[1]汪央,董瑞.尤文肉瘤家族治疗进展[J].临床小儿外科杂志,2022,21(02):191-195.[doi:10.3760/cma.j.cn.101785-201909060-017]
 Wang Yang,Dong Rui.Progress in the treatment of Ewing’s sarcoma family tumor[J].Journal of Clinical Pediatric Surgery,2022,21(02):191-195.[doi:10.3760/cma.j.cn.101785-201909060-017]
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尤文肉瘤家族治疗进展

参考文献/References:

[1] Delattre O,Zucman J,Melot T,et al.The Ewing family of tumors-a subgroup of small-round-cell tumors defined by specific chimeric transcripts[J].N Engl J Med,1994,331(5):294- 299.DOI:10.1056/NEJM199408043310503.
[2] Bernstein M,Kovar H,Paulussen M,et al.Ewing’s sarcoma family of tumors:current management[J].Oncologist,2006,11(5):503- 519.DOI:10.1634/theoncologist.11- 5- 503.
[3] Esiashvili N,Goodman M,Marcus RB.Changes in incidence and survival of Ewing sarcoma patients over the past 3 decades:Surveillance Epidemiology and End Results data[J].J Pediatr Hematol Oncol,2008,30(6):425- 430.DOI:10.1097/MPH.0b013e31816e22f3.
[4] Balamuth NJ,Womer RB.Ewing’s sarcoma[J].Lancet Oncol,2010,11(2):184- 192.DOI:10.1016/S1470- 2045(09)70286- 4.
[5] Jiang Y,Ludwig J,Janku F.Targeted therapies for advanced Ewing sarcoma family of tumors[J].Cancer Treat Rev,2015,41(5):391- 400.DOI:10.1016/j.ctrv.2015.03.008.
[6] Chen S,Kemal D,Sung YS,et al.Ewing sarcoma with ERG gene rearrangements:A molecular study focusing on the prevalence of FUS-ERG and common pitfalls in detecting EWSR1-ERG fusions by FISH[J].Genes Chromosomes Cancer,2016,55(4):340- 349.DOI:10.1002/gcc.22336.
[7] Shing DC,Mcmullan DJ,Roberts P,et al.FUS/ERG gene fusions in Ewing’s tumors[J].Cancer Res,2003,63(15):4568- 4576.
[8] Kilpatrick SE,Reith JD,Rubin B.Ewing sarcoma and the history of similar and possibly related small round cell tumors[J].Adv Anat Pathol,2018,25(5):314- 326.DOI:10.1097/pap.0000000000000203.
[9] Maheshwari AV,Cheng EY.Ewing sarcoma family of tumors[J].J Am Acad Orthop Surg,2010,18(2):94- 107.DOI:10.5435/00124635- 201002000- 00004.
[10] Thacker MM,Temple HT,Scully SP.Current treatment for Ewing’s sarcoma:expert review of anticancer therapy[J].Expert Rev Anticancer Ther,2005,5(2):319- 331.DOI:10.1586/14737140.5.2.319.
[11] Sluga M,Windhager R,Lang S,et al.The role of surgery and resection margins in the treatment of Ewing’s sarcoma[J].Clin Orthop Relat Res,2001,392(392):394- 399.DOI:10.1097/00003086- 200111000- 00051.
[12] Renard AJS,Veth RPH,Schreuder HWB,et al.Functional results and complications after ablative and limb-saving therapy in lower extremity sarcoma of bone[J].Eur J Cancer,1999,35(9):S267- S268.DOI:10.1016/s0959- 8049(99)81486- 5.
[13] Choi Y,Lim DH,Lee SH,et al.Role of radiotherapy in the multimodal treatment of ewing sarcoma family tumors[J].Cancer Res Treat,2015,47(4):904- 912.DOI:10.4143/crt.2014.158.
[14] Paulino AC.Late effects of radiotherapy for pediatric extremity sarcomas[J].Int J Radiat Oncol Biol Phys,2004,60(1):265- 274.DOI:10.1016/j.ijrobp.2004.02.001.
[15] Grier HE,Krailo MD,Tarbell NJ,et al.Addition of ifosfamide and etoposide to standard chemotherapy for Ewing’s sarcoma and primitive neuroectodermal tumor of bone[J].N Engl J Med,2003,348(8):694- 701.DOI:10.1056/NEJMoa020890.
[16] Grünewald TGP,Cidre-Aranaz F,Surdez D,et al.Ewing sarcoma[J].Nat Rev Dis Primers,2018,4(1).DOI:10.1038/s41572- 018- 0003- x
[17] Krasin MJ,Davidoff AM,Rodriguez-Galindo C,et al.Definitive surgery and multiagent systemic therapy for patients with localized Ewing sarcoma family of tumors:local outcome and prognostic factors[J].Cancer,2005,104(2):367- 373.DOI:10.1002/cncr.21160.
[18] Subbiah V,Langanedu-Cgerradi SE,Cuqlievan B,et al.Multimodality treatment of desmoplastic small round cell tumor:chemotherapy and complete cytoreductive surgery improve patient survival[J].Clin Cancer Res,2018,24(19):4865- 4873.DOI:10.1158/1078- 0432.ccr- 18- 0202.
[19] Mctiernan A,Driver D,Michelagnoli MP,et al.High dose chemotherapy with bone marrow or peripheral stem cell rescue is an effective treatment option for patients with relapsed or progressive Ewing’s sarcoma family of tumours[J].Ann Oncol,2006,17(8):1301- 1305.DOI:10.1093/annonc/mdl108.
[20] Whelan J,Le Deley MC,Dirksen U,et al.High-Dose chemotherapy and blood autologous stem-cell rescue compared with standard chemotherapy in localized high-risk ewing sarcoma:results of Euro-E.W.I.N.G.99 and ewing-2008[J].J Clin Oncol,2018,36(31):3110- 3119.DOI:10.1200/jco.2018.78.2516.
[21] Rosenthal J,Pawlowska AB.High-dose chemotherapy and stem cell rescue for high-risk Ewing’s family of tumors[J].Expert Rev Anticancer Ther,2011,11(2):251- 262.DOI:10.1586/era.10.215.
[22] Gaspar N,Hawkins DS,Dirksen U,et al.Ewing sarcoma:current management and future approaches through collaboration[J].J Clin Oncol,2015,33(27):3036- 3046.DOI:10.1200/JCO.2014.59.5256.
[23] Vren A,Toretsky JA.Ewing’s sarcoma oncoprotein EWS-FLI1:the perfect target without a therapeutic agent[J].Future Oncol,2005,1(4):521- 528.DOI:10.2217/14796694.1.4.521.
[24] Magnaghi-Jaulin L,Masutani H,Robin P,et al.SRE elements are binding sites for the fusion protein EWS-FLI-1[J].Nucleic Acids Res,1996,24(6):1052- 1058.DOI:10.1093/nar/24.6.1052..
[25] Siligan C,Ban J,Bachmaier R,et al.EWS-FLI1 target genes recovered from Ewing’s sarcoma chromatin[J].Oncogene,2005,24(15):2512- 2524.DOI:10.1038/sj.onc.1208455.
[26] Kelleher FC,Thomas DM.Molecular pathogenesis and targeted therapeutics in Ewing sarcoma/primitive neuroectodermal tumours[J].Clin Sarcoma Res,2012,2(1):6.DOI:10.1186/2045- 3329- 2- 6.
[27] Shimizu R,Tanaka M,Tsutsumi S,et al.EWS-FLI1 regulates a transcriptional program in cooperation with Foxq1 in mouse Ewing sarcoma[J].Cancer Sci,2018,109(9):2907- 2918.DOI:10.1111/cas.13710.
[28] Selvanathan SP,Graham GT,Grego AR,et al.EWS-FLI1 modulated alternative splicing of ARID1A reveals novel oncogenic function through the BAF complex[J].Nucleic Acids Res,2019,47(18):9619- 9636.DOI:10.1093/nar/gkz699.
[29] Gorthi A,Romero JC,Loranc E,et al.EWS-FLI1 increases transcription to cause R-loops and block BRCA1 repair in Ewing sarcoma[J].Nature,2018,555(7796):387- 391.DOI:10.1038/nature25748.
[30] Anderson PM,Bielack SS,Gorlick RG,et al.A phase II study of clinical activity of SCH 717454(robatumumab) in patients with relapsed osteosarcoma and Ewing sarcoma[J].Pediatr Blood Cancer,2016,63(10):1761- 1770.DOI:10.1002/pbc.26087.
[31] Sun H,Lin DC,Cao Q,et al.CRM1 inhibition promotes cytotoxicity in ewing sarcoma cells by repressing EWS-FLI1-Dependent IGF-1 signaling[J].Cancer Res,2016,76(9):2687- 2697.DOI:10.1158/0008- 5472.can- 15- 1572.
[32] Heitzeneder S,Sotillo E,Shern JF,et al.Pregnancy-Associated plasma Protein-A (PAPP-A) in ewing sarcoma:role in tumor growth and immune evasion[J].J Natl Cancer Inst,2019,111(9):970- 982.DOI:10.1093/jnci/djy209.
[33] Henrich IC,Young R,Quick L,et al.USP6 confers sensitivity to IFN-Mediated apoptosis through modulation of TRAIL signaling in ewing sarcoma[J].Mol Cancer Res,2018,16(12):1834- 1843.DOI:10.1158/1541- 7786.mcr- 18- 0289.
[34] Yan S,Li Z,Thiele CJ.Inhibition of STAT3 with orally active JAK inhibitor,AZD1480,decreases tumor growth in neuroblastoma and pediatric sarcomas in vitro and in vivo[J].Oncotarget,2013,4(3):433- 445.DOI:10.18632/oncotarget.930.
[35] Koppenhafer SL,Kelli LG,William WT,et al.mTORC1/2 and protein translation regulate levels of CHK1 and the sensitivity to CHK1 inhibitors in ewing sarcoma cells[J].Mol Cancer Ther,2018,17(12):2676- 2688.DOI:10.1158/1535- 7163.mct- 18- 0260.
[36] Slotkin EK,Patwardhan PP,Vasudeva SD,et al.MLN0128,an ATP-Competitive mTOR kinase inhibitor with potent in vitro and in vivo antitumor activity,as potential therapy for bone and soft-tissue sarcoma[J].Mol Cancer Ther,2015,14(2):395- 406.DOI:10.1158/1535- 7163.mct- 14- 0711.
[37] Thoenen E,Curl A,Iwakuma T.TP53 in bone and soft tissue sarcomas[J].Pharmacol Ther,2019,202:149- 164.DOI:10.1016/j.pharmthera.2019.06.010.
[38] Huang X,Wu F,Zhang Z,et al.Association between TP53 rs1042522 gene polymorphism and the risk of malignant bone tumors:a meta-analysis[J].Biosci Rep,2019,39(3):1- 9.DOI:10.1042/bsr20181832.
[39] Sand LG,Szuhai K,Hogendoorn PC.Sequencing overview of Ewing sarcoma:a journey across genomic,epigenomic and transcriptomic landscapes[J].Int J Mol Sci,2015,16(7):16176- 16215.DOI:10.3390/ijms160716176.
[40] Thoenen E,Curl A,Iwakuma T.TP53 in bone and soft tissue sarcomas[J].Pharmacol Ther,2019,202:149- 164.DOI:10.1016/j.pharmthera.2019.06.010.
[41] Stolte B,Iniguez AB,Dharia NV,et al.Genome-scale CRI SPR-Cas9 screen identifies druggable dependencies in TP53 wild-type Ewing sarcoma[J].J Exp Med,2018,215(8):2137- 2155.DOI:10.1084/jem.20171066.
[42] Guerzoni C,Fiori V,Terracciano M,et al.CD99 triggering in ewing sarcoma delivers a lethal signal through p53 pathway reactivation and cooperates with doxorubicin[J].Clin Cancer Res,2015,21(1):146- 156.DOI:10.1158/1078- 0432.CCR- 14- 0492.
[43] Fisher JP,Flutter B,Wesemann F,et al.Effective combination treatment of GD2-expressing neuroblastoma and Ewing’s sarcoma using anti-GD2 ch14.18/CHO antibody with Vγ9Vδ2+γδT cells[J].Oncoimmunology,2015,5(1):e1025194.DOI:10.1080/2162402x.2015.1025194.
[44] Grisendi G,Spano C,D’souza N,et al.Mesenchymal progenitors expressing TRAIL induce apoptosis in sarcomas[J].Stem Cells,2015,33(3):859- 869.DOI:10.1002/stem.1903.
[45] Kailayangiri S,Altvater B,Spurny C,et al.Targeting ewing sarcoma with activated and GD2-specific chimeric antigen receptor-engineered human NK cells induces upregulation of immune-inhibitory HLA-G[J].Oncoimmunology,2017,6(1):e1250050.DOI:10.1080/2162402x.2016.1250050.

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备注/Memo

收稿日期:2020-09-23。
通讯作者:董瑞,Email:rdong@fudan.edu.cn

更新日期/Last Update: 1900-01-01