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原发性骨淋巴瘤:化疗免疫治疗时代的13年回顾性机构分析

Primary Bone Lymphoma: A 13 Year Retrospective Institutional Analysis in the Chemo-Immunotherapy Era.

作者信息

Sharma Archana, Ahmed Rayaz, Agrawal Narendra, Kapoor Jyotsna, Sharma Anurag, Khushoo Vishvdeep, Agrawal Pragya, Bhurani Dinesh, Mirgh Sumeet P

机构信息

Department of Hemato-Oncology and Bone Marrow Transplant Unit, Rajiv Gandhi Cancer Institute and Research Centre, Sector-5, Rohini, New Delhi 110085 India.

Department of Research, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.

出版信息

Indian J Hematol Blood Transfus. 2021 Apr;37(2):240-248. doi: 10.1007/s12288-020-01327-3. Epub 2020 Aug 8.

Abstract

Primary Lymphoma of bone (PBL) is an uncommon extranodal tumor accounting for 1% of all malignant lymphomas. The incidence of PBL is so rare that many of its aspects remain unknown. We retrospectively analysed our data in order to know clinical characteristics and treatment outcome in Indian population in chemo-immunotherapy era. We identified 49 patients [2007-2019] (median age 52 years) of which, 35 (71.4%) were males. Nearly one-third patients (n = 18; 36.8%) were elderly (Age > 60). The most common histological subtype was DLBCL. Local pain /swelling (n = 23; 47%) and B symptoms (n = 20; 44.4%) was the most common presentation. Spine was the most frequently involved site (n = 25; 51%) followed by pelvis (n = 17; 34.7%). One third patients had poor ECOG-PS ≥ 2, (n = 16; 32.6). More than 50% of the population presented with IPI score ≥ 2 (n = 25; 55.5%). Majority of the patients presented with Ann-Arbor stage IV disease (n = 31; 63.2%). (n = 32; 71.1%) cases received chemotherapy alone and (n = 13; 28.9%) patients were treated in combination with local radiotherapy. R-CHOP was the most common treatment regimen given to patients (n = 43; 95.5%). Overall, three-fourth patients (n = 36; 80%) achieved a complete response. At a median follow-up of 45 ± 2 (range 3-144) months, 4-year OS (Overall Survival) and PFS (Progression free survival) was 83.1% and 74.5%, respectively, using Kaplan-Meier survival curves. Prognostic factors for OS on multivariate analysis were ECOG-PS 0-1 [p = 0.05], age < 60 [p = 0.03] and achievement of CR [p = 0.001]. PBL in India is usually of DLBCL subtype, with spine as the most common site. It has an excellent prognosis in the R-CHOP era. Chemo-immunotherapy with 6 R-CHOP followed by addition of Radiotherapy if partial response appears to provide good outcomes. However, the exact role of radiation still needs to be confirmed.

摘要

骨原发性淋巴瘤(PBL)是一种罕见的结外肿瘤,占所有恶性淋巴瘤的1%。PBL的发病率极低,其许多方面仍不为人知。我们进行了回顾性数据分析,以了解化疗免疫治疗时代印度人群的临床特征和治疗结果。我们确定了49例患者[2007 - 2019年](中位年龄52岁),其中35例(71.4%)为男性。近三分之一的患者(n = 18;36.8%)为老年人(年龄>60岁)。最常见的组织学亚型是弥漫性大B细胞淋巴瘤(DLBCL)。局部疼痛/肿胀(n = 23;47%)和B症状(n = 20;44.4%)是最常见的表现。脊柱是最常受累的部位(n = 25;51%),其次是骨盆(n = 17;34.7%)。三分之一的患者东部肿瘤协作组(ECOG)体能状态评分≥2分(n = 16;32.6%)。超过50%的患者国际预后指数(IPI)评分≥2分(n = 25;55.5%)。大多数患者表现为Ann-Arbor分期IV期疾病(n = 31;63.2%)。32例(71.1%)患者仅接受化疗,13例(28.9%)患者接受了局部放疗联合治疗。利妥昔单抗联合环磷酰胺、阿霉素、长春新碱、泼尼松(R-CHOP)是给予患者的最常见治疗方案(n = 43;95.5%)。总体而言,四分之三的患者(n = 36;80%)实现了完全缓解。使用Kaplan-Meier生存曲线,在中位随访45±2(范围3 - 144)个月时,4年总生存率(OS)和无进展生存率(PFS)分别为83.1%和74.5%。多因素分析中OS的预后因素为ECOG体能状态评分0 - 1分[p = 0.05]、年龄<60岁[p = 0.03]和达到完全缓解[p = 0.001]。印度的PBL通常为DLBCL亚型,脊柱是最常见的部位。在R-CHOP时代,其预后良好。6周期R-CHOP化疗免疫治疗,若出现部分缓解则加用放疗似乎能带来良好的治疗效果。然而,放疗的确切作用仍需证实。

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