A genetic profiling guideline to support diagnosis and clinical management of lymphomas
暂无分享,去创建一个
M. Sánchez-Beato | L. de la Cruz-Merino | M. Guirado | L. Pedrosa | S. Sequero | M. Provencio | Margarita Sánchez-Beato | Miriam Méndez | María Guirado | Natalia Yanguas-Casás | Luis de la Cruz-Merino | Laura Gálvez | Marta Llanos | Juan Fernando García | Natalia Yanguas-Casás | Mariano Provencio | M. Llanos | Juan F. García
[1] F. Climent,et al. Extranodal natural killer/T‐cell lymphoma nasal type in a western population: Molecular profiling identifies new therapeutic targets , 2023, American journal of hematology.
[2] A. Dogan,et al. Mature T-cell and NK-cell lymphomas: updates on molecular genetic features , 2023, International Journal of Hematology.
[3] T. Baumann,et al. Real-life disease monitoring in follicular lymphoma patients using liquid biopsy ultra-deep sequencing and PET/CT , 2023, Leukemia.
[4] P. Gaulard,et al. Extranodal T- and NK-cell lymphomas , 2022, Virchows Archiv.
[5] W. Chan,et al. Classification and diagnostic evaluation of nodal T- and NK-cell lymphomas , 2022, Virchows Archiv.
[6] Ash A. Alizadeh,et al. Genomic Profiling for Clinical Decision Making in Lymphoid Neoplasms. , 2022, Blood.
[7] A. Rosenwald,et al. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms , 2022, Leukemia.
[8] L. Staudt,et al. The International Consensus Classification of Mature Lymphoid Neoplasms: A Report from the Clinical Advisory Committee. , 2022, Blood.
[9] P. Jain,et al. Mantle cell lymphoma in 2022—A comprehensive update on molecular pathogenesis, risk stratification, clinical approach, and current and novel treatments , 2022, American journal of hematology.
[10] Yeon Jeong Kim,et al. Circulating Tumor DNA–Based Genotyping and Monitoring for Predicting Disease Relapses of Patients with Peripheral T-Cell Lymphomas , 2022, Cancer research and treatment.
[11] Peggy Wu,et al. T-Cell Lymphomas, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology. , 2022, Journal of the National Comprehensive Cancer Network : JNCCN.
[12] C. Ong,et al. Immune pathway upregulation and lower genomic instability distinguish EBV-positive nodal T/NK-cell lymphoma from ENKTL and PTCL-NOS , 2022, Haematologica.
[13] H. Holte,et al. Molecular features encoded in the ctDNA reveal heterogeneity and predict outcome in high-risk aggressive B-cell lymphoma. , 2021, Blood.
[14] L. Leoncini. Epstein–Barr virus positivity as a defining pathogenetic feature of Burkitt lymphoma subtypes , 2021, British journal of haematology.
[15] S. Turner,et al. Genomic abnormalities of TP53 define distinct risk groups of paediatric B-cell non-Hodgkin lymphoma , 2021, Leukemia.
[16] M. Hallek,et al. Chronic lymphocytic leukemia: 2022 update on diagnostic and therapeutic procedures , 2021, American journal of hematology.
[17] A. Evens,et al. Defining and Treating High-grade B-cell lymphoma, NOS. , 2021, Blood.
[18] E. González-Barca,et al. Genomic mutation profile in progressive chronic lymphocytic leukemia patients prior to first-line chemoimmunotherapy with FCR and rituximab maintenance (REM) , 2021, PloS one.
[19] D. Rossi,et al. Circulating tumor DNA for comprehensive noninvasive monitoring of lymphoma treated with ibrutinib plus nivolumab , 2021, Blood advances.
[20] A. Tzankov,et al. Mutational landscape of marginal zone B-cell lymphomas of various origin: organotypic alterations and diagnostic potential for assignment of organ origin , 2021, Virchows Archiv.
[21] J. Ule,et al. Sequential inverse dysregulation of the RNA helicases DDX3X and DDX3Y facilitates MYC-driven lymphomagenesis. , 2021, Molecular cell.
[22] O. Ohara,et al. Genetic subtype classification using a simplified algorithm and mutational characteristics of diffuse large B‐cell lymphoma in a Japanese cohort , 2021, British journal of haematology.
[23] P. Sujobert,et al. How to Obtain a High Quality ctDNA in Lymphoma Patients: Preanalytical Tips and Tricks , 2021, Pharmaceuticals.
[24] Ash A. Alizadeh,et al. Enhanced detection of minimal residual disease by targeted sequencing of phased variants in circulating tumor DNA , 2021, Nature Biotechnology.
[25] P. Kwok,et al. Integrated Genomic Analyses of Cutaneous T Cell Lymphomas Reveal the Molecular Bases for Disease Heterogeneity. , 2021, Blood.
[26] A. López-Guillermo,et al. Genetic and Phenotypic Attributes of Splenic Marginal Zone Lymphoma. , 2021, Blood.
[27] J. Zimmermann,et al. Genomic insights into the pathogenesis of Epstein–Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon sequencing , 2021, Blood Cancer Journal.
[28] M. Piris,et al. Mycosis Fungoides and Sézary Syndrome: An Integrative Review of the Pathophysiology, Molecular Drivers, and Targeted Therapy , 2021, Cancers.
[29] K. Young,et al. Molecular and genetic biomarkers implemented from next-generation sequencing provide treatment insights in clinical practice for Waldenström macroglobulinemia , 2021, Neoplasia.
[30] R. Küppers,et al. Molecular biology of Hodgkin lymphoma , 2021, Leukemia.
[31] Laura E. Brown,et al. New developments in non-Hodgkin lymphoid malignancies. , 2021, Pathology.
[32] Juan F. García,et al. Proposal and validation of a method to classify genetic subtypes of diffuse large B cell lymphoma , 2021, Scientific Reports.
[33] C. Buske,et al. CXCR4 in Waldenström’s Macroglobulinema: chances and challenges , 2020, Leukemia.
[34] Š. Pospíšilová,et al. STAT3 and TP53 mutations associate with poor prognosis in anaplastic large cell lymphoma , 2020, Leukemia.
[35] C. Copie-Bergman,et al. Follicular lymphoma t(14;18)-negative is genetically a heterogeneous disease. , 2020, Blood advances.
[36] E. Campo,et al. IGLV3-21R110 identifies an aggressive biological subtype of chronic lymphocytic leukemia with intermediate epigenetics. , 2020, Blood.
[37] E. Chapiro,et al. The complex karyotype and chronic lymphocytic leukemia. A review of the literature. , 2020, American journal of hematology.
[38] E. Campo,et al. Molecular Pathogenesis of Mantle Cell Lymphoma. , 2020, Hematology/oncology clinics of North America.
[39] Ali F. Alsulami,et al. Whole exome sequencing reveals NOTCH1 mutations in anaplastic large cell lymphoma and points to Notch both as a key pathway and a potential therapeutic target , 2020, Haematologica.
[40] Ryan D. Morin,et al. A Probabilistic Classification Tool for Genetic Subtypes of Diffuse Large B Cell Lymphoma with Therapeutic Implications. , 2020, Cancer cell.
[41] S. Barrans,et al. Targeted sequencing in DLBCL, molecular subtypes, and outcomes: a Haematological Malignancy Research Network report. , 2020, Blood.
[42] A. Salar,et al. Marginal zone lymphomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. , 2020, Annals of oncology : official journal of the European Society for Medical Oncology.
[43] E. Kimby,et al. M7‐FLIPI is not prognostic in follicular lymphoma patients with first‐line rituximab chemo‐free therapy , 2020, British journal of haematology.
[44] M. Darweesh,et al. Follicular lymphoma: Update on management and emerging therapies at the dawn of the new decade , 2019, Hematological oncology.
[45] S. Barrans,et al. Distinct genetic changes reveal evolutionary history and heterogeneous molecular grade of DLBCL with MYC/BCL2 double-hit , 2019, Leukemia.
[46] Yuri Fedoriw,et al. Pathology and diagnosis of follicular lymphoma and related entities. , 2019, Pathology.
[47] S. Hartmann,et al. Nodular lymphocyte predominant Hodgkin lymphoma: pathology, clinical course and relation to T-cell/histiocyte rich large B-cell lymphoma. , 2019, Pathology.
[48] A. López-Guillermo,et al. IRF4-rearranged Large B-cell lymphoma (LBCL) has a genomic profile distinct to other LBCL in children and young adults. , 2019, Blood.
[49] J. Bailey,et al. The whole genome landscape of Burkitt lymphoma subtypes. , 2019, Blood.
[50] D. Rossi,et al. KMT2D mutations and TP53 disruptions are poor prognostic biomarkers in mantle cell lymphoma receiving high-dose therapy: a FIL study , 2019, Haematologica.
[51] L. Bullinger,et al. Venetoclax resistance and acquired BCL2 mutations in chronic lymphocytic leukemia , 2019, Haematologica.
[52] P. Feugier,et al. Prevalence of BTK and PLCG2 mutations in a real‑life CLL cohort still on ibrutinib after three years: a FILO group study. , 2019, Blood.
[53] Michael R. Green,et al. Subtype-specific and co-occurring genetic alterations in B-cell non-Hodgkin lymphoma , 2019, bioRxiv.
[54] S. Pileri,et al. Whole exome sequencing reveals mutations in FAT1 tumor suppressor gene clinically impacting on peripheral T-cell lymphoma not otherwise specified , 2019, Modern Pathology.
[55] L. Staudt,et al. Genetic drivers of oncogenic pathways in molecular subgroups of peripheral T-cell lymphoma. , 2019, Blood.
[56] O. Dereure,et al. Systemic, primary cutaneous, and breast implant-associated ALK-negative anaplastic large-cell lymphomas present similar biologic features despite distinct clinical behavior , 2019, Virchows Archiv.
[57] Jules N. A. Kerssemakers,et al. Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma , 2019, Nature Communications.
[58] Steven J. M. Jones,et al. Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma. , 2019, Blood.
[59] Juan F. García,et al. Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma , 2019, Blood Cancer Journal.
[60] S. Bens,et al. The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma. , 2019, Blood.
[61] Juan F. García,et al. Unraveling transformation of follicular lymphoma to diffuse large B-cell lymphoma , 2019, PloS one.
[62] I. Gut,et al. Clonal dynamics monitoring during clinical evolution in chronic lymphocytic leukaemia , 2019, Scientific Reports.
[63] A. Bordron,et al. 17p deletion strongly influences rituximab elimination in chronic lymphocytic leukemia , 2019, Journal of Immunotherapy for Cancer.
[64] P. Gaulard,et al. Frequent structural variations involving programmed death ligands in Epstein-Barr virus-associated lymphomas , 2019, Leukemia.
[65] L. Bullinger,et al. Nuclear FOXO1 promotes lymphomagenesis in germinal center B cells. , 2018, Blood.
[66] M. Shahjahani,et al. The role of the genetic abnormalities, epigenetic and microRNA in the prognosis of chronic lymphocytic leukemia. , 2018, Experimental oncology.
[67] A. Rosenwald,et al. Duodenal-type and nodal follicular lymphomas differ by their immune microenvironment rather than their mutation profiles. , 2018, Blood.
[68] Michael L. Wang,et al. Long‐term outcomes and mutation profiling of patients with mantle cell lymphoma (MCL) who discontinued ibrutinib , 2018, British journal of haematology.
[69] A. Feldman,et al. Genetic subtyping of breast implant-associated anaplastic large cell lymphoma. , 2018, Blood.
[70] Alexander V Penson,et al. Pervasive mutations of JAK-STAT pathway genes in classical Hodgkin lymphoma. , 2018, Blood.
[71] F. Cavalli,et al. Circulating tumor DNA reveals genetics, clonal evolution, and residual disease in classical Hodgkin lymphoma. , 2018, Blood.
[72] E. Campo,et al. Chronic lymphocytic leukemia and mantle cell lymphoma: crossroads of genetic and microenvironment interactions. , 2018, Blood.
[73] Stefano Monti,et al. Molecular subtypes of diffuse large B cell lymphoma are associated with distinct pathogenic mechanisms and outcomes , 2018, Nature Medicine.
[74] L. de Leval,et al. Dual JAK1 and STAT3 mutations in a breast implant-associated anaplastic large cell lymphoma , 2018, Virchows Archiv.
[75] L. Medeiros,et al. Hepatosplenic T-cell Lymphoma: a review of clinicopathologic features, pathogenesis, and prognostic factors. , 2018, Human pathology.
[76] C. Thieblemont. Improved biological insight and influence on management in indolent lymphoma. Talk 3: update on nodal and splenic marginal zone lymphoma. , 2017, Hematology. American Society of Hematology. Education Program.
[77] M. Davids,et al. IGHV mutational status testing in chronic lymphocytic leukemia , 2017, American journal of hematology.
[78] Juan F. García,et al. Analysis of the mutational landscape of classic Hodgkin lymphoma identifies disease heterogeneity and potential therapeutic targets , 2017, Oncotarget.
[79] Juan F. García,et al. Mutational profile of primary breast diffuse large B-cell lymphoma , 2017, Oncotarget.
[80] Marc L. Mendillo,et al. Genomic analysis of 220 CTCLs identifies a novel recurrent gain-of-function alteration in RLTPR (p.Q575E). , 2017, Blood.
[81] J. D. van der Walt,et al. Mutations of MAP2K1 are frequent in pediatric-type follicular lymphoma and result in ERK pathway activation. , 2017, Blood.
[82] R. Advani,et al. Acquired mutations associated with ibrutinib resistance in Waldenström macroglobulinemia. , 2017, Blood.
[83] R. Foà,et al. Diffuse large B-cell lymphoma genotyping on the liquid biopsy. , 2017, Blood.
[84] P. Gaulard,et al. Integrative clinicopathological and molecular analyses of angioimmunoblastic T-cell lymphoma and other nodal lymphomas of follicular helper T-cell origin , 2017, Haematologica.
[85] M. Du. MALT lymphoma: Genetic abnormalities, immunological stimulation and molecular mechanism. , 2017, Best practice & research. Clinical haematology.
[86] Ali Bashashati,et al. Histological Transformation and Progression in Follicular Lymphoma: A Clonal Evolution Study , 2016, PLoS medicine.
[87] Ash A. Alizadeh,et al. Distinct biological subtypes and patterns of genome evolution in lymphoma revealed by circulating tumor DNA , 2016, Science Translational Medicine.
[88] Gisela Mir Arnau,et al. Whole exome sequencing reveals activating JAK1 and STAT3 mutations in breast implant-associated anaplastic large cell lymphoma anaplastic large cell lymphoma , 2016, Haematologica.
[89] A. Prasad,et al. Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome. , 2016, The Journal of investigative dermatology.
[90] F. Bosch,et al. A high proportion of cells carrying trisomy 12 is associated with a worse outcome in patients with chronic lymphocytic leukemia , 2016, Hematological oncology.
[91] Ryan D. Morin,et al. Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations , 2016, Oncotarget.
[92] E. Zucca,et al. The spectrum of MALT lymphoma at different sites: biological and therapeutic relevance. , 2016, Blood.
[93] P. Gaulard,et al. Breast implant-associated anaplastic large cell lymphoma: two distinct clinicopathological variants with different outcomes. , 2016, Annals of oncology : official journal of the European Society for Medical Oncology.
[94] A. Ferrando,et al. The mutational landscape of cutaneous T cell lymphoma and Sézary syndrome , 2015, Nature Genetics.
[95] M. Pedersen,et al. Peripheral T-cell lymphomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. , 2015, Annals of oncology : official journal of the European Society for Medical Oncology.
[96] M. Sánchez-Beato,et al. Action and resistance of monoclonal CD20 antibodies therapy in B-cell Non-Hodgkin Lymphomas. , 2015, Cancer treatment reviews.
[97] D. Schatz,et al. Genomic landscape of cutaneous T cell lymphoma , 2015, Nature Genetics.
[98] Ash A. Alizadeh,et al. Mutations in early follicular lymphoma progenitors are associated with suppressed antigen presentation , 2015, Proceedings of the National Academy of Sciences.
[99] O. Elemento,et al. Flow sorting and exome sequencing reveal the oncogenome of primary Hodgkin and Reed-Sternberg cells. , 2015, Blood.
[100] Adrien B. Larsen,et al. Loss of signaling via Gα13 in germinal center B cell-derived lymphoma , 2014, Nature.
[101] W. Wilson,et al. ALK-negative anaplastic large cell lymphoma is a genetically heterogeneous disease with widely disparate clinical outcomes. , 2014, Blood.
[102] I. Varela,et al. PLCG1 mutations in cutaneous T-cell lymphomas. , 2014, Blood.
[103] Raul Rabadan,et al. Genetics of follicular lymphoma transformation. , 2014, Cell reports.
[104] M. Calaminici,et al. Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma , 2013, Nature Genetics.
[105] Raul Rabadan,et al. Genetic lesions associated with chronic lymphocytic leukemia transformation to Richter syndrome , 2013, The Journal of experimental medicine.
[106] Manel Juan,et al. Landscape of somatic mutations and clonal evolution in mantle cell lymphoma , 2013, Proceedings of the National Academy of Sciences.
[107] W. Chan,et al. Two main genetic pathways lead to the transformation of chronic lymphocytic leukemia to Richter syndrome. , 2013, Blood.
[108] Ash A. Alizadeh,et al. Hierarchy in somatic mutations arising during genomic evolution and progression of follicular lymphoma. , 2012, Blood.
[109] A. McKenna,et al. Evolution and Impact of Subclonal Mutations in Chronic Lymphocytic Leukemia , 2012, Cell.
[110] L. Staudt,et al. Burkitt lymphoma pathogenesis and therapeutic targets from structural and functional genomics , 2012, Nature.
[111] D. Pisano,et al. New Mutations in Chronic Lymphocytic Leukemia Identified by Target Enrichment and Deep Sequencing , 2012, PloS one.
[112] Steven J. M. Jones,et al. Frequent mutation of histone modifying genes in non-Hodgkin lymphoma , 2011, Nature.
[113] L. Pasqualucci,et al. Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation , 2011, The Journal of experimental medicine.
[114] Steven J. M. Jones,et al. MHC class II transactivator CIITA is a recurrent gene fusion partner in lymphoid cancers , 2011, Nature.
[115] A. López-Guillermo,et al. Clinical activity of bortezomib in relapsed/refractory MALT lymphomas: results of a phase II study of the International Extranodal Lymphoma Study Group (IELSG). , 2011, Annals of oncology : official journal of the European Society for Medical Oncology.
[116] S. Pileri,et al. Gene expression analysis uncovers similarity and differences among Burkitt lymphoma subtypes. , 2010, Blood.
[117] Michael R. Green,et al. Integrative analysis reveals selective 9p24.1 amplification, increased PD-1 ligand expression, and further induction via JAK2 in nodular sclerosing Hodgkin lymphoma and primary mediastinal large B-cell lymphoma. , 2010, Blood.
[118] A. Pettitt,et al. TP53 mutation profile in chronic lymphocytic leukemia: evidence for a disease specific profile from a comprehensive analysis of 268 mutations , 2010, Leukemia.
[119] B. Coiffier,et al. Long-term outcome of patients in the LNH-98.5 trial, the first randomized study comparing rituximab-CHOP to standard CHOP chemotherapy in DLBCL patients: a study by the Groupe d'Etudes des Lymphomes de l'Adulte. , 2010, Blood.
[120] R. Gascoyne,et al. Genome-wide copy number analysis of Hodgkin Reed-Sternberg cells identifies recurrent imbalances with correlations to treatment outcome. , 2010, Blood.
[121] L. Pasqualucci,et al. The NF-{kappa}B negative regulator TNFAIP3 (A20) is inactivated by somatic mutations and genomic deletions in marginal zone lymphomas. , 2008, Blood.
[122] L. Staudt,et al. Follicular lymphomas with and without translocation t(14;18) differ in gene expression profiles and genetic alterations. , 2007, Blood.
[123] R. Siebert,et al. Novel t(5;9)(q33;q22) fuses ITK to SYK in unspecified peripheral T-cell lymphoma , 2006, Leukemia.
[124] Gerard Lozanski,et al. Adult Burkitt leukemia and lymphoma. , 2004, Blood.
[125] M. Piris,et al. Molecular heterogeneity of splenic marginal zone lymphomas: analysis of mutations in the 5′ non-coding region of the bcl-6 gene , 2001, Leukemia.
[126] Ash A. Alizadeh,et al. Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling , 2000, Nature.
[127] M. Piris,et al. Epstein-Barr Virus-Latent Membrane Protein 1 Expression Has a Favorable Influence in the Outcome of Patients with Hodgkin's Disease Treated with Chemotherapy , 2000, Leukemia & lymphoma.
[128] J. Vose,et al. T-Cell Lymphomas in South America and Europe , 2012, Revista brasileira de hematologia e hemoterapia.