School of Pharmacy, College of Health Sciences, University of Zimbabwe, Mount Pleasant, Harare, Zimbabwe.
Newlands Clinic, Highlands, Harare, Zimbabwe.
PLoS One. 2020 Sep 17;15(9):e0239344. doi: 10.1371/journal.pone.0239344. eCollection 2020.
Rituximab in combination with chemotherapy is now widely accepted as standard of care for AIDS-related lymphomas (ARLs) of B-cell origin. However, the clinical impact of rituximab in resource limited settings remains unknown. Different settings and patient heterogeneity may affect the effect of any given treatment. The study objectives were to determine if rituximab use was associated with improved 18-month overall survival (OS) of patients with ARLs and to identify correlates of 18-month OS.
A retrospective review of medical records of adult HIV infected patients treated for high-grade large cell non-Hodgkin's lymphoma with chemotherapy +/- rituximab between 2015-2017 was conducted. Vital status and disease progression/relapse at 18 months were determined. Survival functions were estimated using Kaplan-Meier methodology. Equality of survival functions were assessed using Log-rank tests and Cox regression analysis to identify risk factors for mortality.
One hundred and twenty-four eligible medical records were identified. This was a cohort of black Africans with a median age of 42 (IQR: 33-47) and a 57% male gender distribution. Overall survival at 6, 12 and 18 months for the population was 75.9%, 44.0% and 30.6% respectively. Over the study period, 72.6% of patients were diagnosed with disease progression/ relapse. There was a higher rate of rituximab use in patients who were treated at a private institution and those with medical insurance. Rituximab use was not associated with a reduction in 18-month mortality [adjusted hazard ratio (aHR)1.28, (95% CI 0.63-2.60)]. Risk factors for 18-month mortality were male gender [aHR 1.89, (95% CI 1.04-3.43)], age 40+ years [aHR 2.49, (1.33-4.67)], receipt of <3 chemotherapy cycles [aHR 2.48, (95% CI 1.33-4.60)] and low socioeconomic status [aHR 2.44, (95% CI 1.28-4.67)].
Predictors of mortality were male gender, older age, low socioeconomic status and receipt of a less than half of the recommended number of chemotherapy cycles. Rituximab use was not associated with an improvement in 18-month OS in Zimbabwean patients with ARLs.
利妥昔单抗联合化疗已被广泛接受为 AIDS 相关淋巴瘤(ARL)的标准治疗方法,这些淋巴瘤起源于 B 细胞。然而,在资源有限的环境下,利妥昔单抗的临床影响仍不清楚。不同的环境和患者的异质性可能会影响任何特定治疗的效果。本研究的目的是确定利妥昔单抗的使用是否与 ARL 患者 18 个月总生存率(OS)的提高相关,并确定 18 个月 OS 的相关因素。
对 2015 年至 2017 年间接受化疗联合或不联合利妥昔单抗治疗的成人 HIV 感染患者的医疗记录进行了回顾性分析。确定了 18 个月时的存活状态和疾病进展/复发情况。采用 Kaplan-Meier 方法估计生存函数。采用对数秩检验和 Cox 回归分析评估生存函数的平等性,以确定死亡率的危险因素。
共确定了 124 份符合条件的病历。这是一个由黑人组成的队列,中位年龄为 42 岁(IQR:33-47),男性占 57%。人群的 6、12 和 18 个月总生存率分别为 75.9%、44.0%和 30.6%。在研究期间,72.6%的患者被诊断为疾病进展/复发。在私人机构和有医疗保险的患者中,利妥昔单抗的使用率更高。利妥昔单抗的使用与 18 个月死亡率的降低无关[校正后的危险比(aHR)1.28,(95%置信区间 0.63-2.60)]。18 个月死亡率的危险因素为男性[aHR 1.89,(95%置信区间 1.04-3.43)]、40 岁以上[aHR 2.49,(95%置信区间 1.33-4.67)]、接受<3 个化疗周期[aHR 2.48,(95%置信区间 1.33-4.60)]和低社会经济地位[aHR 2.44,(95%置信区间 1.28-4.67)]。
死亡率的预测因素为男性、年龄较大、社会经济地位较低和接受的化疗周期少于推荐周期的一半。在津巴布韦的 ARL 患者中,利妥昔单抗的使用与 18 个月 OS 的改善无关。