国际肿瘤学杂志››2021,Vol. 48››Issue (7): 385-388.doi:10.3760/cma.j.cn371439-20200923-00075
• 党为人民谋健康的100年 •下一篇
收稿日期:
2020-09-23修回日期:
2020-10-05出版日期:
2021-07-08发布日期:
2021-07-26通讯作者:
刘爱春 E-mail:aichun2002@hotmail.com基金资助:
Received:
2020-09-23Revised:
2020-10-05Online:
2021-07-08Published:
2021-07-26Contact:
Liu Aichun E-mail:aichun2002@hotmail.comSupported by:
摘要:
EB病毒(EBV)阳性弥漫大B细胞淋巴瘤(DLBCL)是与慢性EBV感染相关的一类罕见的B细胞淋巴瘤。主要为活化B细胞亚型,具有侵袭性,对联合化疗的反应较EBV阴性患者差,预后不良。随着对EBV阳性DLBCL发病机制、生物学特征的研究不断深入,新型治疗策略不断出现,如抗病毒治疗、单克隆抗体、信号通路抑制剂以及包括细胞免疫疗法和免疫检查点抑制剂在内的免疫疗法,这些新的治疗策略能够提高疗效,并减少不良反应的发生。
郭奕维, 刘爱春. EB病毒阳性弥漫大B细胞淋巴瘤的治疗[J]. 国际肿瘤学杂志, 2021, 48(7): 385-388.
Guo Yiwei, Liu Aichun. Treatment of EB virus positive diffuse large B cell lymphoma[J]. Journal of International Oncology, 2021, 48(7): 385-388.
[1] | Marques-Piubelli ML, Salas YI, Pachas C, et al. Epstein-Barr virus-associated B-cell lymphoproliferative disorders and lymphomas: a review[J]. Pathology, 2020, 52(1):40-52. DOI: 10.1016/j.pathol.2019.09.006. doi:10.1016/j.pathol.2019.09.006 |
[2] | Zhou Y, Xu Z, Lin W, et al. Comprehensive genomic profifiling of EBV-positive diffuse large B-cell lymphoma and the expression and clinicopathological correlations of some related genes[J]. Front Oncol, 2019, 9:683. DOI: 10.3389/fonc.2019.00683. doi:10.3389/fonc.2019.00683 |
[3] | Amaya D, Moreno JC, Calvache N, et al. Prevalence and clinico-pathological characteristics in patients with Epstein-Barr virus-positive diffuse large B-cell lymphoma in a high complexity hospital in Cali, Columbia[J]. Rev Esp Patol, 2019, 52(3):139-146. DOI: 10.1016/j.patol.2019.01.002. |
[4] | Nicolae A, Pittaluga S, Abdullah S, et al. EBV positive large B-cell lymphomas in young patients: a nodal lymphoma with evidence for a tolerogenic immune environment[J]. Blood, 2015, 126(7):863-872. DOI: 10.1182/blood-2015-02-630632. doi:10.1182/blood-2015-02-630632pmid:25999451 |
[5] | Keane C, Tobin J, Gunawardana J, et al. The tumour microenvironment is immuno-tolerogenic and a principal determinant of patient outcome in EBV-positive diffuse large B-cell lymphoma[J]. Eur J Haematol, 2019, 103(3):200-207. DOI: 10.1111/ejh.13274. doi:10.1111/ejh.13274pmid:31211907 |
[6] | Okamoto A, Yanada M, Inaguma Y, et al. The prognostic significance of EBV DNA load and EBER status in diagnostic specimens from diffuse large B-cell lymphoma patients[J]. Hematol Oncol, 2017, 35(1):87-93. DOI: 10.1002/hon.2245. doi:10.1002/hon.2245pmid:26177728 |
[7] | Witte HM, Merz H, Biersack H, et al. Impact of treatment variability and clinicopathological characteristics on survival in patients with Epstein-Barr-virus positive diffuse large B cell lymphoma[J]. Br J Haematol, 2020, 189(2):257-268. DOI: 10.1111/bjh.16342. doi:10.1111/bjh.v189.2 |
[8] | Hong JY, Yoon DH, Suh C, et al. EBV-positive diffuse large B-cell lymphoma in young adults: is this a distinct disease entity?[J]. Ann Oncol, 2015, 26(3):548-555. DOI: 10.1093/annonc/mdu556. doi:10.1093/annonc/mdu556pmid:25475080 |
[9] | Jöhrens K, Trappe RU, Lenze D, et al. Age and cellular composition influence overall survival in a collective of non-immunocompromised patients with EBV-positive diffuse large B-cell lymphoma from a German lymphoma center[J]. Leuk Lymphoma, 2016, 57(12):2791-2803. DOI: 10.3109/10428194.2016.1169406. doi:10.3109/10428194.2016.1169406 |
[10] | Beltran BE, Castro D, Paredes S, et al. EBV-positive diffuse large B-cell lymphoma, not otherwise specified: 2020 update on diag-nosis, risk-stratification and management[J]. Am J Hematol, 2020, In press. DOI: 10.1002/ajh.25760. |
[11] | Petrara MR, Giunco S, Serraino D, et al. Post-transplant lymphoproliferative disorders: from epidemiology to pathogenesis-driven treatment[J]. Cancer Lett, 2015, 369(1):37-44. DOI: 10.1016/j.canlet.2015.08.007. doi:10.1016/j.canlet.2015.08.007 |
[12] | Chen R, Allibone S, Bartlett NL, et al. Patient-reported outcomes of brentuximab vedotin in Hodgkin lymphoma and anaplastic large-cell lymphoma[J]. Onco Targets Ther, 2016, 9:2027-2034. DOI: 10.2147/OTT.S96175. |
[13] | Pro B, Advani R, Brice P, et al. Five-year results of brentuximab vedotin in patients with relapsed or refractory systemic anaplastic large cell lymphoma[J]. Blood, 2017, 130(25):2709-2717. DOI: 10.1182/blood-2017-05-780049. doi:10.1182/blood-2017-05-780049 |
[14] | Berger GK, McBride A, Lawson S, et al. Brentuximab vedotin for treatment of non-Hodgkin lymphomas: a systematic review[J]. Crit Rev Oncol Hematol, 2017, 109:42-50. DOI: 10.1016/j.critrevonc.2016.11.009. doi:10.1016/j.critrevonc.2016.11.009 |
[15] | Svoboda J, Bair SM, Landsburg DJ, et al. Brentuximab vedotin in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone as frontline treatment for patients with CD30-positive B-cell lymphomas[J]. Haematologica, 2020, haematol. 2019. 238675. DOI: 10.3324/haematol.2019.238675. |
[16] | Jacobsen ED, Sharman JP, Oki Y, et al. Brentuximab vedotin demonstrates objective responses in a phase 2 study of relapsed/refractory DLBCL with variable CD30 expression[J]. Blood, 2015, 125(9):1394-1402. DOI: 10.1182/blood-2014-09-598763. doi:10.1182/blood-2014-09-598763pmid:25573987 |
[17] | Strunz PP, Schmalzing M, Heidemeier A, et al. Response to daratumumab in rituximab-resistant EBV-associated PTLD following allogenic stem cell transplantation from an EBV seronegative donor[J]. Leuk Lymphoma, 2019, 60(14):3573-3576. DOI: 10.1080/10428194.2019.1636981. doi:10.1080/10428194.2019.1636981 |
[18] | Leonard JP, Kolibaba KS, Reeves JA, et al. Randomized phase Ⅱ study of R-CHOP with or without bortezomib in previously untreated patients with non-germinal center B-cell-like diffuse large B-cell lymphoma[J]. J Clin Oncol, 2017, 35(31):3538-3546. DOI: 10.1200/JCO.2017.73.2784. doi:10.1200/JCO.2017.73.2784pmid:28862883 |
[19] | Liu JY, Kenney T, Butterworth L, et al. Abstract 2673: idelalisib has activity at clinically achievable drug concentrations in a subset of ABC and GCB diffuse large B-cell lymphoma and transformed follicular lymphoma cell lines[J]. Cancer Res, 2015, 75(15 Supplement):2673. DOI: 10.1158/1538-7445.AM2015-2673. |
[20] | Maddocks K, Christian B, Jaglowski S, et al. A phase 1/1b study of rituximab, bendamustine, and ibrutinib in patients with untreated and relapsed/refractory non-Hodgkin lymphoma[J]. Blood, 2015, 125(2):242-248. DOI: 10.1182/blood-2014-08-597914. doi:10.1182/blood-2014-08-597914pmid:25355819 |
[21] | Battle-Lopez A, Gonzalez de Villambrosia S, Nuñez J, et al. Epstein-Barr virus-associated diffuse large B-cell lymphoma: diagnosis, difficulties and therapeutic options[J]. Expert Rev Anticancer Ther, 2016, 16(4):411-421. DOI: 10.1586/14737140.2016.1149065. doi:10.1586/14737140.2016.1149065 |
[22] | Yoon SE, Kim SJ, Yoon DH, et al. A phase Ⅱ study of ibrutinib in combination with rituximab-cyclophosphamide-doxorubicin hydrochloride-vincristine sulfate-prednisone therapy in Epstein-Barr virus-positive, diffuse large B cell lymphoma (54179060LYM2003: IVORY study): results of the final analysis[J]. Ann Hematol, 2020, 99(6):1283-1291. DOI: 10.1007/s00277-020-04005-6. doi:10.1007/s00277-020-04005-6 |
[23] | Liu L, Liu Q, Feng S. Management of Epstein-Barr virus-related post-transplant lymphoproliferative disorder after allogeneic hematopoietic stem cell transplantation[J]. Ther Adv Hematol, 2020, 11:2040620720910964. DOI: 10.1177/2040620720910964. |
[24] | Kochenderfer JN, Dudley ME, Kassim SH, et al. Chemotherapy-refractory diffuse large B-cell lymphoma and indolent B-cell malignancies can be effectively treated with autologous T cells expressing an anti-CD19 chimeric antigen receptor[J]. J Clin Oncol, 2015, 33(6):540-549. DOI: 10.1200/JCO.2014.56.2025. doi:10.1200/JCO.2014.56.2025pmid:25154820 |
[25] | He X, Xu C. Immune checkpoint signaling and cancer immunothe-rapy[J]. Cell Res, 2020, 30(8):660-669. DOI: 10.1038/s41422-020-0343-4. doi:10.1038/s41422-020-0343-4 |
[26] | Sakakibara A, Kohno K, Ishikawa E, et al. Age-related EBV-associated B-cell lymphoproliferative disorders and other EBV+ lymphoproliferative diseases: new insights into immune escape and immunodeficiency through staining with anti-PD-L1 antibody clone SP142[J]. Pathol Int, 2020, 70(8):481-492. DOI: 10.1111/pin.12946. doi:10.1111/pin.12946pmid:32367595 |
[27] | Kataoka K, Miyoshi H, Sakata S, et al. Frequent structural variations involving programmed death ligands in Epstein-Barr virus-associated lymphomas[J]. Leukemia, 2019, 33(7):1687-1699.DOI: 10.1038/s41375-019-0380-5. doi:10.1038/s41375-019-0380-5 |
[28] | Kim SJ, Hyeon J, Cho I, et al. Comparison of efficacy of pembro-lizumab between Epstein-Barr virus positive and negative relapsed or refractory non-Hodgkin lymphomas[J]. Cancer Res Treat, 2019, 51(2):611-622. DOI: 10.4143/crt.2018.191. doi:10.4143/crt.2018.191 |
[29] | Quan L, Chen X, Liu A, et al. PD-1 blockade can restore functions of T-cells in Epstein-Barr virus-positive diffuse large B-cell lymphoma in vitro[J]. PLoS One, 2015, 10(9):e0136476. DOI: 10.1371/journal.pone.0136476. doi:10.1371/journal.pone.0136476 |
[30] | Abramson Cancer Center of the University of Pennsylvania. Pembro-lizumab in realpsed or refractory extranodal NK/T-cell lymphoma, nasal type and EBV-associated diffuse large B cell lymphomas[EB/OL]. ClinicalTrials.gov. (2018-07-13) [2020-08-31]. https://clinicaltrials.gov/ct2/show/NCT03586024?term=NCT0358602-4&draw=2&rank=1. |
[31] | The First Affiliated Hospital with Nanjing Medical University. Sinti-limab in combination with R-CHOP in patients with treatment-naive EBV-positive DLBCL, NOS[EB/OL]. ClinicalTrials.gov. ( 2019-11-29) [2020-08-31]. https://clinicaltrials.gov/ct2/show/NCT04181489?term=NCT04181489&draw=2&rank=1. |
[1] | 高凡, 王萍, 杜超, 褚衍六.肠道菌群与结直肠癌非手术治疗的相关研究进展[J]. 国际肿瘤学杂志, 2024, 51(6): 376-381. |
[2] | 范志鹏, 余静, 胡静, 廖正凯, 徐禹, 欧阳雯, 谢丛华.炎症标志物的变化趋势对一线接受免疫联合化疗的晚期非小细胞肺癌患者预后的预测价值[J]. 国际肿瘤学杂志, 2024, 51(5): 257-266. |
[3] | 张文馨, 夏泠, 彭晋, 周福祥.甲胎蛋白升高型胃肝样腺癌1例并文献复习[J]. 国际肿瘤学杂志, 2024, 51(5): 312-315. |
[4] | 杨毫, 施贵冬, 张程城, 张跃, 张力文, 付茂勇.信迪利单抗与替雷利珠单抗在进展期食管鳞状细胞癌新辅助治疗中的疗效及安全性对比[J]. 国际肿瘤学杂志, 2024, 51(4): 210-216. |
[5] | 萨蔷, 徐航程, 王佳玉.乳腺癌免疫治疗研究进展[J]. 国际肿瘤学杂志, 2024, 51(4): 227-234. |
[6] | 张栋岩, 王品, 魏秋亚, 邓成伍, 魏相相, 高远飞, 王琛.索凡替尼靶向联合卡培他滨和奥沙利铂治疗肝内胆管癌术后患者1例及文献复习[J]. 国际肿瘤学杂志, 2024, 51(4): 249-253. |
[7] | 孙维蔚, 姚学敏, 王鹏健, 王静, 贾敬好.基于血液学指标探讨免疫治疗晚期非小细胞肺癌预后因素及列线图构建[J]. 国际肿瘤学杂志, 2024, 51(3): 143-150. |
[8] | 刘玉兰, 井海燕, 孙静, 宋伟, 沙丹.胃癌免疫治疗疗效预测及预后标志物的研究进展[J]. 国际肿瘤学杂志, 2024, 51(3): 175-180. |
[9] | 崔腾璐, 吕璐, 孙鹏飞.放疗联合免疫治疗在头颈部鳞状细胞癌治疗中的应用[J]. 国际肿瘤学杂志, 2023, 50(9): 548-552. |
[10] | 李开春, 丁昌利, 于文艳.安罗替尼联合特瑞普利单抗治疗晚期肺肉瘤样癌1例[J]. 国际肿瘤学杂志, 2023, 50(8): 511-512. |
[11] | 过慈良, 江春平, 吴俊华.肠道菌群与肿瘤免疫治疗[J]. 国际肿瘤学杂志, 2023, 50(7): 432-436. |
[12] | 陈秋, 王雷, 王明琦, 张梅.恩沃利单抗联合阿昔替尼治疗肾癌肺转移1例并文献复习[J]. 国际肿瘤学杂志, 2023, 50(7): 445-448. |
[13] | 李青珊, 谢鑫, 张楠, 刘帅.放疗联合系统治疗在乳腺癌中的应用进展[J]. 国际肿瘤学杂志, 2023, 50(6): 362-367. |
[14] | 顾安琴, 龙金华, 金风.鼻咽癌免疫治疗的临床研究进展[J]. 国际肿瘤学杂志, 2023, 50(5): 299-303. |
[15] | 丁浩, 应劲涛, 付茂勇.CAR-T在食管鳞状细胞癌治疗中的研究进展[J]. 国际肿瘤学杂志, 2023, 50(4): 231-235. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||