Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie Memorial Cancer Center, Institute of Oncology, Warsaw, Poland.
Int J Radiat Oncol Biol Phys. 2010 Oct 1;78(2):494-8. doi: 10.1016/j.ijrobp.2009.07.1704. Epub 2009 Dec 11.
To assess the outcomes of radiotherapy, in terms of local control and treatment complications, of advanced or difficult giant cell tumors of bone (GCTB) that could not be treated by surgery.
Among 122 consecutive patients with confirmed GCTB from 1985 to 2007, 77 patients were treated by megavoltage radiotherapy because they were inappropriate candidates for surgery. We have performed analysis of all data in terms of progression-free survival (PFS) and treatment morbidity. Median follow-up time was 58 months.
In the irradiated group, maximal tumor size ranged from 5 to 18 cm (median, 8.5). Anatomic distribution was as follows: femur, 27 cases; tibia, 19; radial/ulnar bone, 12; sacrum, 9; pelvic bones, 5; other, 5. Twenty-one patients (27%) were referred for local recurrence after ≥1 other treatment procedures. The radiation doses ranged from 26 to 89 Gy (median, 56; administered 1.8-2.0 Gy/fraction with average total duration of treatment of 5-7 weeks); 8 patients (10%) received <50 Gy. All patients tolerated treatment well without acute or late complications. All patients except two are alive. Local control was achieved in 65 patients (84%; bone recalcification/restitution of joint functions), 12 patients showed signs of local progression, all within irradiated fields (9 were treated successfully with salvage surgery). Five- and 10-year local PFS were 83% and 73%, respectively. Three patients developed lungs metastases. Malignant transformation of GCTB occurred in two patients.
GCTB can be safely and effectively treated with megavoltage radiotherapy with local control rate >80% at 5 years. Our study confirms that radiotherapy of GCTB offers an alternative to difficult or complex surgery and may be an option of choice in the treatment of inoperable patients.
评估无法手术治疗的晚期或复杂巨大细胞瘤(GCTB)患者接受放疗的局部控制和治疗并发症的结果。
在 1985 年至 2007 年间,122 例经证实的 GCTB 患者中,有 77 例因不适合手术而接受了兆伏放疗。我们对所有患者的无进展生存(PFS)和治疗并发症进行了分析。中位随访时间为 58 个月。
在放疗组中,最大肿瘤大小范围为 5 至 18 厘米(中位数,8.5 厘米)。解剖分布如下:股骨 27 例,胫骨 19 例,桡骨/尺骨 12 例,骶骨 9 例,骨盆 5 例,其他 5 例。21 例(27%)患者在接受≥1 次其他治疗后出现局部复发。放疗剂量范围为 26 至 89Gy(中位数,56Gy;1.8-2.0Gy/次,平均总治疗时间为 5-7 周);8 例(10%)患者接受<50Gy。所有患者均能很好地耐受治疗,无急性或迟发性并发症。除 2 例患者外,所有患者均存活。65 例(84%)患者达到局部控制(骨再钙化/关节功能恢复),12 例患者出现局部进展迹象,均在照射野内(9 例患者经挽救性手术成功治疗)。5 年和 10 年局部 PFS 分别为 83%和 73%。3 例患者发生肺部转移。2 例患者发生 GCTB 恶变。
巨大细胞瘤采用兆伏放疗可安全有效地治疗,5 年局部控制率>80%。我们的研究证实,放疗是治疗复杂或困难的 GCTB 的一种替代方法,对于无法手术的患者,可能是一种选择。