Clinical characteristics and outcomes of newly diagnosed patients with human immunodeficiency virus-associated Burkitt lymphoma: the Central and Western China AIDS lymphoma league 002 study (CALL-002 study).

IF 3.1 2区 医学 Q3 IMMUNOLOGY Infectious Agents and Cancer Pub Date : 2023-12-05 DOI:10.1186/s13027-023-00559-y
Jinrong Zhao, Haiyan Min, Yunhong Huang, Yaokai Chen, Min Wang, Lirong Xiao, Guo Wei, Yan Wu, Yao Liu, Wei Zhang
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Abstract

Background: Despite the introduction of combined antiretroviral therapy, the clinical outcomes of HIV-associated Burkitt lymphoma (BL) remain poor.

Methods: To evaluate the clinical characteristics, prognostic factors, and outcomes of HIV-associated BL, we conducted a retrospective analysis of patients from multiple centers in China.

Results: The study included 41 patients from 8 medical centers. Among the included population, male patients accounted for 87.8%, with 75.6% in advanced stages. Notably, 46.3% of cases involved bone marrow, while 19.5% involved the central nervous system (CNS). The most commonly used chemotherapy regimen was DA-EPOCH ± R, accounting for 53.6% of cases. The overall response rates for patients receiving DA-EPOCH ± R and R-Hyper-CVAD were 59% and 58.2%, respectively. Interestingly, patients receiving regimens containing rituximab had similar complete remission rates (25% vs. 23.5%) and overall survival time (45.69 ± 11.58 vs. 47.79 ± 11.72 months, P = 0.907) compared to those without rituximab, but differed in progression rates (33.3% vs. 47.1%). For the entire cohort, the 1-year progression-free survival (PFS) and overall survival (OS) rates were 52% and 67%, respectively. CNS involvement was independent risk factors for survival, with 1-year PFS and OS rates of 0% and 38% for patients with CNS involvement, and PFS and OS rates of 66% and 75% for patients without CNS involvement.

Conclusions: HIV-associated BL patients in China have poor prognosis and show limited response to current treatment regimens. The absence of CNS involvement significantly improves clinical outcomes. The use of rituximab is not significantly associated with improved outcomes but can reduce disease progression.

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新诊断的人类免疫缺陷病毒相关伯基特淋巴瘤患者的临床特征和预后:中国中西部艾滋病淋巴瘤联盟002研究(CALL-002研究)。
背景:尽管引入了联合抗逆转录病毒疗法,但艾滋病相关伯基特淋巴瘤(BL)的临床疗效仍然不佳:尽管引入了联合抗逆转录病毒疗法,但HIV相关伯基特淋巴瘤(Burkitt lymphoma,BL)的临床预后仍然不佳:为了评估HIV相关伯基特淋巴瘤的临床特征、预后因素和预后,我们对来自中国多个中心的患者进行了回顾性分析:研究纳入了来自 8 个医疗中心的 41 名患者。其中,男性患者占 87.8%,晚期患者占 75.6%。值得注意的是,46.3%的病例累及骨髓,19.5%累及中枢神经系统(CNS)。最常用的化疗方案是DA-EPOCH±R,占53.6%。接受DA-EPOCH±R和R-Hyper-CVAD治疗的患者的总体反应率分别为59%和58.2%。有趣的是,与未使用利妥昔单抗的患者相比,接受含有利妥昔单抗方案的患者的完全缓解率(25% vs. 23.5%)和总生存时间(45.69 ± 11.58月 vs. 47.79 ± 11.72月,P = 0.907)相似,但进展率(33.3% vs. 47.1%)不同。整个队列的1年无进展生存率(PFS)和总生存率(OS)分别为52%和67%。中枢神经系统受累是影响生存的独立危险因素,中枢神经系统受累患者的1年无进展生存率和总生存率分别为0%和38%,无中枢神经系统受累患者的1年无进展生存率和总生存率分别为66%和75%:结论:中国的艾滋病相关 BL 患者预后较差,对目前的治疗方案反应有限。无中枢神经系统受累可明显改善临床预后。利妥昔单抗的使用与预后改善无明显关联,但可减少疾病进展。
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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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