Radiotherapy and Oncology, ISSN 0167-8140, 03/2020, Volume 144, pp. 101 - 104
Durvalumab after concurrent chemoradiation has significantly improved survival in stage III non-small cell lung cancer (NSCLC). However, there is limited data...
Consolidative durvalumab | Chemoradiation | Non-small cell lung cancer
Consolidative durvalumab | Chemoradiation | Non-small cell lung cancer
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2018, Volume 36, Issue 15_suppl, pp. TPS8581 - TPS8581
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2019, Volume 37, Issue 15_suppl, pp. 2546 - 2546
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 11/2019, p. clincanres.2931.2019
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2016, Volume 17, Issue 3, pp. 299 - 308
Summary Background PD-L1 and CTLA-4 immune checkpoints inhibit antitumour T-cell activity. Combination treatment with the anti-PD-L1 antibody durvalumab and...
Hematology, Oncology and Palliative Medicine | TRIAL | ANTIBODY | ONCOLOGY | NIVOLUMAB | MEDI4736 | IPILIMUMAB | Lung Neoplasms - drug therapy | Follow-Up Studies | Lung Neoplasms - mortality | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Lung Neoplasms - pathology | Male | Dose-Response Relationship, Drug | Young Adult | Neoplasm Invasiveness - pathology | Aged, 80 and over | Adult | Female | Carcinoma, Non-Small-Cell Lung - pathology | Drug Administration Schedule | Survival Rate | Treatment Outcome | Carcinoma, Non-Small-Cell Lung - mortality | Disease-Free Survival | Maximum Tolerated Dose | Antibodies, Monoclonal - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Neoplasm Staging | Viral antibodies | Biological products | Safety and security measures | Oncology, Experimental | Antibodies | Lung cancer, Small cell | Research | T cells | Lung cancer, Non-small cell | Cancer
Hematology, Oncology and Palliative Medicine | TRIAL | ANTIBODY | ONCOLOGY | NIVOLUMAB | MEDI4736 | IPILIMUMAB | Lung Neoplasms - drug therapy | Follow-Up Studies | Lung Neoplasms - mortality | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Lung Neoplasms - pathology | Male | Dose-Response Relationship, Drug | Young Adult | Neoplasm Invasiveness - pathology | Aged, 80 and over | Adult | Female | Carcinoma, Non-Small-Cell Lung - pathology | Drug Administration Schedule | Survival Rate | Treatment Outcome | Carcinoma, Non-Small-Cell Lung - mortality | Disease-Free Survival | Maximum Tolerated Dose | Antibodies, Monoclonal - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Neoplasm Staging | Viral antibodies | Biological products | Safety and security measures | Oncology, Experimental | Antibodies | Lung cancer, Small cell | Research | T cells | Lung cancer, Non-small cell | Cancer
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2015, Volume 33, Issue 15_suppl, pp. 8068 - 8068
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2017, Volume 35, Issue 15_suppl, pp. TPS8577 - TPS8577
Journal Article
Journal of Thoracic Oncology, ISSN 1556-0864, 04/2016, Volume 11, Issue 4, pp. 537 - 544
Although perioperative chemotherapy improves survival in patients with resectable lung cancers, systemic recurrence remains common. Neoadjuvant chemotherapy...
Neoadjuvant therapy | Non–small cell lung cancer | Adaptive clinical trial | 18F-FDG PET | F-FDG PET | Non-small cell lung cancer | non-small cell lung cancer | 18FDG-PET
Neoadjuvant therapy | Non–small cell lung cancer | Adaptive clinical trial | 18F-FDG PET | F-FDG PET | Non-small cell lung cancer | non-small cell lung cancer | 18FDG-PET
Journal Article
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. LB-154 - LB-154
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2017, Volume 35, Issue 15_suppl, pp. 8536 - 8536
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2015, Volume 33, Issue 15_suppl, pp. e19002 - e19002
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 05/2018, Volume 378, Issue 21, pp. 1976 - 1986
In a pilot study, two doses of neoadjuvant nivolumab administered to patients with resectable lung cancer resulted in a major pathological response in 45% and...
MISMATCH-REPAIR DEFICIENCY | TRIAL | MEDICINE, GENERAL & INTERNAL | MULTICENTER | PEMBROLIZUMAB | RESPONSE CRITERIA | SOLID TUMORS | IMMUNE CHECKPOINT BLOCKADE | IMMUNOTHERAPY | OPEN-LABEL | CHEMOTHERAPY | Lung Neoplasms - drug therapy | Adenocarcinoma - pathology | Carcinoma, Squamous Cell - pathology | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Antibodies, Monoclonal - therapeutic use | Lung Neoplasms - pathology | Male | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - adverse effects | Aged, 80 and over | Female | Neoadjuvant Therapy | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Carcinoma, Non-Small-Cell Lung - surgery | Carcinoma, Non-Small-Cell Lung - genetics | Pilot Projects | B7-H1 Antigen - antagonists & inhibitors | Biopsy | Nivolumab | Lung Neoplasms - surgery | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Mutation | Drug therapy | Lung cancer | Peptides | PD-1 protein | Body weight | Lymphocytes T | Cancer therapies | Lymphocytes | Immunotherapy | Surgery | Peripheral blood | Drug dosages | Antigens | Lymphatic system | Cell survival | Cloning | Feasibility studies | Non-small cell lung carcinoma | T cell receptors | Gene expression | Patients | Side effects | Chemotherapy | PD-L1 protein | Tumors | Apoptosis
MISMATCH-REPAIR DEFICIENCY | TRIAL | MEDICINE, GENERAL & INTERNAL | MULTICENTER | PEMBROLIZUMAB | RESPONSE CRITERIA | SOLID TUMORS | IMMUNE CHECKPOINT BLOCKADE | IMMUNOTHERAPY | OPEN-LABEL | CHEMOTHERAPY | Lung Neoplasms - drug therapy | Adenocarcinoma - pathology | Carcinoma, Squamous Cell - pathology | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Antibodies, Monoclonal - therapeutic use | Lung Neoplasms - pathology | Male | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - adverse effects | Aged, 80 and over | Female | Neoadjuvant Therapy | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Carcinoma, Non-Small-Cell Lung - surgery | Carcinoma, Non-Small-Cell Lung - genetics | Pilot Projects | B7-H1 Antigen - antagonists & inhibitors | Biopsy | Nivolumab | Lung Neoplasms - surgery | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Mutation | Drug therapy | Lung cancer | Peptides | PD-1 protein | Body weight | Lymphocytes T | Cancer therapies | Lymphocytes | Immunotherapy | Surgery | Peripheral blood | Drug dosages | Antigens | Lymphatic system | Cell survival | Cloning | Feasibility studies | Non-small cell lung carcinoma | T cell receptors | Gene expression | Patients | Side effects | Chemotherapy | PD-L1 protein | Tumors | Apoptosis
Journal Article
Cell, ISSN 0092-8674, 02/2014, Volume 156, Issue 5, pp. 1002 - 1016
Brain metastasis is an ominous complication of cancer, yet most cancer cells that infiltrate the brain die of unknown causes. Here, we identify plasmin from...
BREAST-CANCER | SYSTEM | FAS LIGAND | LUNG | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | INDUCED APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | MELANOMA-CELLS | ADHESION MOLECULE L1 | EXPRESSION | CELL BIOLOGY | Fas Ligand Protein - metabolism | Plasminogen Activator Inhibitor 2 - genetics | Humans | Plasminogen Activators - metabolism | Lung Neoplasms - pathology | Brain Neoplasms - metabolism | Breast Neoplasms - metabolism | Brain - metabolism | Brain Neoplasms - secondary | Plasminogen Activator Inhibitor 2 - metabolism | Female | Neural Cell Adhesion Molecule L1 - metabolism | Neuropeptides - genetics | Fibrinolysin - metabolism | Carcinoma - secondary | Disease Models, Animal | Serpins - genetics | Serpins - metabolism | Cell Survival | Neuropeptides - metabolism | Adenocarcinoma - secondary | Animals | Breast Neoplasms - pathology | Mice, Nude | Brain - pathology | Cell Line, Tumor | Mice | Astrocytes - metabolism | Lung cancer | Metastasis | Cancer
BREAST-CANCER | SYSTEM | FAS LIGAND | LUNG | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | INDUCED APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | MELANOMA-CELLS | ADHESION MOLECULE L1 | EXPRESSION | CELL BIOLOGY | Fas Ligand Protein - metabolism | Plasminogen Activator Inhibitor 2 - genetics | Humans | Plasminogen Activators - metabolism | Lung Neoplasms - pathology | Brain Neoplasms - metabolism | Breast Neoplasms - metabolism | Brain - metabolism | Brain Neoplasms - secondary | Plasminogen Activator Inhibitor 2 - metabolism | Female | Neural Cell Adhesion Molecule L1 - metabolism | Neuropeptides - genetics | Fibrinolysin - metabolism | Carcinoma - secondary | Disease Models, Animal | Serpins - genetics | Serpins - metabolism | Cell Survival | Neuropeptides - metabolism | Adenocarcinoma - secondary | Animals | Breast Neoplasms - pathology | Mice, Nude | Brain - pathology | Cell Line, Tumor | Mice | Astrocytes - metabolism | Lung cancer | Metastasis | Cancer
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2015, Volume 33, Issue 15_suppl, pp. 8067 - 8067
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2015, Volume 33, Issue 15_suppl, pp. 7548 - 7548
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 10/2011, Volume 17, Issue 19, pp. 6298 - 6303
Purpose: Treatment of patients with oncogene-addicted cancers with tyrosine kinase inhibitors (TKI) is biologically and clinically different than with...
PHASE-II TRIAL | CARBOPLATIN | EVEROLIMUS | EFFICACY | NSCLC | ONCOLOGY | MUTATED EGFR | SAFETY | CELL | IMATINIB MESYLATE | PACLITAXEL | Erlotinib Hydrochloride | Lung Neoplasms - drug therapy | Humans | Middle Aged | ErbB Receptors - genetics | Drug Resistance, Neoplasm | Male | Antineoplastic Agents - therapeutic use | Withholding Treatment | Disease Progression | Time Factors | Protein Kinase Inhibitors - therapeutic use | Quinazolines - therapeutic use | Adult | Female | Aged | Mutation | Gefitinib | EGFR | adenocarcinoma of lung | drug resistance
PHASE-II TRIAL | CARBOPLATIN | EVEROLIMUS | EFFICACY | NSCLC | ONCOLOGY | MUTATED EGFR | SAFETY | CELL | IMATINIB MESYLATE | PACLITAXEL | Erlotinib Hydrochloride | Lung Neoplasms - drug therapy | Humans | Middle Aged | ErbB Receptors - genetics | Drug Resistance, Neoplasm | Male | Antineoplastic Agents - therapeutic use | Withholding Treatment | Disease Progression | Time Factors | Protein Kinase Inhibitors - therapeutic use | Quinazolines - therapeutic use | Adult | Female | Aged | Mutation | Gefitinib | EGFR | adenocarcinoma of lung | drug resistance
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17.
Full Text
Tumor mutational load predicts survival after immunotherapy across multiple cancer types
Nature Genetics, ISSN 1061-4036, 02/2019, Volume 51, Issue 2, pp. 202 - 206
Immune checkpoint inhibitor (ICI) treatments benefit some patients with metastatic cancers, but predictive biomarkers are needed. Findings in selected cancer...
CTLA-4 BLOCKADE | THERAPY | LANDSCAPE | PD-1 BLOCKADE | GENETICS & HEREDITY | SENSITIVITY | NEOANTIGENS | Usage | Research | Gene mutations | Immunotherapy | Oncology, Experimental | Cancer | Laboratories | Lung cancer | Melanoma | Histology | Metastasis | Gene expression | Cancer therapies | Patients | Survival | Metastases | Next-generation sequencing | Immune checkpoint | Biomarkers | Mutation | Tumors
CTLA-4 BLOCKADE | THERAPY | LANDSCAPE | PD-1 BLOCKADE | GENETICS & HEREDITY | SENSITIVITY | NEOANTIGENS | Usage | Research | Gene mutations | Immunotherapy | Oncology, Experimental | Cancer | Laboratories | Lung cancer | Melanoma | Histology | Metastasis | Gene expression | Cancer therapies | Patients | Survival | Metastases | Next-generation sequencing | Immune checkpoint | Biomarkers | Mutation | Tumors
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 09/2012, Volume 18, Issue 18, pp. 4910 - 4918
Purpose: Activating mutations in the tyrosine kinase domain of HER2 (ERBB2) have been described in a subset of lung adenocarcinomas (ADCs) and are mutually...
FACTOR-RECEPTOR | CANCER PATIENTS | MP-412 AV-412 | ONCOLOGY-GROUP | ONCOLOGY | EPIDERMAL-GROWTH-FACTOR | IN-SITU-HYBRIDIZATION | NEU DIFFERENTIATION FACTOR | ONCOGENE MUTATIONS | GENE COPY NUMBER | SOMATIC MUTATIONS | Lung Neoplasms - genetics | Adenocarcinoma - pathology | Prevalence | Prognosis | Receptor, ErbB-2 - genetics | Humans | Middle Aged | Risk Factors | Lung Neoplasms - pathology | Male | DNA Copy Number Variations | Lung Neoplasms - epidemiology | Protein Interaction Domains and Motifs - genetics | Survival Analysis | Aged, 80 and over | Adult | Female | Adenocarcinoma - genetics | Aged | Mutation | Adenocarcinoma - epidemiology | Neoplasm Staging | driver oncogenes | HER2 | EGFR | ERBB2 | lung adenocarcinoma
FACTOR-RECEPTOR | CANCER PATIENTS | MP-412 AV-412 | ONCOLOGY-GROUP | ONCOLOGY | EPIDERMAL-GROWTH-FACTOR | IN-SITU-HYBRIDIZATION | NEU DIFFERENTIATION FACTOR | ONCOGENE MUTATIONS | GENE COPY NUMBER | SOMATIC MUTATIONS | Lung Neoplasms - genetics | Adenocarcinoma - pathology | Prevalence | Prognosis | Receptor, ErbB-2 - genetics | Humans | Middle Aged | Risk Factors | Lung Neoplasms - pathology | Male | DNA Copy Number Variations | Lung Neoplasms - epidemiology | Protein Interaction Domains and Motifs - genetics | Survival Analysis | Aged, 80 and over | Adult | Female | Adenocarcinoma - genetics | Aged | Mutation | Adenocarcinoma - epidemiology | Neoplasm Staging | driver oncogenes | HER2 | EGFR | ERBB2 | lung adenocarcinoma
Journal Article
Journal of Oncology Practice, ISSN 1554-7477, 07/2017, Volume 13, Issue 7, pp. 449 - 451
ONCOLOGY | Carcinoma, Non-Small-Cell Lung - pathology | Carcinoma, Non-Small-Cell Lung - radiotherapy | Lung Neoplasms - drug therapy | United States | Humans | Lung Neoplasms - radiotherapy | Lung Neoplasms - pathology | Societies, Medical | Medical Oncology - standards | Carcinoma, Non-Small-Cell Lung - drug therapy | Chemotherapy, Adjuvant | Neoplasm Staging | Radiotherapy, Adjuvant | Ontario
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2014, Volume 32, Issue 15_suppl, pp. 7515 - 7515
Journal Article
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