Prognostic factors and survival in HHV8 positive diffuse large B cell lymphoma: a national cancer database analysis.

IF 2.1 4区 医学 Q3 HEMATOLOGY
Gaelle C Haddad, You Li, Liang Hong, Chieh-Lin Fu, Yehuda Galili, Chakra P Chaulagain
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引用次数: 0

Abstract

HHV8-positive diffuse large B-cell lymphoma (HHV8+ DLBCL) is a rare and aggressive lymphoma frequently associated with multicentric Castleman disease. Population-based data remain limited. Using the National Cancer Database (2004-2023), we analyzed 262 patients with histologically confirmed HHV8+ DLBCL (ICD-O-3 9738/3), representing the largest cohort to date. The cohort was predominantly male (76.7%), White (66.0%), with a mean age of 52.6 years. The primary site was nodal in 78.6%. Systemic therapy was administered in 72.9% of patients. Median overall survival was 133 months, with 1-, 3-, and 5-year survival rates of 68.2%, 63.1%, and 59.9%, respectively. On multivariable Cox regression, age ≥60 years, Charlson-Deyo score ≥1, HIV-positive status, and lack of systemic therapy and surgery to the primary site were independently associated with worse overall survival. In a subgroup analysis restricted to patients with known HIV status (n = 113), HIV-positive status was the only variable significantly associated with worse overall survival on univariable analysis.

HHV8阳性弥漫性大B细胞淋巴瘤的预后因素和生存率:一项国家癌症数据库分析
HHV8阳性弥漫性大b细胞淋巴瘤(HHV8+ DLBCL)是一种罕见的侵袭性淋巴瘤,常与多中心Castleman病相关。基于人群的数据仍然有限。使用国家癌症数据库(2004-2023),我们分析了262例组织学证实的HHV8+ DLBCL患者(ICD-O-3 9738/3),这是迄今为止最大的队列。该队列以男性(76.7%)为主,白人(66.0%),平均年龄52.6岁。78.6%的主发部位为淋巴结。72.9%的患者接受全身治疗。中位总生存期为133个月,1、3、5年生存率分别为68.2%、63.1%和59.9%。在多变量Cox回归中,年龄≥60岁、Charlson-Deyo评分≥1、hiv阳性状态、缺乏原发部位的全身治疗和手术与较差的总生存期独立相关。在仅限于已知HIV状态患者的亚组分析中(n = 113), HIV阳性状态是单变量分析中唯一与较差的总生存率显著相关的变量。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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