Simonds Hannah M, Neugut Alfred I, Jacobson Judith S
*Division of Radiation Oncology, Tygerberg Hospital/University of Stellenbosch, Stellenbosch, South Africa; †Herbert Irving Comprehensive Cancer Centre, Columbia University, New York, NY; ‡Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY; and §Division of Oncology, Columbia University College of Physicians and Surgeons, New York, NY.
Int J Gynecol Cancer. 2015 Jun;25(5):884-90. doi: 10.1097/IGC.0000000000000441.
Women infected with the human immunodeficiency virus (HIV) have a higher risk of developing cervix carcinoma than do other women who are thought to be more vulnerable to acute toxicities during chemoradiation. We compared HIV-positive/HIV-negative patients with cervix carcinoma at a single institution with respect to cancer treatment toxicities.
Among patients with stage Ib1-IIIb invasive cervical carcinoma who received radiation or chemoradiation with curative intent, we evaluated demographic and clinical characteristics of HIV-positive and HIV-negative patients. Treatment regimens were documented and toxicities scored as per Radiation Therapy Oncology Group guidelines. We developed logistic regression models for the associations of grade 3/4 toxicities with HIV status.
Complete data were available on 213 patients, including 36 (16.8%) who were HIV positive. More than 85% of both HIV-positive and HIV-negative patients received a minimum of 68-Gy equivalent dose in 2-Gy-fraction external beam and high-dose-rate brachytherapy. More HIV-positive than HIV-negative patients were prescribed radiation alone (38.9% vs 24.29%, P = 0.01), experienced at least 1 grade 3/4 toxicity (38.9% vs 26.6%), or developed grade 3/4 leucopenia (30.6% vs 10.2%, P = 0.003).In a multivariable model, patients who developed a grade 3/4 toxicity were 4 times as likely to have received chemotherapy (odds ratio, 4.41 [95% confidence interval, 1.76-11.1]; P = 0.023) and twice as likely to be HIV positive (odds ratio 2.16 [95% confidence interval, 0.98-4.8]; P = 0.05) as women who did not experience such toxicities.
HIV-positive patients with cervical carcinoma received adequate radiotherapy but were less likely than HIV-negative patients to complete chemotherapy. Few HIV-positive or HIV-negative patients who received radiotherapy without chemotherapy experienced grade 3/4 toxicity. However, among patients who received chemotherapy, those who were HIV positive were more likely than others to experience hematologic toxicity.
感染人类免疫缺陷病毒(HIV)的女性患宫颈癌的风险高于其他女性,后者在放化疗期间被认为更容易出现急性毒性反应。我们在一家机构对患有宫颈癌的HIV阳性/阴性患者的癌症治疗毒性进行了比较。
在接受根治性放疗或放化疗的Ib1-IIIb期浸润性宫颈癌患者中,我们评估了HIV阳性和阴性患者的人口统计学和临床特征。记录治疗方案,并根据放射肿瘤学组指南对毒性进行评分。我们建立了logistic回归模型,以分析3/4级毒性与HIV状态之间的关联。
共有213例患者获得了完整数据,其中36例(16.8%)为HIV阳性。超过85%的HIV阳性和阴性患者在2Gy分割的外照射和高剂量率近距离放疗中接受了至少68Gy的等效剂量。接受单纯放疗的HIV阳性患者多于HIV阴性患者(38.9%对24.29%,P = 0.01),经历至少1次3/4级毒性反应的患者更多(38.9%对26.6%),或出现3/4级白细胞减少的患者更多(30.6%对10.2%,P = 0.003)。在多变量模型中,出现3/4级毒性反应的患者接受化疗的可能性是未出现此类毒性反应女性的4倍(比值比,4.41[95%置信区间,1.76 - 11.1];P = 0.023),HIV阳性的可能性是其2倍(比值比2.16[95%置信区间,0.98 - 4.8];P = 0.05)。
患有宫颈癌的HIV阳性患者接受了充分的放疗,但完成化疗的可能性低于HIV阴性患者。很少有未接受化疗而接受放疗的HIV阳性或阴性患者出现3/4级毒性反应。然而,在接受化疗的患者中,HIV阳性患者比其他患者更容易出现血液学毒性。