Casimiro Lucas Coelho, Mauro Geovanne Pedro, Medici Carolina Trindade Mello, Weltman Eduardo
Department of Radiation Oncology, Instituto do Câncer do Estado de São Paulo (ICESP), University of São Paulo Medical School, Brazil.
Department of Radiology and Oncology, University of Sao Paulo Medical School, School of Medicine, Universidade Nove de Julho (UNINOVE), São Paulo, Brazil.
Rep Pract Oncol Radiother. 2020 Nov-Dec;25(6):956-960. doi: 10.1016/j.rpor.2020.09.004. Epub 2020 Oct 1.
Current guidelines tend to treat HIV positive (HIV+) patients as their seronegative counterparts with diffuse large B-cell lymphoma (DLBCL) but little is known about their radiotherapy responses differences.
A retrospective cohort of all consecutive HIV+ DBCL patients treated with chemotherapy between 2004 and 2018 was assessed. All patients had biopsy-proven lymphomas. They were included if the proposed radical treatment was done without progression or death during chemotherapy and had at least 6 months of follow-up or were followed until death.
Fifty-three (53) patients were selected, with a median age at diagnosis of 41.39 years (20-65 years). Median follow-up of 35.16 months (1.4-178.7 months). Male patients accounted for 54.7% and most had a good performance in the ECOG scale at diagnoses (81.1% are ECOG 0-1). Median overall survival was not reached. Mean OS was 41.5 months with 16 deaths. Age had an impact on OS, with patients older than 60 years at more risk (p = 0.044), as did longtime use of HAART, with those that started antiretroviral therapy within the diagnose of the lymphoma at greatest risk (p = 0.044). RT did not have an impact on OS (p = 0.384) or PFS (p = 0.420), although survival curves show better OS in the radiotherapy group. Toxicities were rare, since none of the patients had grade 3 or superior toxicity.
RT did not impact survival or progression in our limited sample, but a longer OS may occur after the first-year post RT. RT should be tested in prospective data in the HIV+ population with DLBCL.
当前指南倾向于将HIV阳性(HIV+)弥漫性大B细胞淋巴瘤(DLBCL)患者与血清学阴性患者同等对待,但对他们放疗反应的差异知之甚少。
对2004年至2018年间接受化疗的所有连续HIV+ DBCL患者进行回顾性队列研究。所有患者均经活检证实患有淋巴瘤。如果在化疗期间进行了拟议的根治性治疗且无进展或死亡,并且至少有6个月的随访或直至死亡,则将他们纳入研究。
共选择了53例患者,诊断时的中位年龄为41.39岁(20 - 65岁)。中位随访时间为35.1个月(1.4 - 178.7个月)。男性患者占54.7%,大多数患者在诊断时ECOG量表评分良好(81.1%为ECOG 0 - 1)。总生存期未达到中位值。平均总生存期为41.5个月,有16例死亡。年龄对总生存期有影响,60岁以上患者风险更高(p = 0.044),长期使用高效抗逆转录病毒治疗(HAART)也是如此,在淋巴瘤诊断时开始抗逆转录病毒治疗的患者风险最大(p = 0.044)。放疗对总生存期(p = 0.384)或无进展生存期(p = 0.420)没有影响,尽管生存曲线显示放疗组的总生存期更好。毒性反应罕见,因为没有患者出现≥3级毒性反应。
在我们的有限样本中,放疗对生存或进展没有影响,但放疗后第一年可能会出现更长的总生存期。应在HIV+ DLBCL人群的前瞻性数据中对放疗进行测试。