Ferreri A J, Reni M, Ceresoli G L, Villa E
Department of Radiochemotherapy, San Raffaele H Scientific Institute, Milan, Italy.
Cancer Invest. 1998;16(8):554-61. doi: 10.3109/07357909809032885.
The best treatment of primary lymphoma of bone (PLB) remains undefined. We reviewed 15 patients with monostotic PLB and 8 with polyostotic PLB. Twenty of the patients were suitable for analysis. All patients but 1 received adriamycin-containing chemotherapy in association with radiation therapy. Radiotherapy for monostotic cases consisted of 40 Gy to long bones, followed by a boost to 45 Gy to bulky lesions or 40-45 Gy to whole flat bones. In cases of polyostotic PLB, bulky sites, fractured lesions, or sites with a high risk of fracture were irradiated with a median dose of 38 Gy. All patients with monostotic disease achieved complete remission (CR): 10 patients were alive and relapse-free at the time of this writing, 1 other patient was alive following a relapse, and 1 patient died while relapse-free. The survival rate for the patients in the study at the time of this writing was 92% at 50 months. Four patients with polyostotic disease achieved CR. Three of them had only two adjacent sites of disease and were treated as cases of monostotic PLB. Two of these 3 patients are alive and relapse-free. Four patients with polyostotic disease achieved PR, relapsed rapidly, and died of progressive disease. The relapse site was invariably the skeleton. The survival rate for patients with polyostotic PLB at the time of writing was 25% at 40 months. No severe late treatment-related toxicity was observed. The treatment of patients with monostotic PLB with adriamycin-containing chemotherapy and whole-bone irradiation with 40 Gy, followed by a boost to 45 Gy to bulky sites, prevented local relapse and produced a more favorable outcome than the use of radiotherapy (RT) alone. Patients with multiple adjacent lesions that can be included within a single radiation field with acceptable toxicity should be treated as cases of monostotic PLB.
原发性骨淋巴瘤(PLB)的最佳治疗方法仍不明确。我们回顾了15名单发性PLB患者和8名多灶性PLB患者。其中20名患者适合进行分析。除1名患者外,所有患者均接受了含阿霉素的化疗并联合放射治疗。单发性病例的放射治疗包括对长骨给予40 Gy的剂量,随后对体积较大的病灶追加至45 Gy,或对整个扁骨给予40 - 45 Gy的剂量。对于多灶性PLB病例,对体积较大的部位、骨折病灶或有高骨折风险的部位进行照射,中位剂量为38 Gy。所有单发性疾病患者均实现完全缓解(CR):在撰写本文时,10名患者存活且无复发,另1名患者复发后存活,1名患者在无复发时死亡。在撰写本文时,该研究中患者的50个月生存率为92%。4名多灶性疾病患者实现CR。其中3名患者仅有两个相邻的病灶部位,被作为单发性PLB病例进行治疗。这3名患者中有2名存活且无复发。4名多灶性疾病患者实现部分缓解(PR),但很快复发,并死于疾病进展。复发部位总是在骨骼。在撰写本文时,多灶性PLB患者的40个月生存率为25%。未观察到严重的晚期治疗相关毒性反应。采用含阿霉素的化疗并对全骨进行40 Gy照射,随后对体积较大的部位追加至45 Gy,治疗单发性PLB患者,可预防局部复发,且比单独使用放射治疗(RT)产生更有利的结果。对于多个相邻病灶且可纳入单一放射野且毒性可接受的患者,应作为单发性PLB病例进行治疗。