AIDS. 2021 Apr 1;35(5):747-757. doi: 10.1097/QAD.0000000000002791.
It is unknown if the carcinogenic effect of smoking is influenced by CD4+ cell count and viral load in persons living with HIV.
RESPOND participants with known smoking status were included. Poisson regression adjusting for baseline confounders investigated the interaction between current CD4+/viral load strata [good (CD4+ cell count ≥500 cells/μl and viral load <200 copies/ml], poor [CD4+ cell count ≤350 cells/μl and viral load >200 copies/ml] and intermediate [all other combinations]), smoking status and all cancers, non-AIDS defining cancers (NADCs), smoking-related cancers (SRCs) and infection-related cancers (IRCs).
Out of 19 602 persons, 41.3% were never smokers, 44.4% current and 14.4% previous smokers at baseline. CD4+/viral load strata were poor in 3.4%, intermediate in 44.8% and good in 51.8%. There were 513 incident cancers; incidence rate 6.9/1000 person-years of follow-up (PYFU) [95% confidence interval (95% CI) 6.3-7.5]. Current smokers had higher incidence of all cancer (adjusted incidence rate ratio 1.45; 1.17-1.79), NADC (1.65; 1.31-2.09), SRC (2.21; 1.53-3.20) and IRC (1.38; 0.97-1.96) vs. never smokers. Those with poor CD4+/viral load had increased incidence of all cancer (5.36; 95% CI 3.71-7.75), NADC (3.14; 1.92-5.14), SRC (1.82; 0.76-4.41) and IRC (10.21; 6.06-17.20) vs. those with good CD4+/viral load. There was no evidence that the association between smoking and cancer subtypes differed depending on the CD4+/viral load strata (P > 0.1, test for interaction).
In the large RESPOND consortium, the impact of smoking on cancer was clear and reducing smoking rates should remain a priority. The association between current immune deficiency, virological control and cancer was similar for never smokers, current smokers and previous smokers suggesting similar carcinogenic effects of smoking regardless of CD4+ cell count and viral load.
目前尚不清楚 CD4+ 细胞计数和病毒载量是否会影响 HIV 感染者的吸烟致癌作用。
纳入已知吸烟状况的 RESPOND 参与者。使用泊松回归调整基线混杂因素,调查了当前 CD4+/病毒载量分层[良好(CD4+ 细胞计数≥500 个/μl 和病毒载量<200 拷贝/ml)、差(CD4+ 细胞计数≤350 个/μl 和病毒载量>200 拷贝/ml)和中等(所有其他组合)]、吸烟状况与所有癌症、非艾滋病定义癌症(NADC)、与吸烟相关癌症(SRC)和与感染相关癌症(IRC)之间的交互作用。
在 19602 人中,41.3%为从不吸烟者,44.4%为当前吸烟者,14.4%为既往吸烟者。CD4+/病毒载量分层差占 3.4%,中等占 44.8%,良好占 51.8%。共有 513 例新发癌症;发病率为 6.9/1000 人年随访(PYFU)[95%置信区间(95%CI)6.3-7.5]。与从不吸烟者相比,当前吸烟者的所有癌症(校正发病率比 1.45;1.17-1.79)、NADC(1.65;1.31-2.09)、SRC(2.21;1.53-3.20)和 IRC(1.38;0.97-1.96)发病率更高。CD4+/病毒载量差的患者所有癌症(5.36;95%CI 3.71-7.75)、NADC(3.14;1.92-5.14)、SRC(1.82;0.76-4.41)和 IRC(10.21;6.06-17.20)的发病率均高于 CD4+/病毒载量良好的患者。没有证据表明吸烟与癌症亚型之间的关联因 CD4+/病毒载量分层而异(P>0.1,交互作用检验)。
在大型 RESPOND 研究联盟中,吸烟对癌症的影响是明确的,降低吸烟率仍应是当务之急。当前免疫缺陷、病毒学控制与癌症之间的关联在从未吸烟者、当前吸烟者和既往吸烟者中相似,这表明无论 CD4+ 细胞计数和病毒载量如何,吸烟的致癌作用相似。