GLOSA LUB KOMENTARZ PRAWNICZY
Zastosowanie immunoterapii u dzieci z neuroblastomą wysokiego ryzyka
Elwira Szychot 1 , Jarosław Peregud-Pogorzelski 2 , Paweł Wawryków 2 , Andrzej Brodkiewicz 31. The Institute of Cancer Research, London, UK.
2. Department of Paediatric Oncology, Pomeranian Medical University, Szczecin, Poland
3. Department of Paediatrics, Nephrology with Dialysis Therapy and Management of Acute Poisoning, Pomeranian Medical University, Szczecin, Poland
Opublikowany: 2016-09-28
DOI: 10.5604/17322693.1220380
GICID: 01.3001.0009.6878
Dostępne wersje językowe: pl en
Wydanie: Postepy Hig Med Dosw 2016; 70 : 1001-1004
Abstrakt
Przypisy
- 1. Anghelescu D.L., Goldberg J.L., Faughnan L.G., Wu J., Mao S., FurmanW.L., Santana V.M., Navid F.: Comparison of pain outcomesbetween two anti-GD2 antibodies in patients with Neuroblastoma.Pediatr. Blood Cancer, 2015; 62: 224-228
Google Scholar - 2. Barone G., Moreno L., Pearson A.D.: CCLG high risk neuroblastomarelapse options and pathway. Children’s Cancer and LeukaemiaGroup; www.cclg.org.uk, 2013; 19: 1-12. http://www.cclg.org.uk/publications/Treatment/Treatment-options-for-relapsed-orrefractory-high-risk-neuroblastoma/NBRELAPS
Google Scholar - 3. Cheng M., Ahmed M,, Xu H., Cheung N.K.: Structural design ofdisialoganglioside GD2 and CD3-bispecific antibodies to redirect Tcells for tumor therapy. Int. J. Cancer, 2015; 136: 476-486
Google Scholar - 4. Cheung N.K., Cheung I.Y., Kushner B.H., Ostrovnaya I., ChamberlainE., Kramer K., Modak S: Murine anti-GD2 monoclonal antibody3F8 combined with granulocyte-macrophage colony-stimulatingfactor and 13-cis-retinoic acid in high-risk patients with stage 4 neuroblastomain first remission. J. Clin. Oncol., 2012; 10; 30: 3264-3270
Google Scholar - 5. Cheung N.K., Dyer M.A.: Neuroblastoma: developmental biology,cancer genomics and immunotherapy. Nat. Rev. Cancer, 2013;13: 397-411
Google Scholar - 6. Cheung N.K., Ostrovnaya I., Kuk D., Cheung I.Y.: Bone marrowminimal residual disease was an early response marker and a consistentindependent predictor of survival after anti-GD2 immunotherapy.J. Clin. Oncol., 2015; 33: 755-763
Google Scholar - 7. Cohn S.L., Pearson A.D., London W.B., Monclair T., Ambros P.F.,Brodeur G.M., Faldum A., Hero B., Iehara T., Machin D., Mosseri V.,Simon T., Garaventa A., Castel V., Matthay K.K.; INRG Task Force:The International Neuroblastoma Risk Group (INRG) classificationsystem: an INRG Task Force report. J. Clin. Oncol. 2009; 27: 289-297
Google Scholar - 8. Kushner B.H., Modak S., Basu E.M., Roberts S.S., Kramer K.,Cheung N.K.: Posterior reversible encephalopathy syndrome in neuroblastomapatients receiving anti-GD2 3F8 monoclonal antibody.Cancer, 2013; 119: 2789-2795
Google Scholar - 9. Kushner B.H., Ostrovnaya I., Cheung I.Y., Kuk D., Kramer K., ModakS., Yataghene K., Cheung N.V.: Prolonged progression-free survivalafter consolidating second or later remissions of neuroblastomawith Anti-GD2 immunotherapy and isotretinoin: a prospective PhaseII study. Oncoimmunology, 2015; 4: e1016704
Google Scholar - 10. Latorre V., Diskin S.J., Diamond M.A., Zhang H., Hakonarson H.,Maris J.M., Devoto M.: Replication of neuroblastoma SNP associationat the BARD1 locus in African-Americans. Cancer Epidemiol.Biomarkers Prev., 2012; 21: 658-663
Google Scholar - 11. Modak S., Kushner B.H., Kramer K., Vickers A., CheungI.Y., Cheung N.K.: Anti-GD2 antibody 3F8 and barley-derived(1→3),(1→4)-β-D-glucan: a phase I study in patients with chemoresistantneuroblastoma. Oncoimmunology, 2013; 2: e23402
Google Scholar - 12. Moreno L., Barone G., Park J.R., Pearson A.D.: About the benefitsof immunotherapy for high-risk Neuroblastoma. J. Clin. Oncol.,2013; 31: 649-650
Google Scholar - 13. Morgenstern D.A., Baruchel S., Irwin M.S.: Current and futurestrategies for relapsed neuroblastoma: challenges on the road toprecision therapy. J. Pediatr. Hematol. Oncol., 2013; 35: 337-347
Google Scholar - 14. Park J.R., Bagatell R., London W.B., Maris J.M., Cohn S.L., MattayKM, Hogarty M.: COG Neuroblastoma Committee. Children’s OncologyGroup’s 2013 blueprint for research: Neuroblastoma. Pediatr.Blood Cancer, 2013; 60: 985-993
Google Scholar - 15. Schulz G., Cheresh D.A., Varki N.M., Yu A., Staffileno L.K., ReisfeldR.A.: Detection of ganglioside GD2 in tumor tissues and sera ofneuroblastoma patients. Cancer Res. 1984; 44: 5914-5920
Google Scholar - 16. Simon T., Hero B., Faldum A., Handgretinger R., Schrappe M.,Berthold F.: No success of anti-GD2 treatment in high risk neuroblastoma?A critical appraisal. Pediatr. Blood Cancer, 2009; 53: 708.Abstract
Google Scholar - 17. Simon T., Hero B., Faldum A., Handgretinger R., Schrappe M.,Niethammer D., Berthold F.: Consolidation treatment with chimericanti-GD2-antibody ch14.18 in children older than 1 year with metastaticneuroblastoma. J. Clin. Oncol., 2004; 22: 3549-3557
Google Scholar - 18. Yu A.L., Gilman A.L., Ozkaynak M.F., London W.B., KreissmanS.G., Chen H.X., Smith M., Anderson B., Villablanca J.G., MatthayK.K., Shimada H., Grupp S.A., Seeger R., Reynolds C.P., Buxton A.,et al.: Children’s Oncology Group: Anti-GD2 antibody with GM-CSF,interleukin-2, and isotretinoin for neuroblastoma. N. Engl. J. Med.,2010; 363: 1324-1334
Google Scholar