收稿日期: 2021-07-27
网络出版日期: 2021-12-25
基金资助
上海市临床重点专科建设项目(shslczdzk03403)
The prognostic value of pretreatment 18F-FDG PET/CT in extranodal natural killer/T-cell lymphoma
Received date: 2021-07-27
Online published: 2021-12-25
目的: 评估治疗前18氟-氟代脱氧葡萄糖(18F-fluorodeoxyglucos,18F-FDG)正电子发射计算机体层显像(positron emission tomography and computed tomography,PET/CT)检查对结外自然杀伤细胞/T细胞淋巴瘤[extranodal natural killer (NK)/T-cell lymphoma,ENKTL]的预后判断价值。方法: 回顾分析60例新诊断为ENKTL并接受治疗前18F-FDG PET/CT检查的患者。所有患者均采用基于培门冬酶的治疗方案。PET/CT检查参数包括最大标准化摄取值(maximum standardized uptake value,SUVmax)、平均SUV(SUVmean)、代谢肿瘤体积(metabolic tumor volume,MTV)、总病灶糖酵解量(total lesion glycolysis,TLG);临床资料包括Ann Arbor分期、鼻部淋巴瘤浸润范围、鼻外淋巴瘤浸润、淋巴结受累、骨髓受累和性别、年龄等。针对上述指标分别进行单因素生存分析,使用对数秩检验比较,筛选出预后相关因素。采用Cox比例风险模型进行多因素分析,评估影响2年总生存(overall survival, OS)期和无进展生存(progression-free survival, PFS)期的独立预后因素。结果: 单因素生存分析提示, MTV(P<0.001)、TLG(P<0.001)、Ann Arbor分期(P<0.001)、鼻外淋巴瘤浸润(P=0.006)、淋巴结受累(P=0.031)和PET/CT上的骨髓受累(P<0.001)能预测患者的2年OS期,而SUVmax(P=0.653)、SUVmean(P=0.446)和鼻部淋巴瘤浸润范围(P=0.308)则无预后预测价值;MTV(P=0.001)、TLG(P=0.009)、Ann Arbor分期(P<0.001)、鼻外淋巴瘤浸润(P<0.001)和PET/CT上的骨髓受累(P<0.001)能预测患者的2年PFS期,而SUVmax (P=0.274)、SUVmean(P=0.213)、鼻部淋巴瘤浸润范围(P=0.621)和淋巴结受累(P=0.069)无预后判断价值。多因素分析显示,PET/CT检查提示骨髓受累和Ann Arbor分期均是患者OS期(分别为P=0.046 和P=0.019)和PFS期(分别为P=0.033和P=0.015)的重要独立预后因素。结论: 18F-FDG PET/CT检查结果提示骨髓受累及Ann Arbor分期是新诊断ENKTL患者OS期和PFS期的重要独立预后因素,可反映患者的预后。
关键词: 结外自然杀伤细胞/T细胞淋巴瘤; 预后; 18氟-氟代脱氧葡萄糖; 正电子发射计算机体层显像
冯国伟, 张晓娟, 郭睿, 关哲, 王越 . 治疗前18F-FDG PET/CT显像对结外NK/T细胞淋巴瘤的预后判断价值[J]. 诊断学理论与实践, 2021 , 20(06) : 533 -539 . DOI: 10.16150/j.1671-2870.2021.06.004
Objective: To assess use of pretreatment 18F-FDG PET/CT in prognosis prediction of extranodal natural killer/T-cell lymphoma(ENKTL). Methods: Sixty consecutive patients with newly diagnosed ENKTL underwent pretreatment 18F-FDG PET/CT were included and all patients received a pegaspargase-based regime. The maximum standardized uptake value (SUVmax), mean SUV (SUVmean), metabolic tumor volume (MTV), total lesion glycolysis (TLG) of the tumor, and clinical parameters including gender, age, ENKTL stage, nasal lymphoma infiltration range, extranasal lymphoma infiltration, lymph node involvement, bone marrow involvement. Survival curves and log-rank test were performed, and Cox proportional hazards model was used to assess the independent risk factors for overall survival(OS) and progression-free survival (PFS). Results: Survival analysis showed that MTV (P<0.001), TLG (P<0.001), PET/CT-based Ann Arbor stage (P<0.001), extranasal lymphoma infiltration (P=0.006), lymph node involvement (P=0.031), and bone marrow involvement on PET/CT (P<0.001) were predictive factors for 2-year OS, while SUVmax (P=0.653), SUVmean (P=0.446), and nasal lymphoma infiltration range (P=0.308) were not. SUVmax (P=0.274), SUVmean (P=0.213), nasal lymphoma infiltration range (P=0.621), and lymph node involvement (P=0.069) were not predictive factors for 2-year PFS,and MTV (P=0.001), TLG (P=0.009), PET/CT-based Ann Arbor stage(P<0.001), extranasal lymphoma infiltration (P<0.001), and bone marrow involvement on PET/CT (P<0.001) were predictive factors. Multivariate analysis showed PET/CT-based bone marrow involvement and Ann Arbor stage were independent prognostic factors for 2-year OS (P=0.046 and 0.019, respectively) and PFS (P=0.033 and 0.015), respectively. Conclusions: It reveals that 18F-FDG PET/CT-based bone marrow involvement and Ann Arbor stage are independent prognostic factors for both OS and PFS of newly diagnosed ENKTL.
[1] | Lee J, Suh C, Park YH, et al. Extranodal natural killer T-cell lymphoma, nasal-type: a prognostic model from a retrospective multicenter study[J]. J Clin Oncol, 2006, 24(4):612-618. |
[2] | Au WY, Ma SY, Chim CS, et al. Clinicopathologic features and treatment outcome of mature T-cell and natural killer-cell lymphomas diagnosed according to the World Health Organization classification scheme: a single center experience of 10 years[J]. Ann Oncol, 2005, 16(2):206-214. |
[3] | Li CC, Tien HF, Tang JL, et al. Treatment outcome and pattern of failure in 77 patients with sinonasal natural killer/T-cell or T-cell lymphoma[J]. Cancer, 2004, 100(2):366-375. |
[4] | 姜璐, 赵维莅, 陈赛娟. 结外鼻型NK/T细胞淋巴瘤研究进展[J]. 诊断学理论与实践, 2012, 11(2):191-195. |
[5] | Foss FM, Zinzani PL, Vose JM, et al. Peripheral T-cell lymphoma[J]. Blood, 2011, 117(25):6756-6767. |
[6] | Chim CS, Ma SY, Au WY, et al. Primary nasal natural killer cell lymphoma: long-term treatment outcome and relationship with the International Prognostic Index[J]. Blood, 2004, 103(1):216-221. |
[7] | Kim SJ, Yoon DH, Jaccard A, et al. A prognostic index for natural killer cell lymphoma after non-anthracycline-based treatment: a multicentre, retrospective analysis[J]. Lancet Oncol, 2016, 17(3):389-400. |
[8] | Cheson BD. Role of functional imaging in the management of lymphoma[J]. J Clin Oncol, 2011, 29(14):1844-1854. |
[9] | 中华医学会核医学分会. 淋巴瘤18F-FDG PET/CT及PET/MR显像临床应用指南(2021版)[J]. 中核医学与分子影像杂志, 2021, 41(3):161-169. |
[10] | Chan WK, Au WY, Wong CY, et al. Metabolic activity measured by F-18 FDG PET in natural killer-cell lymphoma compared to aggressive B- and T-cell lymphomas[J]. Clin Nucl Med, 2010, 35(8):571-575. |
[11] | Khong PL, Pang CB, Liang R, et al. Fluorine-18 fluorodeoxyglucose positron emission tomography in mature T-cell and natural killer cell malignancies[J]. Ann Hematol, 2008, 87(8):613-621. |
[12] | Moon SH, Cho SK, Kim WS, et al. The role of 18F-FDG PET/CT for initial staging of nasal type natural killer/T-cell lymphoma: a comparison with conventional staging methods[J]. J NuclMed, 2013, 54(7):1039-1044. |
[13] | Zhou X, Lu K, Geng L, et al. Utility of PET/CT in the diagnosis and staging of extranodal natural killer/T-cell lymphoma: a systematic review and meta-analysis[J]. Medicine (Baltimore), 2014, 93(28):e258. |
[14] | Fujiwara H, Maeda Y, Nawa Y, et al. The utility of positron emission tomography/computed tomography in the staging of extranodal natural killer/T-cell lymphoma[J]. Eur J Haematol, 2011, 87(2):123-129. |
[15] | Wu HB, Wang QS, Wang MF, et al. Utility of 18F-FDG PET/CT for staging NK/T-cell lymphomas[J]. Nucl Med Commun, 2010, 31(3):195-200. |
[16] | Karantanis D, Subramaniam RM, Peller PJ, et al. The value of [(18)F] fluorodeoxyglucose positron emission tomography/computed tomography in extranodal natural killer/T-cell lymphoma[J]. Clin Lymphoma Myeloma, 2008, 8(2):94-99. |
[17] | Suh C, Kang YK, Roh JL, et al. Prognostic value of tumor 18F-FDG uptake in patients with untreated extranodal natural killer/T-cell lymphomas of the head and neck[J]. J Nucl Med, 2008, 49(11):1783-1789. |
[18] | 沈文斌, 郭睿, 李彪. 18F-FDG PET/CT代谢参数在NK/T细胞淋巴瘤预后价值的评估[J]. 诊断学理论与实践, 2019, 18(3):349-352. |
[19] | Kim SJ, Kim WS. Treatment of localized extranodal NK/T cell lymphoma, nasal type[J]. Int J Hematol, 2010, 92(5):690-696. |
[20] | Ding H, Chang J, Liu LG, et al. High-dose methotrexate, etoposide, dexamethasone and pegaspargase (MEDA) combination chemotherapy is effective for advanced and relapsed/refractory extranodal natural killer/T cell lymphoma: a retrospective study[J]. Int J Hematol, 2015, 102(2):181-187. |
[21] | Liang R, Gao GX, Chen JP, et al. A phase 2 study of methotrexate, etoposide, dexamethasone, and pegaspargase chemotherapy for newly diagnosed, relapsed, or refractory extranodal natural killer/T-cell lymphoma, nasal type: a multicenter trial in Northwest China[J]. Hematol Oncol, 2017, 35(4):619-629. |
[22] | Sabattini E, Bacci F, Sagramoso C, et al. WHO classification of tumours of haematopoietic and lymphoid tissues in 2008: an overview[J]. Pathologica, 2010, 102(3):83-87. |
[23] | Carbone PP, Kaplan HS, Musshoff K, et al. Report of the Committee on Hodgkin′s Disease Staging Classification[J]. Cancer Res, 1971, 31(11):1860-1861. |
[24] | Xu PP, Xiong J, Cheng S, et al. A phase Ⅱ study of methotrexate, etoposide, dexamethasone and pegaspargase sandwiched with radiotherapy in the treatment of newly diagnosed, stage IE to IIE extranodal natural-Killer/T-cell lymphoma, nasal-type[J]. EBioMedicine, 2017, 25:41-49. |
[25] | Schöder H, Noy A, Gönen M, et al. Intensity of 18fluorodeoxyglucose uptake in positron emission tomography distinguishes between indolent and aggressive non-Hodgkin′s lymphoma[J]. J Clin Oncol, 2005, 23(21):4643-4651. |
[26] | Jiang C, Zhang X, Jiang M, et al. Assessment of the prognostic capacity of pretreatment, interim, and post-therapy (18)F-FDG PET/CT in extranodal natural killer/T-cell lymphoma, nasal type[J]. Ann Nucl Med, 2015, 29(5):442-451. |
[27] | Bai B, Huang HQ, Cai QC, et al. Predictive value of pretreatment positron emission tomography/computed tomography in patients with newly diagnosed extranodal natural killer/T-cell lymphoma[J]. Med Oncol, 2013, 30(1):339. |
[28] | 张亚飞, 王珍, 林丽莉, 等. 治疗前18F-FDG PET/CT SUVmax对Ⅰ~Ⅱ期鼻型NK/T细胞淋巴瘤的预后判断价值[J]. 中华核医学与分子影像杂志, 2018, 38(9):602-604. |
[29] | Khong PL, Huang B, Lee EY, et al. Midtreatment 18F-FDG PET/CT scan for early response assessment of SMILE therapy in natural killer/T-cell lymphoma: a prospective study from a single center[J]. J Nucl Med, 2014, 55(6):911-916. |
[30] | Xie M, Zhai W, Cheng S, et al. Predictive value of F-18 FDG PET/CT quantization parameters for progression-free survival in patients with diffuse large B-cell lymphoma[J]. Hematology, 2016, 21(2):99-105. |
[31] | Chang Y, Fu X, Sun Z, et al. Utility of baseline, interim and end-of-treatment(18)F-FDG PET/CT in extranodal natural killer/T-cell lymphoma patients treated with L-asparaginase/pegaspargase[J]. Sci Rep, 2017, 7:41057. |
[32] | Li T, Zhang B, Ye Y, et al. Immunohistochemical and genetic analysis of Chinese nasal natural killer/T-cell lymphomas[J]. Hum Pathol, 2006, 37(1):54-60. |
[33] | Kwong YL, Chan AC, Liang RH. Natural killer cell lymphoma/leukemia: pathology and treatment[J]. Hematol Oncol, 1997, 15(2):71-79. |
[34] | Su YJ, Wang PN, Chang H, et al. Extranodal NK/T-cell lymphoma, nasal type: clinical features, outcome, and prognostic factors in 101 cases[J]. Eur J Haematol, 2018, 101(3):379-388. |
[35] | Xu PP, Wang Y, Shen Y, et al. Prognostic factors of Chinese patients with T/NK-cell lymphoma: a single institution study of 170 patients[J]. Med Oncol, 2012, 29(3):2176-2182. |
/
〈 |
|
〉 |