Titulo:
RANO, más que ficción.
.
Sumario:
Recientemente, el Grupo de Trabajo en Neurooncología RANO (Response assessment in neuro-oncology) introdujo los criterios para la evaluación de la respuesta de los tumores gliales y su implicación clínica. La creación de esta plataforma y de su primer informe representa un importante paso para precisar la evolución del tratamiento en pacientes con gliomas de alto grado, no solo en el escenario de los ensayos clínicos, sino también en la práctica rutinaria. La terapia antiangiogénica y otras nuevas modalidades de tratamiento han aumentado la incidencia de fenómenos imaginológicos como la pseudoprogresión y la pseudorrespuesta. Igualmente, los nuevos criterios de la RANO toman en cuenta parámetros clínicos como el uso de esteroid... Ver más
Guardado en:
2256-2877
2256-2915
2
2013-03-01
34
44
Nicolás Useche - 2013
Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial-CompartirIgual 4.0.
info:eu-repo/semantics/openAccess
http://purl.org/coar/access_right/c_abf2
| id |
metarevistapublica_acho_revistacolombianadehematologiayoncologia_27_article_329 |
|---|---|
| record_format |
ojs |
| spelling |
RANO, más que ficción. RANO, more than fiction. Recientemente, el Grupo de Trabajo en Neurooncología RANO (Response assessment in neuro-oncology) introdujo los criterios para la evaluación de la respuesta de los tumores gliales y su implicación clínica. La creación de esta plataforma y de su primer informe representa un importante paso para precisar la evolución del tratamiento en pacientes con gliomas de alto grado, no solo en el escenario de los ensayos clínicos, sino también en la práctica rutinaria. La terapia antiangiogénica y otras nuevas modalidades de tratamiento han aumentado la incidencia de fenómenos imaginológicos como la pseudoprogresión y la pseudorrespuesta. Igualmente, los nuevos criterios de la RANO toman en cuenta parámetros clínicos como el uso de esteroides y la presencia de síntomas neurológicos. Es importante que los neurorradiólogos, oncólogos y neurooncólogos conozcan estos criterios y adquieran experiencia en su aplicación correcta. Por otra parte, es necesaria más investigación que permita incluir nuevas técnicas de imagen, como la perfusión, difusión y espectroscopia, en el futuro próximo. Recently, the Neuro-oncology Working Group, Response assessment in neuro-oncology (RANO) introduced new response criteria for gliomas and its clinical implication. Establishing this working-progress platform and its first report, represent an important step forward in the accurate assessment of response to therapy in patients with malignant gliomas, not only in clinical trials but also in daily practice. Anti-angiogenic therapy and other new treatment modalities have increased the incidence and our awareness of novel imaging phenomena, such as pseudoprogression and pseudoresponse not only within clinical trials, but also in clinical practice. The new RANO criteria include imaging findings and also clinical parameters, such as steroid medication and neurological symptoms into account. Neuroradiologists, oncologists and neuro-oncologists must know the criteria, apply them to standardized findings communication and gain experience in order to correctly use these information. Further research is needed to allow the inclusion of new imaging techniques, such as perfusion, diffusion-weighted imaging, spectroscopy, and volumetric measurements, which will be probably incorporated in the near future. Useche, Nicolás Bermúdez, Sonia Cardona, Andrés Felipe Jiménez, Enrique Hakim, Fernando Peña, Germán Mejía, Juan Armando Aristizábal, Gerardo Restrepo, Carlos Emilio Bartels, Carlos Quintero, Andrés Carranza, Hernán Otero, Jorge Miguel Vargas, Carlos Ortiz, León Darío criterios de respuesta evaluación de respuesta respuesta radiológica criterios de McDonald criterios RANO glioma de alto grado response criteria response assessment radiographic response McDonald criteria RANO criteria high-grade glioma 2 1 Núm. 1 , Año 2013 : Marzo Artículo de revista Journal article 2013-03-01T00:00:00Z 2013-03-01T00:00:00Z 2013-03-01 application/pdf Asociación Colombiana de Hematología y Oncología (ACHO) Revista Colombiana de Hematología y Oncología 2256-2877 2256-2915 https://revista.acho.info/index.php/acho/article/view/329 10.51643/22562915.329 https://doi.org/10.51643/22562915.329 spa https://creativecommons.org/licenses/by-nc-sa/4.0 Nicolás Useche - 2013 Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial-CompartirIgual 4.0. 34 44 Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, et al. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000;92(3):205-16. Eisenhauer EA, Therase P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45(2):228-47. Levin VA, Crafts DC, Norman DM, Hoffer PB, Spire JP, Wilson CB. Criteria for evaluating patients undergoing chemotherapy for malignant brain tumors. J Neurosurg. 1977;47(3):329-35. Norman D, Enzmann DR, Levin VA, Wilson CB, Newton TH. Computed tomography in the evaluation of malignant glioma before and after therapy. Radiology. 1976;121(1):85-8. Macdonald DR, Cascino TL, Schold SC Jr, Cairncross JG. Response criteria for phase II studies of supratentorial malignant glioma. J Clin Oncol. 1990;8(7):1277-80. Wen PY, Macdonald DR, Reardon DA, Cloughesy TF, Sorensen AG, Galanis E, et al. Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol. 2010;28(11):1963-72. CBTRUS (2009). CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2004-2005. Source: Central Brain Tumor Registry of the United States, Hinsdale, IL. . Van den Bent MJ, Wefel JS, Schiff D, Taphoorn MJ, Jaeckle K, Junck L, et al. Response assessment in neuro-oncology (a report of the RANO group): assessment of outcome in trials of diffuse low-grade gliomas. Lancet Oncol. 2011;12(6):583-93. Vogelbaum MA, Jost S, Aghi MK, Heimberger AB, Sampson JH, Wen PY, et al. Application of novel response/progression measures for surgically delivered therapies for gliomas: Response Assessment in Neuro-Oncology (RANO) Working Group. Neurosurgery. 2012;70(1):234-43. Sorensen AG, Patel S, Harmath C, Bridges S, Synnott J, Sievers A, et al. Comparison of diameter and perimeter methods for tumor volume calculation. J Clin Oncol. 2001;19(2):551-7. Grupo de Trabajo Sociedad Española de Neurorradiología. Criterios de respuesta de los tumores cerebrales (diciembre 2011). Disponible en: http://www.senr.org/pdf/section_4/Criterios_respuesta_Neuroon2011.pdf. Sorensen AG, Batchelor TT, Wen PY, Zhang WT, Jain RK. Response criteria for glioma. Nat Clin Pract Oncol. 2008;5(11):634-44. Henson JW, Ulmer S, Harris GJ. Brain tumor imaging in clinical trials. ANJR Am J Neuroradiol. 2008;29(3):419-24. Van den Bent MJ, Vogelbaum MA, Wen PY, Macdonald DR, Chang SM. End point assessment in gliomas: novel treatments limit usefulness of classical Macdonald’s Criteria. J Clin Oncol. 2009;27(18):2905-8. Cairncross JG, Macdonald DR, Pexman JH, Ives FJ. Steroid-induced CT changes in patients with recurrent malignant glioma. Neurology. 1988;38(5):724-6. Watling CJ, Lee DH, Macdonald DR, Cairncross JG. Corticosteroid-induced magnetic resonance imaging changes in patients with recurrent malignant glioma. J Clin Oncol. 1994;12(9): 1886-9. Brandes AA, Franceschi E, Tosoni A, Blatt V, Pession A, Tallini G, et al. MGMT promoter methylation status can predict the incidence and outcome of pseudoprogression after concomitant radiochemotherapy in newly diagnosed glioblastoma patients. J Clin Oncol. 2008;26(13):2192-7. Pouleau HB, Sadeghi N, Balériaux D, Mélot C, De Witte O, Lefranc F. High levels of cellular proliferation predict pseudoprogression in glioblastoma patients. Int J Oncol. 2012;40(4): 923-8. Motegi H, Kamoshima Y, Terasaka S, Kobayashi H, Yamaguchi S, Tanino M, et al. IDH1 mutation as a potential novel biomarker for distinguishing pseudoprogression from true progression in patients with glioblastoma treated with temozolomide and radiotherapy. Brain Tumor Pathol 2012 Jul 3. [Epub ahead of print]. Ortiz LD, Cardona AF, Fadul C, Londoño A, Becerra H, JiménezHakim E, et al. Clinical outcome of concomitant chemoradiotherapy followed by adjuvant temozolomide (TMZ) therapy for high-grade gliomas (HGG) in Colombia (RedLANO registry). J Clin Oncol. 2011;29:(suppl; abstr 2092). Gunjur A, Lau E, Taouk Y, Ryan G. Early post-treatment pseudoprogression amongst glioblastoma multiforme patients treated with radiotherapy and temozolomide: a retrospective analysis. J Med Imaging Radiat Oncol. 2011;55(6):603-10. Singh AD, Easaw JC. Does neurologic deterioration help to differentiate between pseudoprogression and true disease progression in newly diagnosed glioblastoma multiforme? Curr Oncol. 2012;19(4):e295-8. Knudsen-Baas KM, Moen G, Fluge Ø, Storstein A. Pseudoprogression in high-grade glioma. Acta Neurol Scand Suppl. 2013;(196):31-7. Young RJ, Gupta A, Shah AD, Graber JJ, Chan TA, Zhang Z, et al. MRI perfusion in determining pseudoprogression in patients with glioblastoma. Clin Imaging. 2013;37(1):41-9. Young RJ, Gupta A, Shah AD, Graber JJ, Zhang Z, Shi W, et al. Potential utility of conventional MRI signs in diagnosing pseudoprogression in glioblastoma. Neurology. 2011;76(22): 1918-24. Kong DS, Kim ST, Kim EH, Lim DH, Kim WS, Suh YL, et al. Diagnostic dilemma of pseudoprogression in the treatment of newly diagnosed glioblastomas: the role of assessing relative cerebral blood flow volume and oxygen-6-methylguanine-DNA methyltransferase promoter methylation status. AJNR Am J Neuroradiol. 2011;32(2):382-7. Chinot OL, Macdonald DR, Abrey LE, Zahlmann G, Kerloëguen Y, Cloughesy TF. Response assessment criteria for glioblastoma: practical adaptation and implementation in clinical trials of antiangiogenic therapy. Curr Neurol Neurosci Rep. 2013;13(5):347. Cairncross JG, Pexman JH, Rathbone MP. Post-surgical contrast enhancement mimicking residual brain tumour. Can J Neurol Sci 1985;12(1):75. Nicoletti GF, Barone F, Passanisi M, Mancuso P, Albanese V. Linear contrast enhancement at the operative site on early postoperative CT after removal of brain tumors. J Neurosurg Sci. 1994;38(2):131-5. Ekinci G, Akpinar IN, Baltacioğlu F, Erzen C, Kiliç T, Elmaci I, et al. Early-postoperative magnetic resonance imaging in glial tumors: prediction of tumor regrowth and recurrence. Eur J Radiol. 2003;45(2):99-107. Ulmer S, Spalek K, Nabavi A, Schultka S, Mehdorn HM, Kesari S, et al. Temporal changes in magnetic resonance imaging characteristics of Gliadel wafers and of the adjacent brain parenchyma. Neuro Oncol. 2012;14(4):482-90. Colen RR, Zinn PO, Hazany S, Do-Dai D, Wu JK, Yao K, et al. Magnetic resonance imaging appearance and changes on intracavitary Gliadel wafer placement: A pilot study. World J Radiol. 2011;3(11):266-72. Summary minutes of the Oncologic Drugs Advisory Committee, March 31, 2009. Washington, DC: Center for Drug Evaluation and Research, US Food and Drug Administration; 2009. Winkler F, Kozin SV, Tong RT, Chae SS, Booth MF, Garkavtsev I, et al. Kinetics of vascular normalization by VEGFR2 blockade governs brain tumor response to radiation: role of oxygenation, angiopoietin-1, and matrix metalloproteinases. Cancer Cell. 2004;6(6):553-63. Batchelor TT, Sorensen AG, di Tomaso E, Zhang WT, Duda DG, Cohen KS, et al. AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients. Cancer Cell. 2007;11(1):83-95. Vredenburgh JJ, Desjardins A, Herndon JE 2nd, Marcello J, Reardon DA, Quinn JA, et al. Bevacizumab plus irinotecan in recurrent glioblastoma multiforme. J Clin Oncol. 2007;25(30): 4722-9. Kamoun WS, Ley CD, Farrar CT, Duyverman AM, Lahdenranta J, Lacorre DA, et al. Edema control by cediranib, a vascular endothelial growth factor receptor-targeted kinase inhibitor, prolongs survival despite persistent brain tumor growth in mice. J Clin Oncol. 2009;27(15):2542-52. Norden AD, Drappatz J, Muzikansky A, David K, Gerard M, McNamara MB, et al. An exploratory survival analysis of anti-angiogenic therapy for recurrent malignant glioma. J Neurooncol. 2009;92(2):149-55. Narayana A, Kelly P, Golfinos J, Parker E, Johnson G, Knopp E, et al. Antiangiogenic therapy using bevacizumab in recurrent high-grade glioma: impact on local control and patient survival. J Neurosurg. 2009;110(1):173-80. Wick W, Stupp R, Beule AC, Bromberg J, Wick A, Ernemann U, et al. A novel tool to analyze MRI recurrence patterns in glioblastoma. Neuro Oncol. 2008;10(6):1019-24. Wick A, Dörner N, Schäfer N, Hofer S, Heiland S, Schemmer D, et al. Bevacizumab does not increase the risk of remote relapse in malignant glioma. Ann Neurol. 2011;69(3):586-92. Gruber L. Change in pattern of relapse in newly diagnosed high-grade glioma following bevacizumab therapy. ASCO 2010 (abstract 2020). Brandsma D, van den Bent MJ. Pseudoprogression and pseudoresponse in the treatment of gliomas. Curr Opin Neurol. 2009;22(6):633-8. Hygino da Cruz LC Jr, Rodriguez I, Domingues RC, Gasparetto EL, Sorensen AG. Pseudoprogression and pseudoresponse: imaging challenges in the assessment of posttreatment glioma. AJNR Am J Neuroradiol. 2011;32(11):1978-85. Clarke JL, Ennis MM, Yung WK, Chang SM, Wen PY, Cloughesy TF, et al. Is surgery at progression a prognostic marker for improved 6-month progression-free survival or overall survival for patients with recurrent glioblastoma? Neuro Oncol. 2011;13(10):1118-24. Farace P, Giri MG, Meliadò G, Amelio D, Widesott L, Ricciardi GK, et al. Clinical target volume delineation in glioblastomas: pre-operative versus post-operative/pre-radiotherapy MRI. Br J Radiol. 2011;84(999):271-8. Jansen EP, Dewit LG, van Herk M, Bartelink H. Target volumes in radiotherapy for high-grade malignant glioma of the brain. Radiother Oncol. 2000;56(2):151-6. Gállego Pérez-Larraya J, Lahutte M, Petrirena G, Reyes-Botero G, González-Aguilar A, Houillier C, et al. Response assessment in recurrent glioblastoma treated with irinotecan-bevacizumab: comparative analysis of the Macdonald, RECIST, RANO, and RECIST + F criteria. Neuro Oncol. 2012;14(5):667-73. Clarke JL, Chang SM. Neuroimaging: diagnosis and response assessment in glioblastoma. Cancer J. 2012;18(1):26-31. Pichler J, Pachinger C, Pelz M, Kleiser R. MRI assessment of relapsed glioblastoma during treatment with bevacizumab: Volumetric measurement of enhanced and FLAIR lesions for evaluation of response and progression-A pilot study. Eur J Radiol. 2013;82(5):e240-5. Radbruch A, Lutz K, Wiestler B, Bäumer P, Heiland S, Wick W, et al. Relevance of T2 signal changes in the assessment of progression of glioblastoma according to the Response Assessment in Neurooncology criteria. Neuro Oncol. 2012;14(2):222-9. Gladwish A, Koh ES, Hoisak J, Lockwood G, Millar BA, Mason W, et al. Evaluation of early imaging response criteria in glioblastoma multiforme. Radiat Oncol. 2011;6:121. Wang MY, Cheng JL, Han YH, Li YL, Dai JP, Shi DP. Measurement of tumor size in adult glioblastoma: classical cross-sectional criteria on 2D MRI or volumetric criteria on high resolution 3D MRI? Eur J Radiol. 2012;81(9):2370-4. Hwang EJ, Cha Y, Lee AL, Yun TJ, Kim TM, Park CK, et al. Early response evaluation for recurrent high grade gliomas treated with bevacizumab: a volumetric analysis using diffusionweighted imaging. J Neurooncol. 2013 Feb 17. [Epub ahead of print]. https://revista.acho.info/index.php/acho/article/download/329/295 info:eu-repo/semantics/article http://purl.org/coar/resource_type/c_6501 http://purl.org/redcol/resource_type/ARTREF info:eu-repo/semantics/publishedVersion http://purl.org/coar/version/c_970fb48d4fbd8a85 info:eu-repo/semantics/openAccess http://purl.org/coar/access_right/c_abf2 Text Publication |
| institution |
ASOCIACION COLOMBIANA DE HEMATOLOGIA Y ONCOLOGIA |
| thumbnail |
https://nuevo.metarevistas.org/ASOCIACIONCOLOMBIANADEHEMATOLOGIAYONCOLOGIA/logo.png |
| country_str |
Colombia |
| collection |
Revista Colombiana de Hematología y Oncología |
| title |
RANO, más que ficción. |
| spellingShingle |
RANO, más que ficción. Useche, Nicolás Bermúdez, Sonia Cardona, Andrés Felipe Jiménez, Enrique Hakim, Fernando Peña, Germán Mejía, Juan Armando Aristizábal, Gerardo Restrepo, Carlos Emilio Bartels, Carlos Quintero, Andrés Carranza, Hernán Otero, Jorge Miguel Vargas, Carlos Ortiz, León Darío criterios de respuesta evaluación de respuesta respuesta radiológica criterios de McDonald criterios RANO glioma de alto grado response criteria response assessment radiographic response McDonald criteria RANO criteria high-grade glioma |
| title_short |
RANO, más que ficción. |
| title_full |
RANO, más que ficción. |
| title_fullStr |
RANO, más que ficción. |
| title_full_unstemmed |
RANO, más que ficción. |
| title_sort |
rano, más que ficción. |
| title_eng |
RANO, more than fiction. |
| description |
Recientemente, el Grupo de Trabajo en Neurooncología RANO (Response assessment in neuro-oncology) introdujo los criterios para la evaluación de la respuesta de los tumores gliales y su implicación clínica. La creación de esta plataforma y de su primer informe representa un importante paso para precisar la evolución del tratamiento en pacientes con gliomas de alto grado, no solo en el escenario de los ensayos clínicos, sino también en la práctica rutinaria. La terapia antiangiogénica y otras nuevas modalidades de tratamiento han aumentado la incidencia de fenómenos imaginológicos como la pseudoprogresión y la pseudorrespuesta. Igualmente, los nuevos criterios de la RANO toman en cuenta parámetros clínicos como el uso de esteroides y la presencia de síntomas neurológicos. Es importante que los neurorradiólogos, oncólogos y neurooncólogos conozcan estos criterios y adquieran experiencia en su aplicación correcta. Por otra parte, es necesaria más investigación que permita incluir nuevas técnicas de imagen, como la perfusión, difusión y espectroscopia, en el futuro próximo.
|
| description_eng |
Recently, the Neuro-oncology Working Group, Response assessment in neuro-oncology (RANO) introduced new response criteria for gliomas and its clinical implication. Establishing this working-progress platform and its first report, represent an important step forward in the accurate assessment of response to therapy in patients with malignant gliomas, not only in clinical trials but also in daily practice. Anti-angiogenic therapy and other new treatment modalities have increased the incidence and our awareness of novel imaging phenomena, such as pseudoprogression and pseudoresponse not only within clinical trials, but also in clinical practice. The new RANO criteria include imaging findings and also clinical parameters, such as steroid medication and neurological symptoms into account. Neuroradiologists, oncologists and neuro-oncologists must know the criteria, apply them to standardized findings communication and gain experience in order to correctly use these information. Further research is needed to allow the inclusion of new imaging techniques, such as perfusion, diffusion-weighted imaging, spectroscopy, and volumetric measurements, which will be probably incorporated in the near future.
|
| author |
Useche, Nicolás Bermúdez, Sonia Cardona, Andrés Felipe Jiménez, Enrique Hakim, Fernando Peña, Germán Mejía, Juan Armando Aristizábal, Gerardo Restrepo, Carlos Emilio Bartels, Carlos Quintero, Andrés Carranza, Hernán Otero, Jorge Miguel Vargas, Carlos Ortiz, León Darío |
| author_facet |
Useche, Nicolás Bermúdez, Sonia Cardona, Andrés Felipe Jiménez, Enrique Hakim, Fernando Peña, Germán Mejía, Juan Armando Aristizábal, Gerardo Restrepo, Carlos Emilio Bartels, Carlos Quintero, Andrés Carranza, Hernán Otero, Jorge Miguel Vargas, Carlos Ortiz, León Darío |
| topicspa_str_mv |
criterios de respuesta evaluación de respuesta respuesta radiológica criterios de McDonald criterios RANO glioma de alto grado |
| topic |
criterios de respuesta evaluación de respuesta respuesta radiológica criterios de McDonald criterios RANO glioma de alto grado response criteria response assessment radiographic response McDonald criteria RANO criteria high-grade glioma |
| topic_facet |
criterios de respuesta evaluación de respuesta respuesta radiológica criterios de McDonald criterios RANO glioma de alto grado response criteria response assessment radiographic response McDonald criteria RANO criteria high-grade glioma |
| citationvolume |
2 |
| citationissue |
1 |
| citationedition |
Núm. 1 , Año 2013 : Marzo |
| publisher |
Asociación Colombiana de Hematología y Oncología (ACHO) |
| ispartofjournal |
Revista Colombiana de Hematología y Oncología |
| source |
https://revista.acho.info/index.php/acho/article/view/329 |
| language |
spa |
| format |
Article |
| rights |
https://creativecommons.org/licenses/by-nc-sa/4.0 Nicolás Useche - 2013 Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial-CompartirIgual 4.0. info:eu-repo/semantics/openAccess http://purl.org/coar/access_right/c_abf2 |
| references |
Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, et al. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000;92(3):205-16. Eisenhauer EA, Therase P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45(2):228-47. Levin VA, Crafts DC, Norman DM, Hoffer PB, Spire JP, Wilson CB. Criteria for evaluating patients undergoing chemotherapy for malignant brain tumors. J Neurosurg. 1977;47(3):329-35. Norman D, Enzmann DR, Levin VA, Wilson CB, Newton TH. Computed tomography in the evaluation of malignant glioma before and after therapy. Radiology. 1976;121(1):85-8. Macdonald DR, Cascino TL, Schold SC Jr, Cairncross JG. Response criteria for phase II studies of supratentorial malignant glioma. J Clin Oncol. 1990;8(7):1277-80. Wen PY, Macdonald DR, Reardon DA, Cloughesy TF, Sorensen AG, Galanis E, et al. Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol. 2010;28(11):1963-72. CBTRUS (2009). CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2004-2005. Source: Central Brain Tumor Registry of the United States, Hinsdale, IL. . Van den Bent MJ, Wefel JS, Schiff D, Taphoorn MJ, Jaeckle K, Junck L, et al. Response assessment in neuro-oncology (a report of the RANO group): assessment of outcome in trials of diffuse low-grade gliomas. Lancet Oncol. 2011;12(6):583-93. Vogelbaum MA, Jost S, Aghi MK, Heimberger AB, Sampson JH, Wen PY, et al. Application of novel response/progression measures for surgically delivered therapies for gliomas: Response Assessment in Neuro-Oncology (RANO) Working Group. Neurosurgery. 2012;70(1):234-43. Sorensen AG, Patel S, Harmath C, Bridges S, Synnott J, Sievers A, et al. Comparison of diameter and perimeter methods for tumor volume calculation. J Clin Oncol. 2001;19(2):551-7. Grupo de Trabajo Sociedad Española de Neurorradiología. Criterios de respuesta de los tumores cerebrales (diciembre 2011). Disponible en: http://www.senr.org/pdf/section_4/Criterios_respuesta_Neuroon2011.pdf. Sorensen AG, Batchelor TT, Wen PY, Zhang WT, Jain RK. Response criteria for glioma. Nat Clin Pract Oncol. 2008;5(11):634-44. Henson JW, Ulmer S, Harris GJ. Brain tumor imaging in clinical trials. ANJR Am J Neuroradiol. 2008;29(3):419-24. Van den Bent MJ, Vogelbaum MA, Wen PY, Macdonald DR, Chang SM. End point assessment in gliomas: novel treatments limit usefulness of classical Macdonald’s Criteria. J Clin Oncol. 2009;27(18):2905-8. Cairncross JG, Macdonald DR, Pexman JH, Ives FJ. Steroid-induced CT changes in patients with recurrent malignant glioma. Neurology. 1988;38(5):724-6. Watling CJ, Lee DH, Macdonald DR, Cairncross JG. Corticosteroid-induced magnetic resonance imaging changes in patients with recurrent malignant glioma. J Clin Oncol. 1994;12(9): 1886-9. Brandes AA, Franceschi E, Tosoni A, Blatt V, Pession A, Tallini G, et al. MGMT promoter methylation status can predict the incidence and outcome of pseudoprogression after concomitant radiochemotherapy in newly diagnosed glioblastoma patients. J Clin Oncol. 2008;26(13):2192-7. Pouleau HB, Sadeghi N, Balériaux D, Mélot C, De Witte O, Lefranc F. High levels of cellular proliferation predict pseudoprogression in glioblastoma patients. Int J Oncol. 2012;40(4): 923-8. Motegi H, Kamoshima Y, Terasaka S, Kobayashi H, Yamaguchi S, Tanino M, et al. IDH1 mutation as a potential novel biomarker for distinguishing pseudoprogression from true progression in patients with glioblastoma treated with temozolomide and radiotherapy. Brain Tumor Pathol 2012 Jul 3. [Epub ahead of print]. Ortiz LD, Cardona AF, Fadul C, Londoño A, Becerra H, JiménezHakim E, et al. Clinical outcome of concomitant chemoradiotherapy followed by adjuvant temozolomide (TMZ) therapy for high-grade gliomas (HGG) in Colombia (RedLANO registry). J Clin Oncol. 2011;29:(suppl; abstr 2092). Gunjur A, Lau E, Taouk Y, Ryan G. Early post-treatment pseudoprogression amongst glioblastoma multiforme patients treated with radiotherapy and temozolomide: a retrospective analysis. J Med Imaging Radiat Oncol. 2011;55(6):603-10. Singh AD, Easaw JC. Does neurologic deterioration help to differentiate between pseudoprogression and true disease progression in newly diagnosed glioblastoma multiforme? Curr Oncol. 2012;19(4):e295-8. Knudsen-Baas KM, Moen G, Fluge Ø, Storstein A. Pseudoprogression in high-grade glioma. Acta Neurol Scand Suppl. 2013;(196):31-7. Young RJ, Gupta A, Shah AD, Graber JJ, Chan TA, Zhang Z, et al. MRI perfusion in determining pseudoprogression in patients with glioblastoma. Clin Imaging. 2013;37(1):41-9. Young RJ, Gupta A, Shah AD, Graber JJ, Zhang Z, Shi W, et al. Potential utility of conventional MRI signs in diagnosing pseudoprogression in glioblastoma. Neurology. 2011;76(22): 1918-24. Kong DS, Kim ST, Kim EH, Lim DH, Kim WS, Suh YL, et al. Diagnostic dilemma of pseudoprogression in the treatment of newly diagnosed glioblastomas: the role of assessing relative cerebral blood flow volume and oxygen-6-methylguanine-DNA methyltransferase promoter methylation status. AJNR Am J Neuroradiol. 2011;32(2):382-7. Chinot OL, Macdonald DR, Abrey LE, Zahlmann G, Kerloëguen Y, Cloughesy TF. Response assessment criteria for glioblastoma: practical adaptation and implementation in clinical trials of antiangiogenic therapy. Curr Neurol Neurosci Rep. 2013;13(5):347. Cairncross JG, Pexman JH, Rathbone MP. Post-surgical contrast enhancement mimicking residual brain tumour. Can J Neurol Sci 1985;12(1):75. Nicoletti GF, Barone F, Passanisi M, Mancuso P, Albanese V. Linear contrast enhancement at the operative site on early postoperative CT after removal of brain tumors. J Neurosurg Sci. 1994;38(2):131-5. Ekinci G, Akpinar IN, Baltacioğlu F, Erzen C, Kiliç T, Elmaci I, et al. Early-postoperative magnetic resonance imaging in glial tumors: prediction of tumor regrowth and recurrence. Eur J Radiol. 2003;45(2):99-107. Ulmer S, Spalek K, Nabavi A, Schultka S, Mehdorn HM, Kesari S, et al. Temporal changes in magnetic resonance imaging characteristics of Gliadel wafers and of the adjacent brain parenchyma. Neuro Oncol. 2012;14(4):482-90. Colen RR, Zinn PO, Hazany S, Do-Dai D, Wu JK, Yao K, et al. Magnetic resonance imaging appearance and changes on intracavitary Gliadel wafer placement: A pilot study. World J Radiol. 2011;3(11):266-72. Summary minutes of the Oncologic Drugs Advisory Committee, March 31, 2009. Washington, DC: Center for Drug Evaluation and Research, US Food and Drug Administration; 2009. Winkler F, Kozin SV, Tong RT, Chae SS, Booth MF, Garkavtsev I, et al. Kinetics of vascular normalization by VEGFR2 blockade governs brain tumor response to radiation: role of oxygenation, angiopoietin-1, and matrix metalloproteinases. Cancer Cell. 2004;6(6):553-63. Batchelor TT, Sorensen AG, di Tomaso E, Zhang WT, Duda DG, Cohen KS, et al. AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients. Cancer Cell. 2007;11(1):83-95. Vredenburgh JJ, Desjardins A, Herndon JE 2nd, Marcello J, Reardon DA, Quinn JA, et al. Bevacizumab plus irinotecan in recurrent glioblastoma multiforme. J Clin Oncol. 2007;25(30): 4722-9. Kamoun WS, Ley CD, Farrar CT, Duyverman AM, Lahdenranta J, Lacorre DA, et al. Edema control by cediranib, a vascular endothelial growth factor receptor-targeted kinase inhibitor, prolongs survival despite persistent brain tumor growth in mice. J Clin Oncol. 2009;27(15):2542-52. Norden AD, Drappatz J, Muzikansky A, David K, Gerard M, McNamara MB, et al. An exploratory survival analysis of anti-angiogenic therapy for recurrent malignant glioma. J Neurooncol. 2009;92(2):149-55. Narayana A, Kelly P, Golfinos J, Parker E, Johnson G, Knopp E, et al. Antiangiogenic therapy using bevacizumab in recurrent high-grade glioma: impact on local control and patient survival. J Neurosurg. 2009;110(1):173-80. Wick W, Stupp R, Beule AC, Bromberg J, Wick A, Ernemann U, et al. A novel tool to analyze MRI recurrence patterns in glioblastoma. Neuro Oncol. 2008;10(6):1019-24. Wick A, Dörner N, Schäfer N, Hofer S, Heiland S, Schemmer D, et al. Bevacizumab does not increase the risk of remote relapse in malignant glioma. Ann Neurol. 2011;69(3):586-92. Gruber L. Change in pattern of relapse in newly diagnosed high-grade glioma following bevacizumab therapy. ASCO 2010 (abstract 2020). Brandsma D, van den Bent MJ. Pseudoprogression and pseudoresponse in the treatment of gliomas. Curr Opin Neurol. 2009;22(6):633-8. Hygino da Cruz LC Jr, Rodriguez I, Domingues RC, Gasparetto EL, Sorensen AG. Pseudoprogression and pseudoresponse: imaging challenges in the assessment of posttreatment glioma. AJNR Am J Neuroradiol. 2011;32(11):1978-85. Clarke JL, Ennis MM, Yung WK, Chang SM, Wen PY, Cloughesy TF, et al. Is surgery at progression a prognostic marker for improved 6-month progression-free survival or overall survival for patients with recurrent glioblastoma? Neuro Oncol. 2011;13(10):1118-24. Farace P, Giri MG, Meliadò G, Amelio D, Widesott L, Ricciardi GK, et al. Clinical target volume delineation in glioblastomas: pre-operative versus post-operative/pre-radiotherapy MRI. Br J Radiol. 2011;84(999):271-8. Jansen EP, Dewit LG, van Herk M, Bartelink H. Target volumes in radiotherapy for high-grade malignant glioma of the brain. Radiother Oncol. 2000;56(2):151-6. Gállego Pérez-Larraya J, Lahutte M, Petrirena G, Reyes-Botero G, González-Aguilar A, Houillier C, et al. Response assessment in recurrent glioblastoma treated with irinotecan-bevacizumab: comparative analysis of the Macdonald, RECIST, RANO, and RECIST + F criteria. Neuro Oncol. 2012;14(5):667-73. Clarke JL, Chang SM. Neuroimaging: diagnosis and response assessment in glioblastoma. Cancer J. 2012;18(1):26-31. Pichler J, Pachinger C, Pelz M, Kleiser R. MRI assessment of relapsed glioblastoma during treatment with bevacizumab: Volumetric measurement of enhanced and FLAIR lesions for evaluation of response and progression-A pilot study. Eur J Radiol. 2013;82(5):e240-5. Radbruch A, Lutz K, Wiestler B, Bäumer P, Heiland S, Wick W, et al. Relevance of T2 signal changes in the assessment of progression of glioblastoma according to the Response Assessment in Neurooncology criteria. Neuro Oncol. 2012;14(2):222-9. Gladwish A, Koh ES, Hoisak J, Lockwood G, Millar BA, Mason W, et al. Evaluation of early imaging response criteria in glioblastoma multiforme. Radiat Oncol. 2011;6:121. Wang MY, Cheng JL, Han YH, Li YL, Dai JP, Shi DP. Measurement of tumor size in adult glioblastoma: classical cross-sectional criteria on 2D MRI or volumetric criteria on high resolution 3D MRI? Eur J Radiol. 2012;81(9):2370-4. Hwang EJ, Cha Y, Lee AL, Yun TJ, Kim TM, Park CK, et al. Early response evaluation for recurrent high grade gliomas treated with bevacizumab: a volumetric analysis using diffusionweighted imaging. J Neurooncol. 2013 Feb 17. [Epub ahead of print]. |
| type_driver |
info:eu-repo/semantics/article |
| type_coar |
http://purl.org/coar/resource_type/c_6501 |
| type_version |
info:eu-repo/semantics/publishedVersion |
| type_coarversion |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| type_content |
Text |
| publishDate |
2013-03-01 |
| date_accessioned |
2013-03-01T00:00:00Z |
| date_available |
2013-03-01T00:00:00Z |
| url |
https://revista.acho.info/index.php/acho/article/view/329 |
| url_doi |
https://doi.org/10.51643/22562915.329 |
| issn |
2256-2877 |
| eissn |
2256-2915 |
| doi |
10.51643/22562915.329 |
| citationstartpage |
34 |
| citationendpage |
44 |
| url2_str_mv |
https://revista.acho.info/index.php/acho/article/download/329/295 |
| _version_ |
1811200922850689024 |