Malone S, O'Sullivan B, Catton C, Bell R, Fornasier V, Davis A
Department of Radiation Oncology, Princess Margaret Hospital, University of Toronto, Ontario, Canada.
Int J Radiat Oncol Biol Phys. 1995 Oct 15;33(3):689-94. doi: 10.1016/0360-3016(95)00159-V.
Giant cell tumors of the bone are rare and have variable presentations and natural history. There may be significant functional sequelae as a result of their locally aggressive nature or as a result of treatment. We reviewed the long-term results of radiotherapy for high risk giant cell tumors to assess: the efficacy of radiotherapy and the potential late toxicity of treatment, and to determine indications for radiation treatment.
This report is a retrospective review of 21 localized giant cell tumors of the bone treated with radiotherapy between 1959 and 1991. Radiation was used in the primary management of 13 cases and for recurrent disease in eight cases. In the primary cases, two received radiotherapy as the sole modality (including a massive pelvic lesion and an advanced maxillary sinus tumor with orbital and pterygoid invasion), and in the other 11, 3 had gross residual disease following surgery and 8 had microscopic residual disease. Of eight recurrent cases, five were treated with radiotherapy alone and three with combined surgery and radiation. Sites of origin included extremity bones in nine cases, pelvis in six, spine in four, and skull in two. Extraosseous disease was apparent in 18 tumors and extended to contiguous structures in 14 (including four cases of spinal cord compression, three cases of sacral plexopathy, and one patient with temporal lobe invasion). The most common dose regimen was 35 Gy/15 fractions/3 weeks (14 cases), with varying schedules for the remainder.
Mean follow-up time was 15.4 years (2 to 35 years). Local control was achieved in 19 of 21 patients with radiotherapy. The two failures were subsequently salvaged for an ultimate control rate of 100%. One of the two radiotherapy failures was a marginal failure and was subsequently salvaged with combined surgery and radiotherapy. No patient died of giant cell tumor. Radiotherapy was well tolerated, with no serious late toxicity. There were no cases of malignant transformation or radiation-induced cancer.
Long-term results in this series indicate that radiotherapy in modest doses (35 Gy in 15 fractions or equivalent) is a safe and effective option for primary and recurrent giant cell tumors of the bone. Radiotherapy should be used if surgery would result in significant functional morbidity and should be considered in select sites where the probability of recurrence is high and there is potential for significant morbidity from tumor relapse or subsequent surgery.
骨巨细胞瘤较为罕见,其临床表现和自然病程各异。由于其局部侵袭性或治疗原因,可能会产生严重的功能后遗症。我们回顾了高危骨巨细胞瘤放疗的长期结果,以评估:放疗的疗效和潜在的晚期毒性,并确定放射治疗的适应症。
本报告是对1959年至1991年间接受放疗的21例局限性骨巨细胞瘤的回顾性研究。13例患者将放疗用于初始治疗,8例用于复发病例的治疗。在初始治疗的病例中,2例将放疗作为唯一治疗方式(包括1例巨大盆腔病变和1例侵犯眼眶及翼状胬肉的上颌窦晚期肿瘤),在其他11例中,3例术后有肉眼残留病灶,8例有镜下残留病灶。在8例复发病例中,5例仅接受放疗,3例接受手术联合放疗。肿瘤起源部位包括9例四肢骨、6例骨盆、4例脊柱和2例颅骨。18例肿瘤有骨外病变,14例扩展至相邻结构(包括4例脊髓压迫、3例骶丛神经病变和1例颞叶侵犯)。最常用的剂量方案是35Gy/15次/3周(14例),其余病例采用不同方案。
平均随访时间为15.4年(2至35年)。21例接受放疗的患者中,19例实现了局部控制。随后挽救了2例治疗失败的患者,最终控制率达100%。2例放疗失败患者中的1例为边缘性失败,随后通过手术联合放疗挽救。无患者死于骨巨细胞瘤。放疗耐受性良好,无严重晚期毒性。无恶变或放射诱发癌症病例。
本系列的长期结果表明,中等剂量(15次分割给予35Gy或等效剂量)放疗是原发性和复发性骨巨细胞瘤安全有效的选择。如果手术会导致严重的功能障碍,则应采用放疗,对于复发可能性高且肿瘤复发或后续手术可能导致严重功能障碍的特定部位,也应考虑放疗。