Clinical characteristics and outcomes of primary bone lymphoma in Korea.

The Korean Journal of Hematology Pub Date : 2012-09-01 Epub Date: 2012-09-25 DOI:10.5045/kjh.2012.47.3.213
So Yeon Kim, Dong-Yeop Shin, Seung-Sook Lee, Cheolwon Suh, Jae-Yong Kwak, Hoon-Gu Kim, Jae Hoon Lee, Soon Il Lee, Ye Rim Lee, Seung Hwa Kang, Se Kwon Mun, Min Jae Lee, Hyo-Rak Lee, Sung Hyun Yang, Hye Jin Kang
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引用次数: 9

Abstract

Background: This study evaluates the effectiveness of immunochemotherapy and radiation therapy in the treatment of patients with primary bone lymphoma (PBL).

Methods: We retrospectively reviewed the medical records of 33 patients with PBL who were treated at 6 medical centers in Korea from 1992 to 2010. Clinicopathological features and treatment outcomes were analyzed.

Results: The median age of the patients participating in our study was 40 years. The most common sites of involvement were the pelvis (12.36%) and femur (11.33%). CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) or CHOP-like regimens were administered to 20 patients (61%), and R-CHOP (rituximab plus CHOP) was administered to the remaining 13 patients (39%). The overall response rate was 89% (complete response, 76%; partial response, 12%). The overall survival (OS) of patients with solitary bone lesions was longer than that of patients with multiple bone lesions (median OS: not reached vs. 166 months, respectively; P=0.089). Addition of rituximab to CHOP did not significantly affect either OS or progression-free survival (P=0.53 and P=0.23, respectively). Combining radiation therapy with chemotherapy also did not improve the OS or progression-free survival of patients with solitary bone lesions.

Conclusion: Conventional cytotoxic chemotherapy remains an effective treatment option for patients with PBL. Additional benefits of supplementing chemotherapy with either rituximab or radiation therapy were not observed in this study. Further investigation is needed to characterize the role of immunochemotherapy in treating patients with PBL.

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韩国原发性骨淋巴瘤的临床特点和预后。
背景:本研究评估了免疫化疗和放射治疗原发性骨淋巴瘤(PBL)患者的有效性。方法:回顾性分析1992年至2010年在韩国6个医疗中心治疗的33例PBL患者的病历。分析两组患者的临床病理特征及治疗结果。结果:参与我们研究的患者中位年龄为40岁。最常见的受累部位是骨盆(12.36%)和股骨(11.33%)。20例(61%)患者采用CHOP(环磷酰胺、阿霉素、长春新碱和泼尼松龙)或CHOP样方案,其余13例(39%)患者采用R-CHOP(利妥昔单抗加CHOP)方案。总有效率为89%(完全有效率76%;部分缓解,12%)。单发骨病变患者的总生存期(OS)长于多发性骨病变患者(中位OS:未达到vs. 166个月;P = 0.089)。在CHOP中加入利妥昔单抗对OS和无进展生存期均无显著影响(P分别=0.53和P=0.23)。放疗联合化疗也不能改善孤立性骨病变患者的OS或无进展生存期。结论:传统的细胞毒性化疗仍然是PBL患者的有效治疗选择。在本研究中没有观察到利妥昔单抗或放射治疗补充化疗的其他益处。免疫化疗在PBL患者治疗中的作用有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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