Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden

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Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden is …
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scholarly articleQ13442814

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P6179Dimensions Publication ID1084826380
P356DOI10.1186/S13073-017-0424-2
P932PMC publication ID5395719
P698PubMed publication ID28420421

P50authorYuting HeQ64025704
Juliann ChmieleckiQ66809335
Levi A GarrawayQ89916155
Uri TaboriQ43826656
P2093author name stringSiraj M Ali
Vincent A Miller
Jeffrey S Ross
Adam Shlien
Caitlin F Connelly
Daniel S Lieber
Laurie Gay
Garrett M Frampton
Zachary R Chalmers
David Fabrizio
Brittany Campbell
Alexa Schrock
James Sun
Franklin Huang
Mark Kennedy
Jared White
Phillip J Stephens
Steven Roels
Geoffrey A Otto
Riley Ennis
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Mutational heterogeneity in cancer and the search for new cancer-associated genesQ24606956
Melanoma genome sequencing reveals frequent PREX2 mutationsQ24610463
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomasQ24617520
Safety, activity, and immune correlates of anti-PD-1 antibody in cancerQ24633070
The COSMIC (Catalogue of Somatic Mutations in Cancer) database and websiteQ24645514
Yeast DNA polymerase epsilon participates in leading-strand DNA replicationQ24652913
Fast and accurate short read alignment with Burrows-Wheeler transformQ24653853
Statistical significance for genomewide studiesQ24681264
Analysis of protein-coding genetic variation in 60,706 humansQ26831376
The structural basis of modified nucleosome recognition by 53BP1Q27722410
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing dataQ27860742
The blockade of immune checkpoints in cancer immunotherapyQ27860852
Mutational signatures associated with tobacco smoking in human cancerQ28005544
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancersQ28256331
PD-1 Blockade in Tumors with Mismatch-Repair DeficiencyQ28262647
Enhancement of antitumor immunity by CTLA-4 blockadeQ28275730
Germline and somatic polymerase ε and δ mutations define a new class of hypermutated colorectal and endometrial cancersQ28286394
DNA polymerase ε and δ exonuclease domain mutations in endometrial cancerQ28287769
Signatures of mutational processes in human cancerQ29547191
Highly recurrent TERT promoter mutations in human melanomaQ29614798
Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancerQ29615679
Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 databaseQ29616468
Cancer immunotherapy comes of ageQ29619918
Genetic basis for clinical response to CTLA-4 blockade in melanomaQ29620594
Atezolizumab in patients with locally advanced and metastatic urothelial carcinoma who have progressed following treatment with platinum-based chemotherapy: a single-arm, multicentre, phase 2 trialQ30277192
Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMAQ33713232
p53 and human cancer: the first ten thousand mutations.Q33767112
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samplesQ34327021
Lynch syndrome: genetics, natural history, genetic counseling, and prevention.Q48371688
Drastic genetic instability of tumors and normal tissues in Turcot syndromeQ48570250
Mice defective in the DNA mismatch gene PMS2 are hypersensitive to MNU induced thymic lymphoma and are partially protected by transgenic expression of human MGMT.Q53420486
Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genesQ71733947
Cancer, cadmium and genome integrityQ73588691
Retroviral recombination: what drives the switch?Q73626301
Preferential formation of benzo[a]pyrene adducts at lung cancer mutational hotspots in P53.Q34399850
A first in man phase I trial of the oral immunomodulator, indoximod, combined with docetaxel in patients with metastatic solid tumorsQ34483473
Overexpression of the DNA mismatch repair factor, PMS2, confers hypermutability and DNA damage toleranceQ34486552
Mechanism-driven biomarkers to guide immune checkpoint blockade in cancer therapyQ34522172
Blockade of B7-H1 and PD-1 by monoclonal antibodies potentiates cancer therapeutic immunityQ34554995
Mutations at coding repeat sequences in mismatch repair-deficient human cancers: toward a new concept of target genes for instabilityQ34617569
A role for sunlight in skin cancer: UV-induced p53 mutations in squamous cell carcinomaQ34982679
Role of DNA mismatch repair defects in the pathogenesis of human cancerQ35085461
Recurrent somatic mutations in regulatory regions of human cancer genomesQ35797838
Highly penetrant hereditary cancer syndromes.Q35868041
CTLA-4 blockade with ipilimumab: long-term follow-up of 177 patients with metastatic melanomaQ35871798
PD-1/PD-L1 inhibitors.Q35893753
Fast, scalable prediction of deleterious noncoding variants from functional and population genomic dataQ36306108
Predicting effects of noncoding variants with deep learning-based sequence modelQ36621822
DNA polymerases and cancer.Q37084895
Genomic correlates of response to CTLA-4 blockade in metastatic melanomaQ37319470
Therapeutic targeting of the DNA mismatch repair pathwayQ37786127
CTLA4 blockade in mesothelioma: finally a competing strategy over cytotoxic/target therapy?Q38252348
Comprehensive cancer-gene panels can be used to estimate mutational load and predict clinical benefit to PD-1 blockade in clinical practice.Q38259896
Targeted Next Generation Sequencing Identifies Markers of Response to PD-1 BlockadeQ38377528
Integrated genomic DNA/RNA profiling of hematologic malignancies in the clinical settingQ38381729
PD-L1 blockade for cancer treatment: MEDI4736.Q38475127
Immunologic checkpoints blockade in renal cell, prostate, and urothelial malignancies.Q38475150
Molecular Pathways: Targeting IDO1 and Other Tryptophan Dioxygenases for Cancer Immunotherapy.Q38620878
53BP1 fosters fidelity of homology-directed DNA repairQ38761656
Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers.Q38765494
An integrative approach to predicting the functional effects of non-coding and coding sequence variationQ40518007
Mismatch repair, genetic stability, and cancerQ40556409
Methylation of adenomatous polyposis coli in endometrial cancer occurs more frequently in tumors with microsatellite instability phenotype.Q40720876
Nivolumab versus Everolimus in Advanced Renal-Cell CarcinomaQ41316099
Costimulation of antitumor immunity by the B7 counterreceptor for the T lymphocyte molecules CD28 and CTLA-4Q41589138
A common cancer-associated DNA polymerase ε mutation causes an exceptionally strong mutator phenotype, indicating fidelity defects distinct from loss of proofreadingQ41990410
MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeastQ42427955
Tumor exome analysis reveals neoantigen-specific T-cell reactivity in an ipilimumab-responsive melanomaQ42874163
Mismatch repair deficiency associated with complete remission to combination programmed cell death ligand immune therapy in a patient with sporadic urothelial carcinoma: immunotheranostic considerationsQ43130702
Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumorsQ44383505
Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencingQ47163678
P433issue1
P304page(s)34
P577publication date2017-04-19
P1433published inGenome MedicineQ15816848
P1476titleAnalysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden
P478volume9

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Q55264193Microsatellite instability in prostate cancer by PCR or next-generation sequencing.
Q50049563Microsatellite instability status determined by next-generation sequencing and compared with PD-L1 and tumor mutational burden in 11,348 patients.
Q42353279Microsatellite instability status predicts response to anti-PD-1/PD-L1 therapy regardless the histotype: A comment on recent advances
Q92757665Microsatellite instability: a review of what the oncologist should know
Q92576171Microsatellite-Stable Tumors with High Mutational Burden Benefit from Immunotherapy
Q64990522Mismatch repair deficiency/microsatellite instability-high as a predictor for anti-PD-1/PD-L1 immunotherapy efficacy.
Q64228131Mismatch repair status and high expression of PD-L1 in nasopharyngeal carcinoma
Q97419819Molecular Alterations in Circulating Cell-Free DNA in Patients with Colorectal Adenoma or Carcinoma
Q50027697Molecular Determinants of Response to Anti-Programmed Cell Death (PD)-1 and Anti-Programmed Death-Ligand (PD-L)-Ligand 1 Blockade in Patients With Non-Small-Cell Lung Cancer Profiled With Targeted Next-Generation Sequencing
Q92799371Molecular Neuropathology in Practice: Clinical Profiling and Integrative Analysis of Molecular Alterations in Glioblastoma
Q64086109Molecular Profiling of Hard-to-Treat Childhood and Adolescent Cancers
Q93078485Molecular Subtyping and Prognostic Assessment Based on Tumor Mutation Burden in Patients with Lung Adenocarcinomas
Q63366116Molecular characterisation and liquid biomarkers in Carcinoma of Unknown Primary (CUP): taking the ‘U’ out of ‘CUP’
Q61810151Molecular markers and prediction of response to immunotherapy in non-small cell lung cancer, an update
Q58107960Molecular predictors of response to PD-1/PD-L1 inhibition in urothelial cancer
Q55209571Molecular profiles and tumor mutational burden analysis in Chinese patients with gynecologic cancers.
Q90215713Molecular profiling of cancer patients enables personalized combination therapy: the I-PREDICT study
Q90283161Monoclonal Antibodies in Dermatooncology-State of the Art and Future Perspectives
Q94593616Mucinous Histology, BRCA1/2 Mutations, and Elevated Tumor Mutational Burden in Colorectal Cancer
Q64079285Multi-omics discovery of exome-derived neoantigens in hepatocellular carcinoma
Q55156355Multi-omics profiling of younger Asian breast cancers reveals distinctive molecular signatures.
Q90186863Mutation analysis of multiple pilomatricomas in a patient with myotonic dystrophy type 1 suggests a DM1-associated hypermutation phenotype
Q63499786Mutation burden and other molecular markers of prognosis in colorectal cancer treated with curative intent: results from the QUASAR 2 clinical trial and an Australian community-based series
Q89777376Mutation load and an effector T-cell gene signature may distinguish immunologically distinct and clinically relevant lymphoma subsets
Q55261882Mutation load estimation model as a predictor of the response to cancer immunotherapy.
Q64386735Mutational burden and signatures in 4,000 Japanese cancers provide insights into tumorigenesis and response to therapy
Q92188170Mutational landscape in genetically engineered, carcinogen-induced, and radiation-induced mouse sarcoma
Q64939633Mutational landscape of gastric cancer and clinical application of genomic profiling based on target next-generation sequencing.
Q92684416Mutational landscape of head and neck squamous cell carcinomas in a South Asian population
Q83230246Mutationally-activated PI3'-kinase-α promotes de-differentiation of lung tumors initiated by the BRAF oncoprotein kinase
Q57232070Mutations and PD-1 Inhibitor Resistance in -Mutant Lung Adenocarcinoma
Q92691417Myxoid smooth muscle neoplasia of the uterus: comprehensive analysis by next-generation sequencing and nucleic acid hybridization
Q89121807Nearing saturation of cancer driver gene discovery
Q89965697Neoantigens in Hematologic Malignancies
Q92539066Neoantigens in Hematological Malignancies-Ultimate Targets for Immunotherapy?
Q64989110Neutrophil-lymphocyte ratio (NLR) predicted prognosis for advanced non-small-cell lung cancer (NSCLC) patients who received immune checkpoint blockade (ICB).
Q90428632New insights in predictive determinants of the tumor immune microenvironment for immune checkpoint inhibition: a never ending story?
Q91238280Next Generation Sequencing (NGS): A Revolutionary Technology in Pharmacogenomics and Personalized Medicine in Cancer
Q38599122Next-Generation Sequencing for Patients with Sarcoma: A Single Center Experience
Q47926486Next-generation sequencing (NGS) of cell-free circulating tumor DNA and tumor tissue in patients with advanced urothelial cancer: a pilot assessment of concordance
Q97546037Next-generation sequencing analysis of endometrial screening liquid-based cytology specimens: a comparative study to tissue specimens
Q55209598Next-generation sequencing based detection of germline and somatic alterations in a patient with four metachronous primary tumors.
Q97070215Next-generation sequencing reveals heterogeneous genetic alterations in key signaling pathways of mismatch repair deficient colorectal carcinomas
Q90464942Nivolumab in children and young adults with relapsed or refractory solid tumours or lymphoma (ADVL1412): a multicentre, open-label, single-arm, phase 1-2 trial
Q52586565Nivolumab plus Ipilimumab in Lung Cancer with a High Tumor Mutational Burden.
Q93377901Non-small cell to small cell lung cancer on PD-1 inhibitors: two cases on potential histologic transformation
Q61455084Novel insights into endothelial cell malignancies
Q98282392Olaparib and durvalumab in patients with germline BRCA-mutated metastatic breast cancer (MEDIOLA): an open-label, multicentre, phase 1/2, basket study
Q90065952Overall survival in patients with pancreatic cancer receiving matched therapies following molecular profiling: a retrospective analysis of the Know Your Tumor registry trial
Q47120629PD-1/PD-L1 Blockade: Have We Found the Key to Unleash the Antitumor Immune Response?
Q64066416PD-L1 expression and tumor mutational burden are independent biomarkers in most cancers
Q64056211PD-L1 expression and tumor mutational burden status for prediction of response to chemotherapy and targeted therapy in non-small cell lung cancer
Q94570472PD-L1 expression in malignant pleural effusion samples and its correlation with oncogene mutations in non-small cell lung cancer
Q92932037PIK3CA gene mutations in the helical domain correlate with high tumor mutation burden and poor prognosis in metastatic breast carcinomas with late-line therapies
Q64053621Paired whole exome and transcriptome analyses for the Immunogenomic changes during concurrent chemoradiotherapy in esophageal squamous cell carcinoma
Q99408618Pan-Cancer Landscape Analysis Reveals Recurrent KMT2A-MAML2 Gene Fusion in Aggressive Histologic Subtypes of Thymoma
Q55497366Pan-cancer adaptive immune resistance as defined by the Tumor Inflammation Signature (TIS): results from The Cancer Genome Atlas (TCGA).
Q95933711Pan-sarcoma genomic analysis of KMT2A rearrangements reveals distinct subtypes defined by YAP1-KMT2A-YAP1 and VIM-KMT2A fusions
Q47566281Pancreatic cancer: Next-generation algorithms for neoantigen selection.
Q97545564Pancreatic undifferentiated carcinoma with osteoclast-like giant cells curatively resected after pembrolizumab therapy for lung metastases: a case report
Q64905379Pathogenic and Targetable Genetic Alterations in Resected Recurrent Undifferentiated Pleomorphic Sarcomas Identified by Targeted Next-generation Sequencing.
Q48156858Patient HLA class I genotype influences cancer response to checkpoint blockade immunotherapy
Q98186316Patient specific circulating tumor DNA fingerprints to monitor treatment response across multiple tumors
Q64914214Patients Selection for Immunotherapy in Solid Tumors: Overcome the Naïve Vision of a Single Biomarker.
Q93052152Pediatric patients with acute lymphoblastic leukemia generate abundant and functional neoantigen-specific CD8+ T cell responses
Q92431353Perspectives on Treatment of Metastatic Colorectal Cancer with Immune Checkpoint Inhibitor Therapy
Q55029444Perspectives on the clinical development of immunotherapy in prostate cancer.
Q64086368Phase I study of local radiation and tremelimumab in patients with inoperable locally recurrent or metastatic breast cancer
Q91327123Phase II study of everolimus and bevacizumab in recurrent ovarian, peritoneal, and fallopian tube cancer
Q64114943Phenotype of POLE-mutated endometrial cancer
Q90024264Phenotypic and Genomic Determinants of Immunotherapy Response Associated with Squamousness
Q57461763Phosphoprotein patterns predict trametinib responsiveness and optimal trametinib sensitisation strategies in melanoma
Q64107259Post-neoadjuvant treatment and the management of residual disease in breast cancer: state of the art and perspectives
Q55012383Precision Medicine in Head and Neck Cancer: Myth or Reality?
Q92982809Precision Medicine in Oncology and Immuno-Oncology: Where We Stand and Where We're Headed
Q92991548Preclinical murine tumor models: a structural and functional perspective
Q96155607Predictive Biomarkers of Immune Checkpoint Inhibition in Gastroesophageal Cancers
Q57815797Predictive biomarkers for tumor immune checkpoint blockade
Q57299127Predictive pathology of lung cancer immunotherapy response
Q89497142Presence of allele frequency heterogeneity defined by ctDNA profiling predicts unfavorable overall survival of NSCLC
Q89103577Prevalence of PDL1 Amplification and Preliminary Response to Immune Checkpoint Blockade in Solid Tumors
Q64958062Prevalence of established and emerging biomarkers of immune checkpoint inhibitor response in advanced hepatocellular carcinoma.
Q90579990Primary CNS lymphoma commonly expresses immune response biomarkers
Q89983786Primary mammary angiosarcomas harbor frequent mutations in KDR and PIK3CA and show evidence of distinct pathogenesis
Q99237681Prognosis of Lung Adenocarcinoma Patients With NTRK3 Mutations to Immune Checkpoint Inhibitors
Q57159515Prognostic modeling of the immune-centric transcriptome reveals interleukin signaling candidates contributing to differential patient outcomes
Q64939796RANK-RANKL Signaling in Cancer of the Uterine Cervix: A Review.
Q90441620RNA Transcription and Splicing Errors as a Source of Cancer Frameshift Neoantigens for Vaccines
Q57798069RNA-seq for identification of therapeutically targetable determinants of immune activation in human glioblastoma
Q49797507Rational Design for Cervical Cancer Therapeutics: Cellular and Non-Cellular Based Strategies on the Horizon for Recurrent, Metastatic or Refractory Cervical Cancer.
Q96765678Real world data analysis of next generation sequencing and protein expression in metastatic breast cancer patients
Q94525816Recurrent Metastatic Penile Cancer Patient with Positive PD-L1 Expression Obtained Significant Benefit from Immunotherapy: A Case Report and Literature Review
Q100737233Recurrent urothelial carcinoma-like FGFR3 genomic alterations in malignant Brenner tumors of the ovary
Q90157690Refractory solitary cervical lymph node metastasis after esophageal squamous cell carcinoma surgery and its successful treatment with immune checkpoint inhibitor: A case report and literature review
Q90639891Relationships Between Immune Landscapes, Genetic Subtypes and Responses to Immunotherapy in Colorectal Cancer
Q89537473Resistance Mechanism of PD-1/PD-L1 Blockade in the Cancer-Immunity Cycle
Q42363061Resources for Interpreting Variants in Precision Genomic Oncology Applications
Q88993176Rethinking medulloblastoma from a targeted therapeutics perspective
Q90353808Review and perspective on adjuvant and neoadjuvant immunotherapies in NSCLC
Q62648881Review: Precision medicine and driver mutations: Computational methods, functional assays and conformational principles for interpreting cancer drivers
Q64114357SALMON: Survival Analysis Learning With Multi-Omics Neural Networks on Breast Cancer
Q92691441SMARCA4 inactivation defines a subset of undifferentiated uterine sarcomas with rhabdoid and small cell features and germline mutation association
Q52648065Salivary gland cancer patient-derived xenografts enable characterization of cancer stem cells and new gene fusions associated with tumor progression.
Q55379483Sarcoma-The standard-bearer in cancer discovery.
Q91891970Sex-associated molecular differences for cancer immunotherapy
Q64108704Sex-based heterogeneity in response to lung cancer immunotherapy: a systematic review and meta-analysis
Q49715015Shed Skin Cancer, Not Collagen XVII: A New Approach to Targeting Skin Cancer Progression
Q90172521Significant association between tumor mutational burden and immune-related adverse events during immune checkpoint inhibition therapies
Q92721586Single-molecule detection of cancer mutations using a novel PCR-LDR-qPCR assay
Q92925160Small lung tumor biopsy samples are feasible for high quality targeted next generation sequencing
Q92083308Somatic Alteration Burden Involving Non-Cancer Genes Predicts Prognosis in Early-Stage Non-Small Cell Lung Cancer
Q104486593Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer
Q92593269Somatic genetic aberrations in gallbladder cancer: comparison between Chinese and US patients
Q91612580Somatic mutational profiles of stage II and III gastric cancer according to tumor microenvironment immune type
Q98289241Somatic mutations in genes associated with mismatch repair predict survival in patients with metastatic cancer receiving immune checkpoint inhibitors
Q57813172Somatic mutations in renal cell carcinomas from Chinese patients revealed by whole exome sequencing
Q98613255Spontaneous mutations in the single TTN gene represent high tumor mutation burden
Q89659885Stage IV Colorectal Cancer Patients with High Risk Mutation Profiles Survived 16 Months Longer with Individualized Therapies
Q55282202Stratification of ovarian tumor pathology by expression of programmed cell death-1 (PD-1) and PD-ligand- 1 (PD-L1) in ovarian cancer.
Q59127261Successful response to the combination of immunotherapy and chemotherapy in cholangiocarcinoma with high tumour mutational burden and PD-L1 expression: a case report
Q100504573Systematic analysis of the transcriptome in small-cell carcinoma of the oesophagus reveals its immune microenvironment
Q50001757TGFβ attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells.
Q58054909TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jaw
Q92337932Targeted deep sequencing from multiple sources demonstrates increased NOTCH1 alterations in lung cancer patient plasma
Q92644009Targeted immunotherapy with a checkpoint inhibitor in combination with chemotherapy: A new clinical paradigm in the treatment of triple-negative breast cancer
Q61797340Targeted mutation detection in breast cancer using MammaSeq™
Q89622149Targeted next-generation sequencing to assess tumor mutation burden: ready for prime-time in non-small cell lung cancer?
Q48234912Targeting HER2 in colorectal cancer: The landscape of amplification and short variant mutations in ERBB2 and ERBB3.
Q97905239Targeting Rad51 as a strategy for the treatment of melanoma cells resistant to MAPK pathway inhibition
Q89510215Targeting the Immune system and Epigenetic Landscape of Urological Tumors
Q89668311Testing microsatellite instability in solid tumors: the ideal versus what is real
Q93165232The Biogenesis, Biology, and Clinical Significance of Exosomal PD-L1 in Cancer
Q92533583The Genomic Landscape of Merkel Cell Carcinoma and Clinicogenomic Biomarkers of Response to Immune Checkpoint Inhibitor Therapy
Q90452290The Tumor Microenvironment of Epithelial Ovarian Cancer and Its Influence on Response to Immunotherapy
Q55725588The Tumor Mutational Burden of Chinese Advanced Cancer Patients Estimated by a 381-cancer-gene Panel.
Q98386118The epigenomics of sarcoma
Q90402575The evolving immunotherapeutic landscape in advanced oesophagogastric cancer
Q91520697The evolving landscape of biomarkers for checkpoint inhibitor immunotherapy
Q103728292The evolving landscape of predictive biomarkers in immuno-oncology with a focus on spatial technologies
Q98290541The frequency and inter-relationship of PD-L1 expression and tumour mutational burden across multiple types of advanced solid tumours in China
Q64930481The genomic mutation spectrums of breast fibroadenomas in Chinese population by whole exome sequencing analysis.
Q64079170The gut microbiome and response to immune checkpoint inhibitors: preclinical and clinical strategies
Q102152400The prognostic impact of RAS on overall survival following liver resection in early versus late-onset colorectal cancer patients
Q90281646The prognostic value of tumor mutational burden and immune cell infiltration in esophageal cancer patients with or without radiotherapy
Q93182663The requirement for immune infiltration and organization in the tumor microenvironment for successful immunotherapy in prostate cancer
Q94599849The tumour microenvironment in pancreatic cancer - clinical challenges and opportunities
Q55314072The utilization of next-generation sequencing to detect somatic mutations and predict clinical prognosis of Chinese non-small cell lung cancer patients.
Q64926466Titin mutation associated with responsiveness to checkpoint blockades in solid tumors.
Q91861384Towards quantitative and multiplexed in vivo functional cancer genomics
Q94553390Tracking Neoantigens by Personalized Circulating Tumor DNA Sequencing during Checkpoint Blockade Immunotherapy in Non-Small Cell Lung Cancer
Q99633734Transcriptional and immunohistological assessment of immune infiltration in pancreatic cancer
Q47270933Tumor Mutational Burden and Response Rate to PD-1 Inhibition.
Q90440514Tumor Mutational Burden as a Predictive Biomarker for Response to Immune Checkpoint Inhibitors: A Review of Current Evidence
Q38611235Tumor Mutational Burden as an Independent Predictor of Response to Immunotherapy in Diverse Cancers
Q64063973Tumor genomic alterations in severe-combined immunodeficiency bare-lymphocyte syndrome genes are associated with high mutational burden and disproportional neo-antigen rates
Q92350797Tumor heterogeneity and acquired drug resistance in FGFR2-fusion-positive cholangiocarcinoma through rapid research autopsy
Q91835885Tumor mutation burden and circulating tumor DNA in combined CTLA-4 and PD-1 antibody therapy in metastatic melanoma - results of a prospective biomarker study
Q97524993Tumor mutation burden associated with miRNA-gene interaction outcome mediates the survival of patients with liver hepatocellular carcinoma
Q90612091Tumor mutation burden derived from small next generation sequencing targeted gene panel as an initial screening method
Q98466949Tumor mutation burden in Chinese cancer patients and the underlying driving pathways of high tumor mutation burden across different cancer types
Q92579646Tumor mutation burden: from comprehensive mutational screening to the clinic
Q92593587Tumor mutational and indel burden: a systematic pan-cancer evaluation as prognostic biomarkers
Q92748351Tumor mutational burden
Q89531597Tumor mutational burden and PTEN alterations as molecular correlates of response to PD-1/L1 blockade in metastatic triple-negative breast cancer
Q94475710Tumor mutational burden and immune signatures interplay in renal cell carcinoma
Q59798099Tumor mutational burden assessment as a predictive biomarker for immunotherapy in lung cancer patients: getting ready for prime-time or not?
Q59798130Tumor mutational burden in non-small cell lung cancer-the pathologist's point of view
Q90273707Tumor mutational burden is associated with poor outcomes in diffuse glioma
Q104618320Tumor mutational burden on cytological samples: A pilot study
Q91895975Tumor mutational burden quantification from targeted gene panels: major advancements and challenges
Q91140222Tumor mutational burden standardization initiatives: Recommendations for consistent tumor mutational burden assessment in clinical samples to guide immunotherapy treatment decisions
Q62745707Tumor mutational load predicts survival after immunotherapy across multiple cancer types
Q64106473Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling gene
Q93157712Tumor neoantigens: from basic research to clinical applications
Q98564973Understanding genomics and the immune environment of penile cancer to improve therapy
Q64262617Update on systemic therapy for colorectal cancer: biologics take sides
Q64107768Use of targeted next generation sequencing to characterize tumor mutational burden and efficacy of immune checkpoint inhibition in small cell lung cancer
Q89985173Validation and implementation of a modular targeted capture assay for the detection of clinically significant molecular oncology alterations
Q98613071When, why and how tumour clonal diversity predicts survival
Q92728818[Predictive Value of Tumor Mutation Burden in Immunotherapy for Lung Cancer]
Q58084642[Predictive value of PD-L1 diagnostics]
Q89850600dbPepNeo: a manually curated database for human tumor neoantigen peptides
Q90438932ecTMB: a robust method to estimate and classify tumor mutational burden

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