Kaimila Bongani, van der Gronde Toon, Kasonkanji Edwards, Fox Paula, Chikasema Maria, Tewete Blessings, Gopal Satish
1 UNC Project-Malawi , Lilongwe, Malawi .
2 Department of Medicine, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina.
AIDS Res Hum Retroviruses. 2017 Oct;33(10):1045-1047. doi: 10.1089/AID.2017.0081. Epub 2017 Jun 26.
Given scarce data from sub-Saharan Africa (SSA), we sought to describe CD4 count and HIV RNA trends over time among patients with HIV-positive lymphoproliferative disorders in Malawi. We prospectively enrolled HIV-positive individuals with pathologically confirmed lymphoproliferative disorders between 2013 and 2016. Chemotherapy was standardized with concurrent antiretroviral therapy (ART). We assessed CD4 count and HIV RNA at baseline and every 6 months for up to 2 years. Of 72 HIV-positive patients, 59 had non-Hodgkin lymphoma (NHL), 5 classical Hodgkin lymphoma (CHL), and 8 multicentric Castleman disease (MCD). Median age was 43 years (range 23-64). Fifty-five patients (76%) were on ART at enrollment for a median 47 months (range 1-387), with median CD4 count of 138 cells/μl (range 2-2,235) and median HIV RNA of 2.2 logcopies/ml (range 0.3-7.3). MCD patients had longer median ART durations, higher median CD4 counts, and lower median HIV RNA at baseline than NHL or CHL patients. CD4 count and HIV RNA steadily improved during follow-up, with different patterns in different histological groups. Twelve-month overall survival (OS) was 55% [95% confidence interval (CI) 42%-66%]. There were trends toward baseline CD4 count <100 cells/μl and HIV RNA >2.0 logcopies/ml being associated with worse OS. However, CD4 count and HIV RNA improvements during follow-up were independent of possible effects on OS. Distribution of HIV-positive lymphoproliferative disorders may change with continued ART scale-up in SSA. Chemotherapy and concurrent ART can lead to good immunological and virological outcomes.
鉴于撒哈拉以南非洲(SSA)的数据稀缺,我们试图描述马拉维HIV阳性淋巴增殖性疾病患者的CD4细胞计数和HIV RNA随时间的变化趋势。我们前瞻性地纳入了2013年至2016年间经病理确诊为淋巴增殖性疾病的HIV阳性个体。化疗采用标准化方案并同时进行抗逆转录病毒治疗(ART)。我们在基线时以及之后每6个月评估一次CD4细胞计数和HIV RNA,持续时间长达2年。在72例HIV阳性患者中,59例患有非霍奇金淋巴瘤(NHL),5例患有经典霍奇金淋巴瘤(CHL),8例患有多中心Castleman病(MCD)。中位年龄为43岁(范围23 - 64岁)。55例患者(76%)在入组时接受ART治疗,中位治疗时间为47个月(范围1 - 387个月),中位CD4细胞计数为138个/μl(范围2 - 2235个/μl),中位HIV RNA为2.2 log拷贝/ml(范围0.3 - 7.3 log拷贝/ml)。与NHL或CHL患者相比,MCD患者在基线时的ART中位持续时间更长,CD4细胞计数中位数更高,HIV RNA中位数更低。在随访期间,CD4细胞计数和HIV RNA稳步改善,不同组织学组呈现不同模式。12个月总生存率(OS)为55%[95%置信区间(CI)42% - 66%]。基线CD4细胞计数<100个/μl和HIV RNA>2.0 log拷贝/ml有与较差OS相关的趋势。然而,随访期间CD4细胞计数和HIV RNA的改善与对OS的可能影响无关。随着SSA地区持续扩大ART规模,HIV阳性淋巴增殖性疾病的分布可能会发生变化。化疗和同时进行的ART可带来良好的免疫和病毒学结果。