from spontaneous regression to uncontrolled growth. To investigate whether observation is an appropriate first-line management approach for patients with lung metastases from GCTB, we evaluated the outcomes of patients who were initially managed by observation.
We retrospectively reviewed the data of 22 patients with lung metastases from histologically confirmed GCTB who received observation as a first-line treatment approach. The median follow-up period was 116 months.
Disease progression occurred in 12 patients (54.5%). The median interval between the discovery of lung metastases and progression was 8 months. Eight patients underwent metastasectomy following initial observation. The median interval between the discovery of lung metastases and treatment by metastasectomy was 13.5 months. None of the patients experienced spontaneous regression. Of the 22 patients, 36.4% needed a metastasectomy, and 9.1% required denosumab treatment during the course of the follow-up period. Disease progression occurred in 45.5% of the 11 patients with lung nodules ≤ 5 mm, while all five of the patients with lung nodules > 5 mm experienced disease progression. Progression-free survival was significantly worse in the group with lung nodules > 5 mm compared to the group with lung nodules ≤ 5 mm (p = 0.022).
Observation is a safe first-line method of managing patients with lung metastases from GCTB. According to radiological imaging, approximately half of the patients progressed, and approximately half required a metastasectomy or denosumab treatment. However, patients with lung nodules > 5 mm should receive careful observation because of the high rate of disease progression in this group.
Giant cell tumor of bone (GCTB) accounts for approximately 5% of all primary bone tumors . It usually involves the metaphyseal-epiphyseal region of long bones , and its incidence peaks in the third and fourth decade . The main treatment modality is surgery, consisting of curettage or en bloc resection.
Although benign, GCTB is known to be locally aggressive, with a tendency for local recurrence with occasional metastatic potential . GCTBs metastasize in up to 4% of cases, mainly to the lungs [5,6,7,8,9,10,11,12,13,14,15,16]. While treatment recommendations for lung metastases vary, the most common is a metastasectomy [8, 17,18,19,20,21,22], though chemotherapy (cytotoxic agents [21, 23], denosumab [24,25,26], interferon-α  or bisphosphonates ), radiation [17, 29, 30], and observation  have been reportedly used with varying levels of success. For some patients with lung metastases, uncontrolled growth resulting in death has been reported . However, spontaneous regression or growth arrest has also been reported , and these patients would benefit from a wait-and-see policy to potentially avoid unnecessary surgical or medical treatments. Before 2010, many authors recommended an immediate metastasectomy when feasible [11, 16, 32,33,34,35]. Recently, some authors have proposed that metastasectomy should only be recommended when accompanied by disease progression or symptom development [12, 36,37,38]. The aim of the wait-and-see policy is to observe the biological behavior of the lung metastases to determine further treatment needs based on disease progression. However, there is limited information regarding the ideal treatment approach for patients with metastatic GCTB.
Therefore, this study aimed to evaluate the clinical outcomes of patients with lung metastases from GCTB initially managed by observation only.
We retrospectively reviewed the medical records of 496 patients diagnosed with histologically confirmed GCTB in a single institution between 1984 and 2019. Of these 496 patients, 32 developed lung metastases, confirmed by chest computed tomography (CT). Three of these 32 patients were excluded due to malignant transformation of the GCTB. One of the 32 patients was excluded because no information was available regarding the lung nodules. Fourteen patients underwent metastasectomy and were histologically diagnosed with lung metastases from benign GCTB. The other 14 of the 32 patients were diagnosed with lung metastases from benign GCTB after a chest CT showed well-defined and rounded nodular opacities [11, 38]. Six of the 32 patients were excluded because they received a metastasectomy as the first-line approach (Fig. 1). The remaining 22 patients, who had observation as the first-line approach, were included in this study for further analysis (Fig. 1). In the first-line metastasectomy group, five patients received a metastasectomy 1 month after the discovery of lung metastases, and one patient underwent metastasectomy 3 months after the discovery of the lung metastases. Observation as the first-line approach was defined as observation for 4 months or more after the discovery of lung metastases. Metastasectomy as the first-line approach was performed until around 2003, after which, first-line observation was the standard. We evaluated the primary tumor characteristics, as shown in Table 1. Tumors were graded radiographically according to the Campanacci classification system for GCTB . Primary tumor surgeries were performed by curettage or resection. The tumor cavity after curettage was left alone or packed with bone allografts, cement, or cement with bone allografts, as reported in previous studies [39,40,41]. Resection was indicated for large tumors with soft tissue extension, pathological fractures with joint invasion or an unstable fracture pattern, multiple recurrences, or involvement of expendable bones (head of the fibula or distal end of the ulna), as previously reported .
After primary tumor treatment, the patients were followed up every 4 months for the first 2 years, every 6 months for the next 3 years, and then annually. Follow-up evaluations included radiographs and a chest CT of the primary tumor area. In cases of lung metastases, lung nodules were observed every 2 months by chest CT. Characteristics of the lung metastases, including the number of lung nodules, the size of the maximum nodule, solitary or multiple lesions, and laterality (unilateral or bilateral) were evaluated, as shown in Table 2. Six of the 22 patients had lung metastases at presentation, and the remaining patients had metachronous metastases. The median interval between surgery for the primary tumor and discovery of lung metastases was 22.5 months (interquartile range [IQR], 0 to 40.8 months). Lung metastasectomy was only indicated for patients with metastatic progression, and all lung metastases were determined to be resectable, with adequate surgical margins and future respiratory function, based on mutual consent among members in a multidisciplinary team conference. The basic procedure for lung resection was wedge resection or segmental resection. Regardless of the number of tumors, their size, or their distribution, surgical resection was indicated for patients who met the abovementioned criteria. In two of the 12 patients with disease progression, the progression ceased while they were awaiting metastasectomy (Fig. 1). Recently, denosumab treatment has been indicated for patients with progression of lung metastases. Eight of the 22 patients underwent metastasectomy and two of the 22 patients received denosumab treatment (120 mg) for 1 year and 11 years, respectively, due to progression of lung metastases (Fig. 1). One of the two patients received chemotherapy (ifosfamide, Adriamycin, interferon, or cyclophosphamide) before starting denosumab treatment (case 12).
The size of the lung lesions were assessed by CT and categorized into complete response, partial response, stable disease, or progressive disease, according to the modified Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, which assesses tumor extent through the sum of the longest diameter of the lesions . At least a 20% increase in the sum of the diameters of the lung nodules or the appearance of one or more new lesions was defined as progressive disease . Progression-free survival was defined as the time from the date of occurrence of lung metastases to the date of lung lesion progression or the last follow-up. Progression-free survival was evaluated with the Kaplan-Meier survival analysis; survival curves were compared with a log-rank test. Significance was defined as p < 0.05. Analyses were performed with JMP® 14 (SAS Institute Inc., Cary, NC, USA).
Patient outcomes are shown in Fig. 1 and Table 2. Disease progression occurred in 12 patients (54.5%), and the median interval between the discovery of lung metastases and progression was 8 months (IQR, 5–14.8 months). In the eight patients who underwent metastasectomy following initial observation, the median interval between the discovery of lung metastases and treatment by metastasectomy was 13.5 months (IQR, 2.8–23.8 months). The median follow-up period after the primary tumor surgery was 116 months (IQR, 74.9–142.9 months). The median follow-up period after the discovery of lung metastases was 80.5 months (IQR, 46.5–129.3 months). With respect to the oncological results, five had no evidence of disease and 17 were alive with lung metastases. None of the patients had died from the disease. Among the 12 patients who did not receive any treatment in the overall therapeutic process, no spontaneous regression occurred. Eight (36.4%) of the 22 patients needed a metastasectomy, and two (9.1%) required denosumab treatment over the course of the follow-up period. Of the 22 patients, 14 did not undergo metastasectomy (63.6%), five patients underwent metastasectomy once (22.7%), and three patients had several metastasectomies (13.6%). Disease progression occurred in five of the 11 patients (45.5%) with lung nodules ≤ 5 mm at the median of 11 months (IQR, 5–15 months) after the discovery of lung metastases, while it occurred in all five patients (100%) with lung nodules > 5 mm at the median of 6 months (IQR, 5–14 months). Progression-free survival was significantly worse in the group with lung nodules > 5 mm compared to the group with lung nodules ≤ 5 mm (p = 0.022) (Table 3, Fig. 2). There was no significant difference among any other variables (Table 3). None of the patients with or without disease progression experienced a pleural effusion or respiratory symptoms. None of the patients experienced metastases anywhere other than the lungs. All patients who underwent a metastasectomy had histological confirmation of GCTB lung metastases.
Two patients received denosumab treatment due to disease progression. For one of the two patients, chest CT showed disease progression 1 year after the discovery of lung metastases, and the patient was treated with chemotherapy (ifosfamide, Adriamycin, and interferon). Four months after chemotherapy was initiated, chest CT showed continued disease progression, so the patient underwent cyclophosphamide treatment; however, the lung lesions progressed. Denosumab was initiated 4 years after the discovery of lung metastases and continued for 11 years, and the disease remained stable (case 12). In the other patient, chest CT showed lung lesion progression 3 years after curettage for the primary tumor, and the patient was treated with denosumab for 1 year and was observed to have stable disease until the last follow-up. This was a rechallenge because the patient received denosumab treatment before and after curettage of the primary tumor. The patient had no side effects related to denosumab treatment (case 22, Fig. 3).
This study retrospectively analyzed the clinical outcomes of patients with lung metastases resulting from GCTB who were initially managed by observation alone. It was found that 55% of patients experienced disease progression, 45% had stable disease, and none experienced spontaneous regression. Eventually, almost half of the patients needed a metastasectomy or denosumab treatment after the initial observation period (45%). The disease progression rate was higher in the group with lung nodules > 5 mm compared to the group with lung nodules ≤ 5 mm. To the best of our knowledge, this is the first retrospective study to describe the clinical outcomes of lung metastases from GCTB after an initial period of observation. Before 2010, many authors stressed the importance of early detection of metastasis in GCTB with regular and long-term follow-up and, where possible, appropriate immediate surgical resection, such as metastasectomy, wedge resection, or lobectomy was recommended to prevent progressive pulmonary dysfunction [11, 16, 32,33,34,35]. On the other hand, a few authors have suggested that pulmonary metastases have a good long-term prognosis and should be kept under observation and aggressive treatments such as lobectomy, chemotherapy, and radiotherapy should be avoided [20, 43]. Since 2015, the authors have suggested that it is unnecessary to perform a lung metastasectomy immediately after the diagnosis of metastasis and that it is more appropriate only when there is disease progression in terms of volume and number of metastases [12, 36,37,38]. According to a recent systematic review of metastatic GCTB prognoses, spontaneous regression was observed in 4.5% of patients . There is often no change in volume with GCTB lung metastases . Since it is impossible to predict the behavior of these metastases , it is reasonable to evaluate the tumor biology with observation in each case in order to decide on further treatments, such as a metastasectomy or medical treatments. However, patients with lung nodules > 5 mm require careful observation due to the high rate of disease progression.
The mortality of patients with metastases from GCTB who underwent metastasectomy ranged from 0 to 50% [2, 12,13,14, 20, 31, 32, 34, 37, 45,46,47,48,49,50]. The recurrence rate of patients with metastases from GCTB who underwent metastasectomy ranged from 0 to 50% [2, 13, 14, 20, 31, 32, 37, 45, 46, 49]. The outcomes following metastasectomy varied due to the unpredictable tumor behavior of the GCTB lung metastases. Studies have shown that an aggressive lung metastasectomy might fail to result in a cure .
Since reporting on the efficacy of cytotoxic chemotherapy for lung metastases from GCTB is limited [34, 52], its role is not well defined. However, considering that GCTBs are borderline tumors, they are not responsive to chemotherapy even after the appearance of the lung metastases . There is anecdotal evidence that interferon α-2a can be effective in stabilizing progressive GCTB refractory to other modalities such as surgery, radiation, and cytotoxic chemotherapy [53,54,55]. Interferon may have activity in GCTBs via its antiangiogenic properties. Interferon, however, is not well tolerated and is associated with numerous side effects, including depression and ischemic events .
Feigenberg et al.  reported three patients with lung metastases from GCTB who were treated with whole-lung radiotherapy. One patient’s lung metastasis progressed after treatment, and the patient soon died. The other two patients were long-term survivors (7.5 years and 13 years) with complete resolution of detectable disease. However, radiotherapy may induce secondary malignant transformation, which is a concern, especially because most patients are relatively young. The reported risk of malignant transformation varies between 0 and 5% [58,59,60,61,62].
Denosumab was capable of stopping the progression of lung metastases in two patients. For one of these patients, lung metastases progressed despite chemotherapy, but denosumab halted the progression of lung metastases. Palmerini et al.  reported a series of 15 patients with metastatic GCTB treated with denosumab, and all achieved tumor control. Engellau et al.  reported on 38 patients with metastatic GCTB who achieved tumor control with denosumab treatment. Thus, denosumab could halt disease progression in most metastatic GCTBs. In our study, two patients underwent denosumab treatment and achieved tumor control of lung metastases without side effects. In one of these 2 patients, denosumab was administered twice before surgical management of the primary lesion and then for the treatment of lung nodules. Each of the two denosumab treatments was effective for the patient. However, to date, only two cases have demonstrated that denosumab rechallenge could be effective .
Balke et al.  reported a series of 12 patients with metastatic GCTB who had stable disease following bisphosphonate treatment. Bisphosphonate is also a treatment option for lung metastases from GCTB.
Currently, based on the aforementioned studies and the findings of this study, we determined that observation of the biological behavior of lung metastases is a first-line approach. If the lung metastases progress, denosumab should be administered once every 4 to 6 months to reduce the risk of complications such as osteonecrosis of the jaw . If the denosumab must be discontinued due to complications and the lung metastases progress again, a metastasectomy should be performed. If the lung metastases are inoperable or the patient refuses metastasectomy, a denosumab rechallenge after the patient recovers from the complication or stereotactic radiotherapy treatment is recommended.
This study has several limitations. First, we have histological documentation of lung nodules only for patients who underwent resection of their lung metastases. However, most patients with GCTB are healthy and young and infrequently have lung lesions; therefore, these lung lesions, when observed on imaging studies of GCTB patients, most likely represented GCTB lung metastases. Second, because information on the size of lung nodules was not available in six of the 22 patients, the association between the size of the lung nodule and disease progression should be interpreted with caution. Third, a power analysis was not performed, and there was a risk of type II error due to the small sample size. If an adequate number of patients is gathered in the future, significant differences may appear regarding the other variables in this study. Forth, this is a retrospective study, and patients were treated differently over the long-term following multidisciplinary team meetings. The treatments have also changed in relation to the discovery of new therapies such as denosumab. However, based on the results of this study, we can now recommend a therapeutic strategy for the treatment of lung metastases from GCTB.
This study showed that observation can be used safely as a first-line management approach for patients with lung metastases from GCTB. According to radiological imaging, approximately half of the patients progressed, and approximately half required some form of treatment. However, patients with lung nodules > 5 mm should be carefully observed because of the high rate of disease progression in this group.
Availability of data and materials
The datasets generated and/or analyzed during the current study are not publicly available due to privacy considerations but are available from the corresponding author upon reasonable request.
Giant cell tumor of bone
Response Evaluation Criteria in Solid Tumors
Athanasou NA, Bansal M, Forsyth R, Reid RP, Sapi Z. Giant cell tumour of bone. In: CDM F, Bridge JA, Hogendoorn P, Mertens F, editors. WHO classification of tumours of soft tissue and bone. 4th ed. Lyon: IARC; 2013. p. 321–4.
Deheshi BM, Jaffer SN, Griffin AM, Ferguson PC, Bell RS, Wunder JS. Joint salvage for pathologic fracture of giant cell tumor of the lower extremity. Clin Orthop Relat Res. 2007;459:96–104.
Niu X, Zhang Q, Hao L, Ding Y, Li Y, Xu H, et al. Giant cell tumor of the extremity: retrospective analysis of 621 Chinese patients from one institution. J Bone Joint Surg Am. 2012;94(5):461–7.
Puri A, Gulia A, Hegde P, Verma V, Rekhi B. Neoadjuvant denosumab: its role and results in operable cases of giant cell tumour of bone. Bone Joint J. 2019;101-B(2):170–7.
Quattrini I, Pollino S, Pazzaglia L, Conti A, Novello C, Ferrari C, et al. Prognostic role of nuclear factor/IB and bone remodeling proteins in metastatic giant cell tumor of bone: a retrospective study. J Orthop Res. 2015;33(8):1205–11.
Rock M. Curettage of giant cell tumor of bone. Factors influencing local recurrences and metastasis. Chir Organi Mov. 1990;75(1 Suppl):204–5.
Ghert MA, Rizzo M, Harrelson JM, Scully SP. Giant-cell tumor of the appendicular skeleton. Clin Orthop Relat Res. 2002;400:201–10.
Bertoni F, Present D, Enneking WF. Giant-cell tumor of bone with pulmonary metastases. J Bone Joint Surg Am. 1985;67(6):890–900.
Campanacci M, Baldini N, Boriani S, Sudanese A. Giant-cell tumor of bone. J Bone Joint Surg Am. 1987;69(1):106–14.
Tubbs WS, Brown LR, Beabout JW, Rock MG, Unni KK. Benign giant-cell tumor of bone with pulmonary metastases: clinical findings and radiologic appearance of metastases in 13 cases. AJR Am J Roentgenol. 1992;158(2):331–4.
Viswanathan S, Jambhekar NA. Metastatic giant cell tumor of bone: are there associated factors and best treatment modalities? Clin Orthop Relat Res. 2010;468(3):827–33.
Chan CM, Adler Z, Reith JD, Gibbs CP. Risk factors for pulmonary metastases from giant cell tumor of bone. J Bone Joint Surg Am. 2015;97(5):420–8.
Dominkus M, Ruggieri P, Bertoni F, Briccoli A, Picci P, Rocca M, et al. Histologically verified lung metastases in benign giant cell tumours--14 cases from a single institution. Int Orthop. 2006;30(6):499–504.
Takeuchi A, Tsuchiya H, Niu X, Ueda T, Jeon D-G, Wang EHM, et al. The prognostic factors of recurrent GCT: a cooperative study by the Eastern Asian Musculoskeletal Oncology Group. J Orthop Sci. 2011;16(2):196–202.
Cheng JC, Johnston JO. Giant cell tumor of bone. Prognosis and treatment of pulmonary metastases. Clin Orthop Relat Res. 1997;338:205–14.
Kay RM, Eckardt JJ, Seeger LL, Mirra JM, Hak DJ. Pulmonary metastasis of benign giant cell tumor of bone. Six histologically confirmed cases, including one of spontaneous regression. Clin Orthop Relat Res. 1994;302:219–30.
Maloney WJ, Vaughan LM, Jones HH, Ross J, Nagel DA. Benign metastasizing giant-cell tumor of bone. Report of three cases and review of the literature. Clin Orthop Relat Res. 1989;243:208–15.
Gresen AA, Dahlin DC, Peterson LF, Payne WS. ‘Benign’ giant cell tumor of bone metastasizing to lung. Ann Thorac Surg. 1973;16(5):531–5.
Goldenberg RR, Campbell CJ, Bonfiglio M. Giant-cell tumor of bone. An analysis of two hundred and eighteen cases. J Bone Joint Surg Am. 1970;52(4):619–64.
Bertoni F, Present D, Sudanese A, Baldini N, Bacchini P, Campanacci M. Giant-cell tumor of bone with pulmonary metastases. Six case reports and a review of the literature. Clin Orthop Relat Res. 1988;237:275–85.
Ladanyi M, Traganos F, Huvos AG. Benign metastasizing giant cell tumors of bone. A DNA flow cytometric study. Cancer. 1989;64(7):1521–6.
Mirra JM, Ulich T, Magidson J, Kaiser L, Eckardt J, Gold R. A case of probable benign pulmonary ‘metastases’ or implants arising from a giant cell tumor of bone. Clin Orthop Relat Res. 1982;162:245–54.
Kutchemeshgi AD, Wright JR, Humphrey RL. Pulmonary metastases from a well-differentiated giant cell tumor of bone. Report of a patient with apparent response to cyclophosphamide therapy. Johns Hopkins Med J. 1974;134(4):237–45.
Ueda T, Morioka H, Nishida Y, Kakunaga S, Tsuchiya H, Matsumoto Y, et al. Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial. Ann Oncol. 2015;26(10):2149–54.
Chawla S, Henshaw R, Seeger L, Choy E, Blay J-Y, Ferrari S, et al. Safety and efficacy of denosumab for adults and skeletally mature adolescents with giant cell tumour of bone: interim analysis of an open-label, parallel-group, phase 2 study. Lancet Oncol. 2013;14(9):901–8.
Palmerini E, Chawla NS, Ferrari S, Sudan M, Picci P, Marchesi E, et al. Denosumab in advanced/unresectable giant-cell tumour of bone (GCTB): for how long? Eur J Cancer. 2017;76:118–24.
Wei F, Liu X, Liu Z, Jiang L, Dang G, Ma Q, et al. Interferon alfa-2b for recurrent and metastatic giant cell tumor of the spine: report of two cases. Spine. 2010;35(24):E1418–22.
Balke M, Campanacci L, Gebert C, Picci P, Gibbons M, Taylor R, et al. Bisphosphonate treatment of aggressive primary, recurrent and metastatic giant cell tumour of bone. BMC Cancer. 2010;10:462.
Vanel D, Contesso G, Rebibo G, Zafrani B, Masselot J. Benign giant-cell tumours of bone with pulmonary metastases and favourable prognosis. Report on two cases and review of the literature. Skeletal Radiol. 1983;10(4):221–6.
Stargardter FL, Cooperman LR. Giant-cell tumour of sacrum with multiple pulmonary metastases and long-term survival. Br J Radiol. 1971;44(528):976–9.
Osaka S, Toriyama M, Taira K, Sano S, Saotome K. Analysis of giant cell tumor of bone with pulmonary metastases. Clin Orthop Relat Res. 1997;335:253–61.
Siebenrock KA, Unni KK, Rock MG. Giant-cell tumour of bone metastasising to the lungs. A long-term follow-up. J Bone Joint Surg Br. 1998;80(1):43–7.
Rock MG, Pritchard DJ, Unni KK. Metastases from histologically benign giant-cell tumor of bone. J Bone Joint Surg Am. 1984;66(2):269–74.
Faisham WI, Zulmi W, Halim AS, Biswal BM, Mutum SS, Ezane AM. Aggressive giant cell tumour of bone. Singapore Med J. 2006;47(8):679–83.
Takanami I, Takeuchi K, Naruke M, Kodaira S. Aggressive surgery for treating a pulmonary metastasis of a benign giant cell tumor of the bone: results in four cases. J Thorac Cardiovasc Surg. 1998;116(4):649–51.
Kito M, Matusmoto S, Ae K, Tanizawa T, Gokita T, Kobayashi H, et al. Pulmonary metastasis from giant cell tumor of bone: clinical outcome prior to the introduction of molecular target therapy. Jpn J Clin Oncol. 2017;47(6):529–34.
Chen C-C, Liau C-T, Chang C-H, Hsu Y-H, Shih H-N. Giant cell tumors of the bone with pulmonary metastasis. Orthopedics. 2016;39(1):e68–73.
Rosario M, Kim H-S, Yun JY, Han I. Surveillance for lung metastasis from giant cell tumor of bone. J Surg Oncol. 2017;116(7):907–13.
Errani C, Ruggieri P, Asenzio MAN, Toscano A, Colangeli S, Rimondi E, et al. Giant cell tumor of the extremity: a review of 349 cases from a single institution. Cancer Treat Rev. 2010;36(1):1–7.
Errani C, Tsukamoto S, Leone G, Akahane M, Cevolani L, Tanzi P, et al. Higher local recurrence rates after intralesional surgery for giant cell tumor of the proximal femur compared to other sites. Eur J Orthop Surg Traumatol. 2017;27(6):813–9.
Tsukamoto S, Mavrogenis AF, Tanzi P, Leone G, Akahane M, Tanaka Y, et al. Curettage as first surgery for bone giant cell tumor : adequate surgery is more important than oncology training or surgical management by high volume specialized teams. Eur J Orthop Surg Traumatol. 2020;30(1):3–9.
Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45(2):228–47.
Sanjay BK, Kadhi SM. Giant cell tumour of bone with pulmonary metastases. A report of three cases. Int Orthop. 1998;22(3):200–4.
Itkin B, Straminsky S, De Ronato G, Lewi D, Marantz A, Bardach A. Prognosis of metastatic giant cell tumor of bone in the pre-denosumab era. A systematic review and a meta-analysis. Jpn J Clin Oncol. 2018;48(7):640–52.
Donthineni R, Boriani L, Ofluoglu O, Bandiera S. Metastatic behaviour of giant cell tumour of the spine. Int Orthop. 2009;33(2):497–501.
He H, Zeng H, Luo W, Liu Y, Zhang C, Liu Q. Surgical treatment options for giant cell tumors of bone around the knee joint: extended curettage or segmental resection? Front Oncol. 2019;9:946.
Kremen TJ, Bernthal NM, Eckardt MA, Eckardt JJ. Giant cell tumor of bone: are we stratifying results appropriately? Clin Orthop Relat Res. 2012;470(3):677–83.
Liu J, Yang H, Sun R, Yang Z, Zhu Z. Retrospective analysis of patients with rare-site and metastatic giant cell tumor. Chin J Cancer Res. 2013;25(5):585–92.
Tsukamoto S, Mavrogenis AF, Leone G, Righi A, Akahane M, Tanzi P, et al. Denosumab does not decrease the risk of lung metastases from bone giant cell tumour. Int Orthop. 2019;43(2):483–9.
Wang T, Chan CM, Yu F, Li Y, Niu X. Does wrist arthrodesis with structural iliac crest bone graft after wide resection of distal radius giant cell tumor result in satisfactory function and local control? Clin Orthop Relat Res. 2017;475(3):767–75.
Jacopin S, Viehweger E, Glard Y, Launay F, Jouve J-L, Bouvier C, et al. Fatal lung metastasis secondary to index finger giant cell tumor in an 8-year-old child. Orthop Traumatol Surg Res. 2010;96(3):310–3.
Stewart DJ, Belanger R, Benjamin RS. Prolonged disease-free survival following surgical debulking and high-dose cisplatin/doxorubicin in a patient with bulky metastases from giant cell tumor of bone refractory to ‘standard’ chemotherapy. Am J Clin Oncol. 1995;18(2):144–8.
Kaban LB, Mulliken JB, Ezekowitz RA, Ebb D, Smith PS, Folkman J. Antiangiogenic therapy of a recurrent giant cell tumor of the mandible with interferon alfa-2a. Pediatrics. 1999;103(6 Pt 1):1145–9.
Dickerman JD. Interferon and giant cell tumors. Pediatrics. 1999;103(6 Pt 1):1282–3.
Kaiser U, Neumann K, Havemann K. Generalised giant-cell tumour of bone: successful treatment of pulmonary metastases with interferon alpha, a case report. J Cancer Res Clin Oncol. 1993;119(5):301–3.
Ng VY, Davidson DJ, Kim EY, Pollack SM, Conrad Iii EU, Jones RL. The multidisciplinary management of giant cell tumor of bone. Expert Rev Anticancer Ther. 2014;14(7):783–90.
Feigenberg SJ, Marcus RB, Zlotecki RA, Scarborough MT, Enneking WF. Whole-lung radiotherapy for giant cell tumors of bone with pulmonary metastases. Clin Orthop Relat Res. 2002;401:202–8.
Shi W, Indelicato DJ, Reith J, Smith KB, Morris CG, Scarborough MT, et al. Radiotherapy in the management of giant cell tumor of bone. Am J Clin Oncol. 2013;36(5):505–8.
Ruka W, Rutkowski P, Morysiński T, Nowecki Z, Zdzienicki M, Makula D, et al. The megavoltage radiation therapy in treatment of patients with advanced or difficult giant cell tumors of bone. Int J Radiat Oncol Biol Phys. 2010;78(2):494–8.
Chakravarti A, Spiro IJ, Hug EB, Mankin HJ, Efird JT, Suit HD. Megavoltage radiation therapy for axial and inoperable giant-cell tumor of bone. J Bone Joint Surg Am. 1999;81(11):1566–73.
Malone S, O’Sullivan B, Catton C, Bell R, Fornasier V, Davis A. Long-term follow-up of efficacy and safety of megavoltage radiotherapy in high-risk giant cell tumors of bone. Int J Radiat Oncol Biol Phys. 1995;33(3):689–94.
Nair MK, Jyothirmayi R. Radiation therapy in the treatment of giant cell tumor of bone. Int J Radiat Oncol Biol Phys. 1999;43(5):1065–9.
Engellau J, Seeger L, Grimer R, Henshaw R, Gelderblom H, Choy E, et al. Assessment of denosumab treatment effects and imaging response in patients with giant cell tumor of bone. World J Surg Oncol. 2018;16(1):191.
Raimondi A, Simeone N, Guzzo M, Maniezzo M, Collini P, Morosi C, et al. Rechallenge of denosumab in jaw osteonecrosis of patients with unresectable giant cell tumour of bone: a case series analysis and literature review. ESMO Open. 2020;5(4):e000663.
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Tsukamoto, S., Ciani, G., Mavrogenis, A.F. et al. Outcome of lung metastases due to bone giant cell tumor initially managed with observation. J Orthop Surg Res 15, 510 (2020). https://doi.org/10.1186/s13018-020-02038-1