Title Malignancy in giant cell tumor of bone in the extremities
Authors Liu, Weifeng
Chan, Chung Ming
Gong, Lihua
Bui, Marilyn M.
Han, Gang
Letson, G. Douglas
Yang, Yongkun
Niu, Xiaohui
Affiliation Peking Univ, Beijing Jishuitan Hosp, Dept Orthopaed Oncol Surg, Beijing 100035, Peoples R China
Peking Univ, Med Coll 2, Beijing 100035, Peoples R China
Univ Florida, Dept Orthopaed & Rehabil, Gainesvile, FL 32607 USA
Peking Univ, Beijing Jishuitan Hosp, Dept Pathol, Beijing 100035, Peoples R China
Univ S Florida, Dept Pathol & Cell Biol, Coll Med, Tampa, FL 33612 USA
H Lee Moffitt Canc Ctr & Res Inst, Anat Pathol Dept, Tampa, FL 33612 USA
Texas A&M Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, College Stn, TX 77845 USA
H Lee Moffitt Canc Ctr & Res Inst, Dept Sarcoma Program, Tampa, FL 33612 USA
Issue Date Feb-2021
Publisher JOURNAL OF BONE ONCOLOGY
Abstract Background: Malignancy in giant cell tumor of bone (GCTB) is a rare tumor with relevant literature being sparse. In primary malignant GCTB, distinct areas of benign GCTB are juxtaposed with high-grade sarcoma, while in secondary malignant GCTB sarcoma occurs at the site of previously managed GCTB. This study assesses the distinguishing characteristics of patients with this condition, the time interval for development of secondary malignant GCTB, the outcome of treatment, and explores factors associated with oncologic outcomes. Methods: This is a retrospective case series of patients from a prospectively collected institutional musculoskeletal oncology database. From January 1998 to December 2016, 1365 patients were managed for extremity GCTBs. 32 (2.3%) patients had malignant GCTB, including 12 with primary malignant GCTB and 20 with secondary malignant GCTB. The study population comprised 18 males and 14 females presenting at a mean age of 33.7 years (+/- 13.0) and followed for a mean of 9.5 years (+/- 7.4). Data were collected on patient and treatment-related factors, and the occurrence of local recurrence, metastasis, and death. The time from the diagnosis of GCTB to the secondary malignant GCTB was defined as the latent period. Results: Malignant GCTB most commonly presents in the distal femur and proximal tibia with pain and swelling. Radiologically, they are aggressive Campanacci Grade III tumors with prominent bony destruction and soft tissue extension. In the 20 patients with secondary malignant GCTB, the tumors were osteosarcoma in 15, undifferentiated pleomorphic sarcoma in 4 patients and fibrosarcoma in one patient. The mean latent period in patients with secondary malignant GCTB was 7.9 year (+/- 7.3). The median recurrence-free survival (RFS) of secondary malignant GCTB (latent period) and benign GCTB were 61.5 and 19 months respectively (p < 0.001), receiver operating curve analysis found 49.5 months to be the critical threshold, with a longer interval to recurrence being seen in malignant recurrence. The 5 and 10-year overall survival rate of malignant GCTB were 45.8% and 36.1% respectively. The 5-year survival rates of primary malignant GCTB and secondary malignant GCTB were 56.2% and 40.0% respectively (p = 0.188). Adequate surgical margins decreased the local recurrence (LR) rate (P = 0.006). Pulmonary metastasis developed in 69% of patients. The median distant metastasis-free survival between malignant GCTB and benign GCTB were 9 and 21 months (p = 0.002). Chemotherapy was associated with a longer pulmonary metastasis free survival (13 months Vs 6 months, P = 0.002), but not with increased overall survival (57.0% Vs 33.3%, P = 0.167). Conclusions: Malignant GCTB carries a poor prognosis. Accurate diagnosis is critical to avoid inadequate surgical margins when treating primary malignant GCTB. Aggressive tumors and pulmonary metastasis should raise suspicion for malignant GCTB. Secondary malignant transformation should be suspected in patients presenting with recurrence especially after 4 years. Adjuvant chemotherapy use did not benefit survival, but was associated with increased pulmonary progression-free survival. (c) 2020 The Authors. Published by Elsevier GmbH. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
URI http://hdl.handle.net/20.500.11897/609339
ISSN 2212-1374
DOI 10.1016/j.jbo.2020.100334
Indexed SCI(E)
Appears in Collections: 北京积水潭医院

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