Kim Seok Jin, Choi Joon Young, Hyun Seung Hyup, Ki Chang-Seok, Oh Dongryul, Ahn Yong Chan, Ko Young Hyeh, Choi Sunkyu, Jung Sin-Ho, Khong Pek-Lan, Tang Tiffany, Yan Xuexian, Lim Soon Thye, Kwong Yok-Lam, Kim Won Seog
Division of Hematology and Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Department of Nuclear Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Lancet Haematol. 2015 Feb;2(2):e66-74. doi: 10.1016/S2352-3026(15)00002-2. Epub 2015 Jan 28.
Assessment of tumour viability after treatment is essential for prediction of treatment failure in patients with extranodal natural killer/T-cell lymphoma (ENKTL). We aimed to assess the use of the post-treatment Deauville score on PET-CT and Epstein-Barr virus DNA as a predictor of residual tumour, to establish the risk of treatment failure in patients with newly diagnosed ENKTL.
In a retrospective analysis of patient data we assessed the prognostic relevance of the Deauville score (five-point scale) on PET-CT and circulating Epstein-Barr virus DNA after completion of treatment in consecutive patients with ENKTL who met eligibility criteria (newly diagnosed and received non-anthracycline-based chemotherapy, concurrent chemoradiotherapy, or both together) diagnosed at the Samsung Medical Center in Seoul, South Korea. The primary aim was to assess the association between progression-free survival and risk stratification based on post-treatment Deauville score and Epstein-Barr virus DNA. With an independent cohort from two different hospitals (Hong Kong and Singapore), we validated the prognostic value of our risk model.
We included 102 patients diagnosed with ENKTL between Jan 6, 2005, and Nov 18, 2013, in the study cohort, and 38 patients diagnosed with ENKTL between Jan 7, 2009, and June 27, 2013, in the validation cohort. In the study cohort after a median follow-up of 47·2 months (IQR 30·0-65·5), 45 (44%) patients had treatment failure and 33 (32%) had died. Post-treatment Deauville score and Epstein-Barr virus DNA positivity were independently associated with progression-free and overall survival in the multivariable analysis (for post-treatment Deauville score of 3-4, progression-free survival hazard ratio [HR] 3·607, 95% CI 1·772-7·341, univariable p<0·0001; for post-treatment Epstein-Barr virus DNA positivity, progression-free survival HR 3·595, 95% CI 1·598-8·089, univariable p<0·0001). We stratified patients into three groups based on risk of treatment failure: a low-risk group (post-treatment Epstein-Barr virus negativity and post-treatment Deauville score of 1-2), a high-risk group (post-treatment Epstein-Barr virus negativity with a Deauville score 3-4, or post-treatment Epstein-Barr virus positivity with a Deauville score 1-2), and treatment failure (Deauville score of 5 or post-treatment Epstein-Barr positivity with a Deauville of score 3-4). This risk model showed a significant association with progression-free survival (for low risk vs high risk, HR 7·761, 95% CI 2·592-23·233, p<0·0001; for low risk vs failure, HR 18·546, 95% CI 5·997-57·353, p<0·0001). The validation cohort showed the same associations (for low risk vs high risk, HR 22·909, 95% CI 2·850-184·162, p=0·003; for low risk vs failure, HR 50·652, 95% CI 6·114-419·610, p<0·0001).
Post-treatment Deauville score on PET-CT scan and the presence of Epstein-Barr virus DNA can predict the risk of treatment failure in patients with ENKTL. Our results might be able to help guide clinical practice.
Samsung Biomedical Research Institute.
评估治疗后肿瘤的存活情况对于预测结外自然杀伤/T细胞淋巴瘤(ENKTL)患者的治疗失败至关重要。我们旨在评估治疗后PET-CT的Deauville评分和爱泼斯坦-巴尔病毒DNA作为残留肿瘤预测指标的应用,以确定新诊断的ENKTL患者的治疗失败风险。
在一项对患者数据的回顾性分析中,我们评估了符合入选标准(新诊断且接受了非蒽环类化疗、同步放化疗或两者联合)的韩国首尔三星医疗中心连续诊断的ENKTL患者治疗完成后PET-CT的Deauville评分(五分制)和循环爱泼斯坦-巴尔病毒DNA的预后相关性。主要目的是评估基于治疗后Deauville评分和爱泼斯坦-巴尔病毒DNA的无进展生存期与风险分层之间的关联。我们使用来自两家不同医院(香港和新加坡)的独立队列验证了我们风险模型的预后价值。
我们将2005年1月6日至2013年11月18日诊断为ENKTL的102例患者纳入研究队列,将2009年1月7日至2013年6月27日诊断为ENKTL的38例患者纳入验证队列。在研究队列中,中位随访47.2个月(IQR 30.0 - 65.5)后,45例(44%)患者出现治疗失败,33例(32%)患者死亡。在多变量分析中,治疗后Deauville评分和爱泼斯坦-巴尔病毒DNA阳性与无进展生存期和总生存期独立相关(治疗后Deauville评分为3 - 4,无进展生存期风险比[HR] 3.607,95% CI 1.772 - 7.341,单变量p < 0.0001;治疗后爱泼斯坦-巴尔病毒DNA阳性,无进展生存期HR 3.595,95% CI 1.598 - 8.089,单变量p < 0.0001)。我们根据治疗失败风险将患者分为三组:低风险组(治疗后爱泼斯坦-巴尔病毒阴性且治疗后Deauville评分为1 - 2)、高风险组(治疗后爱泼斯坦-巴尔病毒阴性且Deauville评分为3 - 4,或治疗后爱泼斯坦-巴尔病毒阳性且Deauville评分为1 - 2)和治疗失败组(Deauville评分为5或治疗后爱泼斯坦-巴尔病毒阳性且Deauville评分为3 - 4)。该风险模型与无进展生存期显著相关(低风险组与高风险组相比,HR 7.761,95% CI 2.592 - 23.233,p < 0.0001;低风险组与治疗失败组相比,HR 18.546,95% CI 5.997 - 57.353,p < 0.0001)。验证队列显示了相同的关联(低风险组与高风险组相比,HR 22.909,95% CI 2.850 - 184.162,p = 0.003;低风险组与治疗失败组相比,HR 50.652,95% CI 6.114 - 419.610,p < 0.0001)。
PET-CT扫描的治疗后Deauville评分和爱泼斯坦-巴尔病毒DNA的存在可预测ENKTL患者的治疗失败风险。我们的结果可能有助于指导临床实践。
三星生物医学研究所。